Research scientist jobs in Grand Rapids, MI

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.

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.

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.

Our Taste and Sensory Innovation team is the foundation and driving force of our business through developing new food concepts and flavor formulations to gain new businesses. As a core team member, you will focus on the development and optimization of savory flavors, including reactions, topnotes and EU compliant flavors to ensure that Kalsec remains a leader in delivering high-quality and customized flavor solutions. The successful candidate supports both product innovation and customer-specific projects. Essential Job Responsibilities: Utilize knowledge of flavor science to create complex and authentic savory flavors to meet customer and market demands. Conduct research to explore and understand the functionalities of raw materials and processes that allow the creation of natural flavors for the US, EU and APAC. Stay abreast of the latest trends and innovations in the flavor world, bringing concepts from ideation to commercialization. Ensure compliance with regulatory requirements, customer specifications, and food safety standards during the development of flavor products. Manage innovation projects by collaborating with cross functional teams such as Regulatory, Marketing, Sales, and the Business Unit Leadership teams, and to plan, prioritize, communicate, and execute multiple tasks efficiently. Education/Experience: Required: MS in Food Science or Chemistry or related field. 7-10 years' experience in flavor development. Experience in developing and enhancing top note profiles for savory applications. Experience in designing and optimizing reaction flavor systems, including ingredient interactions, thermal processing, and yield efficiency improvements. Experience in balancing top notes with reaction flavors to achieve complex, authentic flavor profiles. Ability to analyze and interpret data, communicate, and provide recommendations for research projects. Excellent communication skills Excellent project management skills with strong attention to detail. Equipment Operation: Standard and Advanced laboratory equipment and instrumentation Lab scale grinding and extraction equipment Physical Requirements: Domestic and international travel. Lab work will involve standing and walking between lab benches and rooms between 2-8 hours / day. Travel: 15% This job description is not intended to cover every detail or every aspect of the job identified. Other duties may and will be assigned based upon the workload and needs of the department. Kalsec is committed to providing safe food to its customers. This position requires completing annual food safety training. Food safety training is conducted through Kalsec electronic training program and on-the-job training in each department. The organizational chart identifies personnel responsible for covering food safety responsibilities in the absence of this position.

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.

The laboratory of Dr. Michael R. Williams at the Grand Rapids Research Center in the Department of Pediatrics and Human Development, is soliciting applications for the position of Specialist - Research. The incumbent will be expected to take a lead role on biomedical research projects focused on the creation and evaluation of genetically encoded tools to analyze the structure and function of neural circuits in research subjects. Responsibilities include: Assisting in molecular biology techniques, primarily the cloning of recombinant DNA plasmids Assisting in the preparation, organization, and evaluation of replication deficient viral vectors Maintaining a transgenic mouse colony, including breeding, weaning, and genotyping Conducting survival procedures on the same including stereotaxic surgery and other injection paradigms. Conducting terminal procedures including transcardial perfusion for live or fixed brain tissues Conducting patch clamp electrophysiology of neurons and their connected populations Conducting histological procedures for the preparation and evaluation of fixed brain tissues by fluorescent microscopy Conducting data analysis, assist authoring manuscripts and grants, manage trainees, and maintain compliance with health and safety practices in the laboratory Equal Employment Opportunity Statement All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, age, disability or protected veteran status. Required Degree Doctorate -Biology or a related field Minimum Requirements PhD or DVM and at least five (5) years of experience at the level of proficient independence in: All aspects of neuronal patch-clamp electrophysiology Survival procedures in mice including stereotaxic surgery Maintenance of complex transgenic rodent colonies Preparation of fixed tissues for evaluation by fluorescent microscopy Candidates must also demonstrate a track record of peer reviewed, published research, and a basic background in recombinant DNA cloning methods. Required Application Materials Cover Letter CV Review of Applications Begins On 11/10/2025 Summary of Health Risks Work with animals or unfixed animal tissue. Website ****************** MSU Statement Michigan State University has been advancing the common good with uncommon will for more than 160 years. One of the top research universities in the world, MSU pushes the boundaries of discovery and forges enduring partnerships to solve the most pressing global challenges while providing life-changing opportunities to a diverse and inclusive academic community through more than 200 programs of study in 17 degree-granting colleges.

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.

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.

