Senior scientist jobs in Kentwood, MI

Our Research and Development department is on the forefront of product development and innovation. It is easy to be dedicated when you're a part of something much bigger than yourself. We've got an insatiable appetite for making a difference. The ideal candidate will have an integral role in leading the product development of our next wave product innovations, while also lending technical support to our growing base business. We are looking for a candidate with a strong food science foundation, and a demonstrated expertise in product innovation, to help La Colombe advance its' mission of making healthy and delicious coffee beverages Responsibilities * Execute research and development plans and strategies for product development in support of company objectives * Design and execute experiments based on project objectives, excellent record keeping, data collection and analysis and preparing project summaries * Plan and carry out development work in lab and pilot scale; design, develop, and lead tests to qualify new products and to support changes to existing products; while having a mindset to scale-up and production processes * Conduct analytical measurements like, pH, viscosity, density, able to design and execute shelf-life studies, brix, total solids etc. * Manage technical development projects focusing on product development, process, and consumer testing to help La Colombe improve and launch more innovative beverage products * Lead and document development projects all the way from conceptualization to commercialization - this includes budget and target within certain time constraints * Communicate project requirements and recommendations as well as status to internal customers and external stake holders * Lead, assist, and work directly with plant processing and production personnel to ensure trial runs and start-up operations are properly performed * Follow La Colombe's safety procedures and Good Manufacturing procedures and practices Requirements * Minimum B.S. Food Science or related degree. Advanced degree strongly preferred * 5-8 years of food industry experience required, dairy and/or non-dairy is preferred * Extensive ingredient, flavor development, and product stability, and coffee knowledge * Background in process and product development and commercialization of food processes is required. Beverage and Dairy Alternative Beverage processing would be a big bonus. Proven track record of leading product development projects including timeline development / management, testing/trials, operational launch and scale * Familiarity with basic research tools and statistical analysis * Comfortable with ambiguity and are energized by the process of building something from the ground up * Innate curiosity for understanding complex food systems from a physical and chemical perspective * Maintain clean & safe manufacturing environment within all facilities * Excellent written and verbal communication * Must be a self-starter able to work in a fast-paced environment and handle multiple projects/tasks at any given time * Willingness to travel (10-20%) About Us Chobani is a food maker with a mission of making high-quality and nutritious food accessible to more people, while elevating our communities and making the world a healthier place. In short: making good food for all. In support of this mission, Chobani is a purpose-driven, people-first, food-and-wellness-focused company, and has been since its founding in 2005 by Hamdi Ulukaya, an immigrant to the U.S. The Company manufactures yogurt, oat milk, and creamers - Chobani yogurt is America's No.1 yogurt brand, made with natural ingredients without artificial preservatives. Following the 2023 acquisition of La Colombe, a leading coffee roaster with a shared commitment to quality, craftmanship and impact, the Company began selling cold-pressed espresso and lattes on tap at cafés nationwide, as well as Ready to Drink (RTD) coffee beverages at retail. In 2025, Chobani acquired Daily Harvest, a modern brand offering consumers nutritious, delicious and convenient ready-to-make meals. Chobani uses food as a force for good in the world - putting humanity first in everything it does. The company's philanthropic efforts prioritize giving back to its communities and beyond. Chobani manufactures its products in New York, Idaho, Michigan and Australia, and its products are available throughout North America and distributed in Australia and other select markets. For more information, please visit *************** or follow us on Facebook, Twitter, Instagram and LinkedIn. Chobani is an equal opportunity employer. Chobani will not discriminate against any applicant for employment on any basis including, but not limited to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, military and/or veteran status, marital status, predisposing genetic characteristics and genetic information, or any other classification protected by federal, state, and local laws. Chobani provides a comprehensive benefits package, including medical, dental, vision coverage, disability insurance, health savings account, flexible spending accounts, and tuition reimbursement. To help save for the future, all employees are eligible for a 401k match of 100% on up to 5% of eligible pay. To support growing families, we provide fertility and childcare assistance, and 12 weeks of parental leave at full pay after six months of continuous employment. In addition, we provide wellness resources which include an employee assistance program, fitness discounts, a wellness reimbursement, on-site gym access (certain locations) and a monthly wellness newsletter to connect you with resources and timely information. We offer various types of paid time of including: 120 hours of paid time off, 11 holidays, paid volunteer time off and military service leave. Compensation Range: $94,000.00 - $141,000.00, plus bonus. Nearest Major Market: Muskegon Nearest Secondary Market: Grand Rapids

Primarily responsible for planning, conducting, and analyzing protein assay method development, qualification, and validation experiments with a specialized focus in Anti-Drug Antibody ADA and pharmacokinetic (PK) bioanalysis . Uses fundamental concepts, practices, and procedures of protein biology to perform scientific research tasks requiring the application of established bioanalytical techniques, procedures, and criteria. May also act as the Principal Investigator responsible for overall planning and conduct of the study in accordance with applicable regulatory guidelines and contemporary scientific practice. Must Have Qualifications: * Strong understanding of biomarker and anti-drug-antibody (ADA) analysis * Strong understanding of the FDA ADA guidance for Immunogenicity Testing of Therapeutic Protein Products. * Strong understanding of the ICH M10 guideline for bioanalytical method validation and analysis of study samples Role Responsibilities Ability to develop, optimize, qualify, and validate new ADA assays in both pre-clinical and clinical laboratory environments. Ability to develop, optimize, qualify, and validate new assays to assess the pharmacokinetics of large-molecule drug candidates in both pre-clinical and clinical laboratory environments. The scientist must possess a strong understanding of biomarker and anti-drug-antibody (ADA) analysis and be able to execute assays within these areas under the guidance of the Study Director/Principle Investigator, in collaboration with other scientific staff leading the method development and validation procedures. Strong understanding of the FDA ADA guidance for Immunogenicity Testing of Therapeutic Protein Products. Must possess the ability to design assays that meet, or exceed, testing requirements outlined in the available guidance documents and provide scientific justification for deviating from the regulatory testing requirements. Strong understanding of the ICH M10 guideline for bioanalytical method validation and analysis of study samples. Must possess the ability to design assays that meet, or exceed, testing requirements outlined in the available guidance documents and provide scientific justification for deviating from the regulatory testing requirements. Conduct sample analysis of various biological matrices in support of pre-clinical and clinical studies for ADA, PK, and biomarker assays Lead the department in onboarding new instrumentation and applications. This includes, but is not limited to, developing IQOQ documents and working with IT personnel on Computer System Validation (CSV) script development and execution, while simultaneously implementing SOPs and procedures on operation and maintenance Study monitoring as a lead scientist and data review, as needed. The Senior Scientist is expected to have a full understanding of progress and status of method development and validation studies in their purview and relay this information to management and study directors in a timely and comprehensive manner. Ensures that unforeseen circumstances that may affect the quality and integrity of the laboratory study are noted when they occur, and corrective action is taken and documented. Interfacing with Sponsors, Vendors, Contributing Scientists, and Principal Investigators, as needed. Establish relationships with clients and secure trust through high quality scientific execution, with timely and accurate updates provided through sponsors meetings, method development summaries, and presentations. Responsible for providing scientific guidance and direction during interactions with clients, when necessary. Drive efficiencies through automation/new technologies in assay development, validation, sample preparation, analysis, and reporting Write and review reports, methods, and SOPs Maintain laboratory and freezer inventory, manage instrumentation maintenance and troubleshooting Mentor and guide junior scientists and technicians May serve as the Principal Investigator or Study Director for internal and external studies. Maintains the overall responsibility for the technical conduct of the study, interpretation, and reporting of results in accordance with regulatory agencies, protocols, amendments, methods, and standard operating procedures. All other duties as assigned Role Requirements Bachelor's degree or equivalent in a scientific related discipline. Master's degree or Ph.D. preferred Minimum of 6 years of related experience. A combination of education and experience may be accepted Experience with ELISA, MSD, Luminex, GLP-compliant bioanalytical assay development, validation, and sample analysis Familiarity with LIMS, and large molecule bioanalysis is a huge plus Experience with regulated studies and compliance guidelines for bioanalytical assays, including but not limited to the ICH M10 guideline for bioanalytical method validation and analysis Computer skills required: Microsoft Word, Excel, Outlook Behavioral Expectations Excellent analytical and problem-solving skills Excellent verbal and written communication skills; ability to design, interpret, and present complex scientific data in a team environment is required Self-starter, able to prioritize work and work efficiently with minimal supervision Collaboration Teamwork Leadership Special Requirements Individuals will be working in both an office and laboratory setting Ability to lift and carry up to 50lbs. Ability to don and wear personal protective gear, including respirators The person filling this position will spend approximately 20% in an office setting and 80% in the laboratory. There will be exposure to animal pathogens and chemicals. There will be handling of, and/or exposure to animal tissue and zoonotic organisms.

