Scientist jobs in Iowa City, IA - 26 jobs

Q: How much does a scientist earn in Iowa City, IA?

The average scientist in Iowa City, IA earns between $39,000 and $86,000 annually. This compares to the national average scientist range of $67,000 to $140,000.

All

Scientist

Research Associate

Senior Scientist

Chemist

Quality Control Scientist

Technical Scientist

Laboratory Scientist

Food Scientist

Principal Scientist

Senior Laboratory Technician

Research And Development Scientist

Research Scientist

Research And Development Technician

Consumer Goods/Food R&D Senior Scientist
Kelly Services 4.6
Scientist job in Muscatine, IA
**Kelly Science & Clinical is seeking a Senior Scientist, Innovation & Research & Development for a direct-hire (permanent) position with one of our partners in Muscatine, IA.** This role offers the opportunity to lead cutting-edge product innovation within the **pet category** , while also collaborating across **human food and beverage** product lines. The Senior Scientist will drive R&D initiatives from concept through commercialization, develop and test new ingredients, and mentor a high-performing team focused on delivering safe, high-quality, and effective products. **Function:** Research & Development - Innovation, Consumer Goods/Food **Job Type:** Direct Hire (Permanent) **Schedule:** Full-time **Location:** Muscatine, IA (relocation assistance is available) **Target Pay Rate:** approximately $90,000-$120,000/year **Your Impact** + Lead the design, development, and execution of research projects through literature review, experimentation, and cross-functional collaboration. + Stay current on industry trends related to **ingredients and ingredient functionality** , identifying opportunities to expand pet litter and pet treat/supplement product lines. + Design, oversee, and conduct experiments to develop and test **new cat litter and pet food ingredients** , analyzing performance, safety, and commercialization potential. + Lead the execution of **design, optimization, verification, troubleshooting, and validation** of new and existing techniques and methodologies. + Provide technical leadership from **concept development through commercialization** , collaborating with production, quality, regulatory, sales, marketing, and technical services. + Foster a culture of innovation by introducing new product concepts, quality improvements, and productivity enhancements. + Evaluate competitive products and market trends to identify opportunities for new products and applications. + Investigate product and process challenges using **data-driven scientific approaches** to support development, scale-up, and ongoing production. + Collaborate internally with manufacturing, procurement, and quality teams to ensure ingredient and product specifications are met. + Collaborate externally with suppliers and third-party laboratories to expand research capabilities. + Partner with quality and operations teams to troubleshoot **customer complaints, product quality issues, and ingredient concerns** . + Deliver timely and accurate **technical reports, analytical results, and recommendations** to support innovation, benchmarking, and continuous improvement. + Analyze and interpret data using **statistical methods** to drive sound conclusions and product recommendations. + Maintain accurate and complete experimental records. + Mentor and lead team members while promoting collaboration and accountability. **What You'll Bring** **Core Experience:** + **5-10+ years of hands-on industry experience in Consumer Packaged Goods (CPG).** + Experience must be gained in a **commercial, industry-based R&D environment** (e.g., consumer products, food, pet, supplements, ingredients, or related CPG sectors). + **While academic research experience (graduate, postdoctoral, or university laboratory employment) will be consider, this does not count toward the required years of industry experience.** + Proven success in **new product development leading to commercialization** . + Experience leading and managing **R&D and innovation teams** , including direct reports. + Strong project management, time management, and organizational skills. + Ability to communicate complex scientific and innovation concepts to cross-functional stakeholders. + Previous experience as a supervisor, as this position will have 1 direct report. **Technical Qualifications (Required):** + Bachelor of Science degree with **5-10+ years of relevant industry R&D experience** . + Experience working with **ingredients and consumer products** . + Strong analytical, experimental design, and data interpretation skills. **Technical Qualifications (Preferred):** + Master of Science degree. + Experience in **pet products, food, supplements, or ingredient innovation** . + Background working with cross-functional manufacturing, quality, and regulatory teams. **Behaviors & Competencies** + Innovative thinker with strong scientific curiosity. + Results-driven with a high level of accountability. + Collaborative leader and effective mentor. + Detail-oriented with strong problem-solving abilities. + Comfortable operating in fast-paced, product-driven environments. + Promotes a culture of quality, innovation, and continuous improvement.As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.
$90k-120k yearly 36d ago

Looking for a job?

Let Zippia find it for you.

