R&D Chemist II - ECOAT
Associate scientist job in Minneapolis, MN
The Chemist II position is responsible for leading activities related to new product development, continuous improvement of existing product lines and maintenance of business opportunities within the General Industrial Electrodeposition coatings laboratory of the Performance Coatings Group. This role is expected to possess the ability to lead projects of varying levels of complexity with little to no supervision. The Chemist II role will be provided with ample opportunities to demonstrate development of technical expertise while providing support to internal and external customers. Although they are not expected to be a technical expert in any specific technology, they will have opportunities to develop such expertise and demonstrate leadership to lesser experienced chemists within the lab. This position is based in the Minneapolis worksite with approximately 25% -45% travel within North America.
Job duties include contact with other employees and access confidential and proprietary information and/or other items of value, and such access may be supervised or unsupervised. The Company therefore has determined that a review of criminal history is necessary to protect the business and its operations and reputation and is necessary to protect the safety of the Company's staff, employees, and business relationships.
At Sherwin-Williams, our purpose is to inspire and improve the world by coloring and protecting what matters. Our paints, coatings and innovative solutions make the places and spaces in our world brighter and stronger. Your skills, talent and passion make it possible to live this purpose, and for customers and our business to achieve great results. Sherwin-Williams is a place that takes its stability, growth and momentum and translates it to possibility for our people. Our people are behind the strength of our success, and we invest and support you in:
Life … with rewards, benefits and the flexibility to enhance your health and well-being
Career … with opportunities to learn, develop new skills and grow your contribution
Connection … with an inclusive team and commitment to our own and broader communities
It's all here for you... let's Create Your Possible
At Sherwin-Williams, part of our mission is to help our employees and their families live healthier, save smarter and feel better. This starts with a wide range of world-class benefits designed for you. From retirement to health care, from total well-being to your daily commute-it matters to us. A general description of benefits offered can be found at ***************************** Click on “Candidates” to view benefit offerings that you may be eligible for if you are hired as a Sherwin-Williams employee.
Compensation decisions are dependent on the facts and circumstances of each case and will impact where actual compensation may fall within the stated wage range. The wage range listed for this role takes into account the wide range of factors considered in making compensation decisions including skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. The wage range, other compensation, and benefits information listed is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law.
Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable federal, state, and local laws including with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act where applicable.
Sherwin-Williams is proud to be an Equal Employment Opportunity employer. All qualified candidates will receive consideration for employment and will not be discriminated against based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, pregnancy, genetic information, creed, marital status or any other consideration prohibited by law or by contract.
As a VEVRAA Federal Contractor, Sherwin-Williams requests state and local employment services delivery systems to provide priority referral of Protected Veterans.
Please be aware, Sherwin-Williams recruiting team members will never request a candidate to provide a payment, ask for financial information, or sensitive personal information like national identification numbers, date of birth, or bank account numbers during the application process.
• Contribute to the assessment, development, reformulation, quality, maintenance, and enhancement of products through planning, executing, and analysis of experiments with clear and accurate results.
• Accountable for the solutions to technical problems: product or process related.
• Demonstrate significant knowledge and use of chemicals, raw materials, substrates, and instruments used in coatings.
• Ability to complete individual work on simple projects with no direction.
• Accountable for providing timely and accurate solutions to problems of simple-to-moderate complexity.
• This position will develop towards “expert” status in at least one Ecoat technology.
• Adhere to company safety guidelines at all times.
• Project Management to create project timelines and meet required deadlines.
• Provide clear, accurate and timely project progress updates to stakeholders.
• Accountable to develop reports that entail project processes, results, and conclusions.
• Ability to complete projects and daily responsibilities in a timely manner.
• Travel for customer support (product trials and customer line trouble shooting).
• Train and mentor new or lower-level chemists and technicians.
• Participate in paint training sessions for our tech-service as well as customers.
• Monitor customers tank specifications, alert the team of any issues, generate data to support corrective actions with lab work, and compile an action plan for our customers.
BASIC QUALIFICATIONS
• Must be legally authorized to work in the country for which you are applying for employment (without now or in the future needing sponsorship for employment work visa and/or permanent residence status).
• Bachelor's degree in a Science, Technology, Engineering or Math field.
• 3 years of coatings-specific industry experience
• Must be proficient in Microsoft Office (Excel, Word, Power Point)
PREFERRED QUALIFICATIONS
• 5+ years Waterborne or Electrodeposition coatings formulation experience within the industrial coatings market
• Understanding of 1K and 2K Solvent and waterborne coating formulation
• Design for Six Sigma (DFSS)
• Design of Experiment
Travel Requirements: Up to 40%
This position is not eligible for sponsorship for work authorization now or in the future, including conversion to H-1B visa.
Principal Scientist
Associate scientist job in Waterloo, IA
Our pharmaceutical client is seeking a Principal Scientist who will be responsible for evaluating and interpreting analytical results, as well as developing, validating, and transferring analytical methods for APIs, intermediates, and raw materials. If you are someone who wants to be apart of a highly technical environment with a lot of growth, this role may be the one for you!
Responsibilities:
Safely and effectively develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products
Actively participate in teams assembled to investigate and solve analytical technical issues within Analytical Development, Chemical Development, Process Support Group and Quality Control.
Perform analytical chemistry assays based on new and existing methodologies
Operate analytical instrumentation such as HPLC, GC, GC/MS, FTIR, Titrator, Particle Size Analyzer
Write technical reports to document analytical methods
Maintain laboratory notebooks documenting work
Maintain compliance with GMP SOPs and DEA regulations
Transfer documented analytical methods to the QC and Process Support Group departments
Set up new or existing analytical methods for compound identification, purity and potency testing.
Coordinate off-site testing as necessary
Conduct testing of analytical samples for the Chemical Development Department as needed.
Qualify reference materials.
May also perform other duties as required.
Qualifications:
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.
Molecular Biologist
Associate scientist job in Rochester, MN
At my client's cutting-edge biotech organization, innovation fuels discovery in the cell, gene, and virus therapy space. This is your chance to join a collaborative team working to transform scientific breakthroughs into life-saving treatments. You'll help define the molecular backbone of tomorrow's medicines-impacting the future of cancer and rare disease therapies.
