Senior scientist jobs in Grand Rapids, MI

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

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.

The Study Director will engage in serving as the single point of study control and is responsible for the overall planning and conduct of the non-clinical T oxicology investigations in accordance with applicable regulatory guidelines and contemporary scientific practice. Additionally, the RS will ensure that all Good Laboratory Practices (GLP) are met and that the outcome of the study is valid and reliable. *Ideal candidate will have a background in Ophthalmology and Toxicology Role Responsibilities Represent the single point of control for all aspects of a study while serving as Study Director for non-clinical studies. Responsible for the technical conduct of the study as well as for the interpretation, analysis, documentation, and reporting of results Generate protocol and ensure that the protocol, including any changes, are approved and followed. Ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified. Ensure that unforeseen circumstances that may affect the quality and integrity of the nonclinical laboratory study are noted when they occur, and corrective action is taken and documented. Ensure that Test systems are as specified in the protocol. Ensure compliance with the protocol, amendments, and regulatory agencies as identified in the protocol and SOPs Ensure that all raw data, documentation, protocols, specimens, and final reports are archived at the conclusion of a study Interface with Sponsors, Vendors, Contributing Scientists and Principal Investigators Other duties as assigned Role Requirements Master's Degree or equivalent in a related discipline required, PhD preferred. 5 years of experience in a GLP-compliant laboratory preferred. Experience with peer-reviewed publications, presentations, and scientific writing. Proficiency with Microsoft Office core applications and the ability to learn and use additional applications. Good written and oral communication skills. Knowledge of GLPs (FDA, OECD, and MHLW) and other federal regulations relating to the care of laboratory animals. Ability to handle common laboratory species. Strong understanding of study design and protocols. Strong understanding of laboratory operations and data collection. Ability to work under specific time constraints. Behavioral Expectations Communication Decision Making Critical Thinking Special Requirements The person filling this position will spend approximately 90% in an office setting and 10% 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. Ability to don and wear personal protective gear, including N95 masks and respirators. Ability to spend part of the day standing and/or walking. Physical Requirements: Ability to lift and carry up to 50lbs. 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.

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.

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.

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.

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.

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 The Study Director will engage in serving as the single point of study control and is responsible for the overall planning and conduct of the non-clinical Toxicology investigations in accordance with applicable regulatory guidelines and contemporary scientific practice. Additionally, the RS will ensure that all Good Laboratory Practices (GLP) are met and that the outcome of the study is valid and reliable. *Ideal candidate will have a background in Ophthalmology and Toxicology Role Responsibilities Represent the single point of control for all aspects of a study while serving as Study Director for non-clinical studies. Responsible for the technical conduct of the study as well as for the interpretation, analysis, documentation, and reporting of results Generate protocol and ensure that the protocol, including any changes, are approved and followed. Ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified. Ensure that unforeseen circumstances that may affect the quality and integrity of the nonclinical laboratory study are noted when they occur, and corrective action is taken and documented. Ensure that Test systems are as specified in the protocol. Ensure compliance with the protocol, amendments, and regulatory agencies as identified in the protocol and SOPs Ensure that all raw data, documentation, protocols, specimens, and final reports are archived at the conclusion of a study Interface with Sponsors, Vendors, Contributing Scientists and Principal Investigators Other duties as assigned Role Requirements Master's Degree or equivalent in a related discipline required, PhD preferred. 5 years of experience in a GLP-compliant laboratory preferred. Experience with peer-reviewed publications, presentations, and scientific writing. Proficiency with Microsoft Office core applications and the ability to learn and use additional applications. Good written and oral communication skills. Knowledge of GLPs (FDA, OECD, and MHLW) and other federal regulations relating to the care of laboratory animals. Ability to handle common laboratory species. Strong understanding of study design and protocols. Strong understanding of laboratory operations and data collection. Ability to work under specific time constraints. Behavioral Expectations Communication Decision Making Critical Thinking Special Requirements The person filling this position will spend approximately 90% in an office setting and 10% 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. Ability to don and wear personal protective gear, including N95 masks and respirators. Ability to spend part of the day standing and/or walking. Physical Requirements: Ability to lift and carry up to 50lbs. 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.

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 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.

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.

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.