Take the lead in managing and executing critical customer-focused projects related to Colors, while independently conducting applied research in Color Innovation. This work contributes to the advancement of new and improved applications knowledge, driving the development of innovative products, processes, and new business opportunities. Essential Job Responsibilities: Help identify and execute strategic application and customer opportunities. Serve as an independent investigator - planning, designing and conducting experiments and associated research activities directed to the identified, strategic application and customer opportunities. Expectations: Works independently on assignments using knowledge and work experience. Proactively gathers input from colleagues to assist in attaining business objectives. Recognized as a subject matter expert with broad expertise in natural color pigments knowledge, formulation and applications in savory food, along with their use and potential in replacing artificial dies. Applies technical and functional knowledge to design experiments, and independently completes work within own project team, working on multiple sub-projects in parallel. Best-in-class practices on documentation of experiments, and the use of Product Life Cycle Management (PLM) as well as Laboratory Information Management Systems (LIMS). Preparation and dissemination of reports that describe research efforts, customer visits, and when appropriate, presentation of research results to scientific conferences, customers, Kalsec staff and/or other groups. Lead (Project Manager) product development activities through Stage-Gate and customer projects, as needed. To serve as a mentor to Junior Kalsec Ò staff, including occasional leading, guiding and training of staff, student employees, interns, and/or others performing related work. Maintain up to date working knowledge of Kalsec's policies, processes and manufacturing capabilities. May manage scientists, technicians, or interns. Application of extensive product knowledge and experience to troubleshooting product / process problems, investigating customer concerns, developing new processes as needed to meet customer specific needs, and recommendations for correction of non-compliant materials. Use expertise in food science to leverage the use and applications of colors in a wide range of finished products. Education/Experience: Required: Master in Chemistry or related scientific discipline and 2-5 years of experience in natural colors, or equivalent combination of education and industrial experience , along with outstanding communications skills, understanding of business alignment and a drive for growth and development. Desired: Proven track record in: Successful development and commercialization of natural colors formulations. Extensive natural colors applications knowledge, in at least a major savory food category such as meats, alternative protein, sauces, dressings, seasonings or snacks. Equipment Operation: Full lab and/or kitchen equipment including handling of hazardous materials. Computers and general office equipment. Operate color measurement instrumentation, rotary evaporators, lab centrifuges, motorized mortar and pestle and other grinders. Operate pilot plant equipment as needed (extractor, large scale rotary evaporator, pilot/large scale centrifuge, pilot scale still, etc.) Physical Requirements: Laboratory environment; lifting and carrying bulk materials. Travel: 5-15%, domestic and occasionally international.

You want to love what you do and love where you work. Gentex gives you the best of both worlds. A global technology company headquartered in Zeeland, Michigan, Gentex is an 8-time winner of the Top Workplaces in Michigan. Contribute to the discovery, development, and improvement of Gentex technology and engage in research and development, testing, and evaluation of novel technologies, processes, and/or applications. The role involves optimizing and implementing polymer coatings, sealants, and adhesive chemistries and formulations to support both existing and future electrochromic products. It requires conducting research and driving formulation improvements through effective experimental planning, troubleshooting, and interpretation of analytical test results. A background in polymer science, materials science, or chemistry is preferred to successfully perform in this position. This position is working onsite at a Gentex facility. WHAT YOU'LL DO Responsible for developing new materials, devices and/or processes that help to advance the company's new and current product offerings. Assist in the solving of problems associated with production processes, materials and/or products as needed. Analyze competitor and related patents pertinent to the company's initiatives, support patent filings and prosecutions and other related activities. Work with suppliers to find products or technologies which can improve quality, reduce cost, or simplify manufacturing. Document and analyze experimental data, including maintaining an accurate notebook and/or database of experimental results. Manage project teams, lead meetings, write minutes, track progress and report finding to senior leadership Perform various laboratory activities relating to research projects within the various R&D groups. When needed, aid other group members in the performance of their research and development duties. Work closely with key disciplines to smoothly execute projects. Coordinate assembly and testing of new products and/or processes. Participate in technical collaboration with members from other sections and/or divisions. Continue to learn and build expertise in a particular technical field, providing consulting to others as needed. Other duties as assigned. HOW YOU'LL DO IT Analytical thinking - Tackling a problem by using a logical, systematic, and sequential approach. Nimble learning - Actively learning through experimentation when tackling new problems, using both successes and failures as learning experiences. Action oriented - Taking on new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm. Problem solving - Defining a problem, determining the cause, identifying, prioritizing and selecting alternatives for a solution, and implementing a solution. Communicating effectively - Developing and delivering multi-mode communications that convey clear understanding, taking into account the unique needs of different audiences. Building teams - Working with staff to strengthen the team. Leading by example and going beyond the expected to ensure the success of all involved. Maintaining a high level of honesty, integrity, and confidentiality with respect to company matters. Complying with all Company policies and procedures, safety regulations, company safety policies and safely perform all duties, including but not limited to, promoting a safe workplace. WHAT TO BRING Bachelor's degree in Mechanical, Electrical, or Chemical Engineering, Chemistry, Material Science, Mathematics or a related field. 2+ years of relevant research experience. Proven creativity and strong problem-solving abilities and track record. Strong written and verbal communication skills. Proven problem-solving skills. Proficiency in Microsoft Office Suite. WHAT WILL HELP Master's degree or a PhD in Engineering, Science or a related field. Ability to quickly comprehend and apply new technology and be proactive. Demonstrated technical interdisciplinary skills. Project management skills. Knowledge of statistics and data analysis, particularly using programming languages such as Python or R. Ability to communicate with those with different types and levels of skills. Motivated by discovery and problem solving moderated by a developing business sense. Gentex is an equal opportunity employer Gentex extends equal employment opportunities to qualified applicants and employees regardless of an individual's race, color, religion, national origin, age, sex (including pregnancy, gender identity, and sexual orientation), disability, marital status, military service, height, weight, genetic information, or any other reason protected by law. Assistance Gentex is committed to working with and providing reasonable accommodation to applicants with disabilities. For accommodation requests, email us at *********************. Gentex will not discriminate against any qualified individual who can perform the essential functions of the job with or without a reasonable accommodation. Understand your right to work At Gentex, we use E-verify to confirm you're authorized to work in the U.S. E-Verify - English & Spanish Right to Work - English Right to Work - Spanish

