Scientist Jobs in Bellefontaine Neighbors, MO

We're a Little Different Our mission is clear. We bring to life a healing ministry through our compassionate care and exceptional service. At Mercy, we believe in careers that match the unique gifts of unique individuals - careers that not only make the most of your skills and talents, but also your heart. Join us and discover why Modern Healthcare Magazine named us in its “Top 100 Places to Work.” Overview: The Senior Clinical Quality Measure Specialist is responsible for the data abstraction/review, submission and validation of clinical quality data obtained from the electronic health record as required by their assignment to CMS, the Joint Commission and/or other state or national registries for public reporting and/or internal reporting. As assigned, the position is responsible for mentoring and teaching new clinical quality measure specialists, leading the learning of new measures and/or projects (pilots, state quality programs, quality improvement or others), and providing expertise for EPIC optimization applying to their measure assignments. Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards. Qualifications: Experience: 5-7 years of healthcare experience. Clinical chart review and abstraction experience required. Preferred experience with Stroke Care/Registry (American Heart Association Get with the Guidelines Stroke and/or The Joint Commission Stroke). Required Education: BA/BS in relevant field or ADN; Master level education adds one additional year towards Senior credit of experience Preferred Licensure: RN Other Skills & Knowledge: Must be analytical, resourceful, and possess excellent problem-solving skills Strong project management skills Computer, Electronic Health Record and Internet experience Familiarity and comfort with MS Office products are essential for success in this position (i.e. Word and Excel - required; PowerPoint - preferred) Ability to work as a team player with excellent communication skills Basic statistical knowledge We Offer Great Benefits: Day-one comprehensive health, vision and dental coverage, PTO, tuition reimbursement and employer-matched retirement funds are just a few of the great benefits offered to eligible co-workers, including those working 32 hours or more per pay period! We're bringing to life a healing ministry through compassionate care. At Mercy, our supportive community will be behind you every step of your day, especially the tough ones. You will have opportunities to pioneer new models of care and transform the health care experience through advanced technology and innovative procedures. We're expanding to help our communities grow. Join us and be a part of it all. What Makes You a Good Match for Mercy? Compassion and professionalism go hand-in-hand with us. Having a positive outlook and a strong sense of advocacy is in perfect step with our mission and vision. We're also collaborative and unafraid to do a little extra to deliver excellent care - that's just part of our commitment. If that sounds like a good fit for you, we encourage you to apply. EEO/AA/Minorities/Females/Disabled/Veterans

Contribute to groundbreaking scientific advancements in AgriFood. Scientist with in depth Plant Transformation expertise required (with progression to Leadership level in future) KEY SKILLS / EXPERIENCE REQUIRED: Extensive post Degree or PhD experience - 5+ years' - in the realm of Plant Transformation and Tissue Culture. The ability to implement new and more effective Plant Transformation systems and processes (as opposed to purely following an existing blueprint). The ability to balance being a hands-on scientist in a lab environment, while undertaking leadership responsibilities such as guiding and mentoring other scientists and technicians, and contributing to scientific direction of the business. Knowedge of Corn, Soybean or other row crops would be highly valued. OVERVIEW: This agri-biotech start-up has strong backing and, while still small, is already operating in partnership with some household names in the AgriFood sector. Through their breakthroughs in plant bioengineering and transformation, they are on a mission to contribute to the next biotech revolution in agriculture through the genetic enhancement of some of the world's most commercialised and consumed crop varieties. They are seeking a Senior / Lead Scientist in Plant Transformation, somebody who can showcase a track record of devising novel solutions and implenting new and improved systems for transformation in row crops. This role could suit somebody who is equally at home in a lab as they are contributing to strategic decisions and liaising with commercial partners - including some of the largest agrifood players in the world. While a very hands on role, there is a progression route in place that could see this individual developing into a key leadership post in the company in a few years' time. Extensive experience in the fields of Plant Transformationd Tissue Culture will be required - this could be somebody with a PhD background and 5+ years' subsequent relevant experience, or an individual with a related MS / BS and 7-10+ years domain exposure on top. For an opportunity to contribute to groundbreaking impactful solutions where you can genuinely make your mark on the future of the AgriFood domain, get in touch!

We're a Little Different Our mission is clear. We bring to life a healing ministry through our compassionate care and exceptional service. At Mercy, we believe in careers that match the unique gifts of unique individuals - careers that not only make the most of your skills and talents, but also your heart. Join us and discover why Modern Healthcare Magazine named us in its “Top 100 Places to Work.” Overview: The Senior Clinical Quality Measure Specialist is responsible for the data abstraction/review, submission and validation of clinical quality data obtained from the electronic health record as required by their assignment to CMS, the Joint Commission and/or other state or national registries for public reporting and/or internal reporting. As assigned, the position is responsible for mentoring and teaching new clinical quality measure specialists, leading the learning of new measures and/or projects (pilots, state quality programs, quality improvement or others), and providing expertise for EPIC optimization applying to their measure assignments. Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards. Qualifications: Experience: 5-7 years of healthcare experience. Clinical chart review and abstraction experience required. Preferred experience with Stroke Care/Registry (American Heart Association Get with the Guidelines Stroke and/or The Joint Commission Stroke). Required Education: BA/BS in relevant field or ADN; Master level education adds one additional year towards Senior credit of experience Preferred Licensure: RN Other Skills & Knowledge: Must be analytical, resourceful, and possess excellent problem-solving skills Strong project management skills Computer, Electronic Health Record and Internet experience Familiarity and comfort with MS Office products are essential for success in this position (i.e. Word and Excel - required; PowerPoint - preferred) Ability to work as a team player with excellent communication skills Basic statistical knowledge We Offer Great Benefits: Day-one comprehensive health, vision and dental coverage, PTO, tuition reimbursement and employer-matched retirement funds are just a few of the great benefits offered to eligible co-workers, including those working 32 hours or more per pay period! We're bringing to life a healing ministry through compassionate care. At Mercy, our supportive community will be behind you every step of your day, especially the tough ones. You will have opportunities to pioneer new models of care and transform the health care experience through advanced technology and innovative procedures. We're expanding to help our communities grow. Join us and be a part of it all. What Makes You a Good Match for Mercy? Compassion and professionalism go hand-in-hand with us. Having a positive outlook and a strong sense of advocacy is in perfect step with our mission and vision. We're also collaborative and unafraid to do a little extra to deliver excellent care - that's just part of our commitment. If that sounds like a good fit for you, we encourage you to apply. EEO/AA/Minorities/Females/Disabled/Veterans