Applies broad scientific knowledge to produce research results that support Kalsec's research and development efforts in Food Protection. Executes studies with direction on design from supervisor or project leaders. Organizes own results and prepares draft reports for supervisor review. May train technicians and interns in various techniques. Reviews internal research reports and scientific literature to enhance job knowledge. Essential Job Responsibilities: Independently conduct routine microbiological assays and collects data in support of Food Protection research and development activities. Perform antimicrobial testing of designated substances in media and food systems. Extract of raw materials such as plant matter. Make and sterilize microbiological media (broth and agar). Isolate and identify microorganisms from contaminated food sources or fermented foods and add to the strain library as needed. Work collaboratively with members of the Food Protection team. Support new product development activities for Food Protection. Experience with running a Bioreactor (fermenter) is a plus. Carefully records experimental observations in an electronic laboratory notebook kept in a sufficient manner to protect Kalsec's intellectual property rights. Organizes own results as specified by project design for review by supervisor or project leader. Train technicians and interns in various laboratory techniques. Maintains a safe and clean work area, complying with corporate safety and environmental policies. Participates in training programs deemed necessary to either develop job skills and laboratory capabilities or meet company policies and directives. Education/Experience: Required: B.S in Food Science, Microbiology, or other related fields. Desired: Formal schooling in microbiology, food science, biochemistry (or other related disciplines). Prior lab experience in food microbiology or microbiology related fields. Equipment Operation: Computer-controlled scientific instrumentation. Operate lab safety equipment such as biosafety hoods and fume hoods for proper handling of potentially hazardous materials. Operate precision measurement tools such as pipets and balances. Operate autoclave, incubators, lab centrifuges, 5 L bioreactor, etc. Physical Requirements: Working with BSL1 microorganisms, liquids, dry powders, solvents, and reagents in a microbiology lab environment. Basic motions of bending, leaning, lifting, twisting and turning with the need to lift 4 oz to 10 lbs on a frequent basis and up to 25 lbs on an infrequent basis. Lab work will involve standing and walking between lab benches and rooms between 4-8 hours / day. Travel: 0-10% travel