Why You Should Apply
Join a mission-driven team accelerating the next generation of cell and gene therapies
Hands-on innovation with viral vectors, CRISPR tools, and molecular assay design
Work in a collaborative, PhD-led environment that values discovery and scientific integrity
Comprehensive benefits including health, dental, vision, life insurance, PTO, and employer-matched IRA
What You'll Be Doing
Design, develop, and optimize molecular assays to support gene and cell therapy programs
Perform advanced PCR (qPCR, dPCR), cloning, and NGS-based analyses
Conduct CRISPR-based screening and vector validation projects
Interpret data, generate technical reports, and present findings to cross-functional teams
Support assay development and QC testing within a dynamic, discovery-focused lab
About You
Strong expertise in molecular biology, including qPCR/dPCR and NGS workflows
Comfortable with CRISPR systems and viral vector design
Adept at bioinformatics and data interpretation for molecular assays
Thrive in a fast-paced, collaborative environment focused on innovation
How To Apply
We'd love to see your resume, but we don't need it to have a conversation. Send us an email to ************************* and tell me why you're interested. Or, feel free to email your resume. Please include Job#19593.
Food Scientist- New Product Development
Associate scientist job in West Liberty, IA
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
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor
Senior Food Scientist
Associate scientist job in Monticello, MN
The Senior Food Scientist will lead technical projects that support Karlsburger Foods' strategic business goals, including new product development, product optimization, cost savings, quality improvement, and troubleshooting. This role will focus on a range of product forms including dry powders, broths concentrate, stocks concentrate, sauces, and gravies. The ideal candidate is a self-starter with deep experience in savory product development and commercialization, especially in powdered and concentrated formats.
Essential Functions and Responsibilities:
Lead new product development projects with emphasis on dry powders, soup/broth bases, and seasoning blends.
Optimize existing powdered, liquid and paste products for quality, shelf-life, and cost.
Execute plant trials, product validations, and troubleshooting in both dry and wet processing environments.
Maintain accurate and detailed technical documentation, including formulations, batching instructions, and product specifications.
Participate in sensory panels and lead evaluations for taste, appearance, and texture.
Serve as a technical resource for powder blending, ingredient functionality, and processing parameters to operations and sales.
Partner with supply chain, operations, and procurement to support scale-up and identify alternative ingredients.
Apply food science principles to support sensory performance and commercializability.
Ensure formulations meet food safety, regulatory, and labeling requirements.
Manage multiple projects concurrently, delivering on time and within scope.
Other Duties and Responsibilities:
Contribute to ideation and concept development for new powdered and liquid product formats.
Collaborate with culinary, QA, and sales teams to align technical execution with customer needs.
Mentor junior scientists and support continuous improvement in lab and pilot operations.
Required Qualifications:
Bachelor's degree in food science or a related field (Master's preferred).
9-10 years of food product development experience, with at least 3+ years focused on powdered food systems and or food bases.
Proven track record leading projects from benchtop through commercialization.
Strong formulation and process development skills, especially with food bases and/or powders.
Hands-on experience in pilot and manufacturing environments.
Strong communication, organization, and leadership skills.
Self-starter who takes initiative, works well cross-functionally, and thrives in a fast-paced setting.
Tools and Technology:
Microsoft Office Suite (Excel, Outlook, Word, PowerPoint).
Specification and PLM systems.
Lab and pilot-scale powder blending equipment.
Moisture analyzers, sieves, and sensory evaluation tools.
Preferred Qualifications:
Experience with savory product building blocks including bases, bouillons, seasonings, and dry mixes.
Knowledge of powder flow, agglomeration, and moisture control in dry blends.
Familiarity with aseptic, retort, and spray drying processes.
Experience collaborating with chefs or other culinary professionals.
Experience with GMP, HACCP, SQF, and FDA labeling standards.
Experience with products requiring Organic, Kosher, NON GMO, GAP certifications.
Physical Requirements:
Stand and work at lab bench or pilot area for extended periods.
Use hands to operate blending and lab equipment.
Lift and carry containers of powder ingredients (up to 25 lbs.).
Occasional travel to support trials or customer meetings (up to 20%).
Associate Scientist
Associate scientist job in Brookings, SD
RTI is a leading biomedical contract research organization, providing global clients in both animal health and human health, biopharma, and advanced feed/nutrition industries with premier quality services and product development support.
Job Purpose
The Associate Scientist will perform laboratory assays, maintain laboratory equipment, assist with facility maintenance and completion of testing for submitted samples.
Responsibilities
Perform laboratory assays according to Standard Operating Procedures, or other standard methodologies such as FDA BAM, in areas including but not limited to, bacteriology, virology, mycology, and immunology.
Document laboratory work in accordance with RTI Lab's Standard Operating Procedures on appropriate forms and report out results and/or author reports.
Assist with and at times manage laboratory projects, research and order supplies and equipment, and help lab team meet project deadlines.
Ensure diagnostic laboratory processes maintain compliance with ISO 17025 requirements and complete record keeping in compliance with RTI Lab's Standard Operating Procedures.
Train to perform daily tests processes such as media preparation, sample processing, VIs, SNs, and ELISA
Perform Equipment and facility maintenance, equipment calibration/verification, laboratory cleaning, and other general laboratory inventories
Maintain, and perform QC for, RTI Lab's stock cells, viruses, and/or bacteria. Assist in maintaining RTI Lab's stock of monoclonal antibodies (MABs) and pulmonary alveolar macrophages (PAMs)
Document work accurately, appropriately and make timely corrections to errors. Assist with internal review of laboratory data
Maintain competency in diagnostic lab processes and cross train on other laboratory procedures.
Maintain training record, review, and assist with SOP (Standard Operating Procedures) revisions, and/or writing of new SOP's and perform literature reviews.
Qualification, Training, and Experience Requirements
Undergraduate degree in biological sciences or equivalent required and 0-4 years of experience, or
Graduate degree and 0-2 years' relevant experience and demonstration of competency in job role-specific requirements
Associate Scientist
Associate scientist job in Minneapolis, MN
Job Description
:
Claros Technologies is a venture backed, deep-tech company solving the worldwide challenge of destroying PFAS in the environment. PFAS remediation is rapidly becoming a multi-billion-dollar, global market and is at the center of regulatory action in the US, Europe and Asia that requires the removal of this carcinogen from drinking water, industrial processes and waste sites. Claros has developed a patented, scalable destruction technology proven to fully destroy 99.99% of PFAS in customers' samples.