This position resides within the Pharmaceutical Research and Development department at Client. The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing analytical characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, and report writing. RESPONSIBILITIES: The responsibilities of this position include but are not limited to: • Support the development of parenteral formulations for biotherapeutic modalities such as monoclonal antibodies, antibody drug conjugates, proteins, and vaccines. • Perform rapid, comprehensive characterization of candidate molecules to determine the stability profile. This will be achieved by applying various biophysical, biochemical, particulates characterization techniques such as HPLC (SE-HPLC, IEX, HIC, RP-HPLC), Capillary Gel electrophoresis (CGE), imaged Capillary Electrophoresis (iCE), Spectroscopy techniques, light obscuration, microflow imaging and additional characterization techniques. • The incumbent must be able to interact effectively with a multidisciplinary team of scientists for formulation optimization and overall candidate progression. • This position will be responsible for preparing data summary presentations, compiling data and using lab-based systems for data collection such as empower and electronic laboratory notebooks. • Effective communication skills are desirable for interactions with laboratory scientists, project managers and colleagues from numerous functions. TECHNICAL SKILLS: Essential: • Familiarity with biologics such as proteins, enzymes, monoclonal antibodies, vaccines, or antibody drug conjugates and how to characterize them with analytical techniques Desirable: • Familiarity with HPLC, Capillary electrophoresis, and other analytical techniques • Strong computer skills and experience with lab-based computer systems • Ability to collect and analyze data sets EDUCATION & EXPERIENCE: Minimum: B.S. in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology or equivalent with 0-3 years of work experience Intake Notes Hard Skills: 1. Material weighing 2. Lab scale balance use 3. Buffer preparation 4. Pipetting

This position resides within the Pharmaceutical Research and Development department. The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing analytical characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, and report writing. Job Responsibilities: The responsibilities of this position include but are not limited to: • Support the development of parenteral formulations for biotherapeutic modalities such as monoclonal antibodies, antibody drug conjugates, proteins, and vaccines. • Perform rapid, comprehensive characterization of candidate molecules to determine the stability profile. This will be achieved by applying various biophysical, biochemical, particulates characterization techniques such as HPLC (SE-HPLC, IEX, HIC, RP-HPLC), Capillary Gel electrophoresis (CGE), imaged Capillary Electrophoresis (iCE), Spectroscopy techniques, light obscuration, microflow imaging and additional characterization techniques. • The incumbent must be able to interact effectively with a multidisciplinary team of scientists for formulation optimization and overall candidate progression. • This position will be responsible for preparing data summary presentations, compiling data and using lab-based systems for data collection such as empower and electronic laboratory notebooks. • Effective communication skills are desirable for interactions with laboratory scientists, project managers and colleagues from numerous functions. Education & Qualifications: TECHNICAL SKILLS: Essential: • Familiarity with biologics such as proteins, enzymes, monoclonal antibodies, vaccines, or antibody drug conjugates and how to characterize them with analytical techniques Desirable: • Familiarity with HPLC, Capillary electrophoresis, and other analytical techniques • Strong computer skills and experience with lab-based computer systems • Ability to collect and analyze data sets EDUCATION & EXPERIENCE: Minimum: • B.S. in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry, Bioengineering, Biotechnology, Biology or equivalent with 0-3 years of work experience Intake Notes Hard Skills: 1. Material weighing 2. Lab scale balance use 3. Buffer preparation 4. Pipetting Soft Skills 1. Oral/Written Comms 2. Team Environment 3. Critical Thinking/Problem Solving