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Technical support for projects Provide routine cell culture work in support of clinical programs and vaccine construct development Provide in vivo clinical support in the preparation and testing of biologic specimens such as serum, tissues, swabs, and fecal material Run basic analytical instruments such as plate readers, microplate washers, automated workstations etc. Perform analytical techniques upon biological specimens such as qPCR, ELISAs, Western, virus isolation, etc Analyze and interpret experimental data with guidance Contribute to writing of SOPs, study reports, and protocols Write up laboratory notebooks regularly in compliance with guidelines Take care of general housekeeping activities such as cleaning bench spaces, processing equipment and glass Perform process characterization studies (including Bioreactor, Metabolic profiling, and DOE approaches) to identify and define acceptable parameter ranges for egg-based, CEF and tissue culture origin viruses Order, maintain, and stock lab supplies such as common reagents, primary packaging materials, gloves, cleaning agents, safety glasses, etc. Hands on study support including Necropsy and other in-vivo work Qualifications Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) Computer skills required: Microsoft Word, Excel, Outlook Minimum 1 year microbiology laboratory experience and proven skills in cell culturing techniques Experience with livestock or lab animals strongly preferred Bench experience in basic molecular biology, cell culture and viral propagation Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, first shift, Monday-Friday 8AM-5PM. Candidates located within a commutable distance of Kalamazoo, MI are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holiday #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Van Andel Institute (VAI), a world-class biomedical research institute, located in Grand Rapids, Michigan, is dedicated to improving human health. We are pioneers in the fight against cancer, Parkinson's, and other diseases. We are committed to inspiring the next generation of scientists and educators. Van Andel Institute is hiring a cryo-EM Core Scientist to assist in the daily operations of our state-of-the-art cryo-EM facility, which includes the latest Titan Krios microscope and Arctis cryo-PFIB. The cryo-EM Core provides both transmission electron microscopy (TEM) and cryo-EM sample preparation and data collection services to researchers. As our cryo-EM Core Scientist, you will work with the cryo-EM Core Director and will be responsible for the following Key Areas: * Operate and maintain the Thermo Fisher Arctis cryo-PFIB system and related cryo-EM instrumentation. * Develop, optimize, and document cryo-FIB milling workflows for a variety of biological samples. * Lead method development to integrate FIB-SEM workflows with light microscopy and tomography pipelines. * Collaborate with faculty, postdocs, and students on sample preparation and data acquisition for in situ cryo-ET studies. * Participate in grant and manuscript writing with VAI faculty * Provide training and technical support to internal and external users. * Coordinate service, maintenance, and upgrades with Thermo Fisher engineers. * Maintain detailed experimental and maintenance records to ensure optimal system performance and data integrity. * May serve as a co-mentor to interns and VAIGS graduate students * Perform other duties as assigned. What skills and qualifications should you possess? * We would expect you to possess a Ph.D. Degree (or equivalent) in Biochemistry, Structural Biology, Cell and Molecular Biology, or related field. * 2 - 5 years of hands-on experience in single particle cryo-EM and cryo-ET is required and you should be familiar with modern electron microscopes, electron detectors, and cryo-ET data collection procedures and single particle and cryo-ET image processing pipeline. Most importantly, you should be a person with the following traits and characteristics: * A good communicator who is flexible and has a customer service-oriented personality. We expect you to have a strong commitment to building and maintaining a positive work environment. * A motivated and hardworking individual who has excellent organizational and time management skills. * Demonstrate excellent organizational and multitasking skills and athe bility to meet deadlines. * A strong desire and capability to learn new technologies. * The ability to work alone or as a team member. * Strong critical thinking and troubleshooting skills. Compensation and Benefits All full-time employees of Van Andel Institute are eligible for benefits, effective Day One! This is a salaried position targeting $80,000 - $90,000 commensurate with experience, skills and qualifications. How to apply: If you possess these attributes and the desire to help us provide best-in-class service to our researchers, we would welcome speaking with you and strongly encourage you to apply today. In your application, provide us the following in a single combined PDF: * cover letter highlighting key qualifications * current curriculum vitae with complete bibliography * names and contact information of 3 references This position will be open until filled. Applications will be reviewed on an ongoing basis. If you have any difficulty uploading your application or any questions, please email Megan Doerr at *******************. About Van Andel Institute Established in Grand Rapids, Michigan, in 1996 by the Van Andel family, VAI is now home to nearly 500 scientists, educators and support staff, who work with national and international collaborators to foster discovery. The Institute's scientists study the origins of cancer, Parkinson's and other diseases and translate their findings into breakthrough prevention and treatment strategies. Our educators develop inquiry-based approaches for K-12 education to help students and teachers prepare the next generation of problem-solvers, while our Graduate School offers a rigorous, research-intensive Ph.D. program in molecular and cellular biology. VAI is committed to excellence through broad participation and diverse perspectives. We welcome applications from individuals of all backgrounds and experiences who share our passion for innovation and collaboration. Van Andel Institute is an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. As Van Andel Institute is a drug free employer, all prospective new employees undergo a urinalysis/drug test as part of our pre-employment process. This is a 7-panel drug screen and it includes testing for Marijuana, Cocaine, Amphetamines, Opiates, PCP, Barbiturates, and Benzodiazepines. About Grand Rapids, MI Van Andel Institute is in downtown Grand Rapids, Michigan in the center of the Medical Mile. A remarkable combination of a cosmopolitan atmosphere and small-town warmth, Grand Rapids is known for its philanthropic and sustainability-driven community. It's fun affordable and family-friendly. Located on the banks of the Grand River, Grand Rapids offers all the big-city excitement you'd expect from a million-resident metropolis, featuring hundreds of restaurants and nightspots, theaters, museums, sports and concerts. The safe and clean downtown is surrounded by an eclectic mix of walkable neighborhoods and natural areas. The downtown area is safe and clean with an eclectic mix of walkable neighborhoods and natural areas.