Zoetis is the largest animal health company in the world with an industry-leading research and development team. Zoetis Veterinary Medicine Research and Development, Biologics Analytical Sciences in Kalamazoo, MI is seeking an assay development professional at the Senior Scientist/Principal Scientist level. This position requires a highly motivated and independent contributor who can effectively collaborate with other team members to develop fit for purpose analytical methods, advance projects, develop program strategies and answer questions from regulatory authorities. The candidate must be highly motivated to contribute to the characterization of biopharmaceutical products. Agility in data analytics is highly preferred. Self-motivation, excellent problem-solving skills and communication, and an ability to work independently and within a group are essential to this role. Responsibilities Responsibilities include, but are not limited to the following: * Lead, design and conduct laboratory experiments including analytical method development, validation and transfer. Primary assays will be HPLC, mass spectrometry, electrophoresis, spectrophotometric, and microplate assays. * Represent Analytical Sciences at project team meetings and provide analytical support for antigen or antibody characterization in support of process development and establishment of analytical methods for release testing. * Perform analytical methods necessary for the characterization and release of active biological ingredients, vaccine and biopharmaceutical products. * Design, set up, and conduct stability and other hypothesis driven studies. * Trend and report method/critical reagent performance data. * Develop and/or adopt new analytical technology, as appropriate, to advance programs with significant analytical and timeline challenges. * Documentation, reporting, and communication of results in electronic laboratory notebooks, technical reports, PowerPoint presentations, and oral presentations. * Interface with other scientists in a variety of technical disciplines including process development, formulation development, clinical operations, quality control, quality assurance, discovery, and manufacturing. * Have a basic understanding of and utilize the statistical methods employed in process control and method development. Partner with Statistics group to design experiments and report data. * Assist in the preparation and writing of regulatory filings. Minimum Qualifications: * PhD or BS/MS in chemistry, biochemistry, engineering, biology or other related discipline, at least 1-3 years (PhD) or 8+ years (MS or BS) experience preferably in the biopharmaceutical or vaccine industry. * Motivated self-starter with excellent oral and written communication skills * Experience with HPLC, mass spectrometry, electrophoresis * Experience in developing, and validating biopharmaceutical analytical methods * Prepare comprehensive analytical reports and presentations, conveying findings to both technical and non-technical stakeholders. * Strong problem-solving skills and a proactive attitude toward process improvement Desired Qualifications: * Proficiency in data analytics tools such as JMP, Tableau, and Minitab, with the ability to manipulate, analyze, and visualize complex data sets * Individual contributor with experience in multiple analytical techniques (HPLC, mass spectrometry, immunoassays, CGE, cIEF) used to assess quality attributes of biopharmaceutical or vaccines products in development. * Familiarity with peptide mapping by LC-MS/MS (UHPLC and nano LC), intact mass analysis, MS/MS for protein and carbohydrate structural elucidation * Skills and experience in statistical analysis of assays, design of experiments (DOE), technical problem solving and continuous improvement. * Experience with biopharmaceutical development and product licensure. * Familiarity with biopharmaceutical manufacturing processes, including cell culture, purification, and formulation * Knowledge of the regulatory requirements (ICH, FDA, EMA, USDA) that apply to the development of tests for products tested under GMP release. 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 The Surgical Scientist I will perform surgical services in support of research protocols. They will offer support in the form of surgical protocol review and development. The Surgical Scientist I will help research and implement new surgical capabilities and train or coordinate surgical-related training of Research Technicians. Role Responsibilities Provide surgical services to support research protocols including performing surgery, study set-up, pre-operative functions, or supervision and post-operative follow-up. Assist in writing anesthesia protocols for study. Support Study Directors and IACUC on study design as it pertains to surgical models. Assist in developing and refining surgical models under direct supervision as necessary. Train or coordinate training of Surgery Technicians. Provide mentorship to In-Life Technicians. Evaluate and amend procedures to keep up with the best practices in the industry. Help with procuring the equipment necessary to perform surgical services. Other duties as assigned. Role Requirements Bachelor's degree, master's degree, or equivalent in animal or life science-related discipline. Minimum of 5 years of surgical-related research experience preferred. SRT or SRS Certification through the Academy of Surgical Research. Preferred rodent stereotaxic and canulation experience. Ability to demonstrate the scientific relevance of using surgical models for development of treatments. Ability to independently perform, direct, and assist with minor and major surgical procedures. Ability to troubleshoot surgical techniques and associated surgical equipment. Proficiency with Microsoft Office core applications and the ability to learn and use additional applications. Excellent written and oral communication skills. Understanding of operational procedures in a pre-clinical environment and the ability to resolve complex issues. Ability to handle common laboratory species. Assist with or perform humane euthanasia procedures as necessary. Excellent understanding of study design and protocols. Knowledge of GLPs and other federal regulations relating to care of laboratory animals. Behavioral Expectations Responsibility Critical Thinking Resourcefulness/Creativity Special Requirements The person filling this position will spend approximately 35% in an office setting and 65% in the laboratory/operating room. There will be exposure to animal pathogens and chemicals. There will be handling of, and/or exposure to, animal tissue and zoonotic organisms. Ability to don and wear personal protective gear, including N95 masks and respirators. Ability to stand for long periods of time. Physical activity includes lifting (up to 50lbs), carrying (up to 40lbs for up to 50 feet), pushing/pulling (up to 75lbs force), reaching, gripping/pinching, standing, and ascending the ladder without restriction. Ability to work beyond typical work schedule including evenings, weekends, and extended shifts with short notice.