We are a diverse team of scientists, business-builders, and impact leaders committed to solving problems without creating new ones. The company has just closed a $20M financing round with leading environment venture capital firms, which provides the credibility and resources required to convert current pilot users into full scale commercial customers as well as to sell easy-to-identify prospects across the globe.
If you are a mission driven, highly motivated, positively aggressive scienist, join us as we solve one of the greatest environmental challenges of our time.
Position Overview:
The Associate Scientist will work closely with the technological development team focused on industrial PFAS wastewater treatment on the lab scale. The duty of this position includes the evaluation of our destruction system performance on customer-specific wastewater and the fundamental exploration of reaction chemistry. The Associate Scientist will also assist in processing data, preparing customer reports, and patent e. The selected candidate will receive thorough training in experimental procedures and data presentation techniques.
Essential Job Functions:
Become the expert on the operation of Claros PFAS destruction technology
Evaluate and execute adjustments as necessary to Claros solutions to ensure the technology meets customer specifications
Complete experiments in aid of customer proposals, implementations, and continued operation of Claros PFAS destruction technology
Partner with internal stakeholders to ensure the successful implementation and operation of Claros solutions
Perform experiments independently with occasional guidance from senior team members
Keep a clean and safe workplace both inside and outside of the laboratory
Competencies & Skills:
Adequate knowledge of water/wastewater treatment processes
Strong background in water chemistry
An eagerness to learn new skills and acquire new knowledge in the field of water treatment
Strong writing skills
Excellent teamwork skills, with a collaborative spirit and the ability to work effectively in a diverse team environment
Management of multiple projects timelines/tasks
Preferred Experience:
Bachelor's or master's degree in environmental engineering/chemical engineering/chemistry/atomic physics or a related field
1-2 years experience working with wastewater treatments, preferably with PFAS (inclusive of academic experience)
Attention to detail
Job Specifications
Compensation: $62,000 - $72,000
Location: In person at the Claros Headquarters in Minneapolis, Minnesota.
Travel: none
Claros Technologies offers attractive salary and benefits including health, vision, and dental insurance, PTO as well as 401k plans and options.
For more information, please visit ******************
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Integrated Photonics R&D Scientist
Associate scientist job in Plymouth, MN
The future is what you make it. When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers and doers who make the things that make the future. That means changing the way we fly, fueling jets in an eco-friendly way, keeping buildings smart and safe and even making it possible to breathe on Mars. Working at Honeywell isn't just about developing cool things. That's why all of our employees enjoy access to dynamic career opportunities across different fields and industries.
Are you ready to help us make the future?
Honeywell's Advanced and Applied Technology organization is seeking an exceptional Photonics Research Scientist to join our Advanced Sensing Technology group. In this role, you'll have the unique opportunity to explore new paradigm-changing technologies that could shape future products for the Aerospace industry. In this position you will develop resonant Fiber Optic Gyroscopes, and support a wide variety of other projects and programs which evolve and grow to meet the evolving needs of our customers and sponsors
As an Integrated Photonics Scientist here at Honeywell, you will be at the forefront of innovation, driving the advancement of cutting-edge technologies and solutions, ensuring that Honeywell remains a leader in technological advancements. In this role, you will impact the future of Aerospace technologies by contributing to the ideation, conceptualization, research, and development of innovative new solutions.
* Work as part of our team of scientists and engineers to develop advanced Sensor technologies and then demonstrate them for mission critical systems.
* Engage with customers and partners to define their needs and requirements, then apply your skills to find creative solutions through rigorous analysis, engineering, and experimentation.
* Effectively communicate your ideas and results to research sponsors, scientific peers, and business leadership, through effective presentations, publications, and the writing of proposals.
* Develop new concepts, write proposals, and create and test hardware prototypes.
YOU MUST HAVE
* Master's Degree
* R&D experience or academic research experience in one of the following areas:
* Optics
* Atomic physics
* Inertial sensors
* Precision measurement
WE VALUE
* Ph.D. degree in Electrical Engineering, Physics, Applied Physics, Optical Engineering, or equivalent
* Demonstrated expertise in 2 or more of the fields below and/or skills within the last 4 years:
* Optical Sensing
* Fiber and guided wave optics
* Signal processing and feedback
* Data Collection and analysis
* Enthusiasm for learning about new technologies and engaging difficult technical problems
* Excellent written and communication skills
* Track record of innovation and ability to solve complex problems through analysis and innovation
* Ability to manage and understand complex customer requirements and manage stakeholders
U.S. PERSON REQUIREMENTS
Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status or have the ability to obtain an export authorization.
BENEFITS OF WORKING FOR HONEYWELL
In addition to a competitive, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays .For more Honeywell Benefits information visit: *******************************
The annual base salary range for this position is $134,000 - $167,000. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations.
The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Job Posting Date: Oct 28th, 2025
Scientist I
Associate scientist job in Saint Paul, MN
We are looking for a motivated Scientist to join our client's team. In this role, you will apply your scientific training to support product development, manufacturing, and quality testing in a fast-paced, GMP-regulated laboratory environment.
Perform wet chemistry testing of incoming chemicals and raw materials following USP methodologies.
Operate and maintain analytical instrumentation, including HPLC, UPLC, GC, FT-IR, ICP, DSC, and TGA, in a high-throughput environment.
Execute routine and non-routine laboratory tests according to written procedures and GMP standards.
Analyze, interpret, and report results through LabVantage LIMS, ensuring accuracy and compliance.
Conduct daily and monthly laboratory maintenance, verification, and inventory management.
Collaborate with senior scientists to develop and validate analytical methods.
Communicate effectively across teams, providing clear updates and technical insights.
Expand technical expertise in analytical techniques and troubleshooting.
Cross-train on additional methods and instrumentation as needed.
Requirements
Bachelor's degree in Chemistry or related scientific discipline with 1-3 years of laboratory experience, or a Master's degree with 0-2 years of relevant experience.