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus Executing method transfer protocols Performing monthly maintenance of laboratory equipment Working efficiently, documenting work clearly, and performing tests accurately Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Reads and understands analytical procedures (compendial and client supplied) and internal SOPs Processes data, generates reports, and evaluates data Trains others in laboratory procedures Performs laboratory maintenance Communicates with vendors and repair personnel Writes investigations Leads project/test areas and perform method transfers/feasibility studies Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus Qualifications The Ideal Candidate would possess: Good dexterity; positive attitude; solution driven Due to the size of the site, employees are required to flex into positions and activities outside their normally assigned duties as workload requires and as trained. These activities require working in all departments including QA, microbiology, chemistry, and general support for laboratory operations Conducts all activities in a safe and efficient manner Performs other duties as assigned Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Minimum Qualifications: Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) 1-2 years of previous laboratory experience Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information Position is full-time position, Monday - Thursday 8:00am - 6:00pm, 4*10 schedule. Candidates currently living within a commutable distance of Portage, MI are encouraged to apply. 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 BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Technical support for projects Provide routine cell culture work in support of clinical programs and vaccine construct development Provide in vivo clinical support in the preparation and testing of biologic specimens such as serum, tissues, swabs, and fecal material Run basic analytical instruments such as plate readers, microplate washers, automated workstations etc. Perform analytical techniques upon biological specimens such as qPCR, ELISAs, Western, virus isolation, etc Analyze and interpret experimental data with guidance Contribute to writing of SOPs, study reports, and protocols Write up laboratory notebooks regularly in compliance with guidelines Take care of general housekeeping activities such as cleaning bench spaces, processing equipment and glass Perform process characterization studies (including Bioreactor, Metabolic profiling, and DOE approaches) to identify and define acceptable parameter ranges for egg-based, CEF and tissue culture origin viruses Order, maintain, and stock lab supplies such as common reagents, primary packaging materials, gloves, cleaning agents, safety glasses, etc. Hands on study support including Necropsy and other in-vivo work Qualifications Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) Computer skills required: Microsoft Word, Excel, Outlook Minimum 1 year microbiology laboratory experience and proven skills in cell culturing techniques Experience with livestock or lab animals strongly preferred Bench experience in basic molecular biology, cell culture and viral propagation Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, first shift, Monday-Friday 8AM-5PM. Candidates located within a commutable distance of Kalamazoo, MI are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holiday #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Fortis Life Sciences is a strategic platform providing capital, expertise, and operational resources enabling the growth and success of founder-led life sciences tools companies. Fortis Life Sciences was founded in 2020, with the vision of creating a unique life sciences company focused on offering world class products coupled with the best customer experience in the life science tools industry. We have an incredibly talented group of intelligent, down-to-earth individuals who are committed to developing and manufacturing only the highest quality products. Our mission: “Pursuing a Healthier World by Creating Tomorrow's Science Today” Job Description The Field Application Scientist (FAS) is responsible for supporting the technical business functions of Fortis Life Sciences in a pre-sales and post-sales manner with an emphasis on the clinical diagnostics, proteomics, and genomics portfolio. The purpose of the role is to support customers with applications questions related to the Fortis portfolio in a pre-sales and post-sales manner. The FAS will communicate internally with the commercial organization on the technical applications of products with the goal of supporting continued growth of the Fortis portfolio and brand. Potential to travel within the US up to 75% What You'll Do Become an expert in all applications supported by Fortis products including proficient knowledge in experimental set-up, troubleshooting, and accessory products/instrumentation Conduct ongoing product and application presentations and trainings for customers Provide consultation to customers seeking product support as it relates to their application Participate in internal global field application calls to maintain knowledge and proficiency of all products and applications Troubleshoot issues with on-market products as needed Communicate with customers and commercial organization on a routine basis, keeping all parties informed and up to date Learn new product portfolios as they become available and train internal team and customers on new offerings Pre-Sales Functions Understand the technical details of open opportunities and be able to discuss a technical strategy with the account manager and internal science team to ensure a successful win Draft and edit custom project proposals based on the customer's needs and Fortis Life Science capabilities Conduct product demonstrations and technical presentations remotely and in-person Technically compare the benefits of Fortis products and highlight the shortcomings of competitive products Assist in mapping out bulk strategy for key accounts by recommending product type and volume based on customer's needs and workflow Post-Sales Functions Support customers with understanding the necessary analytical validation required for their laboratory developed tests· Answer e-mails and phone calls from customers in timely manner Escalate issues to manager when necessary and design customer facing plans to help customer troubleshoot and resolve issue within timely manner Document knowledge in solutions within Salesforce.com for field team to access and reference as needed Host remote trainings and presentations for customers Follow-up with customers to ensure customer adopting product into workflow successfully Qualifications Education and Experience 4-year bachelor's degree in the life sciences required with a preference for biochemistry or molecular biology degrees. 2+ year Masters or PhD preferred. 2+ years working in a technical commercial role supporting customers in pre-sales and post-sales situations 2+ years practical experience working with genetic and proteomic life science applications (e.g. NGS, ELISA, Lateral Flow Assays) Proficiency in understanding CLIA requirements as they relate to Laboratory Developed Tests High degree of computer literacy in Microsoft Word, Excel and PowerPoint and ability to utilize computer-based tools for reports, email and for general communication Skills & Knowledge Life sciences, molecular biology, biotechnology, genetics, PCR, next-generation sequencing, bioinformatics, diagnostics, antibody-based assays, flow cytometry, imaging, lateral flow assays, ELISA Excellent oral and written English communication, including communicating in a way that a non-technical end user can understand Ability to think, learn, and solve problems quickly Ability to operate independently and remotely with at least 1 weekly meeting with supervisor Organized, well prepared, and maintains a professional appearance and conduct Ability to maintain flexible travel schedule during the work week Other Information This position requires up to 75% travel Additional Information What We Offer We have an incredibly talented group of intelligent, down-to-earth individuals who are committed to developing and manufacturing only the highest quality products. Our mission: “Pursuing a Healthier World by Creating Tomorrow's Science Today” is complemented by our core values: § Customer First - We prioritize the experience and outcomes of our customers above all. § Integrity - We are honest and accountable, holding ourselves to a high standard of ethical conduct. § Trust - We believe an engaged, empowered team begins with a foundation of trust. We trust our team members to make the right decisions and to be driven by and evaluated on results. § Entrepreneurship - We encourage smart risk taking. We value novel mistakes in the pursuit of innovation. § Excellence - We believe in solving for root cause. No shortcuts, no “band-aids”. Fortis provides a competitive salary, success-sharing bonus plan, medical, dental, disability and life insurance, and a 401(k) plan. We are an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. We are an E-Verify Employer in the United States.