The Research Technician I will engage in basic research functions, and facility and equipment maintenance while supporting the larger operations team in completing studies in a safe, efficient, and accurate manner. Role Responsibilities Assist with restraint, handling, and manipulation of animal species. Perform animal observations to monitor and assess animal health and monitor the study. Collect and record data on paper and/or in an electronic laboratory information management system (LIMS) in accordance with Good Laboratory Practices (GLP). Introduction to data review for GLP compliance. Sample collection including, but not limited to, non-sterile scrub of collection sites, blood draws, and urine collections. Drug administration including, but not limited to, eye drops, tablets, subcutaneous injections, intramuscular injections, and drug calculations. Basic anesthesia monitoring including intubation/extubation and use of animal warming systems. May serve as a secondary Point Technician on a study. May assist with animal husbandry, including but not limited to cleaning, feeding, watering and enrichment as needed. Perform other training or duties as assigned. Role Requirements High School Diploma/GED required Minimum 1 year experience required ALAT Certification Preferred Proficient with Microsoft Office core applications and the ability to learn and use additional applications Behavioral Expectations Decision Making/Problem-Solving Team Player Coachable Special Requirements This role works predominately in a laboratory setting. There will be exposure to animal pathogens and chemicals. There will be handling of and/or exposure to animal tissues and zoonotic organisms. Ability to don and wear personal protective gear, including N95 respirators. 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 a ladder without restriction. Ability to work beyond typical work schedule including, but not limited to, evenings, weekends, holidays, and extended shifts with short notice.

The Teixeira Lab investigates how disruptions in cell signaling, transcriptomics, chromatin structure, and the epigenome contribute to reproductive tract pathologies. Dr. Teixeira is an experienced mentor with a history of guiding postdoctoral fellows who have gone on to receive prestigious NIH awards (NRSA, K99/R00) and secure faculty positions globally. The ideal candidate will have a strong record of research productivity and experience with standard molecular biology, biochemistry, and cell culture techniques. Proficiency in documenting laboratory procedures and results, along with familiarity with standard computer software, is essential. While prior experience with bioinformatics is preferred, a strong willingness to learn is also acceptable. As the lab fosters a collaborative environment, the successful candidate must be an effective communicator and team player. Trainees will be part of the MSU Reproductive and Developmental Sciences Program, a well-established and internationally recognized consortium of diverse researchers committed to advancing human and veterinary reproductive health. This is a full-time position with an initial one-year appointment, renewable annually based on performance and funding availability. The starting salary is competitive and includes a standard MSU benefits package. MSU offers comprehensive professional development resources through its Office of Postdoctoral Affairs, including customized development plans, grant writing support, travel funding for national/international conferences, and opportunities for training in computer programming, leadership, and career advancement. Fellows will meet regularly with a Postdoc Advisory Committee (PAC) composed of senior researchers to support their career trajectory. Equal Employment Opportunity Statement All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, age, disability or protected veteran status. Required Degree Doctorate -Genetics, epigenetics, molecular biology, genomics, or a related discipline in the basic sciences Minimum Requirements Ph.D. in genetics, epigenetics, molecular biology, genomics, or a related discipline in the basic sciences. Strong foundation in molecular biology techniques, including experience with cell culture and biochemistry. Highly motivated, independent, and committed to hypothesis-driven, disease-focused research. Demonstrated publication record and a keen interest in reproductive biology. Willingness to work with mouse models. Desired Qualifications Experience with next-generation sequencing and/or bioinformatics is a plus; however, a willingness to learn these techniques is sufficient. Strong problem-solving skills and the ability to critically design and execute experiments. Eagerness to mentor junior lab members and collaborate with peers and clinical fellows. Excellent written and verbal communication skills. Capable of working independently while also contributing to a team-oriented lab culture. Required Application Materials Candidates should submit a cover letter outlining their interests, along with a CV or resume and list of three references. Review of Applications Begins On 07/29/2025 Website obgyn.msu.edu MSU Statement Michigan State University has been advancing the common good with uncommon will for more than 160 years. One of the top research universities in the world, MSU pushes the boundaries of discovery and forges enduring partnerships to solve the most pressing global challenges while providing life-changing opportunities to a diverse and inclusive academic community through more than 200 programs of study in 17 degree-granting colleges.

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.

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.

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.