Strong foundation in wet chemistry and familiarity with analytical instrumentation.
Experience working in GMP or other regulated laboratory environments.
Skilled in documentation practices, electronic/paper notebooks, and data integrity standards.
Proficient in MS Office, especially Excel, with ability to perform statistical/data analysis.
Excellent problem-solving skills, attention to detail, and ability to thrive in a dynamic, fast-moving environment.
Advanced R&D Quantum & Optical Scientist
Associate scientist job in Plymouth, MN
The future is what you make it.
When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers and doers who make the things that make the future. That means changing the way we fly, fueling jets in an eco-friendly way, keeping buildings smart and safe and even making it possible to breathe on Mars. Working at Honeywell isn't just about developing cool things. That's why all of our employees enjoy access to dynamic career opportunities across different fields and industries.
Are you ready to help us make the future?
Honeywell's Advanced and Applied Technology organization is seeking an exceptional Atomic, Molecular, and Optical (AMO) experimentalist to join our Advanced Sensing Technology group located in Plymouth, Minnesota. We are a team of scientists and engineers translating today's research into tomorrow's sensors for air and space applications.
We are currently developing and deploying such cutting-edge technology as: ultra-stable inertial sensors based on atom interferometry, precision timing references based on laser cooled atoms, compact magnetometers based on NV diamond, and ultra-wideband electromagnetic sensors based on Rydberg atoms, among a wide variety of other projects and programs which evolves and grows to meet the evolving needs of our customers and sponsors.
YOU MUST HAVE
Ph.D. in physics, applied physics
Research experience in one or more of the following areas:
Experimental Atomic, Molecular, and Optical (AMO) Physics
Atomic Sensors
Atomic Clocks
Precision Measurement
Atom Interferometry
Track record of solving difficult, complex problems through innovation, analysis, engineering, and experimentation.
Excellent written and oral communication skills reflected in a record of published results and public presentations in your field of research.
WE VALUE
Hardware experience with some of the following is of value:
Laser systems including diode lasers and ultra-stable optical cavities.
Microwave frequency (>6 GHZ) test and measurement equipment.
UHV (
Fiber optic components
Analog and digital circuitry
Integrated photonics
Software experience with any of the following is of value:
COMSOL or other multiphysics simulation software
LabView or other experimental control software
BENEFITS OF WORKING FOR HONEYWELL
In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information visit: Benefits at Honeywell
The annual base salary range for this position is $115,000 - $144,000. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations.
The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Job Posting Date: Oct 10, 2025.
Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status or have the ability to obtain an export authorization.
Work as part of our team of scientists and engineers to develop new atomic sensor technology concepts, and then demonstrate them in practical devices.
Engage with customers and partners to define their needs and requirements, then apply your skills to find creative solutions through rigorous analysis, engineering, and experimentation.
Effectively communicate your ideas and results to research sponsors, scientific peers, and business leadership, through effective presentations, publications, and the writing of proposals.
Use your expertise to spur the growth of our technology portfolio in new directions, shaping the future of sensing technology.
As an Advanced R&D Quantum & Optical Scientist here at Honeywell, you will be at the forefront of innovation, driving the advancement of cutting-edge technologies and solutions, ensuring that Honeywell remains a leader in technological advancements. In this role, you will impact the future of Honeywell Sensing technologies by contributing to the ideation, conceptualization, research, and development of innovative new solutions.
Auto-ApplyScientist/ Associate Scientist of Laboratory Automation
Associate scientist job in Lincoln, NE
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion is hiring a Scientist/ Associate Scientist of Laboratory Automation to join our Lincoln, NE Bioanalytical team. This role will work onsite daily with our Hamilton, Tecan and Sciclone instruments.
In this role, you will perform research and/or development in collaboration with scientific teams and automated systems based on new and existing methodologies. This hands-on role focuses on programming and operating laboratory automation systems with the objective of becoming the subject matter expert for all laboratory automation technologies within our organization.Essential Functions:
Operate and program software for automated liquid handling and instrument tending laboratory robots
Collaborate with Scientists to translate scientific protocol requirements into application software
Develop and validate automated methods according to established standards
Prepare and review comprehensive documentation for method validation protocols and reports
Troubleshoot method and equipment-related issues with a systematic approach
Perform scheduled and preventative maintenance on all automation equipment
Maintain proficient knowledge of all automation equipment within the laboratory
Process samples both manually and using automation to support client timelines
Ensure compliance with applicable GLPs/GMPs, SOPs, policies, safety and regulatory requirements
Utilize computer programs efficiently to perform daily functions
Work collaboratively in a team environment while maintaining professional communication
Manage independent projects with minimal supervision
Provide training and mentorship to colleagues on automation systems
Qualifications:
Education: Minimum of an Associate's degree in science or engineering-related field with 2 years of industry experience, or a Bachelor's degree with 1 year of industry experience
Experience: 1 or more years of Laboratory and/or GLP knowledge preferred
Technical Skills: Previous experience with automated systems (Hamilton, Tecan, Sciclone, etc.) preferred
Computer Proficiency: Strong skills in relevant software applications
Communication: Excellent oral and written communication abilities
Work Style: Demonstrated ability to work both independently and as part of a collaborative team
Work Location: Works onsite in Lincoln, NE daily, with the ability to travel occasionally for training
Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Auto-ApplyNew Product Development Scientist
Associate scientist job in Owatonna, MN
Job Title: New Product Development Scientist Location: Owatonna, MN Summary This position will be based out of Owatonna, MN manufacturing plant reporting to the Technical Director. NPD Scientist is responsible for overseeing and executing product development activities and providing technical support to internal and external stakeholders related to the Duraco Specialty Tapes & Liners business. This includes recommending, planning, prioritizing, and conducting experimental lab work, product prototyping and optimization, product testing, literature research, as well as data gathering, processing, and reporting. NPD Scientist will also be responsible for maintaining relationships with key suppliers, new raw material qualifications, supporting secondary raw material qualifications, cost savings efforts, and working closely with other functional teams on NPD trial, scale-up, and new product commercialization activities. Responsibilities
Oversee and execute development and technical support for Duraco Specialty Tapes & Liners New Product Development (NPD) pipeline, with ability to deliver minimum 5 product launches per year