Bioinformatics Research Scientist III
Danaher Corporation 4.6
Scientist job in Coralville, IA
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's (*********************************** 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Our team at Integrated DNA Technologies (IDT), is united by a commitment to collaboration and scientific excellence, building on a strong foundation of innovation, expertise, and reliability. Guided by our vision to help researchers rapidly move from the lab to life-changing advances, we work closely with global partners to accelerate progress and genomics breakthroughs across fields like cancer, infectious disease, rare genetic disorders, and more. At IDT, you'll be part of a culture rooted in continuous learning and improvement-where your growth fuels our mission to accelerate the pace of genomics and helps shape a healthier, brighter future for all. Learn about the Danaher Business System (************************************************************ which makes everything possible. The Bioinformatics Research Scientist III will work closely with fellow scientists to innovate next-generation sequencing (NGS) applications, enabled by oligonucleotide design, chemistry, analysis software, or other technologies. In this role, you will develop novel algorithms and pipelines, provide data analysis support to collaborators, and be a key contributor to the product development team. This position reports to the Director of Bioinformatics and Computational Biology and is part of the Bioinformatics Team l ocated in Sunnyvale, CA or Coralville, IA. It is an on-site role. In this role, you will have the opportunity to: + Design, develop and implement novel algorithms and data analysis workflows + Collaborate with internal and external researchers to develop novel chemistry, enzymes, and oligonucleotide designs + Contribute to the development of cutting-edge technologies that support genomics research, disease diagnosis, and epidemiological tracking + Prepare and deliver scientific presentations to collaborators and at professional conferences The essential requirements of the job include: + Bachelor's degree (in Biology, Computer Science, Mathematics, Statistics or a related field) with 5+ years of relevant work experience; Master's with 3+ years of relevant work experience; a PhD in a relevant field + Some hands-on experience in NGS bioinformatic, which might include methods development, software implementation, or workflow design + Foundational knowledge of genomics and computational biology + Proficiency with python, Linux OS, NGS bioinformatics tools (e.g., minimap2, Pandas/Polars, etc) and genomics databases (e.g., RefSeq, UCSC, ClinVar, etc) + Excellent oral and written communication skills, with the ability to clearly and efficiently summarize complex scientific topics Travel, Motor Vehicle Record & Physical/Environment Requirements: + Ability to travel to other IDT sites or scientific conferences (< %5) It would be a plus if you also possess previous experience in: + Publication record in peer-reviewed scientific journals + Familiarity with statistical analysis methods and their application in biological research + Hands-on experience developing with a workflow language, such as snakemake, nextflow, CWL, or AWS Batch + Use of large language models (LLMs) like Claude to accelerate coding, documentation, or other tasks + Development of AI applications (e.g., heuristic, machine learning, deep learning) + Experience analyzing oncology biomarkers, DNA methylation, RNA-seq, or long read sequencing data IDT, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info (**************************************************************************************** . The annual salary range for this role is $100,000 - $117,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. #LI-LM3 Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit *************** . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here (********************************************************************************************** . We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com .
$100k-117k yearly 7d ago
Robotics and AI Scientist, Iowa Technology Institute
Uiowa
Scientist job in Iowa City, IA
The Iowa Technology Institute within the College of Engineering is seeking a Robotics Simulation Engineer. This role will focus on the development and control of Santos, the virtual soldier, within the NVIDIA Isaac platform and will apply advanced robotics principles to a humanoid model, creating and validating complex virtual human behaviors for simulation environments. This will be a two year specified term appointment, (anticipated end date 8/31/2027), and is funded by the US Army I-STRIKE project. Specific Job Duties and Tasks: Utilize and process motion capture (MoCap) data to animate and validate Santos's movements, ensuring the virtual soldier's behavior is both physically accurate and realistic. Perform basic and complex procedures and techniques as outlined in research protocol, assure fidelity to protocols, may propose modifications to protocols and/or assist in the design of research protocols. Design portions of research plan. Monitor, test, and evaluate current procedures. Supervise adherence to safety and compliance guidelines when necessary. Contribute to progress reports required by funding agencies. Participate in the development of new proposals for research and obtain external funding support for new and/or continuing research activities. Perform experiments, simulations, or theoretical investigations. Collect data and evaluate relevance of data. Work independently on basic research tasks with oversight by Faculty or Principal Investigator (PI). Contribute to documentation of equipment and procedures. Prepare manuscripts for contributing author for publication. Present results in departmental seminars and at professional meetings. Participate in public outreach activities as required by funding sources. May participate in national and international meetings within the discipline. To obtain the full job description including key areas of responsibility, technical competencies, and desirable qualifications, please contact *************************** About the College of Engineering The College of Engineering at the University of Iowa is driven by talented faculty, staff, and students who are dedicated to producing knowledge that addresses grand challenges in advanced technologies, health sciences, sustainability, energy, and the environment. We pride ourselves on producing ethical, globally aware engineers whose work makes the world safer and more efficient. As a center of innovation and discovery, the College of Engineering is committed to improving the quality of life for our Iowa community, as well as for people across the United States and around the world. We uphold the values of respect, community, and collaboration in all our endeavors, fostering a welcoming and respectful environment where members are valued and supported. Joining our team means becoming part of a supportive environment that values work-life balance and personal well-being. The University of Iowa offers a comprehensive benefits package, including health and wellness resources, dual career support, and opportunities for professional development. Learn more about working at the University of Iowa: Build A Career/Build a Life. Education Requirement: Bachelor's degree in related field and a minimum of 3 years of experience or equivalent combination of education and experience. Required Qualifications: Expert knowledge of robotic kinematics, including humanoid kinematics and locomotion, control theory, and advanced motion planning for complex, multi-degree-of-freedom systems. Strong Proficiency in Python for simulation scripting, and exceptional skills in C++ for developing high-performance, real-time control modules. Extensive experience with NVIDIA Isaac Sim and the broader Omniverse platform. This includes building and configuring virtual worlds, importing assets, and using the core APIs to create and test human-centric scenarios. Specific experience with humanoid robotics or virtual characters, with a focus on implementing inverse kinematics and bipedal control systems. Practical experience with virtual sensor creation and data processing, specifically for use in perception and navigation tasks within a simulated environment. Application Details In order to be considered for an interview, applicants must upload: Resume Cover Letter Job openings are posted for a minimum of 7 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. 5 professional references will be requested at a later step in the recruitment process. For questions, contact Adrian Cunningham at *************************** Benefits Highlights Regular salaried position. Pay level 5B. Located in Iowa City, Iowa. Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans. For more information about Why Iowa? Click here. About Iowa Joining the University of Iowa means becoming a vital part of the Hawkeye community, where your work directly impacts education, research, and student success. Enjoy exceptional health coverage, university-paid life insurance, robust retirement plans, and generous leave policies. Benefit from 24/7 support services, well-being resources, and access to UI Health Care specialists. Grow professionally with advanced training, leadership development, and tuition assistance. Iowa City offers a great quality of life with world-class performances at Hancher Auditorium, Big Ten athletics, top-ranked public schools, and outdoor recreation. Join us in making a difference at a leading Big Ten university and premier public research institution. Additional Information Compensation Contact Information
$62k-89k yearly est. Easy Apply 4d ago
SR SCIENTIST
Precision Food Service, Inc.
Scientist job in Muscatine, IA
KENT Worldwide is seeking a dynamic Senior Scientist of Innovation, Research & Development to lead cutting-edge product innovation in the pet category, while also collaborating across our human food and beverage lines. This leadership role will drive R&D initiatives, develop and test new ingredients, and mentor a talented team-all with a focus on delivering high-quality, safe, and effective products. * This role will be based in Muscatine, Iowa. PRIMARY DUTIES & RESPONSIBILITIES: * Demonstrate innovative design, development, and execution of research projects through literature review and scientific teamwork. * Stay up to date through continued learning on industry developments and trends related to ingredients and ingredient functionality and identify new ingredients that can expand the litter and pet treat/supplement product lines. * Design, oversee, and conduct experiments to develop and test new cat litter and pet food ingredients, analyze data to evaluate the performance and safety of different ingredients and the opportunity for using within pet litter products or expanding the litter portfolio. * Leads the execution of design, optimization, verification, troubleshooting and validation of current and new techniques and provides input into the design, implementation and interpretation of experimental studies with respect to the pet product platforms. * Provide technical leadership on projects from concept development through successful commercialization, interacting with production, quality, regulatory, sales, marketing, and technical services. * Foster a culture of innovation by continually introducing ideas and product concepts for new products, quality improvements, and productivity. * Familiarize and evaluate competitive products in the marketplace to determine market opportunities for new products and application recommendations for current products. * Investigate product and process challenges, provide creative solutions using sound scientific techniques and data-based decision making to solve challenges in development and commercialization and ongoing product production. * Collaborate internally with other departments, such as manufacturing, procurement and quality control, to ensure that the ingredients meet product specifications. * Collaborate externally with suppliers and laboratories to extend our research capabilities. * Troubleshoot with quality and operations on issues of customer complaints, product quality, ingredient quality or anything related to consumer feedback. * Deliver timely and accurate analytical results and technical reports to support research projects, resolve customer complaints, benchmark competitive products, develop new products, improve existing products, and support various business teams. * Analyze and interpret data using proven statistical methods to provide conclusions and recommendations for product development, problem-solving, and continuous product improvement. * Maintain accurate records of experiments and results. * Display team focus and collaboration in both innovating new products and ensuring current products are performing optimally. * Perform other duties or special projects as needed. EDUCATION, EXPERIENCE AND/OR QUALIFICATIONS: * Bachelors of Science degree with 10+ years of experience, a Master of Science degree is a plus * Experience working with ingredients and consumer products is preferred * Attention to detail and effective time management and project management skills are vital to meet deadlines * Ability to manage and engage direct reports, along with leading a culture of collaboration * 10+ years of experience in a research and development role, preferably in the consumer goods industries * Experience leading and managing team members in R&D and innovation discipline * Experience in developing new products and ideas that led to commercialization * Experience communicating innovation and research to other groups in a manner that is understandable and leads to insights * Experimental design and statistical analysis competency * Demonstrated ability to use scientific instruments for measuring ingredient properties * Knowledge of quality control and formulation in the pet or food products industry is a plus TRAVEL EXPECTED: * Some travel may be required - estimated 25% of the time or less * Some international travel to customers or company divisions * Travel for team meetings, other Kent campuses, technical meetings, conferences and training courses OTHER: * While this role is primarily in the office environment, there will be time spent in the plant laboratory and plant facility working with the R&D Scientist.
$60k-89k yearly est. 60d+ ago
Sr Scientist
Kent Worldwide 4.7
Scientist job in Muscatine, IA