Job Title: Clinical-Scientific - Research Associate Duration : 18+ months • This role is part of Client's Bioprocess Research & Development Cell Banking team responsible for the manufacturing and testing of GMP cell banks used to produce clinical and commercial biopharmaceutical product POSITION RESPONSIBILITIES: • Conduct cell bank manufacturing operations as required. Follow and adhere to cGMP documentation practices, operational procedures, and compliance procedures. • Perform cell bank distribution and shipping activities, as required. • Adhere to safety procedures and guidelines by practicing and promoting safe work habits. • Review and Archive GMP documents [SOPs, master batch records and campaign summary reports]. • Maintain cell banking facility and equipment in a constant state of operational and audit readiness. • Collaborate with partners from diverse cross-functional lines to effectively resolve events and issues. • Understand scientific principles in order to identify and solve moderately complex problems. • Make sound and compliant decisions with minimal input that may require choosing from limited options. • Think critically and facilitate the drive towards continuous improvement. • Effectively manage own time and balance workload priorities. ORGANIZATIONAL RELATIONSHIPS Provide the primary groups or key positions that this position will have interaction with as a regular part of the position responsibilities. Include any external interactions as appropriate. • Cell Bank testing team • Client's QA • PharmSci Cell Bank team • Client's shipping and logistics teams • Client's calibration and validation colleagues EDUCATION AND EXPERIENCE: Minimum: • High School Diploma or GED with 1-3 years of experience in a biotechnology manufacturing or laboratory environment. Preferred: • Bachelor's degree in biology or related scientific discipline with 1-3 years of relevant experience TECHNICAL SKILLS REQUIREMENTS: Must-Have • Knowledge of mammalian cell culture and/or microbial fermentation processes. • Operational knowledge of computerized systems. • Ability to follow Standard Operating Procedures and work under minimal supervision. • Understanding of scientific principles, ability to think critically and demonstrate troubleshooting and problem-solving skills. • Strong interpersonal, teamwork, and collaboration skills with the ability to work in a complex, multi-discipline organization under minimal supervision. • Excellent oral and written communication skills. • Strong computer skills in Microsoft Office required, especially MS Word, MS Excel. Nice-to-Have : • Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting. • Familiarity with business systems (e.g. Document Management Systems, LIMS, SAP, electronic Notebook, etc.) • Experience in mammalian and microbial cell culture in a GMP setting with strong aseptic technique. • Experience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologics. PHYSICAL POSITION REQUIREMENTS: • Must be able to gown into cleanroom environment and be standing for ~1-2 hours at a time. • Must be able to manipulate screw-cap vials inside a BSC and aseptically fill at least 200 vials in a single setting. • Must have practical knowledge of the use of Personal Protective Equipment (PPE) to handle hazardous materials throughout site. • Must be able to gracefully manage non-ideal situations under stress. • Must have a change-agile growth mindset for navigating changing needs and priorities. Hard Skills: 1. Knowledge of mammalian cell culture and/or microbial fermentation processes. 2. Operational knowledge of computerized systems. 3. Ability to follow Standard Operating Procedures and work under minimal supervision. Soft Skills: 1. Communication (Oral, Written) 2. Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting. 3. Familiarity with business systems (e.g. Document Management Systems, LIMS, SAP, electronic Notebook, etc.) 4. Experience in mammalian and microbial cell culture in a GMP setting with strong aseptic technique. 5. Experience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologics. Interview Process: 1st Teams Bridge Phone interview 2nd Panel Teams (camera on)

Job Title: Cell Bank Testing Associate Duration: 18 Months Contract Pay rate: $27/hours Responsibilities: This role is part of Client's Bioprocess Research & Development Cell Banking team responsible for the manufacturing and testing of GMP cell banks used to produce clinical and commercial biopharmaceutical product POSITION RESPONSIBILITIES: • Conduct cell bank manufacturing operations as required. Follow and adhere to cGMP documentation practices, operational procedures, and compliance procedures. • Perform cell bank distribution and shipping activities, as required. • Adhere to safety procedures and guidelines by practicing and promoting safe work habits. • Review and Archive GMP documents [SOPs, master batch records and campaign summary reports]. • Maintain cell banking facility and equipment in a constant state of operational and audit readiness. • Collaborate with partners from diverse cross-functional lines to effectively resolve events and issues. • Understand scientific principles in order to identify and solve moderately complex problems. • Make sound and compliant decisions with minimal input that may require choosing from limited options. • Think critically and facilitate the drive towards continuous improvement. • Effectively manage own time and balance workload priorities. ORGANIZATIONAL RELATIONSHIPS: Provide the primary groups or key positions that this position will have interaction with as a regular part of the position responsibilities. Include any external interactions as appropriate. • Cell Bank testing team • Client QA • PharmSci Cell Bank team • Client shipping and logistics teams • Client calibration and validation colleagues EDUCATION AND EXPERIENCE: Minimum: • High School Diploma or GED with 1-3 years of experience in a biotechnology manufacturing or laboratory environment. Preferred: • Bachelor's degree in biology or related scientific discipline with 1-3 years of relevant experience TECHNICAL SKILLS REQUIREMENTS: Must-Have • Knowledge of mammalian cell culture and/or microbial fermentation processes. • Operational knowledge of computerized systems. • Ability to follow Standard Operating Procedures and work under minimal supervision. • Understanding of scientific principles, ability to think critically and demonstrate troubleshooting and problem-solving skills. • Strong interpersonal, teamwork, and collaboration skills with the ability to work in a complex, multi-discipline organization under minimal supervision. • Excellent oral and written communication skills. • Strong computer skills in Microsoft Office required, especially MS Word, MS Excel. Nice-to-Have : • Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting. • Familiarity with business systems (e.g. Document Management Systems, LIMS, SAP, electronic Notebook, etc.) • Experience in mammalian and microbial cell culture in a GMP setting with strong aseptic technique. • Experience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologics. PHYSICAL POSITION REQUIREMENTS: • Must be able to gown into cleanroom environment and be standing for ~1-2 hours at a time. • Must be able to manipulate screw-cap vials inside a BSC and aseptically fill at least 200 vials in a single setting. • Must have practical knowledge of the use of Personal Protective Equipment (PPE) to handle hazardous materials throughout site. • Must be able to gracefully manage non-ideal situations under stress. • Must have a change-agile growth mindset for navigating changing needs and priorities. Hard Skills: 1. Knowledge of mammalian cell culture and/or microbial fermentation processes. 2. Operational knowledge of computerized systems. 3. Ability to follow Standard Operating Procedures and work under minimal supervision. Soft Skills: 1. Communication (Oral, Written) 2. Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting. 3. Familiarity with business systems (e.g. Document Management Systems, LIMS, SAP, electronic Notebook, etc.) 4. Experience in mammalian and microbial cell culture in a GMP setting with strong aseptic technique. 5. Experience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologics. Interview Process: 1st Teams Bridge Phone interview 2nd Panel Teams (camera on).