Conduct required laboratory experimentation and testing, provide leadership in Silicone release coating formulation development, new release liner prototyping, materials design, process optimization, and product testing that aligns with Duraco Specialty Tapes & Liners site capabilities and strategic initiatives
Provide technical assistance in related regulatory compliance matters related to Silicone release coatings and liner products
Engage and collaborate with customers as well as Marketing and Sales Teams to identify key development opportunities and appropriately prioritize projects and initiatives
Strong collaboration with Production, Quality, and other functional teams to ensure efficient product development, scale-up, performance optimization, consistent quality, and successful commercialization
Establishing and cultivating relationships with suppliers of key raw materials
Provide technical leadership in support of cost-savings initiatives including, but not limited to, alternate raw material identification, insource/outsource decisions, and Silicone release coating formulation enhancements for increased throughput and efficiencies
Provide timely data processing, organizing, and reporting to superiors and functional teams, including generating and sharing ideas for NPD projects and opportunities
Proactively identify and implement best safety practices in both laboratory and manufacturing settings
Enhance NPD and Project Management processes and establishing improved IP protection practices
Other duties as assigned
Personal Attributes:
Results driven and able to focus on, prioritize, and execute individual activities
Curious and eager to learn - enjoys leveraging new knowledge to enhance current Silicone release coating chemistries, release liner constructions, and products
Excellent written and verbal communication skills
Excellent laboratory and analytical skills including FTIR, XRF, and basic Release Liner testing
Comfortable working in a high-pace manufacturing and laboratory environments, and navigating changing priorities
Effective in engaging and collaborating with cross-functional teams, including production floor supervisors, operators and QC technicians
Outstanding personal integrity and ethics
Understands and easily connects products, technologies, and capabilities across a diverse portfolio of customers and markets
Demonstrated ability to work across different systems and adapt to new processes
Strong planning and organizational skills and high degree of comfort working in and around production / manufacturing settings
Qualifications: Required Skills, Education, and Experience
BS or MS in a Technical field; preferably Chemistry, Polymer Science, Chemical Engineering, Material Science, or Plastics Engineering with excellent hands-on lab experience
3-5 Years of proven track record of developing new Silicone release coating formulations and paper and film release liner products
Understanding and experience with PSAs and PSTC testing methods is desired to help complement release liner and Silicone coating formulation development
Experience with development methodologies including project management, stage-gate, ideation, Design of Experiments (DOE), IP management, and literature and patent research
Good knowledge of additives, formulation processing, applications, and analytical test methods as they relate to the development of Si release coating formulations
Experience in Silicone release coating and web handling processes is highly desirable
Knowledge of Microsoft Office products with advanced experience in Excel and analytics programs (e.g., Minitab, JMP, etc.)
Travel
Must be able to travel within the US
10-15% Domestic Travel
The job description is not an exhaustive listing of all responsibilities and may be revised at any time.
R&D Post License Scientist
Associate scientist job in Brookings, SD
Job Description
At Medgene Labs, we are advancing animal health through science, innovation, and dedication. Based in Brookings, South Dakota, our team is proud to develop and deliver next-generation vaccines that protect animal populations and support producers across the country. With a passion for discovery and a commitment to excellence, we are shaping the future of animal health one breakthrough at a time.
Our work is guided by five core values that define who we are and how we work:
Safety - We prioritize a safe environment for our people, partners, and the animals we serve.
Quality - We hold ourselves to the highest standards to ensure the reliability and impact of our products.
Respect - We value our people and their diverse contributions, treating every team member with dignity and fairness.
Transparency - We build trust through open communication and shared accountability.
Innovation - We constantly seek new and better ways to solve challenges and deliver value.
If you're looking to join a collaborative, mission-driven team that's making a real difference in animal health and beyond, we'd love to hear from you.
POSITION SUMMARY
A Research and Development (R&D) Post License Scientist (level dependent on experience) will be responsible for performing experiments and tasks in support of R&D projects involving vaccine research for various diseases in multiple species to address customers' needs. In particular, the scientist will be responsible for conducting, modifying, and developing immunological assays, as well as supporting other teams within R&D and throughout the company. The position requires the ability to perform detail-oriented work, trouble-shoot effectively, ability to review literature and adapt both methodology and scientific principles and successfully integrate within a strong R&D team. The scientist will report to the R&D Post License Manager and will not have direct reports.
JOB DUTIES
Perform in both an individual and team setting
Process clinical samples according to protocol with a high level of detail/accuracy
Perform laboratory experiments according to a written method (with supervision level commensurate with experience)
Design and execute experiments (with supervision level commensurate with experience)
Perform data analysis, troubleshooting, data presentation, and discussion
Perform basic microscopy
Ability to learn and utilize software for set tasks including but not limited to Smartsheet, Compass, SoftMax, Gen5
Treat experiments and data witha high level of integrity and ethics
Able to follow detailed instructions, scientific protocols, and Standard Operating Procedures
Strong understanding and application of aseptic technique, biosafety level requirements, and strong adherence to biosecurity practices
Keep laboratory documents and logs as needed, following ALCOA+ principles
Maintain quality control checks and a safe environment in compliance with all governmental and laboratory policies, rules, regulations, and codes
Trains other scientists as appropriate for their knowledge and skill level
Performs routine laboratory maintenance and upkeep, including cleaning glassware, autoclaving, waste disposal, and equipment maintenance/monitoring as necessary
Performs literature searches to bring in new techniques or improve current assays
Coordinates with various teams within R&D as well as teams external to R&D
Perform other duties as needed
MINIMUM QUALIFICATIONS:
An associate degree will be considered; however, a bachelor's degree from an accredited university in microbiology, virology, molecular biology, or a related field is preferred.
Knowledge of:
General laboratory principles and equipment
Biosafety (BSL1 / BSL2) and biosecurity practices
Immunological methods and techniques involving both live and inactivated cultures
Cell culture methods, including cryopreservation.
Viral propagation techniques and identification
Bacterial propagation techniques and identification
Microsoft Word and Excel computer skills
Ability to:
Perform various cell culture growth methods, tests, and analyses.