KENT Worldwide™ is seeking a dynamic Senior Scientist of Innovation, Research & Development to lead cutting-edge product innovation in the pet category, while also collaborating across our human food and beverage lines. This leadership role will drive R&D initiatives, develop and test new ingredients, and mentor a talented team-all with a focus on delivering high-quality, safe, and effective products. This role will be based in Muscatine, Iowa. PRIMARY DUTIES & RESPONSIBILITIES: Demonstrate innovative design, development, and execution of research projects through literature review and scientific teamwork. Stay up to date through continued learning on industry developments and trends related to ingredients and ingredient functionality and identify new ingredients that can expand the litter and pet treat/supplement product lines. Design, oversee, and conduct experiments to develop and test new cat litter and pet food ingredients, analyze data to evaluate the performance and safety of different ingredients and the opportunity for using within pet litter products or expanding the litter portfolio. Leads the execution of design, optimization, verification, troubleshooting and validation of current and new techniques and provides input into the design, implementation and interpretation of experimental studies with respect to the pet product platforms. Provide technical leadership on projects from concept development through successful commercialization, interacting with production, quality, regulatory, sales, marketing, and technical services. Foster a culture of innovation by continually introducing ideas and product concepts for new products, quality improvements, and productivity. Familiarize and evaluate competitive products in the marketplace to determine market opportunities for new products and application recommendations for current products. Investigate product and process challenges, provide creative solutions using sound scientific techniques and data-based decision making to solve challenges in development and commercialization and ongoing product production. Collaborate internally with other departments, such as manufacturing, procurement and quality control, to ensure that the ingredients meet product specifications. Collaborate externally with suppliers and laboratories to extend our research capabilities. Troubleshoot with quality and operations on issues of customer complaints, product quality, ingredient quality or anything related to consumer feedback. Deliver timely and accurate analytical results and technical reports to support research projects, resolve customer complaints, benchmark competitive products, develop new products, improve existing products, and support various business teams. Analyze and interpret data using proven statistical methods to provide conclusions and recommendations for product development, problem-solving, and continuous product improvement. Maintain accurate records of experiments and results. Display team focus and collaboration in both innovating new products and ensuring current products are performing optimally. Perform other duties or special projects as needed. EDUCATION, EXPERIENCE AND/OR QUALIFICATIONS: Bachelors of Science degree with 10+ years of experience, a Master of Science degree is a plus Experience working with ingredients and consumer products is preferred Attention to detail and effective time management and project management skills are vital to meet deadlines Ability to manage and engage direct reports, along with leading a culture of collaboration 10+ years of experience in a research and development role, preferably in the consumer goods industries Experience leading and managing team members in R&D and innovation discipline Experience in developing new products and ideas that led to commercialization Experience communicating innovation and research to other groups in a manner that is understandable and leads to insights Experimental design and statistical analysis competency Demonstrated ability to use scientific instruments for measuring ingredient properties Knowledge of quality control and formulation in the pet or food products industry is a plus TRAVEL EXPECTED: Some travel may be required - estimated 25% of the time or less Some international travel to customers or company divisions Travel for team meetings, other Kent campuses, technical meetings, conferences and training courses OTHER: While this role is primarily in the office environment, there will be time spent in the plant laboratory and plant facility working with the R&D Scientist.
$47k-68k yearly est. 60d+ ago
Robotics and AI Scientist, Iowa Technology Institute
University of Iowa 4.4
Scientist job in Iowa City, IA
The Iowa Technology Institute within the College of Engineering is seeking a Robotics Simulation Engineer. This role will focus on the development and control of Santos, the virtual soldier, within the NVIDIA Isaac platform and will apply advanced robotics principles to a humanoid model, creating and validating complex virtual human behaviors for simulation environments. This will be a two year specified term appointment, (anticipated end date 8/31/2027), and is funded by the US Army I-STRIKE project. Specific Job Duties and Tasks: * Utilize and process motion capture (MoCap) data to animate and validate Santos's movements, ensuring the virtual soldier's behavior is both physically accurate and realistic. * Perform basic and complex procedures and techniques as outlined in research protocol, assure fidelity to protocols, may propose modifications to protocols and/or assist in the design of research protocols. * Design portions of research plan. Monitor, test, and evaluate current procedures. * Supervise adherence to safety and compliance guidelines when necessary. * Contribute to progress reports required by funding agencies. * Participate in the development of new proposals for research and obtain external funding support for new and/or continuing research activities. * Perform experiments, simulations, or theoretical investigations. Collect data and evaluate relevance of data. Work independently on basic research tasks with oversight by Faculty or Principal Investigator (PI). Contribute to documentation of equipment and procedures. * Prepare manuscripts for contributing author for publication. Present results in departmental seminars and at professional meetings. * Participate in public outreach activities as required by funding sources. May participate in national and international meetings within the discipline. To obtain the full job description including key areas of responsibility, technical competencies, and desirable qualifications, please contact *************************** About the College of Engineering The College of Engineering at the University of Iowa is driven by talented faculty, staff, and students who are dedicated to producing knowledge that addresses grand challenges in advanced technologies, health sciences, sustainability, energy, and the environment. We pride ourselves on producing ethical, globally aware engineers whose work makes the world safer and more efficient. As a center of innovation and discovery, the College of Engineering is committed to improving the quality of life for our Iowa community, as well as for people across the United States and around the world. We uphold the values of respect, community, and collaboration in all our endeavors, fostering a welcoming and respectful environment where members are valued and supported. Joining our team means becoming part of a supportive environment that values work-life balance and personal well-being. The University of Iowa offers a comprehensive benefits package, including health and wellness resources, dual career support, and opportunities for professional development. Learn more about working at the University of Iowa: Build A Career/Build a Life. Education Requirement: * Bachelor's degree in related field and a minimum of 3 years of experience or equivalent combination of education and experience. Required Qualifications: * Expert knowledge of robotic kinematics, including humanoid kinematics and locomotion, control theory, and advanced motion planning for complex, multi-degree-of-freedom systems. * Strong Proficiency in Python for simulation scripting, and exceptional skills in C++ for developing high-performance, real-time control modules. * Extensive experience with NVIDIA Isaac Sim and the broader Omniverse platform. This includes building and configuring virtual worlds, importing assets, and using the core APIs to create and test human-centric scenarios. * Specific experience with humanoid robotics or virtual characters, with a focus on implementing inverse kinematics and bipedal control systems. * Practical experience with virtual sensor creation and data processing, specifically for use in perception and navigation tasks within a simulated environment. Application Details In order to be considered for an interview, applicants must upload: * Resume * Cover Letter Job openings are posted for a minimum of 7 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. 5 professional references will be requested at a later step in the recruitment process. For questions, contact Adrian Cunningham at *************************** Benefits Highlights Regular salaried position. Pay level 5B. Located in Iowa City, Iowa. Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans. For more information about Why Iowa? Click here. About Iowa Joining the University of Iowa means becoming a vital part of the Hawkeye community, where your work directly impacts education, research, and student success. Enjoy exceptional health coverage, university-paid life insurance, robust retirement plans, and generous leave policies. Benefit from 24/7 support services, well-being resources, and access to UI Health Care specialists. Grow professionally with advanced training, leadership development, and tuition assistance. Iowa City offers a great quality of life with world-class performances at Hancher Auditorium, Big Ten athletics, top-ranked public schools, and outdoor recreation. Join us in making a difference at a leading Big Ten university and premier public research institution. Additional Information * Classification Title: Engineering Specialist * Appointment Type: Professional and Scientific * Schedule: Full-time * Work Modality Options: On Campus Compensation * Pay Level: 5B Contact Information * Organization: College of Engineering * Contact Name: Alex Schutman * Contact Email: ***********************
$52k-73k yearly est. Easy Apply 6d ago
Research Associate, Molecular Biology/Genome Editing
Precigen, Inc. 3.9
Scientist job in Iowa City, IA
Job Description Exemplar Genetics, a leader in innovative biomedical animal models, is seeking a highly motivated and creative Research Associate at our Coralville, Iowa facility. This position will report to the Chief Scientific Officer and be responsible for the development of genetically modified cell lines for the purpose of developing novel animal models of human disease. The candidate should have strong expertise in molecular biology and cell culture techniques. Excellent interpersonal, organizational, and communication skills are required. Exemplar Genetics is a wholly owned subsidiary of Precigen Corporation. DUTIES AND RESPONSIBILITIES Coordinate parallel tasks across multiple projects, demonstrating the ability to manage timelines and deliverables Develop reports for various projects to be presented in both oral and written form Utilize technology, i.e. Outlook, PowerPoint, and other programs to create and distribute reports and key information Interpret and effectively execute upon a variety of instructions provided in written, oral, diagram or schedule formats Maintain a high degree of accuracy and attention to detail Demonstrate ability to achieve high performance in independent work as well as in team setting EDUCATION AND EXPERIENCE B.S. in biology (or related field) with a minimum of 6 years relevant experience or M.S. in molecular biology (or related field) with a minimum of 4 years relevant experience Expertise in molecular and cell biology Expertise in mammalian cell genome modification Strong knowledge of genome editing Strong knowledge of cell culture Good understanding of gene delivery technologies and their applications DESIRED KEY COMPETENCIES Ability to understand and execute on the company's mission and values Maintain a high degree of ethical standard and trustworthiness Capable of fostering change in an organization Deals with conflict in a direct, positive manner Ability to think and adapt to a rapidly changing environment and demands Able to reach rational conclusions through complex processing of information Fosters innovation through creative solutions Energized by accomplishments and excellence in the workplace Self-motivated and independently minded Positive interpersonal skills with the ability to interact with individuals from a variety of levels and function Strong quantitative and analytical skills Responsive, can-do attitude PHYSICAL DEMANDS Prolonged standing and/or sitting Manual dexterity required to operate office equipment, standard laboratory equipment (i.e., pipette, detector, etc.), and heavy lab equipment. Carrying, handling, lifting, and reaching for objects up to 25 pounds Exposure to hazardous/toxic/radioactive reagents and potentially to experimental animals For more information about Exemplar Genetics or to apply for this position, please visit our website at ************************
$51k-66k yearly est. 12d ago
Laboratory Scientist - Hospital (Part Time Evenings)
Unitypoint Health 4.4
Scientist job in Cedar Rapids, IA