BYK Additives & Instruments is one of the world's leading suppliers in the field of additives and measuring instruments. Around the world, the additives of BYK ensure that coatings and plastics precisely obtain the desired properties and the correct quality. We're looking for a highly motivated, experienced Senior Chemist to join our production team! Excellent Medical, Dental, and Vision Benefit plans eligible to enroll within 30 days of hire Annual Merit increases, Bonuses, and 401K Discretionary company match up to 5%! Opportunity for advancement and training opportunities for all employees. SUMMARY: The ADP Sr. Chemist will primarily be responsible for new product development that addresses the needs of different thermoplastic end-use applications, e.g. automotive, industrial, etc. This role will report to the head of ADP and work to provide technical leadership and direction to the ADP team. DUTIES: New product development through the design and development novel plastic additive formulations Design experiments to evaluate performance of additive formulations using plastics processing and testing equipment and reporting data from such studies Perform testing on competitive products, commercial products, and plastics samples as needed work directly with manufacturing to address production issues and process optimization Author technical reports for internal and external customers Perform plastic processing, compounding and plastics forming Responsible for shipping high-quality customer samples in a timely manner, in accordance with domestic and international regulations The successful candidate will write work instructions and Standard Operating Procedures. The successful candidate will interface with operations to translate successful lab-scale projects to production. Maintain laboratory equipment Responsible for working with, handling, shipping, ordering, and storing chemicals in a safe and environmentally responsible manner as outlined in Safety Data Sheets, and in accordance with company and governmental regulations Special assignments, projects, and process improvement initiatives; as assigned by ADP management Will be responsible for managing direct reports QUALIFICATIONS: Working knowledge relating to chemical processes, plastic applications or laboratory applications Understand safety implications with respect to equipment, processes, and chemicals in the laboratory and manufacturing environments Highly skilled in the use of computer programs necessary for data entry and data analysis (e.g. Microsoft Word, PowerPoint, Excel, etc.) Good verbal and written communication skills Ability to drive self-directed projects to completion in a team-oriented collaborative work environment Able to lift 50 pounds. Able to travel both domestically and internationally Working knowledge of formulation ingredients and the processing of thermoplastics or thermosets is preferred EDUCATION AND EXPERIENCE: PhD Preferred Practical experience in a lab or production setting is necessary. Ideally, two years of experience in industrial manufacturing and knowledge of the plastics industry. Experience with analytical lab testing, data analysis and presentations are required Experience with plastic processing technologies (extrusion, molding and testing) is preferred. Experience working with mechanical equipment is preferred. This role is not eligible for sponsorship. In the ALTANA Group, you will work in a unique culture of innovation where the utmost importance is attached to promoting individual ideas and abilities as well as open, trusting interaction. ALTANA AG and its subsidiaries is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Lab Chemist I Our client is a manufacturer and distributor of 4000+ specialty and industrial chemicals. They are looking for a Lab Chemist to join their growing team! Shift: Overnight, M-Th 4:30pm-3:00am Pay: $21with $0.75 shift differential Key Responsibilities: Perform routine testing and approval of chemicals and chemical blends. Conduct inspections of incoming, intermediate, and finished goods, including raw materials, intermediates, and finished products. Inspect USP containers and tankers, when applicable. Gauge, sample, and document incoming ethanol shipments, when applicable. Maintain accurate records of test results, product status, and chemical nonconformances. Ensure that all quality records are properly documented and maintained. Verify raw materials, in-process materials, and finished goods against established specifications. Generate certificates of analysis for materials and products. Conduct USP testing and routine monograph testing, when applicable. Adhere to safety policies and maintain a clean and organized work environment. Qualifications: A BS/BA degree in Chemistry or a related science field, or an Associate's degree in Chemistry or a related science field with laboratory experience. Knowledge of modern industrial quality principles and practices is preferred. Strong communication skills, both written and verbal. Proficiency in typing, filing, and basic PC skills (Windows, Microsoft Office). Attention to detail and ability to follow established specifications and procedures.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description T he qualified candidate will join the Bioassay and Impurities Testing group, which is part of the Analytical R&D organization located in STL, MO to enable the development of biological therapeutics at Pharmaceutical. • The position will be part of a highly matrixed team responsible for developing analytical methodologies (Cell Based, ELISA, DNA) and strategies needed to progress biotherapeutic products through the pipeline. Responsibilities include specific method development and method testing via ELISA and Cell-Based assays, as well as host cell impurity testing. The deliverables of the project are to complete method development, implementation and transfer to partners as needed. • The scientist filling this position will work within a highly matrixed team setting on variety of modalities including vaccines, viral constructs, therapeutic proteins and monoclonal antibodies. The contractor will work in a cGMP testing environment doing method development, qualification, and testing. Qualifications Experience with ELISA, Cell-Based assays, Luminex (or Bioplex), cell culture, DNA (qPCR) method development, and method qualification. Must have ELISA based experience in biotherapeutics. Cell based is preferable. Looking for intermediate candidate with at least 3 years of experience Skills: ELISA experience is required Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