Some roles ask you to follow a process. This one asks you to shape it. At Zoetis, we're advancing the science of animal health-and we're looking for a scientist or engineer who can run bioreactors, think in models, and turn data into decisions. At the junction of upstream bioprocess development and modern analytics, you'll own study design with DoE, translate CFD into practical scaling and control, and explore multivariate analytics and pragmatic models to drive gravity‑defying yields and process improvements. You'll partner across functions by listening well, learning quickly, and communicating clearly to deliver decisions and solutions. If you're ready to take ownership, share success with teams that value clear thinking, and accelerate your career in a space where science meets purpose, we'd love to meet you. Responsibilities: Design, run, and interpret mammalian cell culture experiments in shake flasks and bioreactors for monoclonal antibodies and proteins Apply DoE, statistical models, and scale‑up principles to optimize processes Design, execute, and translate CFD modeling into actionable scaling and control strategies Champion multivariate analyses and modeling (e.g., PCA, time‑series analytics), and explore mechanistic models and hybrid/ML approaches where they add value Leverage digital tools and data systems to improve process understanding and decision‑making Collaborate across upstream, downstream, formulation, and analytical teams Document work in electronic lab notebooks and author high‑quality technical reports Support tech transfers and regulatory filings with clear, traceable documentation Drive innovation by evaluating new bioprocess technologies and modeling approaches to improve workflows Basic Qualifications: Biochemistry, Molecular Biology, Biotechnology, Chemical/Biological/Biomedical Engineering, or related field. BS and 4-7+ years industry experience, or MS and 1-3+ years industry experience, or PhD with relevant research and/or 0-3+ years industry experience Preferred Qualifications: Strong upstream bioprocess foundation: cell culture and bioreactor operation (fed‑batch, perfusion) Scale-up/scale-down fluency and mass transfer fundamentals DoE and MVDA literacy; experience with statistical tools a plus CFD literacy with applied impact; hands‑on experience a plus Familiarity with scientific computing and data analysis tools and languages; capacity to interpret and adopt quickly Exposure to mechanistic/kinetic modeling (e.g. Monod growth kinetics) and practical ML Clear, first‑principles reasoning; can explain assumptions and design validation experiments Success bridging bench science, process engineering, and data science; strong communication and organization 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 Research Technician I will engage in basic research functions, and facility and equipment maintenance while supporting the larger operations team in completing studies in a safe, efficient, and accurate manner. Role Responsibilities Assist with restraint, handling, and manipulation of animal species. Perform animal observations to monitor and assess animal health and monitor the study. Collect and record data on paper and/or in an electronic laboratory information management system (LIMS) in accordance with Good Laboratory Practices (GLP). Introduction to data review for GLP compliance. Sample collection including, but not limited to, non-sterile scrub of collection sites, blood draws, and urine collections. Drug administration including, but not limited to, eye drops, tablets, subcutaneous injections, intramuscular injections, and drug calculations. Basic anesthesia monitoring including intubation/extubation and use of animal warming systems. May serve as a secondary Point Technician on a study. May assist with animal husbandry, including but not limited to cleaning, feeding, watering and enrichment as needed. Perform other training or duties as assigned. Role Requirements High School Diploma/GED required Minimum 1 year experience required ALAT Certification Preferred Proficient with Microsoft Office core applications and the ability to learn and use additional applications Behavioral Expectations Decision Making/Problem-Solving Team Player Coachable Special Requirements This role works predominately in a laboratory setting. There will be exposure to animal pathogens and chemicals. There will be handling of and/or exposure to animal tissues and zoonotic organisms. Ability to don and wear personal protective gear, including N95 respirators. 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 a ladder without restriction. Ability to work beyond typical work schedule including, but not limited to, evenings, weekends, holidays, and extended shifts with short notice.