The laboratory scientist plays an important role in the lab.The laboratory scientist is the face of the lab interacting with patients and nursing personnel. The laboratory scientist is a Bachelor degreed individual who supports preanalytic, analytic and post analytic laboratory workflows. Responsibilities may include the following:1) registration; 2) registration/billing work queues; 3) inpatient, outpatient or outreach phlebotomy; 4) sample processing/aliqouting/ accessioning; and 5) CLIA waived and moderate complexity testing. Testing areas may include hematology, chemistry, coagulation, urinalysis, and microbiology. Why UnityPoint Health? At UnityPoint Health, you matter. We're proud to be recognized as a Top 150 Place to Work in Healthcare by Becker's Healthcare several years in a row for our commitment to our team members. Our competitive Total Rewards program offers benefits options that align with your needs and priorities, no matter what life stage you're in. Here are just a few: Expect paid time off, parental leave, 401K matching and an employee recognition program. Dental and health insurance, paid holidays, short and long-term disability and more. We even offer pet insurance for your four-legged family members. Early access to earned wages with Daily Pay, tuition reimbursement to help further your career and adoption assistance to help you grow your family. With a collective goal to champion a culture of belonging where everyone feels valued and respected, we honor the ways people are unique and embrace what brings us together. And, we believe equipping you with support and development opportunities is a vital part of delivering an exceptional employment experience. Find a fulfilling career and make a difference with UnityPoint Health. Responsibilities Pre-Analytic workflows Greets everyone with a pleasant and professional manner, using patient experience best practice guidelines (AIDET, 5/10 Rule and No-Point, etc). Identifies patients and samples using two patient identifiers, always labeling samples in the presence of the patient. May perform venous and capillary blood collections independently for patients of all ages within specified safety parameters, timelines and pace. Assists with sample transport, receiving, processing, aliqouting, accessioning and delivery of specimens to testing areas. Demonstrates knowledge of computer programs for patient identification, registration, registration work queues, order, and sample tracking. Utilizes supply items in a cost effective manner, recognizing when to reorder, and assisting with unpacking and/or restocking items. Achieves basic understanding of lab tests to answer patient questions in an easy to understand way. Analytic workflows Performs CLIA waived and moderate complex testing in accordance with manufacturer specifications using good laboratory practice. Works closely with MT/MLS/MLT with lab procedures/tests/training Works efficiently with the work flow and work load Documents routine instrument maintenance Troubleshoots and resolves instrument and equipment issues Documents, reviews and writes technical procedures for department Monitors technical practices to meet necessary standards, recommendations and requirements of voluntary and government agencies (CAP, TJC, CLIA). Strong knowledge of computer systems used on analyzers, Sunquest and EPIC Post-Analytic workflows Appropriate reporting protocols Able to review reports for errors Understanding of Quality Management system Committed Team Prioritizes work in the best interest of the patient, sharing the work with team members. Assists with training new employees and students, being helpful and supportive in their teaching. Demonstrates knowledge that patient and workplace safety is a priority by preventing errors, accidents and infections and reporting potential or actual concerns immediately. Attends department huddles, staff meetings and other required training. Checks emails regularly for huddle minutes and important communications relevant to assignment. Qualifications Bachelor's degree in a chemical, physical or clinical laboratory science or medical technology from an accredited institution College or post-graduate laboratory experience Writes, reads, comprehends and speaks fluent English. Technical Aptitude- ability to learn new systems quickly Medical Terminology Basic laboratory skills Accountability Adaptability Professionalism Decision making skills Planning and Organizing skills Problem solving Use of usual and customary equipment used to perform essential functions of the position.
$37k-49k yearly est. Auto-Apply 7d ago
Food Scientist - New Product Development
West Liberty Foods 4.3
Scientist job in West Liberty, IA
OUR TEAM IS OUR BEST ASSET West Liberty Foods manufactures hundreds of meat and poultry products that can be found in well-known grocery stores and top restaurant chains nationwide. Recognized as one of the top protein processors in North America, we have the capacity to produce over 650 million pounds of food products per year across our facilities. We are The Surprisingly Big Company, and we're right in your backyard. Build your career with West Liberty Foods and be a part of an exciting, collaborative team environment! We are currently hiring for: Job Title: Food Scientist - New Product Development Salary Range: $65,000 to $90,000+ depending on experience Job Summary: The Research and Development Team are expanding and is looking for an Inventor to join their team as a Food Scientist. We focus on developing and perfecting new product offerings for the grocery, deli, restaurant industries and ready to eat packaged sandwiches. The position is based out the corporate office in West Liberty, Iowa and the Pilot Plant across town. You will have the ability to create, test, and improve upon existing formulations and commercialization of products. Job Responsibilities: * Focus on development of meat formulations focusing on deli meat applications. * Apply science and technology to meat research and development. * Conduct and sensory studies and interpret data that is collected. * Plan and design product processes working with operations and engineering teams. * Lead research within the R & D Team towards new new product development. * Lead cost reduction initiatives as it relates to development of current and new products. * Other duties as assigned. Job Requirements: * Minimum of 3 years of related research and development experience in the food and beverage industry is required. * Bachelor's Degree in Science is required. * Experience in a pilot plant setting is preferred. * Education and formal training in the food development and manufacturing process is preferred. * Sandwich development experience would be a plus. * Ability to travel for production facility needs and customer meetings. * Candidates must successfully pass a post-offer/pre-employment drug test and background screen. West Liberty Foods is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. West Liberty Foods is committed to providing all team members with predictable work schedules that accommodate the universal need to spend time away from work to rest, relax, and spend time with family and friends. However, as a food manufacturer, West Liberty Foods is responsible for producing perishable products. To help ensure that our food products meet the quality and safety standards our customers expect, team members may, at times, be asked or expected to work overtime, weekends, or holidays. West Liberty Foods remains committed to its overtime, weekend, and holiday pay policies, and will schedule team members for those hours on a volunteer-first basis, whenever possible. To be considered an applicant for this position, you must apply online on our career site at ***************************** The following benefits are available: * Medical, Dental, Vision & Prescription Coverage * Paid Time Off * Life Insurance * Short Term Disability * Flexible Spending Account and Health Savings Account * 401(k) Retirement Savings Plan * Employee Assistance Program * Educational Assistance Program * Discount Benefits * Additional Voluntary Benefits
$65k-90k yearly 4d ago
Chemical Development Principal Scientist I
Cambrex 4.4
Scientist job in Homestead, IA
Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs. Your Work Matters. At Cambrex, we strive to build a culture where all colleagues have the opportunity to: engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more! Your Future Matters. Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today! Job Overview Position is directed toward optimization of existing chemical routes and development of alternate chemistry toward key synthetic intermediates and APIs. Carries out multistep chemical synthesis and product isolation/purification operations in the laboratory, independently or as part of an integrated team. Chemist utilizes modern analytical tools to determine identity and purity of products made during projects. Communication with clients in regular team meetings; prepares R&D reports at the conclusion of projects. Responsibilities Design and carry out multistep organic syntheses, isolation, and purification of targeted products. Must possess a strong understanding of modern organic synthesis methodologies. Must have a thorough understanding of modern analytical and spectroscopic techniques and be able to interpret the corresponding data and spectra. Ability to conduct literature searches for specific target compounds and be able to use the literature to base a design of alternate routes to these compounds. Requires ongoing professional development to keep abreast of current scientific literature and discuss these findings with colleagues. Must demonstrate a proficiency to carry out laboratory syntheses and purification techniques on scales ranging from milligrams to several kilograms, and design and implement process modifications. Requires excellent time management with the ability to manage projects on-time without supervision. Ability to author and review comprehensive reports at the conclusion of projects for internal and customer use. Work closely with other chemistry and analytical laboratory staff to coordinate project activities and resource usage. Work to ensure that a spirit of teamwork and cooperation always exists within the group. Conduct laboratory operations in a safe manner. Maintain familiarity with the company's chemical hygiene plan. Exhibit safety awareness and safe work practices. Follow responsible actions regarding chemical disposal. Maintain compliance with all regulations at the federal, state, and local levels. Must demonstrate effective communication skills (both interpersonal and presentations). Participate in project team meetings with customers. Work closely with manufacturing and GMP operations to coordinate project related equipment and activities. Qualifications/Skills Demonstrated ability to scale up pharmaceutical processes. Excellent verbal and written communication/interpersonal skills, organizational skills, and the ability to work in a diverse team environment are essential. Education, Experience & Licensing Requirements Ph. D. in Chemistry or related field with minimum 6 years of experience or M. S. in Chemistry or related field with minimum 10 years of experience or B. S. degree in Chemistry or related field with 14 years of experience in lab environment, pharmaceutical experience preferred. Cambrex is committed to providing a safe and productive work environment. All offers of employment are contingent on the successful completion of a comprehensive pre-employment screen. The pre-employment screen may consist of several components including but not limited to a drug test, criminal record check, identity verification, reference checks, education and employment verification, and may vary based on federal, state, and local laws. Refusal to submit to testing will result in disqualification of further employment consideration. All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law. #LI-RD1Ph. D. in Chemistry or related field with minimum 6 years of experience or M. S. in Chemistry or related field with minimum 10 years of experience or B. S. degree in Chemistry or related field with 14 years of experience in lab environment, pharmaceutical experience preferred. Design and carry out multistep organic syntheses, isolation, and purification of targeted products. Must possess a strong understanding of modern organic synthesis methodologies. Must have a thorough understanding of modern analytical and spectroscopic techniques and be able to interpret the corresponding data and spectra. Ability to conduct literature searches for specific target compounds and be able to use the literature to base a design of alternate routes to these compounds. Requires ongoing professional development to keep abreast of current scientific literature and discuss these findings with colleagues. Must demonstrate a proficiency to carry out laboratory syntheses and purification techniques on scales ranging from milligrams to several kilograms, and design and implement process modifications. Requires excellent time management with the ability to manage projects on-time without supervision. Ability to author and review comprehensive reports at the conclusion of projects for internal and customer use. Work closely with other chemistry and analytical laboratory staff to coordinate project activities and resource usage. Work to ensure that a spirit of teamwork and cooperation always exists within the group. Conduct laboratory operations in a safe manner. Maintain familiarity with the company's chemical hygiene plan. Exhibit safety awareness and safe work practices. Follow responsible actions regarding chemical disposal. Maintain compliance with all regulations at the federal, state, and local levels. Must demonstrate effective communication skills (both interpersonal and presentations). Participate in project team meetings with customers. Work closely with manufacturing and GMP operations to coordinate project related equipment and activities.
$71k-101k yearly est. Auto-Apply 60d+ ago
Radiochemist
Perspective Therapeutics
Scientist job in Coralville, IA