(Rank commensurate with experience) The Missouri Botanical Garden (MBG) is excited to announce a full-time position for a Scientist to join our Latin America Program. We are searching for a dedicated, forward-thinking researcher with a background in one or more of the following areas of focus: plant systematics, taxonomy, conservation, and restoration ecology. The successful candidate will leverage MBG's strengths and build new initiatives to advance science in support of our mission to understand and protect plant diversity in Latin America. The ideal candidate will develop a robust collaborative research program and be eager to bridge their science with conservation or restoration practice. The scientist's research may focus on plant groups well represented in MBG's herbarium or in regions where MBG is actively engaged in Latin America. Preference will be given to candidates whose work targets the Tropical Andes. This is a unique opportunity to join a growing interdisciplinary research team at MBG and contribute to meaningful research in Latin America. We look forward to welcoming a new scientist to our team who will help us advance our mission and impact. Application Instructions The process of reviewing applications will start on February 3, 2025, and will continue until the candidate has been selected for the position. While the preferred start date is before August 2025, there is flexibility, and the exact start date is negotiable. To apply, candidates need to compile the following documents and submit them in a single PDF file: * A cover letter * A research statement that should not exceed two pages * Their CV * The contact information for three references Rank and compensation will be commensurate with experience and qualifications. The salary will be accompanied by a comprehensive benefits package. Essential Duties and Responsibilities Leadership and Research: * Assume a leadership role in developing and executing research projects that advance biodiversity science and conservation in Latin America. * Publish research results in high-quality peer-reviewed journals and other publications. * Share research findings at scientific meetings and with the public through talks and other outreach initiatives. * Support colleagues and students in the development and execution of collaborative research projects. Funding and Management: * Identify funding sources and write competitive grant proposals. * Manage funded projects including budget oversight and supervision of support staff, contractors, or volunteers as necessary. Mentorship and Collaboration: * Provide mentorship to undergraduate, Master's, Ph.D. students, interns, volunteers, and Post-Doctoral Fellows. * Collaborate with other Departments and Divisions within MBG such as the Herbarium, Horticulture, and Education. * Foster external collaborations and partnerships to enhance MBG's Latin American Program. Representation and Reporting: * Serve on scientific panels or committees as needed. * Represent MBG at scientific and non-scientific meetings, events, and outreach activities. * Prepare detailed reports on projects for internal and external stakeholders. * Review and contribute to various documents including grant proposals and journal articles. Teamwork and Compliance: * Contribute to a positive culture of teamwork, cooperation, and respect. * Adhere to MBG's guidelines for budgets, contracts, agreements, and projects. * Follow established policies and procedures. Education and Training * Ph.D. training in one or more fields of focus for the Latin America Program: plant systematics, taxonomy, conservation and restoration ecology. * An equivalent combination of education, skills, and experience may be considered. Qualifications/Experience * Documented scientific record with a minimum of three (3) years' experience in one or more of the following fields: plant systematics, taxonomy, conservation and restoration ecology. * Demonstrated capacity to conceive, develop and execute research projects and initiatives. * Demonstrated ability to publish research in high-quality peer-reviewed journals. * Demonstrated ability in grant proposal writing and managing projects. * Ability to work effectively and respectfully with diverse teams including international colleagues. * Ability to travel domestically and internationally up to 25% of the time. * Excellent communication and interpersonal skills: professionalism; ability to speak clearly and persuasively in positive or negative situations, to listen and get clarification, and to respond well to questions; is tactful and treats others with respect. * Scheduling flexibility is required to work evenings, weekends, or holidays as needed. The Garden is committed to the safety and well-being of our employees, volunteers, and guests. All staff are strongly encouraged to receive all vaccinations as recommended by your healthcare provider prior to hire date. The Garden reserves the right to require future proof of current vaccination status based on local health department guidelines. When international travel is necessary for Garden business, staff must be able to obtain required travel clearances, driving permits, and vaccinations for all countries where travel is required. The requirements and duties listed are representative and not exhaustive of the knowledge, skill, and/or abilities required. Core Competencies * Communication: Combines listening skills, verbal and written communication skills and visitor relation skills. * Collaboration: Incorporates teamwork, mutual respect, active engagement, and cooperation. * Accountability: Initiative to take ownership of responsibilities, the ability to prioritize and the working knowledge and skills to take action. * Problem Solving: Blends problem solving skills, judgement and decision making skills along with creativity and resourcefulness. * Stewardship: Merges the practical application of the Garden values and support for a positive organizational climate. * Leadership: Leadership competency incorporates a cluster of knowledge, skills and abilities required for management of people, budgets and assigned business functions/operations. Other Skills and Abilities Language Skills: * Ability to communicate effectively in English (oral/written). * Ability to communicate effectively in Spanish, or other languages spoken in Latin America, is highly desirable. * Excellent public speaking skills. Reasoning Ability: * Requires ability to conduct independent research and to actively participate in team work; apply facts and principles for developing approaches and techniques to problem resolution; represent the interests and projects a positive image of the Missouri Botanical Garden. Mathematical Skills: * Proficiency in basic statistics and statistical programming. * Advanced quantitative skills is highly desirable. * Ability to track and analyze budgets. * Advanced college math aptitude - requires the ability to perform algebra/calculus equations, addition, subtraction, multiplication and division; calculate percentages and decimals, etc. Computer Skills: * Proficiency using Microsoft Office Word and Excel programs required; strong working knowledge of Outlook features required and PowerPoint preferred. * Solid Internet research skills. * Ability to use e-mail to communicate with MBG staff in order to answer questions and service their needs. Certificates, Licenses, Registrations: * Must be able to obtain and maintain a passport for international travel. * Must be able to obtain visas, vaccinations and immunizations for all countries where travel is required. Physical Demands: * Ability to travel independently for long periods on airplanes, trains and other conveyances both domestic and international. * May be required to perform tasks at varying heights and at high altitudes. * Ability to lift up to 10 lbs. * Ability to utilize computer keyboard (typing), and operates copiers, printers, fax machines and computers. * Ability to sit for extended periods (up to 50% of workday). * Ability to move about facility frequently throughout workday. * Ability to walk, stand, kneel, or climb as required and move about for extended periods. * Ability to understand travel safety requirements and wear personal protective equipment, as needed. * May require working long hours to meet deadlines. Work Environment: * Office and laboratory environment in St. Louis and overseas; overseas assignments, including in developing countries. * Outdoor setting; ability to work outdoors in all weather conditions (i.e., in temperatures over 100°F as well as temperatures below 0°F, in rain, snow and other inclement weather conditions as needed). * Comfortable working in immediate proximity to general public, in a safe and friendly manner, answering questions. Contacts with Individuals/Organizations inside/outside the Missouri Botanical Garden: * Garden employees and volunteers * Collaborators, Guests and International Scientists * Professional Organizations * Governmental Officials * Colleges/Universities Supervisor: Director of the Latin America Department