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays, such as enzyme-linked immunosorbent assay, to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic assays to measure drug and Immunogenicity assay to measure anti-drug antibodies and neutralizing antibodies. Other assay types also performed are branched DNA and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery, Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. Essential Functions: * Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight * Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area * Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight * Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations * Assist in problem solving for technical and/or regulatory issues with oversight Responsible for writing and preparing study plans/protocols/amendments with minimal oversight * Participate in Sponsor visits/tours with minimal oversight * Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with minimal oversight * Perform data analysis using appropriate software with minimal oversight * Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas * Demonstrate effective communication skills through informal discussions with peers, supervisor, and team * Function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD with minimal oversight * Ensure scientific integrity of studies with minimal oversight * Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight * Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data * Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.) * Write, review and approve deviations with oversight; Develop knowledge of regulatory and GXP requirements, industry standards and company SOPs within one operational area * Effectively manage a small portfolio of research projects including method development and validation while ensuring timelines are met in a single operational area with oversight * Performs all other related duties as assigned Job Qualifications * Bachelor's degree (BA/BS) with 5-7 years of relevant working experience. Master's degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with no experience * Experience with micropipetting (Required) * Experience building assays, assay development (Preferred) * Elisa and Luminex experience (Preferred) * Flow Cytometry experience (Preferred) * An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above * Ability to communicate verbally and in writing at all levels inside and outside the organization * Basic familiarity with Microsoft Office Suite; Computer skills, commensurate with Essential Functions, including the ability to learn a validated system * Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice * Ability to work under specific time constraints Salary for this role is $80k/year. About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. Equal Employment Opportunity Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit *************** 231506

Roskam Foods Sr Food Scientist Reports to: Director of R&D About Us Founded in 1923 and headquartered in Grand Rapids, Michigan, Roskam Foods is a leading, scaled, and rapidly growing contract manufacturing partner for world-renowned food brands. We currently operate 8 manufacturing facilities in the U.S. and Canada where we produce a wide array of frozen and ready-to-eat breakfast products, snacks, frozen meals, confections, and custom dry blends. At Roskam Foods, we believe in the power of purpose-driven leadership to generate value for all. And we're on a mission to optimize the potential of our people and the brands we serve. We rely on the exceptional leadership, talent, and passion of over 2,400 team members to fuel our growth and “multiply possibilities” for each of our stakeholders. Position Description and Purpose Our growth has created an opening for a new Senior Food Scientist on the Research and Development (R&D) team. In this role, you will play a crucial role in the creation, enhancement, and optimization of food products. You will lead research initiatives, drive innovation, and collaborate with cross-functional teams and customers to develop market-leading food solutions. This role requires a deep understanding of food science principles, extensive experience in product development, and a passion for helping our customers grow their brands through high-quality, safe, and delicious food products. This is an excellent opportunity for someone who shares our passion for “multiplying possibilities” and wants to be part of a winning team! ESSENTIAL FUNCTIONS: Research and Innovation: Lead research efforts to identify emerging food trends, ingredients, and technologies. Drive innovation by conceptualizing and developing new product ideas aligned with consumer preferences and market demands. Recommend and advocate new product concepts to take to the next level of product development. Product Development: Oversee all aspects of product development from concept to commercialization. Develop prototypes, conduct sensory evaluations, and refine formulations to meet desired taste, texture, nutritional, and regulatory requirements. Translate concepts into manufacturing friendly products. Conduct pilot plant and production line trials. Provide production start-up support. Conduct shelf-life testing and sensory evaluations. Recipe Formulation: Develop and optimize product formulations, considering factors such as ingredient functionality, cost, shelf-life stability, and production scalability. Utilize scientific principles to achieve desired product attributes and ensure consistency across batches. Ingredient Sourcing and Evaluation: Identify and evaluate raw materials and ingredients for use in product formulations. Collaborate with procurement and suppliers to source high-quality ingredients that meet quality, safety, and sustainability standards. Initiate alternate ingredient evaluations. Process Optimization: Optimize manufacturing processes to improve product quality, efficiency, and cost-effectiveness. Collaborate with operations teams to scale up production processes and troubleshoot any issues that arise during manufacturing. Regulatory Compliance: Stay abreast of food safety regulations and ensure product compliance with relevant food laws and standards. Work closely with regulatory affairs teams to navigate regulatory requirements and obtain necessary approvals for product launches. Cross-functional Collaboration: Collaborate with cross-functional teams including marketing, sales, quality assurance, and supply chain to align product development initiatives with business objectives. Communicate effectively and coordinate activities to ensure successful project execution. Project Management: Manage multiple complex projects simultaneously, prioritizing tasks and deadlines effectively. Develop project timelines, track progress, and proactively address any challenges to ensure timely delivery of project milestones. Technical Expertise: Serve as a subject matter expert in food science and product development. Stay updated on industry advancements, scientific research, and technological innovations to drive continuous improvement and innovation in product development processes. Team Leadership and Mentorship: Provide guidance, mentorship, and technical support to junior team members. Help foster a collaborative and innovative work environment, encouraging knowledge sharing and professional development within the R&D team. EDUCATION & EXPERIENCE: Bachelor's degree in Food Science, Food Engineering, or related field. Minimum of 5 years of experience in food product development, preferably in a consumer-packaged goods (CPG) or food manufacturing environment. Experience with Roskam Foods' product categories preferred including bakery products, wet goods and coating systems or related product adjacencies. Strong understanding of food chemistry, microbiology, sensory evaluation, and food processing principles. Proficiency in recipe formulation, ingredient functionality, and product optimization. Experience with food regulations, food safety standards, and quality assurance protocols. Excellent project management, communication, and leadership skills. Ability to thrive in a fast-paced, dynamic environment and adapt to changing priorities. Creative problem-solving skills and a passion for innovation in the food industry. Demonstrated ability to successfully lead multiple complex development project simultaneously Excellent analytical and organizational skills. Ability to collaborate and interact with all levels and functional areas (internally and with customers). Knowledgeable in Microsoft Office applications including Word, Excel, PowerPoint, and Outlook. Roskam Foods offers a competitive compensation package including medical, dental and vision benefits, life and disability insurance, and a 401K plan with company match. AAP/EEO Statement: Roskam Foods is a recognized veteran friendly and equal opportunity employer.

Zoetis Veterinary Medicine Research and Development (VMRD) seeks a skilled Toxicologist to join the Toxicology Group within Clinical Pharmacology and Safety Sciences based in Kalamazoo, MI. This challenging and dynamic role provides global toxicology and safety assessment support. The successful candidate will collaborate across VMRD and Global Manufacturing and Supply (GMS) to develop scientifically rigorous safety assessments supporting product safety across therapeutic areas, veterinary species, human health, and manufacturing processes. Responsibilities: Toxicological Assessment for Drug Products: Conduct safety assessments for formulation excipients, degradants, raw materials, and residual solvents in active pharmaceutical ingredients (APIs) and drug products Toxicological Assessment for Manufacturing: Qualify impurities in the manufacturing process of APIs and drug products; conduct safety assessments for extractables and leachables, cross-contamination of products in shared facilities, and establish cleaning limits. Occupational Safety: Develop Occupational Exposure Limits (OELs/ OEBs) following Zoetis processes and procedures. User and Worker Safety: Provide product user and worker safety support for project teams, including risk assessments, exposure scenario calculations, risk mitigation proposals, packaging recommendations and label language development. Safe Exposure Level Development: Establish Threshold of Toxicological Concern (TTC) and health-based exposure limits, including Permitted Daily Exposure (PDE), Acceptable Daily Intake (ADI), and Margin of Exposure (MoE). Health Hazard/ Medical Assessments: Support pharmacovigilance, product quality, and qualification of out-of-specification batches. Regulatory Support: Assist with REACH registration for API intermediates and raw materials, and address global regulatory queries related to the safety of registered products. Toxicology Data Analysis & Literature Review: Perform rigorous toxicology gap analysis, literature data mining, and critical evaluation of toxicological information to support product development and registration. Hazard Communication and Chemical Regulatory Compliance (Preferred): Experience in preparing Safety Data Sheets (SDS), classifying drug substances and process intermediates according to the Globally Harmonized System (GHS) and national requirements, and horizon scanning and monitoring of chemical regulations. Cross-Collaboration and Technical Leadership: Engage in multidisciplinary collaboration within R&D, and with Manufacturing, Product Quality, and Sustainability, to develop and integrate key knowledge areas and expertise into actionable business insights. Regulatory & Scientific Engagement: Support regulatory compliance, trade association participation, and involvement in professional organizations relevant to toxicology. Travel Requirement: This role involves up to 10% travel for collaborations, regulatory engagements, or conferences as needed. Minimum Qualifications Ph.D. (or