Follow detailed directions and instructions.
Work safely with dangerous and contagious materials and specimens.
Operate general lab equipment and computers.
Perform mathematical computations.
Interpret subject matter.
Establish and maintain effective working relationships with others.
Perform various tests and adapt techniques as required.
Maintain accurate and up-to-date laboratory notebook records.
Communicate information clearly and concisely.
Please note that submission of an application does not guarantee employment. As part of our hiring process, Medgene reserves the right to conduct background investigations, which may include verification of education, past employment, and professional references, as well as criminal history checks where permitted by law. Background checks will be conducted when deemed necessary and appropriate for the role being considered, and any such inquiries will be handled in accordance with all applicable federal, state, and local laws. A criminal conviction does not automatically disqualify a candidate from employment consideration. Each situation will be evaluated on a case-by-case basis, considering the nature of the offense, its relevance to the role, and the time that has passed since the conviction. By submitting an application, you acknowledge that the information provided is accurate to the best of your knowledge and understand that falsification of information may result in removal from the hiring process or termination if already employed.
Job Posted by ApplicantPro
Scientist - Virology
Associate scientist job in Lincoln, NE
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you're looking for a rewarding career, apply with us today!
Job Description
Maintenance of mammalian cell culture stocks to support process development experiments.
Perform viral infection experiments in a BSL-2 setting with veterinary pathogens.
Support the set-up and running of bioreactors including single-use and glass.
Use of automated robotic equipment including Biomeks and Multimeks.
Maintain a research laboratory notebook to document all lab-based work, write basic study reports and delivery memos and assist process team members with more complicated report writing.
Order and stock laboratory equipment and supplies for the Virology laboratory.
Work with multiple scientists within the group to effectively schedule work.
Requires minimal supervision or guidance in technical work.
Understand techniques and instrumentation enough to explain to another in informal or formal training.
Understand technical aspects enough to perform non-routine work with moderate guidance from supervision or others.
Perform high quality non-routine work.
Qualifications
Bachelor's Degree with course work and laboratory experience in biology, biochemistry, microbiology or related disciplines.
Training in aseptic techniques and cell culture.
Familiarity in working with BL-2 pathogens and the use of appropriate PPE.
Highly computer literate. Capable of quickly learning and adapting to new computer programs.
Excellent oral and written communication skills required.
Other Computer skills required: Microsoft Word, Excel, Powerpoint and Outlook.
Capable of interpreting and carrying-out experimental design and protocols.
Individual must have good organizational skills and attention to detail. Individual should be highly motivated, must be a team player, and capable of working with minimal oversight in a cross-functional environment
Authorization to work in the US unrestricted and without sponsorship
Candidates currently living in a commutable distance to Lincoln, NE are encouraged to apply.
Additional Information
Position is Monday-Friday, 8:00 AM - 5:00 PM.
What We Offer:
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Scientist - Virology
Associate scientist job in Lincoln, NE
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you're looking for a rewarding career, apply with us today!
Job Description
Maintenance of mammalian cell culture stocks to support process development experiments.
Perform viral infection experiments in a BSL-2 setting with veterinary pathogens.
Support the set-up and running of bioreactors including single-use and glass.
Use of automated robotic equipment including Biomeks and Multimeks.
Maintain a research laboratory notebook to document all lab-based work, write basic study reports and delivery memos and assist process team members with more complicated report writing.
Order and stock laboratory equipment and supplies for the Virology laboratory.
Work with multiple scientists within the group to effectively schedule work.
Requires minimal supervision or guidance in technical work.
Understand techniques and instrumentation enough to explain to another in informal or formal training.
Understand technical aspects enough to perform non-routine work with moderate guidance from supervision or others.
Perform high quality non-routine work.
Qualifications
Bachelor's Degree with course work and laboratory experience in biology, biochemistry, microbiology or related disciplines.
Training in aseptic techniques and cell culture.
Familiarity in working with BL-2 pathogens and the use of appropriate PPE.
Highly computer literate. Capable of quickly learning and adapting to new computer programs.
Excellent oral and written communication skills required.
Other Computer skills required: Microsoft Word, Excel, Powerpoint and Outlook.
Capable of interpreting and carrying-out experimental design and protocols.
Individual must have good organizational skills and attention to detail. Individual should be highly motivated, must be a team player, and capable of working with minimal oversight in a cross-functional environment
Authorization to work in the US unrestricted and without sponsorship
Candidates currently living in a commutable distance to Lincoln, NE are encouraged to apply.
Additional Information
Position is Monday-Friday, 8:00 AM - 5:00 PM.
What We Offer:
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
R&D Scientist I
Associate scientist job in Stillwater, MN
Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world.
Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist."
Why Join Diasorin?
* Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.
* Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.
Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.
Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!
Job Scope
Conduct, analyze and document experiments for the development and validation of automated immunodiagnostic assays as part of a project team under direction of a Project Leader.
Key Duties and Responsibilities
* Support new and current diagnostic product lines.
* Successfully complete complex research work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process studies, research investigations, and report preparation.
* Summarize, analyze and draw conclusions from complex test results
* Conduct experiments for the development of immunodiagnostic assays
* Contribute to multiple product development projects
* Maintain accurate and complete records through computer systems and laboratory notebooks according to QSR/ISO requirements
* Conduct work according to Good Manufacturing Practices and Safety Procedures
* Provide analysis and reporting of data and results using Microsoft Excel, Word and PowerPoint.
* Maintain laboratory equipment.
Education, Experience, and Qualifications
* Bachelor's degree in Biology, Chemistry, Biochemistry, Chemical Engineering or related discipline.
* 1 year of Experience working in an academic, government or industrial life sciences laboratory setting
* Experience in the development of immunodiagnostic assays preferred
* Experience working in the medical device/diagnostics industry preferred
* Understanding of immunology, gastroenterology, infectious disease, endocrinology, protein chemistry, laboratory automation, or ELISA-based assays
* Ability to execute experiments related to the development of immunodiagnostic products
* Self-motivation with a passion for solving problems.
What we offer
Receive a competitive salary and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world.
This position is $60,000 - $70,000 . The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance.
Diasorin 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.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.
Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation.
The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements.
Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations.
Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations.
This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.
IVF Embryologist
Associate scientist job in Hull, IA
Trans Ova Genetics is seeking a full-time IVF Embryologist to join their team in Hull, IA! As an IVF Embryologist, you will be responsible for a crucial and valuable component of our Advanced Reproductive Technology (ART) toolbox. This role will allow for a team member to become specialized in embryo evaluation, grading, & freezing, and other laboratory procedures within the IVF lab. Data entry, excellent communication, and teamwork are also vital aspects this role.
Our ideal candidate would be passionate about laboratory procedures, client satisfaction, and, of course, embryos! Trans Ova Genetics provides in-depth training that provides a solid foundation prior to supporting client production and would require eight-twelve weeks at our training facility, which is critical to the success of this role.
Key Responsibilities:
Embryo stripping.
Embryo evaluation, grading and freezing.
Fertilization and culture plate preparation.
Semen handling and preparation for IVF.
Recordkeeping/Data Entry.
Embryology training.
Quality Control.
Maintain good laboratory technique and follow lab protocols.
Follow Trans Ova's policies and procedures.
Maintain a professional image reflective of Trans Ova's industry position.
Other duties as assigned by supervisor.
Education Requirements:
B.S. in Agriculture, Animal Science, Biology or a related field; or a Veterinary Technician degree.
Physical Requirements/Working Conditions:
Ability to sit for long periods of time behind a microscope, in a clean lab setting. Ability to work under a laminar flow hood. Good hand-eye coordination. Handling dexterity is required for manipulation of equipment and small objects. Ability to lift up to 30 lbs. Specific vision abilities required by this job include close, distance, and peripheral vision, color/pattern recognition, depth perception, and ability to adjust to focus. Ability to work with liquid nitrogen. Some travel may be required.
Other skills/experience:
Strong attention to detail and organization.
Auto-ApplyAssociate Scientist - Diagnostics
Associate scientist job in Worthington, MN
Associate Scientist - Diagnostics
Vaxxinova US is seeking an individual to join our team as an Associate Scientist - Diagnostics in Worthington, Minnesota.
At Vaxxinova US, you'll be part of a passionate team dedicated to making a difference. We offer competitive pay and benefits, opportunities for growth, and a supportive work culture.
About the role
The Associate Scientist, reporting to the Diagnostic Team Leader, is responsible for assisting and supporting; cell culture, virus isolation, bacteriology, PCR and Sequencing, in the preparation of isolates for autogenous vaccine production, within the guidelines set by regulatory agencies.
Main Responsibilities:
Work under minimal supervision to assist with projects while maintaining a high level of process clarity with direct management
Follow SOPS in an efficient and accurate manner
Initiate and maintain continuous cell lines for use in virus isolation
Produce primary cells for virus isolation
Develop, perform, and optimize fluorescent antibody detection
Perform viral and bacterial antigen isolation for use in autogenous products
Receive and accession bacterial and viral clinical samples into LIMS
Maintain updates in LIMS on status of viral and bacterial samples
Assist in molecular laboratories as needed.
Clean and maintain the aseptic environment; maintain cleanliness of facilities
Assist with necessary documentation, ensuring accurate and complete information
Maintain inventory of laboratory consumables and clinical samples
Assist in investigation of laboratory error to identify root cause and prevent repeated errors
Assist other departments as requested and complete other duties as assigned
Qualifications and Capabilities:
Hands on experience in basic cell culture, virology, and/or bacteriology. Experience in virology and bacteriology preferred.
Understanding of molecular techniques
Familiar with the principles of veterinary microbiology
Proficient in cell culture, viral propagation and titration Bacterial isolation and propagation
Proficient in bacterial isolation, identification, and propagation.
Attention to detail
Strong organizational and time management skills
Good laboratory practices; aseptic techniques
Communications skills to effectively work with teams and across departments
Ability to follow department written SOP's (Standard Operating Procedure)
Ability to read, write, comprehend, and follow verbal & written instructions in English
Ability to stand on feet for long periods of time; bending, twisting, and preforming fine motor manipulations required
Ability to lift 50 lbs.
Familiarity with regulatory agencies including the USDA/CVB, C-CVB, VICH, OSHA, Federal, State, and Local Agencies is a plus
Experience/Educational Requirements:
Associate's degree in microbiology, virology or related field and 7+ years of relevant work experience, or
Bachelor's degree in microbiology, virology or related field and 5+ years of relevant work experience
Benefits at Vaxxinova:
We are proud to offer a generous benefit package in addition to competitive compensation. Our benefits include:
Medical
Dental
Vision
Health Savings Account with company match
401K plan with company match
Paid time off accrual
Holiday pay
Company Shutdown December 25 to December 31
Short- and long-term disability
Company paid life insurance
About Vaxxinova
Vaxxinova provides a wide range of both autogenous and licensed vaccines combined with high-level diagnostic services, supported by strong R&D. Our focus is on livestock including cattle, poultry, swine and aqua. Vaxxinova US, formerly known as Epitopix and Newport Laboratories, is the US operating unit of Vaxxinova International, headquartered in the Netherlands. Vaxxinova US has a strong market presence making autogenous vaccines for cattle, swine, and poultry as well as a state-of-the-art diagnostic laboratory. Vaxxinova currently has facilities in fourteen countries including Brazil, Canada, Chile, Colombia, Croatia, Italy, Germany, Japan, Jordan, Norway, South Africa, Thailand, the USA, and the Netherlands. Vaxxinova is part of the family-owned EW Group, headquartered in Germany. The EW Group specializes in animal genetics, animal nutrition and animal health, operates in over 100 countries and records consistent international growth.
Recruiting Agencies
Vaxxinova US does not accept unsolicited CVs from recruiters or employment agencies in response to job postings on social media or Vaxxinova US websites. Vaxxinova US will not consider or agree to payment of any referral compensation or recruiter fee relating to these unsolicited CVs. Vaxxinova US explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited CVs, including those submitted to hiring managers, are deemed to be the property of Vaxxinova US. Phone calls or emails from recruiters or employment agencies are not appreciated.