What do "Mad Scientists" do? At Mad Science, we are having a BLAST! We pay you to have fun! Build and fly rockets, demonstrate lasers, explore the states of matter using dry ice, and help children create slime and other polymers. You will inspire the next generation of scientists through our innovative activities that show kids what science is really all about. As a Mad Scientist, you will inspire students through an inquiry-based discovery method involving instructor demonstrations, hands-on activities, and amazing take-home projects that will illustrate how science affects the world around us. Mad Science is the world's leading provider of fun science programs for elementary-aged children. We are currently looking for energetic individuals to join our growing team to conduct exciting science programs during the school year including after-school programs, birthday parties, and science shows. You do NOT need to be a certified teacher, nor do you need to be a science major. Available Mad Science Positions: After-School Instructor Science Show Presenter Birthday Party Presenter Science Workshop Presenter To learn more about our programs, please visit our website at stlouis.madscience.org Qualifications: Experience working with groups of elementary-age (4-12) children (such as CCD instructor or camp counselor) Experience performing/presenting in front of large groups Must have a reliable car All employees will be fingerprinted for criminal background checks(required) Have a fun & outgoing personality We train you in the curriculum and provide all materials. This is part-time and rewarding work if it fits with your schedule and lifestyle. Learn more and apply online at ***************************************** Click here to fill out our online application. Compensation: $12.00 - $30.00 per hour Mad Science is a powerhouse brand with locations around the globe! For over 35 years, we have sparked imaginative learning through our summer camps, birthday parties, in-class workshops, after-school programs, and special events for kids ages 3-12. Become part of our team and help us inspire the next generation of scientists and engineers. Our locations are always looking for part-time instructors and full-time office staff.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: As the Associate Production Scientist with MilliporeSigma, your role is to support our large-scale Enzymes and Proteins product lines. You will work with other production scientists and operators, and SMEs to ensure successful manufacturing of an established line of products and troubleshoot and investigate process issues that arise. You will write and modify procedures consistent with quality guidelines and identify potential process improvements while interacting cross-functionally with Quality Control, Quality Assurance, Packaging, Materials Management, Engineering and Maintenance. * Day Shift- Monday-Friday 8am-4pm * Safely perform operations to meet quality expectations. * Perform multi-disciplined, established processes, assays and/or unit operations, primarily those requiring a higher level of skill and knowledge. * Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). * Clean-up equipment and working areas during and after operations. * Communicate the status of operations and bring deviations to the attention of supervisor. * Ensure all applicable logbooks have been filled out completely as required by current procedures. * Participate as needed in quality audits. * Accurately perform in-process testing and assays. * Identify problems and limitations of analysis. * Perform routine troubleshooting. * In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. * Participate in process improvements under the guidance of a Supervisor or Scientist. * Take the necessary action to resolve any unsafe conditions. * Perform and interpret analytical evaluations of products and intermediates. Physical Attributes: * Wearing of personal protective equipment such as respirator or chemical protective clothing for extended periods. * Lifting and pushing up to 50 pounds. Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or other life science discipline. Preferred Qualifications: * Knowledge in chemistry or biochemistry, math, and general science. * Knowledge of protein extraction and purification. * Familiar with laboratory instruments and production equipment. * Analytical techniques and equipment. * Safe chemical handling methods experience. * Good communication skills, verbal and written. * Mechanical skills. * Troubleshooting skills. * Interpersonal skills. * Organizational skills. RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

The incumbent will participate in the formulation and process development of biotherapeutics. This position will be responsible for performing analytical characterization of candidate molecules by using various biophysical, biochemical and particulates characterization techniques. This is a laboratory-based position performing formulation and process development activities specifically for biotherapeutic products from pre-clinical and Ph I clinical trials through late stage, license application and commercialization. Furthermore, this position will assist in data compilation, data presentations, and report writing. Support the development of parenteral formulations for biotherapeutic modalities such as monoclonal antibodies, antibody drug conjugates, proteins, and vaccines. Perform rapid, comprehensive characterization of candidate molecules to determine the stability profile. This will be achieved by applying various biophysical, biochemical, particulates characterization techniques such as HPLC (SE-HPLC, IEX, HIC, RP-HPLC), Capillary Gel electrophoresis (CGE), imaged Capillary Electrophoresis (iCE), Spectroscopy techniques, light obscuration, microflow imaging and additional characterization techniques. The incumbent must be able to interact effectively with a multidisciplinary team of scientists for formulation optimization and overall candidate progression. This position will be responsible for preparing data summary presentations, compiling data and using lab-based systems for data collection such as empower and electronic laboratory notebooks. Technical Skills: Familiarity with biologics such as proteins, enzymes, monoclonal antibodies, vaccines, or antibody drug conjugates and how to characterize them with analytical techniques Desirable: Familiarity with HPLC, Capillary electrophoresis, and other analytical techniques. Strong computer skills and experience with lab-based computer systems. Ability to collect and analyze data sets. Hard Skills: Material weighing Lab scale balance use Buffer preparation Pipetting What is the minimum education experience required: Bachelor's of Science (or Arts) in Chemistry, Biology, Chemical Biology, Biochemistry, Biomedical Engineering, Chemical Eng, Microbiology Basic Lab techniques learned in classroom lab and/or research/academic/industry laboratory. Minimum 2 years in academic lab and 0-3 yrs in industrial lab.