equivalent) plus at least 2-3 years of experience in toxicology or closely related discipline is critical. Master's degree in toxicology or closely related discipline with 8 years of relevant experience shall be considered. Demonstrated experience in preparing regulatory-quality technical documents or toxicology dossiers, with strong technical writing skills (e.g., protocols, reports, journal articles) Experience in study design, implementation, and interpretation of studies evaluating in vivo and in vitro toxicity or similar experience. Highly organized with strong problem-solving skills, capable of performing rigorous scientific assessments. Ability to prioritize tasks, make informed decisions, and collaborate effectively in a global matrix environment. Excellent verbal and written communication skills in English. Proficiency in MS Office, and toxicology databases for literature research and data analysis Desirable Skills, Experience, and Attributes: Board certification in toxicology (e.g., DABT, ERT) and/or DVM. Knowledge of global regulatory requirements for toxicology risk assessment and documentation to support product safety and chemical registrations. Experience in preparing safety data sheets. The following base pay range reflects the anticipated base pay for this position if a selected candidate were to be located in (Colorado). Base pay may vary based on location and other factors. Base Pay Range: $91,000 - $131,000 The following base pay range reflects the anticipated base pay for this position if a selected candidate were to be located in (California), (NJ Remote), (NY Remote), or (Washington). Base pay may vary based on location and other factors. Base Pay Range: $103,000 - $148,000 [This position is eligible for short-term incentive compensation.] [The position is also eligible for long-term incentive.] We offer a competitive and comprehensive benefits package, which includes healthcare, dental coverage, and retirement savings benefits along with paid holidays, vacation and disability insurance. Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Job Description Primarily responsible for planning, conducting, and analyzing protein assay method development, qualification, and validation experiments with a specialized focus in Anti-Drug Antibody ADA and pharmacokinetic (PK) bioanalysis. Uses fundamental concepts, practices, and procedures of protein biology to perform scientific research tasks requiring the application of established bioanalytical techniques, procedures, and criteria. May also act as the Principal Investigator responsible for overall planning and conduct of the study in accordance with applicable regulatory guidelines and contemporary scientific practice. Must Have Qualifications: * Strong understanding of biomarker and anti-drug-antibody (ADA) analysis * Strong understanding of the FDA ADA guidance for Immunogenicity Testing of Therapeutic Protein Products. * Strong understanding of the ICH M10 guideline for bioanalytical method validation and analysis of study samples Role Responsibilities Ability to develop, optimize, qualify, and validate new ADA assays in both pre-clinical and clinical laboratory environments. Ability to develop, optimize, qualify, and validate new assays to assess the pharmacokinetics of large-molecule drug candidates in both pre-clinical and clinical laboratory environments. The scientist must possess a strong understanding of biomarker and anti-drug-antibody (ADA) analysis and be able to execute assays within these areas under the guidance of the Study Director/Principle Investigator, in collaboration with other scientific staff leading the method development and validation procedures. Strong understanding of the FDA ADA guidance for Immunogenicity Testing of Therapeutic Protein Products. Must possess the ability to design assays that meet, or exceed, testing requirements outlined in the available guidance documents and provide scientific justification for deviating from the regulatory testing requirements. Strong understanding of the ICH M10 guideline for bioanalytical method validation and analysis of study samples. Must possess the ability to design assays that meet, or exceed, testing requirements outlined in the available guidance documents and provide scientific justification for deviating from the regulatory testing requirements. Conduct sample analysis of various biological matrices in support of pre-clinical and clinical studies for ADA, PK, and biomarker assays Lead the department in onboarding new instrumentation and applications. This includes, but is not limited to, developing IQOQ documents and working with IT personnel on Computer System Validation (CSV) script development and execution, while simultaneously implementing SOPs and procedures on operation and maintenance Study monitoring as a lead scientist and data review, as needed. The Senior Scientist is expected to have a full understanding of progress and status of method development and validation studies in their purview and relay this information to management and study directors in a timely and comprehensive manner. Ensures that unforeseen circumstances that may affect the quality and integrity of the laboratory study are noted when they occur, and corrective action is taken and documented. Interfacing with Sponsors, Vendors, Contributing Scientists, and Principal Investigators, as needed. Establish relationships with clients and secure trust through high quality scientific execution, with timely and accurate updates provided through sponsors meetings, method development summaries, and presentations. Responsible for providing scientific guidance and direction during interactions with clients, when necessary. Drive efficiencies through automation/new technologies in assay development, validation, sample preparation, analysis, and reporting Write and review reports, methods, and SOPs Maintain laboratory and freezer inventory, manage instrumentation maintenance and troubleshooting Mentor and guide junior scientists and technicians May serve as the Principal Investigator or Study Director for internal and external studies. Maintains the overall responsibility for the technical conduct of the study, interpretation, and reporting of results in accordance with regulatory agencies, protocols, amendments, methods, and standard operating procedures. All other duties as assigned Role Requirements Bachelor's degree or equivalent in a scientific related discipline. Master's degree or Ph.D. preferred Minimum of 6 years of related experience. A combination of education and experience may be accepted Experience with ELISA, MSD, Luminex, GLP-compliant bioanalytical assay development, validation, and sample analysis Familiarity with LIMS, and large molecule bioanalysis is a huge plus Experience with regulated studies and compliance guidelines for bioanalytical assays, including but not limited to the ICH M10 guideline for bioanalytical method validation and analysis Computer skills required: Microsoft Word, Excel, Outlook Behavioral Expectations Excellent analytical and problem-solving skills Excellent verbal and written communication skills; ability to design, interpret, and present complex scientific data in a team environment is required Self-starter, able to prioritize work and work efficiently with minimal supervision Collaboration Teamwork Leadership Special Requirements Individuals will be working in both an office and laboratory setting Ability to lift and carry up to 50lbs. Ability to don and wear personal protective gear, including respirators The person filling this position will spend approximately 20% in an office setting and 80% in the laboratory. There will be exposure to animal pathogens and chemicals. There will be handling of, and/or exposure to animal tissue and zoonotic organisms.

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Prepare standards and samples for analysis Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, and dissolution apparatus; perform monthly maintenance of laboratory equipment Prepare reagents, samples, and standards according to procedures Understand and perform calculations as required by test methods Process data, generate reports, and evaluate data Understand and utilize computers for information access, calculations, and report preparation Read and understand analytical procedures (compendial and client supplied) and internal SOPs Execute validation projects and write validation reports Applies GMP/GLP in all areas of responsibility, as appropriate Qualifications The ideal candidate would possess : Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications : Bachelor's degree in Biology, Chemistry, Biochemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) At least three years related experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Portage, MI are encouraged to apply. 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 BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Prepare standards and samples for analysis Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, and dissolution apparatus; perform monthly maintenance of laboratory equipment Prepare reagents, samples, and standards according to procedures Understand and perform calculations as required by test methods Process data, generate reports, and evaluate data Understand and utilize computers for information access, calculations, and report preparation Read and understand analytical procedures (compendial and client supplied) and internal SOPs Execute validation projects and write validation reports Applies GMP/GLP in all areas of responsibility, as appropriate Qualifications The ideal candidate would possess : Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications : Bachelor's degree in Biology, Chemistry, Biochemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) At least three years related experience Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Portage, MI are encouraged to apply. 