ObjectiveWe are seeking an experienced and motivated Radiochemist to join our dynamic team. The successful candidate will be responsible for the development of radiolabeling, purification, and characterization methods for various compounds for use in preclinical and clinical studies. This role will involve close collaboration with multidisciplinary teams, including biologists, pharmacologists, and clinicians, to support the development of our radiopharmaceutical products.Essential Functions Synthesis of Radiolabeled Compounds: Design, synthesize, and optimize radiolabeling methods of compounds (e.g., PET, SPECT, and alpha emitting isotopes) for use in preclinical and clinical studies. Radiochemical Purity and Quality Control: Perform and develop analytical methods to ensure the radiochemical purity, stability, and quality of radiolabeled compounds. Contribute to the development of critical quality attributes of various products. Process Development: Contribute to the development and optimization of radiolabeling processes through identification of critical process parameters, including scale-up for clinical production. Regulatory Compliance: Ensure all radiochemical activities comply with relevant regulations, including GMP, GLP, and safety protocols. Documentation: Maintain accurate records of all experiments, procedures, and results. Prepare technical reports and contribute to regulatory submissions. Cross-Functional Collaboration: Work closely with other departments, including Manufacturing, Pharmacology, and Clinical Development, to support the integration of radiochemistry into the drug development process. Safety: Uphold strict safety standards in handling radioactive materials, and participate in the maintenance of radiation safety procedures and protocols. Innovation: Stay abreast of the latest advancements in radiochemistry and radiopharmaceutical development, and apply this knowledge to drive innovation within the company. QualificationsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Education / Experience Education: Ph.D. in Radiochemistry, Chemistry, or a related field. Exceptional candidates with a Master's degree and significant experience will also be considered. Experience: 3+ years of experience in radiochemistry, preferably in a pharmaceutical or clinical research environment. Proficiency in the synthesis and handling of radioactive isotopes (e.g., Pb-203, Pb-212, Ga-68, Cu-64, Cu-67 and F-18). Strong background in analytical techniques such as HPLC, TLC, GC, NMR, and mass spectrometry. Experience with automated radiochemistry synthesis modules is a plus. Thorough understanding of radiopharmaceutical development, including regulatory requirements for use of products in clinical trials (e.g., 21CFR Part 211, 21CFR Part 212, etc.). Knowledge / Skill / Ability Deep understanding of radiochemistry techniques related to the radiolabeling of molecules and their purification Knowledge of radioactive decay, RAM transportation regulations and international shipments Effective communication, including writing, speaking and interpersonal communication. Rapid critical thinking and problem-solving abilities. Excellent customer service and client relations skills. Organizational and time management skills. Great collaboration and teamwork abilities. Great leadership skills. Adaptable to work in a fast-paced environment. Advanced data analysis and data visualization. Expert inventory management. Ability to use computers, software and other technology for inventory and communication purposes. Understanding of the supply chain, including common obstacles and effective solutions. Flexibility to work various shifts as required. Flexible and willing to perform other tasks as assigned. Ability to lift 60 lbs. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Work EnvironmentThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels. Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require. May be required to sit or stand for long periods of 8+ hours a day while performing duties. Occasional kneeling, crouching, twisting the upper body, bending, stooping, pushing, pulling, or reaching may be required. Must possess good hand-eye coordination; close attention to detail is required. Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including radioactive, corrosive, flammable and toxic material, dust, dirt, odors, and irritants. Must be willing to wear a variety of Personal Protective Equipment (PPE), including eye and hearing protection, as needed. Willingness to complete safety training within allotted timeframes, and work in a team-based environment. For information on Perspective Therapeutics, visit our website at: ******************************** Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. For information on Perspective Therapeutics, visit our website at: ********************************
$49k-72k yearly est. Auto-Apply 60d+ ago
Scientist/Senior Scientist
Zoetis 4.9
Scientist job in Homestead, IA
Role Description Zoetis is seeking an enthusiastic, innovative, and highly motivated professional to significantly contribute to the efficient manufacture and process optimization of animal health biologics. The candidate will work at the interface of R&D and manufacturing to optimize manufacturing processes at scale, focusing on yield improvement, cycle time reduction, and overall process efficiency. The Scientist/Senior Scientist will work autonomously and/or in small groups executing experiments and reporting results to multi-disciplinary project teams. This role supports a strategic process improvement program aimed at increasing supply capacity and reducing cost of goods for key biologic products in the swine portfolio. Collaboration will be extensive with colleagues in Global Manufacturing Technology, Global Biologics Research, Quality, Regulatory, and manufacturing operations. The position is based in Charles City (Iowa, USA), with frequent interactions with Zoetis' R&D headquarters in Kalamazoo (Michigan, USA) and other global manufacturing sites. This is a term position with an intended duration of 2 years. Position Responsibilities * Apply knowledge of bacteriology, biological, analytical, and process optimization principles to improve manufacturing efficiency and capacity. * Conduct laboratory experiments at scales ranging from bench to commercial quantities, focusing on process innovation and efficiency gains. * Document experiments and results in electronic laboratory notebooks and reports in accordance with GMP quality management systems. * Assess and implement novel equipment, methods, and procedures to enhance existing manufacturing processes. * Participate in cross-functional project teams driving licensing, supply strategy, and commercial readiness of animal health biologics. * Support strategic decision-making through data-driven insights on process improvements impacting supply and cost. Organizational Relationships * The position is within the Global Biologics Research line and collaborates with manufacturing technology, vaccine research, process development, analytical development, quality control, regulatory affairs, and manufacturing teams. * Interaction with global colleagues to ensure compliance with GMP and regulatory standards. * Contribute to process improvement programs that enable supply capacity expansion and portfolio growth. Education and Experience * Minimum: BS in biology, animal science, immunology, bacteriology, bioengineering, or related biotechnology fields with 3-5 years' experience in relevant process development or manufacturing. * MS or PhD with commensurate experience is also acceptable. * Desirable: Experience in bacterial propagation, cell culture, vaccine development, analytical and immunology methods. * Experience working in GMP/GLP environments and bioprocessing is preferred. Technical Skills Requirements * Excellent organizational and communication skills, including scientific writing and data presentation. * Self-motivated, collaborative, and able to work effectively in a global, multi-disciplinary team. * Hands-on experience with sterile bacterial culture and independent lab operation. * Critical scientific thinking with openness to new technologies and process improvements. * Familiarity with quality regulated environments and process optimization. Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.
$65k-95k yearly est. Auto-Apply 60d+ ago
Research Associate - Anesthesia, Smith Lab
Uiowa
Scientist job in Iowa City, IA
The Research Associate will work in a research lab focused on the acute inflammation and endothelial response to acute surgical stress. Clinical outcomes of interest include postoperative acute kidney injury and delirium. Study techniques include clinical studies of surgical patients, in vivo mechanistic studies (mice), and in vitro human primary cell experiments. The successful candidate should have experience in an academic medical-science focused laboratory with a wet-lab component, along with excellent record keeping ability and organization skills. Prior experience with wet-lab methods including but not limited to next-generation sequencing and data analysis, spatial transcriptomic sequencing and analysis, single-cell studies, cell culture, DNA/RNA work, and animal husbandry (mice) is highly desired, but not a requirement. The candidate must exhibit a great deal of independence and be able to independently design experiments, carry them out and assist with analyzing and presenting data. What you will do: • Plan and perform existing experiments in support of ongoing research projects based on extensive knowledge of scientific theory. Interpret and perform analyses of results and their possible implications • Analyze and interpret literature on an ongoing basis to remain current with new procedures and related research, interpret new findings and analyze their validity • Demonstrate in depth knowledge of and offer suggestions regarding modifications to procedures and protocols. Advise on advanced research analysis methods • Design, write, and publish findings as needed. Participate in the preparation of written documents, including procedures, presentations, and proposals. Edit and revise as needed • Coordinate and evaluate general lab maintenance as needed; maintain lab stock, manage chemical inventory and safety records, and coordinate lab support when required • Responsible for following guidelines and maintaining required documentation in support of safety programs for laboratory members For a full job description, please send an e-mail to the contact listed below. About The Department of Anesthesia: The Department of Anesthesia provides exceptional patient experiences and a positive work environment through excellence, compassionate care, continuous improvement, innovative research, and collaborative learning. What you will need: Required Qualifications: • Bachelor's Degree or equivalent combination of education and experience in related scientific field • One year of related experience • Extensive understanding of scientific principles. • Ability to maintain detailed records of experiments and outcomes. Edit and revise as needed • Advanced computer skills and ability to quickly learn computer programs, databases, and scientific applications • Excellent organizational skills and demonstrated ability to accurately complete detailed work Desired Qualifications: • A Bachelor of Science related to molecular medicine or related discipline or equivalent experience • Two years' experience • Experience in wet-lab methods • Technical writing experience in SOP's, protocols, and reports • Experience with laboratory animal experiments, in particular, s.c. injection of drugs • Ability to communicate effectively with team members and collaborators • Experimental design, execution of plan and presentation of data to team • Utilization of good documentation practices Dual Postings: The department intends to hire for one position from either: Research Assistant - Anesthesia, Smith Lab #25006461 or Research Associate - Anesthesia, Smith Lab #25006460, based on the qualifications of the successful candidate. Please apply to the specific position for which you wish to be considered or both. Position and Application details: In order to be considered for an interview, applicants must upload the following documents and mark them as a “Relevant File” to the submission: Resume Cover Letter Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process. This position is not eligible for University sponsorship for employment authorization. For additional questions, please contact Charlie Miner at ***********************. Additional Information Compensation Contact Information
$35k-53k yearly est. Easy Apply 46d ago
Laboratory Scientist - Hospital (Part Time Evenings)
Unitypoint Health 4.4
Scientist job in Cedar Rapids, IA
* Area of Interest: Laboratory * FTE/Hours per pay period: 0.6 * Department: Lab-General/Point Of Care * Shift: Part Time - 24 hours per week evenings, variable start times, weekend/holiday rotation * Job ID: 177283 The laboratory scientist plays an important role in the lab.The laboratory scientist is the face of the lab interacting with patients and nursing personnel. The laboratory scientist is a Bachelor degreed individual who supports preanalytic, analytic and post analytic laboratory workflows. Responsibilities may include the following:1) registration; 2) registration/billing work queues; 3) inpatient, outpatient or outreach phlebotomy; 4) sample processing/aliqouting/ accessioning; and 5) CLIA waived and moderate complexity testing. Testing areas may include hematology, chemistry, coagulation, urinalysis, and microbiology. Why UnityPoint Health? At UnityPoint Health, you matter. We're proud to be recognized as a Top 150 Place to Work in Healthcare by Becker's Healthcare several years in a row for our commitment to our team members. Our competitive Total Rewards program offers benefits options that align with your needs and priorities, no matter what life stage you're in. Here are just a few: * Expect paid time off, parental leave, 401K matching and an employee recognition program. * Dental and health insurance, paid holidays, short and long-term disability and more. We even offer pet insurance for your four-legged family members. * Early access to earned wages with Daily Pay, tuition reimbursement to help further your career and adoption assistance to help you grow your family. With a collective goal to champion a culture of belonging where everyone feels valued and respected, we honor the ways people are unique and embrace what brings us together. And, we believe equipping you with support and development opportunities is a vital part of delivering an exceptional employment experience. Find a fulfilling career and make a difference with UnityPoint Health. Responsibilities Pre-Analytic workflows * Greets everyone with a pleasant and professional manner, using patient experience best practice guidelines (AIDET, 5/10 Rule and No-Point, etc). * Identifies patients and samples using two patient identifiers, always labeling samples in the presence of the patient. * May perform venous and capillary blood collections independently for patients of all ages within specified safety parameters, timelines and pace. * Assists with sample transport, receiving, processing, aliqouting, accessioning and delivery of specimens to testing areas. * Demonstrates knowledge of computer programs for patient identification, registration, registration work queues, order, and sample tracking. * Utilizes supply items in a cost effective manner, recognizing when to reorder, and assisting with unpacking and/or restocking items. * Achieves basic understanding of lab tests to answer patient questions in an easy to understand way. Analytic workflows * Performs CLIA waived and moderate complex testing in accordance with manufacturer specifications using good laboratory practice. * Works closely with MT/MLS/MLT with lab procedures/tests/training * Works efficiently with the work flow and work load * Documents routine instrument maintenance * Troubleshoots and resolves instrument and equipment issues * Documents, reviews and writes technical procedures for department * Monitors technical practices to meet necessary standards, recommendations and requirements of voluntary and government agencies (CAP, TJC, CLIA). * Strong knowledge of computer systems used on analyzers, Sunquest and EPIC Post-Analytic workflows * Appropriate reporting protocols * Able to review reports for errors * Understanding of Quality Management system Committed Team * Prioritizes work in the best interest of the patient, sharing the work with team members. * Assists with training new employees and students, being helpful and supportive in their teaching. * Demonstrates knowledge that patient and workplace safety is a priority by preventing errors, accidents and infections and reporting potential or actual concerns immediately. * Attends department huddles, staff meetings and other required training. * Checks emails regularly for huddle minutes and important communications relevant to assignment. Qualifications * Bachelor's degree in a chemical, physical or clinical laboratory science or medical technology from an accredited institution * College or post-graduate laboratory experience * Writes, reads, comprehends and speaks fluent English. * Technical Aptitude- ability to learn new systems quickly * Medical Terminology * Basic laboratory skills * Accountability * Adaptability * Professionalism * Decision making skills * Planning and Organizing skills * Problem solving * Use of usual and customary equipment used to perform essential functions of the position.