Seeking a highly productive and self-motivated individual to participate in research centered on understanding how to moderate striatal pathology as a means of improving quality of life for individuals afflicted with Parkinson's disease (PD). Post doc research associate will work on one NIH-funded and one private foundation funded translational project, employing rat and non-human primate (NHP) models of PD. The NIH funded studies involve examining the ability of a recombinant adeno associated virus (AAV)-mediated short hairpin RNA (sh RNA) to provide potent, target-selective mRNA-level silencing of striatal and/or substantia nigra CaV1.3 channels to provide disease modifying and pharmacotherapy enhancing benefits. These studies are aimed at understanding the molecular, anatomical and functional consequences associated with this gene modulation in producing functional efficacy, with the goal of bringing this therapy to clinical application. The private foundation funded project involves extensive, fast-paced postmortem analyses of NHP samples examining the potency and safety a variety of humanized RNA-interference viral vectors. Multi-disciplinary approaches include, but are not limited to, stereotaxic surgery; animal behavior/analysis; dual/triple labeled fluorescent immunohistochemistry and in situ hybridization; advanced microscopy including confocal; stereological &/or computer-assisted image analyses. Candidate must be capable of working independently but importantly must be willing to work as part of a team. Fellow will participate actively in bench research as well as data/statistical analyses; they will be encouraged to develop & submit stage-appropriate grants; they will participate/lead in the preparation of publications & presentations. This position is located in the state-of-the-art Grand Rapids Research Center, 400 Monroe Ave NW, Grand Rapids, MI 49503. Equal Employment Opportunity Statement All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, age, disability or protected veteran status. Required Degree Doctorate -Neuroscience, Neurodegeneration, Gene Therapy Minimum Requirements Post doc research associate must have a doctoral degree in neuroscience or biological science, and at least four years of experience working in a basic science laboratory. Advanced knowledge of neuroscience and/or neurodegeneration, and strong understanding of statistics and data analysis are required. A strong background with advanced microscopy (e.g.: confocal, stereology, etc.), brain tissue handling and processing (e.g.: immunohistochemistry, in situ hybridization), and a willingness to participate in small animal (e.g., rat) handling and survival stereotaxic surgery are also required. Must have excellent communication skills (verbal and written). Desired Qualifications In addition to the required skills above, knowledge of brain anatomy, molecular biology, image analysis & visualization software (e.g.: Imaris ) are desired. Required Application Materials Curriculum Vitae 2-3 Letters of Recommendations Review of Applications Begins On 05/18/2025 Summary of Health Risks Work with animals or unfixed animal tissue. Website https://translationalscience.msu.edu/ MSU Statement Michigan State University has been advancing the common good with uncommon will for more than 160 years. One of the top research universities in the world, MSU pushes the boundaries of discovery and forges enduring partnerships to solve the most pressing global challenges while providing life-changing opportunities to a diverse and inclusive academic community through more than 200 programs of study in 17 degree-granting colleges.

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. Maulik Patel is seeking to hire an Assistant Research Technician to be a key part of our research team. Our research focuses on how cells maintain mitochondrial homeostasis and the consequences that occur when these processes break down. Understanding mitochondrial homeostasis is crucial, as mitochondrial dysregulation is a hallmark of many diseases and the aging process. Additionally, the Patel Lab boasts a supportive research environment and has a strong track record of training early-career scientists for their next steps, including graduate and medical school. More information can be found at ************************* QUALIFICATIONS * A Bachelor's degree in life sciences, focusing on genetics, cell biology, molecular biology, or related biomedical fields. * Prior research experience (undergraduate research, summer internships, etc.) in a life science research laboratory. Previous experience with C. elegans or another genetic model system (e.g. yeast, flies, etc.) would be a plus. * Demonstrated ability to take initiative and handle responsibility and tasks in a reliable, high-quality, and efficient manner. * A motivated individual who shows strong interest in research and can work independently and in a team environment. * Excellent organizational and communication (oral and written) skills. RESPONSIBILITIES * Plan and coordinate experiments directly and under the supervision of senior scientists in the lab. * Work with C. elegans as a genetic model system, including conducting CRISPR injections for gene editing. * Conduct molecular biology experiments (e.g. PCR, restriction digests, gel electrophoresis, DNA extraction, etc.) * Cell microscopy experiments (brightfield and fluorescence) * Data analysis * Keep detailed records of experiments and other lab procedures. * General lab maintenance (e.g., order supplies, assess inventory, equipment maintenance) and make common lab reagents and solutions as required (e.g., media, buffers, plates). * Liaison with facilities and operations staff and outside vendors. * Serve as an emergency contact (e.g., in case of freezer alarm). * Additional opportunities will be available commensurate with effort and interest. HOW TO APPLY Interested candidates should submit a single PDF file containing the following items: * A brief cover letter outlining your research experience and interests * A recent Curriculum Vitae * A list of 2-3 individuals and their contact details who have agreed to act as references This position will remain open until it is filled, and we will be reviewing applications on an ongoing basis. If you experience any difficulties uploading your application or have questions, please email *******************. 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.