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 BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Technical support for projects Provide routine cell culture work in support of clinical programs and vaccine construct development Provide in vivo clinical support in the preparation and testing of biologic specimens such as serum, tissues, swabs, and fecal material Run basic analytical instruments such as plate readers, microplate washers, automated workstations etc. Perform analytical techniques upon biological specimens such as qPCR, ELISAs, Western, virus isolation, etc Analyze and interpret experimental data with guidance Contribute to writing of SOPs, study reports, and protocols Write up laboratory notebooks regularly in compliance with guidelines Take care of general housekeeping activities such as cleaning bench spaces, processing equipment and glass Perform process characterization studies (including Bioreactor, Metabolic profiling, and DOE approaches) to identify and define acceptable parameter ranges for egg-based, CEF and tissue culture origin viruses Order, maintain, and stock lab supplies such as common reagents, primary packaging materials, gloves, cleaning agents, safety glasses, etc. Hands on study support including Necropsy and other in-vivo work Qualifications Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) Computer skills required: Microsoft Word, Excel, Outlook Minimum 1 year microbiology laboratory experience and proven skills in cell culturing techniques Experience with livestock or lab animals strongly preferred Bench experience in basic molecular biology, cell culture and viral propagation Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, first shift, Monday-Friday 8AM-5PM. Candidates located within a commutable distance of Kalamazoo, MI are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holiday #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Van Andel Institute (VAI), a world-class biomedical research institute, located in Grand Rapids, Michigan, is dedicated to improving human health. We are pioneers in the fight against cancer, Parkinson's, and other diseases. We are committed to inspiring the next generation of scientists and educators. The Van Andel Institute (VAI) Laboratory of Dr. Adelheid Lempradl and the Laboratory of Andrew Pospisilik, Ph.D. is hiring a Postdoctoral Fellow or Research Scientist (depending on qualifications) for a combined research project focusing on dissection of two unique and powerful models of paternal epigenetic inheritance. The labs focus on understanding the epigenetic processes that drive interindividual variability, epigenetic inheritance, developmental programming and thereby disease heterogeneity. We intersect functional fly and mouse genetics, epigenomics, machine learning, human cohort analysis and physiology to define novel disease processes. You will be responsible for establishing and profiling male germline epigenomes and linking those to programming of early embryos of the next generation. Our other projects focus on defining human disease sub-types and disease regulatory modules via machine learning approaches, understanding the molecular architecture that buffers against interindividual susceptibility to disease, and identifying mechanistic insights into how developmental / intergenerational programming underpins human disease. Why choose the Lempradl and Pospisilik Labs: The Lempradl and Pospisilik Labs form a long-standing partnership at the forefront of epigenetics, developmental programming, and disease heterogeneity. Working jointly for more than 14 years, we combine complementary strengths in functional mouse and Drosophila genetics, human big-data analysis, chromatin biology, and systems-level modeling of metabolic and developmental processes. Together, our teams have delivered many firsts in the field: * discovery of chromatin-encoded intergenerational metabolic programming (Cell 2014), * the first demonstration that Trim28-dependent developmental heterogeneity drives alternate obesity and cancer susceptibilities (Cell 2016; Nat Cancer 2025), * identification of human probabilistic disease subtypes using machine learning on twin and cohort data (Nat Metab 2022), and * deconstruction of β-cell epigenetic subtypes relevant to diabetes (Cell Metab 2023). * temporally resolved concomitant single-embryo metabolomic and transcriptomic analysis of early embryo development (Nat Metab 2025) Our laboratories have been recognized internationally with honors including the NIH Director's Transformative Research Award (2021), two European Research Council Grants (Starting 2011; Consolidator 2016), the GSK-Stiftung Prize for Basic Medical Research (2015), the EASD Rising Star Award (2013), and the HeIDI Helmholtz Investigator Award (2016). Dr. Pospisilik also serves on the Editorial Board of Science Advances and is a standing NIH POMD study-section member. Both groups are funded through multi-year NIH, NSF and startup awards (R01 HG012444, R01 DK132216, NSF 2346622 and internal), ensuring strong project support and access to advanced genomic, animal, and computational resources. Postdoctoral researchers benefit from the combined infrastructure of two fully integrated teams and the collaborative environment of VAI's Departments of Epigenetics and Metabolism. About the Principal Investigators: Adelheid Lempradl, Ph.D. and Andrew Pospisilik, Ph.D. are long-term collaborators whose complementary expertise spans epigenomic technology, developmental biology, and integrative physiology. Their joint mentoring philosophy emphasizes independence, creativity, and cross-disciplinary training. Each postdoc has the opportunity to develop projects that bridge Drosophila and mouse models with human genomic data, gaining exposure from molecular bench work to big-data analysis. Mentoring excellence is reflected in high success rate of Postdocs achieving independent PI positions in academia, sustained trainee success and roles as organizers of multiple international epigenetics, development and metabolism symposia as well as leadership of VAI's Epigenomics R25 training program. With nearly 15 years of productive collaboration, the Lempradl-Pospisilik partnership offers an unusually stable and synergistic environment for early-career scientists eager to explore how epigenetic systems shape development and disease. Required qualifications: * PhD in molecular / cellular / physiological sciences * Team player * Highly organized * Demonstrates proactive communication and coordination skills to manage the complexities of working across two research groups. * Self-motivated and driven * Experience leading a project from start to publication Desired qualifications: * Experience in Embryology, germline and developmental biology * Research experience in chromatin biology and epigenomics * Data science/command line/bioinformatics * Mouse physiology * CRISPRa / CRIPSRi * Strengths in biochemistry, genomics and molecular biology Qualities, traits and characteristics of an ideal candidate for the Lempradl and Pospisilik Labs: * Innate abilities include self-motivation, creativity, hard work, a can-do attitude, empathy, and a humble and communicative team player. * Collaborative team player who proactively shares knowledge and expertise with lab members. * Ability to independently design and carry out complex research projects. * Excitement to pursue interesting new research directions and willingness to take scientific risks. * Excellent verbal and written scientific communication skills. Why join Van Andel Institute as a Postdoctoral Fellow? Postdoctoral Fellows are full-time employees and receive a competitive annual salary beginning at $71,000. Postdoctoral fellows are a crucial part of Van Andel Institute's efforts to improve the health and enhance the lives of current and future generations. Along with the competitive salary, our Postdoctoral Fellows are eligible for VAI benefits: * Medical, dental and vision coverage * Employer-sponsored life and AD&D insurance * Additional voluntary life and AD&D insurance for employees and dependents * Short-term and long-term disability insurance * Flexible-spending accounts for health and child/elder care * 401 K retirement savings plans with employee/employer contributions * Paid vacation, holidays, personal days * Relocation Assistance VAI recognizes that selecting where to complete a postdoctoral fellowship is a significant decision for postdoctoral fellows. VAI has a dedicated Office of Postdoctoral Affairs, which provides a comprehensive professional development program. How to Apply If you possess these attributes and enjoy working with motivated and committed people, we encourage you to apply today. We ask you to submit your online application with a single combined PDF, including the following: * A cover letter describing your research interests, experience, and how you might contribute to the Lempradl and Pospisilik Labs. * An up-to-date Curriculum Vitae. * A list of 2-3 individuals who have agreed to act as professional references, along with their contact details. Please contact Megan Doerr (*******************) for further information or questions, or if you have any difficulty with the application process. About Van Andel Institute Established in Grand Rapids, Michigan, in 1996 by the Van Andel family, VAI is now home to nearly 500 scientists, educators and support staff, who work with national and international collaborators to foster discovery. The Institute's scientists study the origins of cancer, Parkinson's and other diseases and translate their findings into breakthrough prevention and treatment strategies. Our educators develop inquiry-based approaches for K-12 education to help students and teachers prepare the next generation of problem-solvers, while our Graduate School offers a rigorous, research-intensive Ph.D. program in molecular and cellular biology. VAI is committed to excellence through broad participation and diverse perspectives. We welcome applications from individuals of all backgrounds and experiences who share our passion for innovation and collaboration. Van Andel Institute is an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. As Van Andel Institute is a drug free employer, all prospective new employees undergo a urinalysis/drug test as part of our pre-employment process. This is a 7-panel drug screen and it includes testing for Marijuana, Cocaine, Amphetamines, Opiates, PCP, Barbiturates, and Benzodiazepines. About Grand Rapids, MI Van Andel Institute is in downtown Grand Rapids, Michigan in the center of the Medical Mile. A remarkable combination of a cosmopolitan atmosphere and small-town warmth, Grand Rapids is known for its philanthropic and sustainability-driven community. It's fun affordable and family-friendly. Located on the banks of the Grand River, Grand Rapids offers all the big-city excitement you'd expect from a million-resident metropolis, featuring hundreds of restaurants and nightspots, theaters, museums, sports and concerts. The safe and clean downtown is surrounded by an eclectic mix of walkable neighborhoods and natural areas. The downtown area is safe and clean with an eclectic mix of walkable neighborhoods and natural areas.