Role Description Senior Scientist/Principal Scientist - Clinical Veterinarian Kalamazoo, Michigan is the world headquarters for Veterinary Medicine Research and Development (VMRD) for Zoetis. The Kalamazoo/Richland Veterinary Service group, within Global Animal Science and Welfare, at Zoetis, has the mission and responsibility of developing and implementing the program of veterinary care and providing veterinary support to VMRD projects at the Richland and Kalamazoo sites. We are seeking an experienced, innovative and highly motivated veterinarian to contribute towards delivering an exceptional animal care program as well as partnering with VMRD researchers to produce high quality research studies. EDUCATION AND EXPERIENCE: Suitable candidates will have a DVM/VMD from an accredited College of Veterinary Medicine and a minimum of 3 years of experience in clinical veterinary practice with a primary focus on livestock (horses, cattle, swine, small ruminant, poultry), companion animal medicine and surgery, and familiarity with traditional lab animal species (rats, mice, guinea pig) Licensed to practice in at least one state with the expectation to become licensed in Michigan Federally accredited or the ability to become federally accredited. Strong hands-on expertise in a range of animal techniques including handling, restraint, dosing, venipuncture, clinical examination and diagnosis, dental surgery, minor surgical procedures and necropsy. OTHER DESIRABLE ATTRIBUTES Previous experience in research setting as a clinical veterinarian. A diplomate of the American College of Laboratory Medicine (DACLAM) Experience with development of animal models for research. Experience working in biocontainment facilities and development of biosecurity programs. Additional academic training in an allied field (infectious diseases, immunology, epidemiology). Knowledge of animal welfare compliance oversight Experience working in animal programs regulated by USDA APHIS and visited by AAALAC. Network of research veterinarians and/or experts in a variety of veterinary disciplines. High motivation, demonstrated initiative, independent and flexible in thinking, strong interpersonal skills, and attention to detail. Strong documentation, writing, teaching and oral communication skills. Experience with multiple software platforms, including electronic data capture and data management. Experience with livestock and/or traditional lab animal species POSITION RESPONSIBILITIES: Primary responsibility is to provide clinical veterinary support to research animals at the Richland and/or Kalamazoo sites in support of VMRD. Clinical Veterinary responsibility includes but is not limited to: development and/or implementation of population medicine programs and preventive medicine procedures provision of training to animal care technicians and/or study personnel study oversight by reviewing protocols and ensuring compliance with approved procedures attendance and participation in pre-study activities preparation of health certificates assessment of animals prior to shipment and after receipt authoring and reviewing SOPs performing necropsies serving as a non-voting Institutional Animal Care and Use Committee ad hoc member (ex. Animal Use Protocol review, semiannual facility inspections) participate in veterinary on-call duty on weekends and holidays on a rotational basis participation in facility design/renovation planning Additional responsibilities may include: providing support to the Animal Welfare and Compliance Team by assisting with animal welfare audits of animal suppliers and contract research organizations; and participating in internal and external animal welfare audits (AAALAC International, USDA, and internal audits.). ADDITIONAL INFORMATION: Work environment: The person filling this position will work with research scientists, study monitors, line managers and technical staff. May be required to work with zoonotic and animal pathogens and chemicals. There may be handling of zoonotic organisms and working in BSL-2 and BSL-3 facilities requiring shower in/out procedures. Veterinary support is about 25% in support of research projects and 75% in support of the animal care program. Participate in veterinary on-call duty on weekends and holidays on a rotational basis including some work outside of core business hours. Some travel (10%) to off-site locations may be required Support for tuition reimbursement, continuing education and career development is available. 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.

The Surgical Scientist I will perform surgical services in support of research protocols. They will offer support in the form of surgical protocol review and development. The Surgical Scientist I will help research and implement new surgical capabilities and train or coordinate surgical-related training of Research Technicians. Role Responsibilities Provide surgical services to support research protocols including performing surgery, study set-up, pre-operative functions, or supervision and post-operative follow-up. Assist in writing anesthesia protocols for study. Support Study Directors and IACUC on study design as it pertains to surgical models. Assist in developing and refining surgical models under direct supervision as necessary. Train or coordinate training of Surgery Technicians. Provide mentorship to In-Life Technicians. Evaluate and amend procedures to keep up with the best practices in the industry. Help with procuring the equipment necessary to perform surgical services. Other duties as assigned. Role Requirements Bachelor's degree, master's degree, or equivalent in animal or life science-related discipline. Minimum of 5 years of surgical-related research experience preferred. SRT or SRS Certification through the Academy of Surgical Research. Preferred rodent stereotaxic and canulation experience. Ability to demonstrate the scientific relevance of using surgical models for development of treatments. Ability to independently perform, direct, and assist with minor and major surgical procedures. Ability to troubleshoot surgical techniques and associated surgical equipment. Proficiency with Microsoft Office core applications and the ability to learn and use additional applications. Excellent written and oral communication skills. Understanding of operational procedures in a pre-clinical environment and the ability to resolve complex issues. Ability to handle common laboratory species. Assist with or perform humane euthanasia procedures as necessary. Excellent understanding of study design and protocols. Knowledge of GLPs and other federal regulations relating to care of laboratory animals. Behavioral Expectations Responsibility Critical Thinking Resourcefulness/Creativity Special Requirements The person filling this position will spend approximately 35% in an office setting and 65% in the laboratory/operating room. There will be exposure to animal pathogens and chemicals. There will be handling of, and/or exposure to, animal tissue and zoonotic organisms. Ability to don and wear personal protective gear, including N95 masks and respirators. Ability to stand for long periods of time. Physical activity includes lifting (up to 50lbs), carrying (up to 40lbs for up to 50 feet), pushing/pulling (up to 75lbs force), reaching, gripping/pinching, standing, and ascending the ladder without restriction. Ability to work beyond typical work schedule including evenings, weekends, and extended shifts with short notice.