Job title: Cell Bank Testing Associate Duration:- 12 Months Pay rate: $27/hr Minimum education experience: High School Diploma or GED with 1-3 years of experience in a biotechnology manufacturing or laboratory environment. Preferred:• Bachelor's degree in biology or related scientific discipline with 1-3 years of relevant experience POSITION SUMMARY: • This role is part of Client's Bioprocess Research & Development Cell Banking team responsible for the manufacturing and testing of GMP cell banks used to produce clinical and commercial biopharmaceutical product POSITION RESPONSIBILITIES: • Conduct cell bank manufacturing operations as required. Follow and adhere to cGMP documentation practices, operational procedures, and compliance procedures. • Perform cell bank distribution and shipping activities, as required. • Adhere to safety procedures and guidelines by practicing and promoting safe work habits. • Review and Archive GMP documents [SOPs, master batch records and campaign summary reports]. • Maintain cell banking facility and equipment in a constant state of operational and audit readiness. • Collaborate with partners from diverse cross-functional lines to effectively resolve events and issues. • Understand scientific principles in order to identify and solve moderately complex problems. • Make sound and compliant decisions with minimal input that may require choosing from limited options. • Think critically and facilitate the drive towards continuous improvement. • Effectively manage own time and balance workload priorities. ORGANIZATIONAL RELATIONSHIPS Provide the primary groups or key positions that this position will have interaction with as a regular part of the position responsibilities. Include any external interactions as appropriate. • Cell Bank testing team • Client QA • PharmSci Cell Bank team • Client shipping and logistics teams • Client calibration and validation colleagues EDUCATION AND EXPERIENCE: • High School Diploma or GED with 1-3 years of experience in a biotechnology manufacturing or laboratory environment. Preferred: • Bachelor's degree in biology or related scientific discipline with 1-3 years of relevant experience Must-Have • Knowledge of mammalian cell culture and/or microbial fermentation processes. • Operational knowledge of computerized systems. • Ability to follow Standard Operating Procedures and work under minimal supervision. • Understanding of scientific principles, ability to think critically and demonstrate troubleshooting and problem-solving skills. • Strong interpersonal, teamwork, and collaboration skills with the ability to work in a complex, multi-discipline organization under minimal supervision. • Excellent oral and written communication skills. • Strong computer skills in Microsoft Office required, especially MS Word, MS Excel. Nice-to-Have : • Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting. • Familiarity with business systems (e.g. Document Management Systems, LIMS, SAP, electronic Notebook, etc.) • Experience in mammalian and microbial cell culture in a GMP setting with strong aseptic technique. • Experience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologics. PHYSICAL POSITION REQUIREMENTS: • Must be able to gown into cleanroom environment and be standing for ~1-2 hours at a time. • Must be able to manipulate screw-cap vials inside a BSC and aseptically fill at least 200 vials in a single setting. • Must have practical knowledge of the use of Personal Protective Equipment (PPE) to handle hazardous materials throughout site. • Must be able to gracefully manage non-ideal situations under stress. • Must have a change-agile growth mindset for navigating changing needs and priorities. Hard Skills: 1. Knowledge of mammalian cell culture and/or microbial fermentation processes. 2. Operational knowledge of computerized systems. 3. Ability to follow Standard Operating Procedures and work under minimal supervision. Soft Skills: 1. Communication (Oral, Written) 2. Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting. 3. Familiarity with business systems (e.g. Document Management Systems, LIMS, SAP, electronic Notebook, etc.) 4. Experience in mammalian and microbial cell culture in a GMP setting with strong aseptic technique. 5. Experience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologics. What will the resource be working with, or, have exposure to?: • Biohazardous Agent work (such as menigiditis, staph aureus, Lenti Virus, streph pneumoniae) • Neisseria meningitidis serogroup A,C, Y,W • Neisseria meningitidis serogroup B • Strep Pneumoniae Interview Process: 1st Teams Bridge Phone interview 2nd Panel Teams (camera on)

LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada. Title: Bench Scientist Location: Chesterfield, MO Duration: 18 Months Job Description: • The scientist filling this position will work within a highly-matrixed team setting on gene therapy modalities. The contractor will work in a cGMP environment performing sample testing by qPCR. Experience with DNA techniques (qPCR) is required. Intermediate proficiency in Microsoft Office (Excel, Word, and Outlook) is required. Must be able to understand and follow standard operating procedures. Responsibilities: • Analytical testing by qPCR in a cGMP environment • Analysis and documentation of results • Routine lab duties (ex. reagent preparation, consumable stocking) The qualified candidate will join the Bioassay and Impurities Testing group, which is part of the Analytical R&D organization located to enable the development of biological therapeutics at Pfizer. The position will be part of a highly matrixed team responsible for developing analytical methodologies (qPCR, ELISA) and strategies needed to progress biotherapeutic products through the pipeline. Tech Skills Required: • qPCR (required) • Proficiency in Microsoft Office (Excel and Word) required • cGMP experience (preferred) • LIMS experience (preferred) Additional Information Regards, Anuj Mehta ************