Fortis Life Sciences is a strategic platform providing capital, expertise, and operational resources enabling the growth and success of founder-led life sciences tools companies. Fortis Life Sciences was founded in 2020, with the vision of creating a unique life sciences company focused on offering world class products coupled with the best customer experience in the life science tools industry. We have an incredibly talented group of intelligent, down-to-earth individuals who are committed to developing and manufacturing only the highest quality products. Our mission: “Pursuing a Healthier World by Creating Tomorrow's Science Today” Job Description The Field Application Scientist (FAS) is responsible for supporting the technical business functions of Fortis Life Sciences in a pre-sales and post-sales manner with an emphasis on the clinical diagnostics, proteomics, and genomics portfolio. The purpose of the role is to support customers with applications questions related to the Fortis portfolio in a pre-sales and post-sales manner. The FAS will communicate internally with the commercial organization on the technical applications of products with the goal of supporting continued growth of the Fortis portfolio and brand. Potential to travel within the US up to 75% What You'll Do Become an expert in all applications supported by Fortis products including proficient knowledge in experimental set-up, troubleshooting, and accessory products/instrumentation Conduct ongoing product and application presentations and trainings for customers Provide consultation to customers seeking product support as it relates to their application Participate in internal global field application calls to maintain knowledge and proficiency of all products and applications Troubleshoot issues with on-market products as needed Communicate with customers and commercial organization on a routine basis, keeping all parties informed and up to date Learn new product portfolios as they become available and train internal team and customers on new offerings Pre-Sales Functions Understand the technical details of open opportunities and be able to discuss a technical strategy with the account manager and internal science team to ensure a successful win Draft and edit custom project proposals based on the customer's needs and Fortis Life Science capabilities Conduct product demonstrations and technical presentations remotely and in-person Technically compare the benefits of Fortis products and highlight the shortcomings of competitive products Assist in mapping out bulk strategy for key accounts by recommending product type and volume based on customer's needs and workflow Post-Sales Functions Support customers with understanding the necessary analytical validation required for their laboratory developed tests· Answer e-mails and phone calls from customers in timely manner Escalate issues to manager when necessary and design customer facing plans to help customer troubleshoot and resolve issue within timely manner Document knowledge in solutions within Salesforce.com for field team to access and reference as needed Host remote trainings and presentations for customers Follow-up with customers to ensure customer adopting product into workflow successfully Qualifications Education and Experience 4-year bachelor's degree in the life sciences required with a preference for biochemistry or molecular biology degrees. 2+ year Masters or PhD preferred. 2+ years working in a technical commercial role supporting customers in pre-sales and post-sales situations 2+ years practical experience working with genetic and proteomic life science applications (e.g. NGS, ELISA, Lateral Flow Assays) Proficiency in understanding CLIA requirements as they relate to Laboratory Developed Tests High degree of computer literacy in Microsoft Word, Excel and PowerPoint and ability to utilize computer-based tools for reports, email and for general communication Skills & Knowledge Life sciences, molecular biology, biotechnology, genetics, PCR, next-generation sequencing, bioinformatics, diagnostics, antibody-based assays, flow cytometry, imaging, lateral flow assays, ELISA Excellent oral and written English communication, including communicating in a way that a non-technical end user can understand Ability to think, learn, and solve problems quickly Ability to operate independently and remotely with at least 1 weekly meeting with supervisor Organized, well prepared, and maintains a professional appearance and conduct Ability to maintain flexible travel schedule during the work week Other Information This position requires up to 75% travel Additional Information What We Offer We have an incredibly talented group of intelligent, down-to-earth individuals who are committed to developing and manufacturing only the highest quality products. Our mission: “Pursuing a Healthier World by Creating Tomorrow's Science Today” is complemented by our core values: § Customer First - We prioritize the experience and outcomes of our customers above all. § Integrity - We are honest and accountable, holding ourselves to a high standard of ethical conduct. § Trust - We believe an engaged, empowered team begins with a foundation of trust. We trust our team members to make the right decisions and to be driven by and evaluated on results. § Entrepreneurship - We encourage smart risk taking. We value novel mistakes in the pursuit of innovation. § Excellence - We believe in solving for root cause. No shortcuts, no “band-aids”. Fortis provides a competitive salary, success-sharing bonus plan, medical, dental, disability and life insurance, and a 401(k) plan. We are an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. We are an E-Verify Employer in the United States.

Roskam Foods Sr Food Scientist Reports to: Director of R&D About Us Founded in 1923 and headquartered in Grand Rapids, Michigan, Roskam Foods is a leading, scaled, and rapidly growing contract manufacturing partner for world-renowned food brands. We currently operate 8 manufacturing facilities in the U.S. and Canada where we produce a wide array of frozen and ready-to-eat breakfast products, snacks, frozen meals, confections, and custom dry blends. At Roskam Foods, we believe in the power of purpose-driven leadership to generate value for all. And we're on a mission to optimize the potential of our people and the brands we serve. We rely on the exceptional leadership, talent, and passion of over 2,400 team members to fuel our growth and “multiply possibilities” for each of our stakeholders. Position Description and Purpose Our growth has created an opening for a new Senior Food Scientist on the Research and Development (R&D) team. In this role, you will play a crucial role in the creation, enhancement, and optimization of food products. You will lead research initiatives, drive innovation, and collaborate with cross-functional teams and customers to develop market-leading food solutions. This role requires a deep understanding of food science principles, extensive experience in product development, and a passion for helping our customers grow their brands through high-quality, safe, and delicious food products. This is an excellent opportunity for someone who shares our passion for “multiplying possibilities” and wants to be part of a winning team! ESSENTIAL FUNCTIONS: Research and Innovation: Lead research efforts to identify emerging food trends, ingredients, and technologies. Drive innovation by conceptualizing and developing new product ideas aligned with consumer preferences and market demands. Recommend and advocate new product concepts to take to the next level of product development. Product Development: Oversee all aspects of product development from concept to commercialization. Develop prototypes, conduct sensory evaluations, and refine formulations to meet desired taste, texture, nutritional, and regulatory requirements. Translate concepts into manufacturing friendly products. Conduct pilot plant and production line trials. Provide production start-up support. Conduct shelf-life testing and sensory evaluations. Recipe Formulation: Develop and optimize product formulations, considering factors such as ingredient functionality, cost, shelf-life stability, and production scalability. Utilize scientific principles to achieve desired product attributes and ensure consistency across batches. Ingredient Sourcing and Evaluation: Identify and evaluate raw materials and ingredients for use in product formulations. Collaborate with procurement and suppliers to source high-quality ingredients that meet quality, safety, and sustainability standards. Initiate alternate ingredient evaluations. Process Optimization: Optimize manufacturing processes to improve product quality, efficiency, and cost-effectiveness. Collaborate with operations teams to scale up production processes and troubleshoot any issues that arise during manufacturing. Regulatory Compliance: Stay abreast of food safety regulations and ensure product compliance with relevant food laws and standards. Work closely with regulatory affairs teams to navigate regulatory requirements and obtain necessary approvals for product launches. Cross-functional Collaboration: Collaborate with cross-functional teams including marketing, sales, quality assurance, and supply chain to align product development initiatives with business objectives. Communicate effectively and coordinate activities to ensure successful project execution. Project Management: Manage multiple complex projects simultaneously, prioritizing tasks and deadlines effectively. Develop project timelines, track progress, and proactively address any challenges to ensure timely delivery of project milestones. Technical Expertise: Serve as a subject matter expert in food science and product development. Stay updated on industry advancements, scientific research, and technological innovations to drive continuous improvement and innovation in product development processes. Team Leadership and Mentorship: Provide guidance, mentorship, and technical support to junior team members. Help foster a collaborative and innovative work environment, encouraging knowledge sharing and professional development within the R&D team. EDUCATION & EXPERIENCE: Bachelor's degree in Food Science, Food Engineering, or related field. Minimum of 5 years of experience in food product development, preferably in a consumer-packaged goods (CPG) or food manufacturing environment. Experience with Roskam Foods' product categories preferred including snacks, confections, frozen breakfast/ meals, cereal, granola or related product adjacencies. Strong understanding of food chemistry, microbiology, sensory evaluation, and food processing principles. Proficiency in recipe formulation, ingredient functionality, and product optimization. Experience with food regulations, food safety standards, and quality assurance protocols. Excellent project management, communication, and leadership skills. Ability to thrive in a fast-paced, dynamic environment and adapt to changing priorities. Creative problem-solving skills and a passion for innovation in the food industry. Demonstrated ability to successfully lead multiple complex development project simultaneously Excellent analytical and organizational skills. Ability to collaborate and interact with all levels and functional areas (internally and with customers). Knowledgeable in Microsoft Office applications including Word, Excel, PowerPoint, and Outlook. Roskam Foods offers a competitive compensation package including medical, dental and vision benefits, life and disability insurance, and a 401K plan with company match. AAP/EEO Statement: Roskam Foods is a recognized veteran friendly and equal opportunity employer.