$37k-49k yearly est. Auto-Apply 6d ago
Food Scientist - New Product Development
West Liberty Foods Jobs 4.3
Scientist job in West Liberty, IA
OUR TEAM IS OUR BEST ASSET About West Liberty Foods West Liberty Foods manufactures hundreds of meat and poultry products that can be found in well-known grocery stores and top restaurant chains nationwide. Recognized as one of the top protein processors in North America, we have the capacity to produce over 650 million pounds of food products per year across our facilities. We are The Surprisingly Big Company , and we're right in your backyard. Build your career with West Liberty Foods and be a part of an exciting, collaborative team environment! We are currently hiring for: Job Title: Food Scientist - New Product Development Salary Range: $65,000 to $90,000+ depending on experience Job Summary: The Research and Development Team are expanding and is looking for an Inventor to join their team as a Food Scientist. We focus on developing and perfecting new product offerings for the grocery, deli, restaurant industries and ready to eat packaged sandwiches. The position is based out the corporate office in West Liberty, Iowa and the Pilot Plant across town. You will have the ability to create, test, and improve upon existing formulations and commercialization of products. Job Responsibilities: Focus on development of meat formulations focusing on deli meat applications. Apply science and technology to meat research and development. Conduct and sensory studies and interpret data that is collected. Plan and design product processes working with operations and engineering teams. Lead research within the R & D Team towards new new product development. Lead cost reduction initiatives as it relates to development of current and new products. Other duties as assigned. Job Requirements: Minimum of 3 years of related research and development experience in the food and beverage industry is required. Bachelor's Degree in Science is required. Experience in a pilot plant setting is preferred. Education and formal training in the food development and manufacturing process is preferred. Sandwich development experience would be a plus. Ability to travel for production facility needs and customer meetings. Candidates must successfully pass a post-offer/pre-employment drug test and background screen. West Liberty Foods is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. West Liberty Foods is committed to providing all team members with predictable work schedules that accommodate the universal need to spend time away from work to rest, relax, and spend time with family and friends. However, as a food manufacturer, West Liberty Foods is responsible for producing perishable products. To help ensure that our food products meet the quality and safety standards our customers expect, team members may, at times, be asked or expected to work overtime, weekends, or holidays. West Liberty Foods remains committed to its overtime, weekend, and holiday pay policies, and will schedule team members for those hours on a volunteer-first basis, whenever possible. To be considered an applicant for this position, you must apply online on our career site at ***************************** The following benefits are available: Medical, Dental, Vision & Prescription Coverage Paid Time Off Life Insurance Short Term Disability Flexible Spending Account and Health Savings Account 401(k) Retirement Savings Plan Employee Assistance Program Educational Assistance Program Discount Benefits Additional Voluntary Benefits
$65k-90k yearly 4d ago
Research Associate - Dept of Surgery
University of Iowa 4.4
Scientist job in Iowa City, IA
The Research Associate will work as a member of the research team supporting Dr. Vikas Dudeja's Surgical Oncology research program through the Department of Surgery at the University of Iowa Health Care. Responsibilities include support for research by conducting experiments, investigations, and/or evaluations; collecting and analyzing data and performing operational duties associated with the laboratory; and other research related actions and duties. * Perform research activities in a specialized area. * Research literature as requested. Adapt and perform protocols from the literature. * Critically review literature for the purposes of furthering the research and developing new hypotheses in conjunction with other investigators. * Perform basic and complex procedures and techniques as outlined in research protocol, assure fidelity to protocols, propose modifications to protocols, and/or assist in the design of research protocols. * Design portions of research plan. Monitor, test, and evaluate current procedures. * Identify and adhere to Quality Assurance practices to maintain validity and integrity of research data. Apply new methods/theories. * Perform statistical analysis of data and qualitative analysis. * Assist in the design of manuals, questionnaires, and forms. * Assist in preparing publications and presentations. Contribute to the technical writing of papers, manuscripts, grant applications, and published materials as evidenced by documented recognition. * Present results/findings at team and departmental meetings; present at local and national meetings. * Make recommendations regarding the validity of research subjects and data. * Submit routine IRB, ACURF, or similar protocol submissions, if applicable. * Responsible for following guidelines and maintaining required documentation in support of safety programs. * Coordinate and manage equipment and facilities. * Monitor environmental risks and quality control. * Test new equipment, troubleshoot, and resolve complex equipment failures and perform repairs. Coordinate software licenses as necessary to complete projects. * Provide ongoing training on basic and new lab techniques and protocols for employees. * Provide direction, assignments, feedback, coaching, and counseling to track progress and assure outcomes are achieved. Department of Surgery: The University of Iowa Health Care Department of Surgery is committed to saving lives and improving our patient's quality of life through excellent surgical techniques and extraordinary patient care. Our surgeons and medical professionals address a wide variety of complex medical issues, from matching donors with recipients in the Organ Transplant Center to providing continuous care for both adult and pediatric trauma victims in the state's only designated Level I Trauma Center and certified regional Burn Treatment Center. Percent of Time: 100% Schedule: Monday through Friday, 8:00 am to 5:00 pm Location: UIHC Medical Center University Campus Pay Grade: 4A Pay Structure Benefit Highlights: * Regular salaried position located in Iowa City, Iowa. * Fringe benefit package including paid vacation; sick leave; health, dental, life, and disability insurance options; and generous employer contributions into retirement plans. For more information on benefits, please visit UI Health Care Benefits. * For more information about Why Iowa?, click here. Required Qualifications: * Bachelor's degree in science or health science field related to study, or an equivalent combination of related education and experience. * Minimum of 1 year of experience in research. * Excellent interpersonal, written, and verbal communication skills. Proven interpersonal and organizational skills. * Experience working on multiple projects at a given time with some level of independent decision making and responsibility. * Demonstrated ability to enter data into and manage research databases according to best practices. * Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, and Adobe Acrobat. Desired Qualifications: * Previous experience in routine molecular biology, cell culture, and mice handling techniques. * Knowledge of University policies, procedures, and regulations. Application Process: In order to be considered for an interview, applicants must upload a resume and cover letter and mark them as a "Relevant File" to the submission. Job openings are posted for a minimum of 14 calendar days and may be removed from posting and filled any time after the original posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 references will be requested at a later step in the recruitment process. This position is not eligible for University sponsorship for employment authorization. For additional questions, please contact Katie Pontious-Vanhxay at ************** or ********************************. Additional Information * Classification Title: Research Associate * Appointment Type: Professional and Scientific * Schedule: Full-time * Work Modality Options: On Campus Compensation * Pay Level: 4A Contact Information * Organization: Healthcare * Contact Name: Katie Pontious-Vanhxay * Contact Email: ********************************
$35k-47k yearly est. Easy Apply 8d ago
Radiochemist
Perspective Therapeutics
Scientist job in Coralville, IA
ObjectiveWe are seeking an experienced and motivated Radiochemist to join our dynamic team. The successful candidate will be responsible for the development of radiolabeling, purification, and characterization methods for various compounds for use in preclinical and clinical studies. This role will involve close collaboration with multidisciplinary teams, including biologists, pharmacologists, and clinicians, to support the development of our radiopharmaceutical products.Essential Functions Synthesis of Radiolabeled Compounds: Design, synthesize, and optimize radiolabeling methods of compounds (e.g., PET, SPECT, and alpha emitting isotopes) for use in preclinical and clinical studies. Radiochemical Purity and Quality Control: Perform and develop analytical methods to ensure the radiochemical purity, stability, and quality of radiolabeled compounds. Contribute to the development of critical quality attributes of various products. Process Development: Contribute to the development and optimization of radiolabeling processes through identification of critical process parameters, including scale-up for clinical production. Regulatory Compliance: Ensure all radiochemical activities comply with relevant regulations, including GMP, GLP, and safety protocols. Documentation: Maintain accurate records of all experiments, procedures, and results. Prepare technical reports and contribute to regulatory submissions. Cross-Functional Collaboration: Work closely with other departments, including Manufacturing, Pharmacology, and Clinical Development, to support the integration of radiochemistry into the drug development process. Safety: Uphold strict safety standards in handling radioactive materials, and participate in the maintenance of radiation safety procedures and protocols. Innovation: Stay abreast of the latest advancements in radiochemistry and radiopharmaceutical development, and apply this knowledge to drive innovation within the company. QualificationsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Education / Experience Education: Ph.D. in Radiochemistry, Chemistry, or a related field. Exceptional candidates with a Master's degree and significant experience will also be considered. Experience: 3+ years of experience in radiochemistry, preferably in a pharmaceutical or clinical research environment. Proficiency in the synthesis and handling of radioactive isotopes (e.g., Pb-203, Pb-212, Ga-68, Cu-64, Cu-67 and F-18). Strong background in analytical techniques such as HPLC, TLC, GC, NMR, and mass spectrometry. Experience with automated radiochemistry synthesis modules is a plus. Thorough understanding of radiopharmaceutical development, including regulatory requirements for use of products in clinical trials (e.g., 21CFR Part 211, 21CFR Part 212, etc.). Knowledge / Skill / Ability Deep understanding of radiochemistry techniques related to the radiolabeling of molecules and their purification Knowledge of radioactive decay, RAM transportation regulations and international shipments Effective communication, including writing, speaking and interpersonal communication. Rapid critical thinking and problem-solving abilities. Excellent customer service and client relations skills. Organizational and time management skills. Great collaboration and teamwork abilities. Great leadership skills. Adaptable to work in a fast-paced environment. Advanced data analysis and data visualization. Expert inventory management. Ability to use computers, software and other technology for inventory and communication purposes. Understanding of the supply chain, including common obstacles and effective solutions. Flexibility to work various shifts as required. Flexible and willing to perform other tasks as assigned. Ability to lift 60 lbs. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Work EnvironmentThe work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels. Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require. May be required to sit or stand for long periods of 8+ hours a day while performing duties. Occasional kneeling, crouching, twisting the upper body, bending, stooping, pushing, pulling, or reaching may be required. Must possess good hand-eye coordination; close attention to detail is required. Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including radioactive, corrosive, flammable and toxic material, dust, dirt, odors, and irritants. Must be willing to wear a variety of Personal Protective Equipment (PPE), including eye and hearing protection, as needed. Willingness to complete safety training within allotted timeframes, and work in a team-based environment. For information on Perspective Therapeutics, visit our website at: ******************************** Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. For information on Perspective Therapeutics, visit our website at: ******************************** Powered by JazzHR WLee8mInAn