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: Perform production operations: * Shift: 7am-3:30pm- may require shift work. * Schedule, set-up and prepare products, both those with and without established protocols. * Ensure quality and quantity of product throughout production process. * Clean-up equipment and working areas after production operation. * Coordinate appropriate disposal of waste with Environmental Services personnel and complete compliance documentation. * Assuring, he/she is adequately trained to perform the tasks/assignments. * Communicate and document status of processes, products, and equipment. * Participate as needed in quality audits. * Interface with management and customers to collaborate, design, and execute methods, technologies, systems, and processes. * Communicate the status of production operations and bring deviations to the attention of supervisor. * Provide a complete and accurate batch record at the conclusion of production operations consistent with quality guidelines including Non-Conformance Reports (NCR) if applicable * Enter deviations in TrackWise as necessary. * Complete quaility investigations in compliance with quality standards and guidelines. * Enter and complete Change Control records in Trackwise in compliance with quality standards and guidelines. * Write and modify production procedures consistent with quality guidelines. * Enter hours worked and raw materials used into SAP. * Ensure all applicable log books have been filled out completely as required by current procedures. * Perform and interpret analytical evaluations of products and intermediates. * Review analytical procedures to ensure that they are currently used by Analytical Services. * Perform necessary analytical tests and evaluate results during the process and at the completion of the run. * Develop analytical methods to assist process development. * Ensure purity of starting material, intermediates and final products are consistent with history and product specifications. * Improve manufacturing processes through application of scientific knowledge and principals. * Conduct independent investigations to solve production problems. * Develop and implement process improvements. * Implement the scale-up of improvement ideas on new products and processes. * Identify opportunities for process improvement. * Evaluate and justify new instrumentation, equipment, or technology. * Perform daily and production operations in a safe and orderly manner. * Follow production procedures and safety policies at all times. * Label all in-process equipment and containers properly. * Take the necessary action to resolve any unsafe conditions. * Participate in required safety and quality training and other related activities. * Maintain good housekeeping in laboratory and working areas. * Independently conduct investigations and implement ideas to develop processes and technology. * Help in the training of individual co-workers. * Give technical direction as necessary during operations. Physical Attributes: * Must be able to perform tasks while wearing personal protective equipment such as respirator or chemical protective clothing for extended times. * Materials movement and equipment set-up and operation may require ability to lift to 80 lbs. and apply significant force to push or pull objects occasionally to successfully complete essential responsibility 1. Who you are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or related Life Science. * 3+ years production experience. Preferred Qualifications: * Knowledge in chemistry or biochemistry, math and general science. * Familiar with laboratory instruments and production equipment. * Process techniques and unit operations. * Analytical techniques and equipment. * Safe chemical handling methods. * Scientific method. * Knowledge in quality systems. * Laboratory and analytical. * Communication skills, oral and written and experience with computers. * Mechanical skills * Troubleshooting skills. * Interpersonal skills. * Organizational skills. * Chemical production environment. RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Candidate must be proficient with wet chemistry and analytical instrumentation (emphasis on proteins desired). • Primary roles include routine analytical testing (HPLC, colorimetric assays) and GMP testing (qualification and validation) for a high throughput protein analytics laboratory. • Responsible for general laboratory and operational support, including assisting scientific staff with lab maintenance activities. Strong interpersonal skills are required to communicate effectively with our partner lines. • Basic laboratory skills including use of balances and adjustable pipets, ability to work with Excel spreadsheets and laboratory notebook software, and attention to detail are required. Additional Information Akriti Gupta Associate Recruiter Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Website: ******************

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your role: As the Associate Production Scientist with MilliporeSigma, your role is to support our large-scale Enzymes and Proteins product lines. You will work with other production scientists and operators, and SMEs to ensure successful manufacturing of an established line of products and troubleshoot and investigate process issues that arise. You will write and modify procedures consistent with quality guidelines and identify potential process improvements while interacting cross-functionally with Quality Control, Quality Assurance, Packaging, Materials Management, Engineering and Maintenance. * Day Shift- Monday-Friday 8am-4pm * Safely perform operations to meet quality expectations. * Perform multi-disciplined, established processes, assays and/or unit operations, primarily those requiring a higher level of skill and knowledge. * Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). * Clean-up equipment and working areas during and after operations. * Communicate the status of operations and bring deviations to the attention of supervisor. * Ensure all applicable logbooks have been filled out completely as required by current procedures. * Participate as needed in quality audits. * Accurately perform in-process testing and assays. * Identify problems and limitations of analysis. * Perform routine troubleshooting. * In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. * Participate in process improvements under the guidance of a Supervisor or Scientist. * Take the necessary action to resolve any unsafe conditions. * Perform and interpret analytical evaluations of products and intermediates. Physical Attributes: * Wearing of personal protective equipment such as respirator or chemical protective clothing for extended periods. * Lifting and pushing up to 50 pounds. Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or related life science discipline. Preferred Qualifications: * Knowledge in chemistry or biochemistry, math, and general science. * Familiar with laboratory instruments and production equipment. * Analytical techniques and equipment. * Safe chemical handling methods experience. * Good communication skills, verbal and written. * Mechanical skills. * Troubleshooting skills. * Interpersonal skills. * Organizational skills. RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************