Regulatory Affairs Jobs in Kalamazoo, MI

Role DescriptionThe Parasitology Research Team is seeking a highly skilled and experience Ectoparasite Technical Specialist to lead and manage the in vitro ectoparasite assays including establishment optimization and data management. This individual will also execute in vivo studies across species i...

Use Your Power for PurposeAt Pfizer everything we do every day is driven by an unwavering commitment to delivering high-quality safe and effective products to patients. Our adaptable innovative and customer-focused quality culture ensures that your contributions in development maintenance compliance...

POSITION SUMMARY:We are seeking an experienced Regulatory Affairs Contractor to support our Human Health Division specifically focused on medical device regulatory submissions and compliance. This role is ideal for a detail-oriented professional with a strong understanding and experience of global r...

Preference will be given to within Central & Eastern Time ZoneHome Therapies interest requiredPURPOSE AND SCOPE:Leads regulatory surveys and promotes utilization of continuous quality improvement (CQI) principles methods and tools. Directs investigates and resolves regulatory compliance concerns. Le...

The VMRD Clinical Project Associate (VCPA) interfaces with R&D study teams to provide support in the successful planning development implementation conduct documentation and archive of a wide range of R&D studies. The VCPA serves as the point of contact with clinical project leads clinicians monitor...

Eurofins PSS is lookin for a new member for our team to help working with preparation of publication submissions and document management!This role will help with following:Prepare submissions in eSubmitter or relevant Agency web-based systems.Provide electronic document importing support and archivi...

Role DescriptionThe Kalamazoo Site Quality Lead role is accountable for product quality and the sites regulatory compliance standing ensuring adherence to all regulatory compliance requirements and cGMPs maintaining a state of Inspection Readiness and ensuring a continuous supply of high-quality pro...

Zoetis Veterinary Medicine Research and Development (VMRD) is seeking a highly accomplished Sr. Project Toxicologist to join the Toxicology group within Clinical Pharmacology and Safety Sciences in Kalamazoo MI. This senior scientific role provides technical strategy regulatory expertise and project...

Role DescriptionWe are seeking a veterinary professional with strong global regulatory expertise to join our Global Pharmacovigilance team ensuring rigorous post-marketing surveillance of veterinary medicinal products in compliance with evolving regulatory requirements worldwide. This role requires...

Role DescriptionWe are seeking a veterinary professional with strong global regulatory expertise to join our Global Pharmacovigilance team ensuring rigorous post-marketing surveillance of veterinary medicinal products in compliance with evolving regulatory requirements worldwide. This role requires...

Location: MichiganLincoln NERole Description: This is an exciting opportunity to join the Supply Chain and Distribution team in Veterinary Medicine Research and Development (VMRD). In this role you will be accountable for the active development and management of supply plans to guarantee a precise a...