$49k-72k yearly est. 12d ago
Quality Control Scientist III
Zoetis 4.9
Scientist job in Homestead, IA
This Quality Control Scientist III serves as a vital influencer within the Biologics Quality Control team, shaping the team's approach to quality, compliance, and animal care through expertise and example. In this role, the colleague performs essential product release testing and maintains the highest standards in laboratory animal care, consistently demonstrating best practices and attention to detail. Daily contributions from the colleague help elevate the team's proficiency by sharing knowledge, offering guidance on routine challenges, and providing training to peers. By assisting the team leader with testing coordination and animal distribution, the colleague helps streamline operations and fosters a collaborative, solutions-focused atmosphere. Position Responsibilities: * Conduct potency, identity, inactivation, and extraneous agent testing on antigen stocks and final product vaccines using both egg-based and tissue culture methodologies, adhering to strict aseptic techniques, and operating independently without supervision. * Perform essential product release safety and potency testing in accordance with regulatory and company standards. * Maintain the highest standards of laboratory animal care, consistently demonstrating best practices and ethical responsibility in accordance with IACUC, AAALAC, and other regulatory guidelines. * Accurately record laboratory observations and test results, recognizing and reporting deviations promptly. * Offer support and guidance on laboratory challenges, helping troubleshoot, and resolve routing issues. * Monitor and maintain optimal inventory levels of laboratory supplies and equipment to ensure uninterrupted workflow and compliance with operational standards. * Support the upkeep, cleanliness, and routine maintenance of laboratory facilities to promote a safe, organized, and regulatory-compliant working environment. * Assist the team leader with coordinating testing schedules and animal distribution to optimize workflow. * Foster a collaborative, solutions-focused atmosphere and encourage continuous improvement and ethical standards within the department. * Assist with writing and reviewing Animal Usage Protocols (AUPs) to ensure compliance with IACUC guidelines. * Contribute to the onboarding and performance training of new team members by providing technical guidance, sharing best practices, and supporting skill development to ensure effective integration into laboratory operations. * Help revise departmental methods and protocols, including animal usage procedures and change controls. * Participate in laboratory investigations when necessary. Education and Experience: BS/BA plus 2 years' experience OR AA plus 5-7 years' experience. * Animal care and handling experience * Experienced with the following software programs: Word, Excel, and PowerPoint * Strong technical writing skills * Knowledge of USDA, EU, and Animal Welfare Act guidelines * Experience with maintenance, ordering, testing, and other company-based programs * Willingness to positively embrace change and flexibility in adjusting to changing priorities * Strong attention to detail, ability to work well independently and as a part of a team, and to work effectively with people at all levels within the organization * Trouble-shooting skills Technical Requirements: * Proficient in Microsoft Word, Excel, and PowerPoint, with the ability to leverage advanced features for data analysis, reporting, and presentation development. * Strong attention to detail, ability to work well independently and as a part of a team, and to work effectively with people at all levels within the organization. * Proactively seeks out opportunities for improvements and takes action with minimal direction. * Applies problem solving skills in a team environment. * High level of understanding of multiple technologies and/or assays within the workgroup. * Proficiency of 90% of the testing within the workgroup. Physical Requirements: * Must be able to walk, sit, or stand for long periods of time. * Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently. * Must be able to work scheduled 40 hours with the ability to work overtime as needed. * Must be able to work weekends as needed. * Frequent lifting and carrying of 5 to 25 lbs. * Regular reaching, bending, stooping, and twisting. * Repetitive motion and substantial movement of the wrists, hands, and/or fingers. * Ability to grasp and manipulate objects like pipettors, flasks, and bottles. * Flexibility to cover rotating weekend duties. Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.
$60k-81k yearly est. Auto-Apply 8d ago
Quality Control Data Review Scientist - Nights
Cambrex 4.4
Scientist job in Homestead, IA
Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing. Your Work Matters. At Cambrex, we strive to build a culture where all colleagues have the opportunity to: engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more! Your Future Matters. Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today! Job Overview The Data Review Scientist will be responsible for reviewing laboratory data and supporting documentation to ensure that they are compliant with SOPs, and compendial and CGMP requirements. This individual must have knowledge of instrument theory in order to thoroughly vet and review data and draw conclusions based on collected data. Responsibilities Reviews raw technical data provided by technicians, chemists and laboratory supervision to ensure accuracy, completeness and correct scientific conclusions have been drawn. Data may include Analytical Records, notebooks, logbooks, spectra, chromatograms, other instrument output and any other information supporting Analytical Records. Identifies data inaccuracies, incomplete inferences and works directly with laboratory staff to provide guidance and direction on the correction of laboratory data packages. Verifies and ensures that conclusions drawn on laboratory data are sound and accurate and representative of materials under examination. Maintains and manages cGMP and controlled substance systems in all QC/PSG labs at defined levels of compliance in accordance with site approved procedures and protocols. Maintains open communication within and across departments to ensure timely delivery and approval of laboratory documents. Works alternative schedules to support output and data review of laboratories based on business need. All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned. Qualifications/Skills Strong chemistry knowledge with proven ability to handle various project loads is beneficial. Education, Experience & Licensing Requirements Bachelor's degree in chemistry with three years' experience in a pharmaceutical and cGMP environment highly preferred. Experience in a laboratory environment highly preferred. Knowledge of analytical instrumentation (GC, HPLC, FTIR, UV-VIS, etc. ) required. Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the 'Arthur I. Mendolia Scholarship Program. ' Relocation assistance will be offered for this position. Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. #LI-RD1 All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Bachelor's degree in chemistry with three years' experience in a pharmaceutical and cGMP environment highly preferred. Experience in a laboratory environment highly preferred. Knowledge of analytical instrumentation (GC, HPLC, FTIR, UV-VIS, etc. ) required. Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the 'Arthur I. Mendolia Scholarship Program. ' Relocation assistance will be offered for this position. Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. #LI-RD1Reviews raw technical data provided by technicians, chemists and laboratory supervision to ensure accuracy, completeness and correct scientific conclusions have been drawn. Data may include Analytical Records, notebooks, logbooks, spectra, chromatograms, other instrument output and any other information supporting Analytical Records. Identifies data inaccuracies, incomplete inferences and works directly with laboratory staff to provide guidance and direction on the correction of laboratory data packages. Verifies and ensures that conclusions drawn on laboratory data are sound and accurate and representative of materials under examination. Maintains and manages cGMP and controlled substance systems in all QC/PSG labs at defined levels of compliance in accordance with site approved procedures and protocols. Maintains open communication within and across departments to ensure timely delivery and approval of laboratory documents. Works alternative schedules to support output and data review of laboratories based on business need. All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.
$49k-72k yearly est. Auto-Apply 60d+ ago
Research Associate - Dept of Surgery
Uiowa
Scientist job in Iowa City, IA
The Research Associate will work as a member of the research team supporting Dr. Vikas Dudeja's Surgical Oncology research program through the Department of Surgery at the University of Iowa Health Care. Responsibilities include support for research by conducting experiments, investigations, and/or evaluations; collecting and analyzing data and performing operational duties associated with the laboratory; and other research related actions and duties. Perform research activities in a specialized area. Research literature as requested. Adapt and perform protocols from the literature. Critically review literature for the purposes of furthering the research and developing new hypotheses in conjunction with other investigators. Perform basic and complex procedures and techniques as outlined in research protocol, assure fidelity to protocols, propose modifications to protocols, and/or assist in the design of research protocols. Design portions of research plan. Monitor, test, and evaluate current procedures. Identify and adhere to Quality Assurance practices to maintain validity and integrity of research data. Apply new methods/theories. Perform statistical analysis of data and qualitative analysis. Assist in the design of manuals, questionnaires, and forms. Assist in preparing publications and presentations. Contribute to the technical writing of papers, manuscripts, grant applications, and published materials as evidenced by documented recognition. Present results/findings at team and departmental meetings; present at local and national meetings. Make recommendations regarding the validity of research subjects and data. Submit routine IRB, ACURF, or similar protocol submissions, if applicable. Responsible for following guidelines and maintaining required documentation in support of safety programs. Coordinate and manage equipment and facilities. Monitor environmental risks and quality control. Test new equipment, troubleshoot, and resolve complex equipment failures and perform repairs. Coordinate software licenses as necessary to complete projects. Provide ongoing training on basic and new lab techniques and protocols for employees. Provide direction, assignments, feedback, coaching, and counseling to track progress and assure outcomes are achieved. Department of Surgery: The University of Iowa Health Care Department of Surgery is committed to saving lives and improving our patient's quality of life through excellent surgical techniques and extraordinary patient care. Our surgeons and medical professionals address a wide variety of complex medical issues, from matching donors with recipients in the Organ Transplant Center to providing continuous care for both adult and pediatric trauma victims in the state's only designated Level I Trauma Center and certified regional Burn Treatment Center. Percent of Time: 100% Schedule: Monday through Friday, 8:00 am to 5:00 pm Location: UIHC Medical Center University Campus Pay Grade: 4A Pay Structure Benefit Highlights: Regular salaried position located in Iowa City, Iowa. Fringe benefit package including paid vacation; sick leave; health, dental, life, and disability insurance options; and generous employer contributions into retirement plans. For more information on benefits, please visit UI Health Care Benefits. For more information about Why Iowa?, click here. Required Qualifications: Bachelor's degree in science or health science field related to study, or an equivalent combination of related education and experience. Minimum of 1 year of experience in research. Excellent interpersonal, written, and verbal communication skills. Proven interpersonal and organizational skills. Experience working on multiple projects at a given time with some level of independent decision making and responsibility. Demonstrated ability to enter data into and manage research databases according to best practices. Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, and Adobe Acrobat. Desired Qualifications: Previous experience in routine molecular biology, cell culture, and mice handling techniques. Knowledge of University policies, procedures, and regulations. Application Process: In order to be considered for an interview, applicants must upload a resume and cover letter and mark them as a "Relevant File" to the submission. Job openings are posted for a minimum of 14 calendar days and may be removed from posting and filled any time after the original posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 references will be requested at a later step in the recruitment process. This position is not eligible for University sponsorship for employment authorization. For additional questions, please contact Katie Pontious-Vanhxay at ************** or ********************************. Additional Information Compensation Contact Information
$35k-53k yearly est. Easy Apply 9d ago