Auto-ApplySenior Research Associate 1, Product Development
Associate scientist job in Sioux Falls, SD
The Senior Research Associate 1, PD is responsible for executing experiments, immunoassays, and technical procedures. Working under the supervision of the Manager, this role involves leading the preparation of antigen, vaccine and/or adjuvant formulations, and leading and performing the development, optimization, and qualification of analytical assays. The Senior Research Associate 1, PD will lead research projects, document and interpret research data, write research protocols, SOPs, GR and related documentation and ensure accurate records and reporting of experimental data.
Responsibilities:
· Lead the preparation of antigen, vaccine and/or adjuvant formulations according to project requirements as needed.
· Lead and perform the development, optimization, and/or qualification of analytical assays.
· Lead and perform routine laboratory assays, including ELISAs, cell-based assays, serological assays, and bioassays according to established protocols.
• Write and document research protocols, SOPs, GR and other related documentation.
• Lead the preparation of antigen, vaccine and/or adjuvant formulations according to project requirements as needed.
• Collect, evaluate, interpret, and document research data, maintaining Electronic Lab Notebook in accordance with scientific objectives and company principles.
• Responsible for the proper logging, storing, and maintenance of research samples and materials, ensuring accurate records in Electronic Lab Notebook and databases.
· Manage general laboratory operations, including ordering supplies and equipment maintenance.
Requirements:
· M.S. in a relevant field with 0-2 years of experience or a Bachelor's degree with 5+ years of experience in life sciences related field.
· Strong written and verbal communication skills. Writing skills include routine communications and technical reports detailing procedures, outcomes, and observations. Ability to effectively present information in one-on-one, small groups and lab meetings
· Demonstrated proficiency using Microsoft Office applications (Word, Excel, PPT) as well as job related electronic systems/applications.
· Proficient in applying established mathematical and scientific techniques to compile and analyze data.
· Knowledge of laboratory techniques and protocol development, with adherence to Good Laboratory Practice (GLP) standards.
Physical Demands:
While performing the duties of this job, the employee is regularly required to walk, stand and sit. The employee will be able to use the pipettes for long periods at any given time. The employee must regularly lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, peripheral vision, and the ability to adjust focus.
Working Environment and Travel: Normal laboratory working conditions. Business travel is not typical for this position.
ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.
Auto-ApplyJunior Embryologist
Associate scientist job in Minneapolis, MN
Job Description
Come join CCRM Fertility, a global pioneer in fertility treatment, research, science, specializing in IVF, fertility testing, egg freezing, preimplantation genetic testing, third party reproduction and egg donation. As a member of CCRM Fertility's diverse team of professionals, you will be a part of helping families grow and changing lives. We take pride in providing our employees with meaningful employment, a supportive culture, and a well-balanced personal & work life alignment. For more information, visit ***************
Location Address:
Department: Embryology (IVF) Lab
Work Schedule: Monday - Friday and weekends as needed
What We Offer Our Team Members:
Generous Paid time-off (PTO) and paid holidays
Medical, Dental, and Vision Insurance
Health benefits eligible the first day of the month following your start date.
401(k) Plan with Company Match (first of the month following 2 months of service)
Basic & Supplement Life Insurance
Employee Assistance Program (EAP)
Short-Term Disability
Flexible spending including Dependent Care and Commuter benefits.
Health Savings Account
CCRM Paid Family Medical Leave (eligible after 1 year)
Supplemental Options (Critical Illness, Hospital Indemnity, Accident)
Bonus Potential
401(k) Plan with Company Match (first of the month following 2 months of service)
Professional Development, Job Training
The Junior Embryologist plays a crucial role in the field of reproductive medicine, focusing on the development and management of embryos in a clinical setting. This position involves working closely with senior embryologists and medical professionals to ensure the highest standards of care and success rates in assisted reproductive technologies. The primary end result of this role is to contribute to the successful conception and birth of healthy babies, providing hope and support to families. The Junior Embryologist will be responsible for performing laboratory procedures, maintaining equipment, and adhering to strict protocols to ensure the safety and quality of embryonic development. Ultimately, this role is vital in advancing reproductive health and helping individuals achieve their family-building goals.
Minimum Qualifications:
Bachelor's degree in Biology, Biochemistry, or a related field.
Experience in a laboratory setting, preferably in a clinical or reproductive health environment.
Strong attention to detail and ability to follow strict protocols and procedures.
Preferred Qualifications:
Master's degree in Reproductive Biology or a related field.
Familiarity with assisted reproductive technologies and embryology laboratory techniques.
Certification from a recognized professional organization in embryology or reproductive technology.
Responsibilities:
Assist in the preparation and analysis of gametes and embryos for in vitro fertilization (IVF) procedures.
Perform routine laboratory tasks such as media preparation, cryopreservation, and embryo culture.
Maintain accurate records of laboratory procedures and patient information in compliance with regulatory standards.
Collaborate with senior embryologists and medical staff to optimize laboratory protocols and improve patient outcomes.
Participate in quality control measures and contribute to the maintenance of a clean and organized laboratory environment.
Skills:
The required skills for this position include strong analytical abilities and attention to detail, which are essential for accurately performing laboratory procedures and analyzing results. Effective communication skills are also important, as the Junior Embryologist will need to collaborate with a diverse team of medical professionals and provide updates on patient progress. Time management skills are crucial for balancing multiple tasks and ensuring that all laboratory processes are completed efficiently. Preferred skills, such as familiarity with advanced laboratory techniques, will enhance the candidate's ability to contribute to innovative practices within the team. Overall, both required and preferred skills will be utilized daily to ensure the highest quality of care for patients undergoing fertility treatments.
CCRM's Compensation: The salary range represents the national average compensation for this position. The base salary offered will vary based on location, experience, skills, and knowledge. The pay range does not reflect the total compensation package. Our rewards may include an annual bonus, flexible work arrangements, and many other region-specific benefits.
Pre-Employment Requirements: All offers of employment are conditional upon the successful completion of the CCRM Fertility onboarding process, including verification of eligibility and authorization to work in the United States. This employer participates in the E-Verify Program in order to verify the identity and work authorization of all newly hired employees.
Equal Employment/Anti-Discrimination: We are an equal-opportunity employer. In all aspects of employment, including the decision to hire, promote, discipline, or discharge, the choice will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.