Learn more about scientist jobs

How much does a scientist earn in Iowa City, IA?

The average scientist in Iowa City, IA earns between $39,000 and $86,000 annually. This compares to the national average scientist range of $67,000 to $140,000.

Average scientist salary in Iowa City, IA

$58,000

$39,00010%

$58,000Median

$86,00090%

Job type you want

Full Time

Part Time

Internship

Temporary

Zippia Careers
Life, Physical, and Social Science Industry
Scientist Jobs
Locations
Iowa City, IA
Scientist Iowa City, IA Jobs

Scientist jobs in Iowa City, IA - 26 jobs

Consumer Goods/Food R&D Senior Scientist

Bioinformatics Research Scientist III

Robotics and AI Scientist, Iowa Technology Institute

SR SCIENTIST

Sr Scientist

Robotics and AI Scientist, Iowa Technology Institute

Research Associate, Molecular Biology/Genome Editing

Laboratory Scientist - Hospital (Part Time Evenings)

Food Scientist - New Product Development

Chemical Development Principal Scientist I

Radiochemist

Scientist/Senior Scientist

Research Associate - Anesthesia, Smith Lab

Laboratory Scientist - Hospital (Part Time Evenings)

Food Scientist - New Product Development

Research Associate - Dept of Surgery

Radiochemist

Quality Control Scientist III

Quality Control Data Review Scientist - Nights

Research Associate - Dept of Surgery

Learn more about scientist jobs

How much does a scientist earn in Iowa City, IA?