Regulatory Jobs | Search & Apply Today

Found 17 jobs
    • Hessen
    • Negotiable
    • Posted 3 days ago

    EPM are searching for a team of QC Consultants to support a project with our Pharmaceutical client in Hesse, Germany. * QC Specialist * Experience in regulated environment (GLP) * HPLC experience (methods + testing experience) * "Hands on" Project * Start: June * 3 month contract (initially) ...

    • Cleveland
    • Negotiable
    • Posted 5 days ago

    Sr. Process Chemist for a Leading Pharmaceutical Organization * Greater Cleveland Area * Competitive Salary + Benefits + Long Term Incentives A fast-growing Contract Development and Manufacturing Pharmaceutical Company has just had a number of key retirements and are looking to add top talent a...

    • New Concord
    • Negotiable
    • Posted 5 days ago

    Sr. Process Chemist for a Leading Pharmaceutical Organization * Greater Cleveland Area * Competitive Salary + Benefits + Long Term Incentives A fast-growing Contract Development and Manufacturing Pharmaceutical Company has just had a number of key retirements and are looking to add top talent a...

    • San Diego
    • Negotiable
    • Posted 8 days ago

    Company summary: An exciting biotech down in San Diego is looking to add a key member to their Regulatory team. This Senior Director will oversee all CMC activities, and work across several therapeutic areas, including oncology. This mid-sized biotech boasts a great company culture, and has a l...

    • New Jersey
    • US$100000 - US$100001 per annum
    • Posted 8 days ago

    A pharmaceutical company with a diverse portfolio of products and a wealth of opportunity for growth is looking to hire for a Manager of Regulatory Affairs with strong CMC experience for their New Jersey based office (relocation assistance provided if needed). This role has opened up because the...

    • New Jersey
    • US$170000 - US$170001 per annum
    • Posted 8 days ago

    Our client is looking to hire for a Director of Regulatory Affairs with expertise in complex products and complex generics. This position has opened up because the former Director of Regulatory Affairs has been promoted to a Senior Director level, reflecting a common trend this company has of en...

    • Munich
    • Negotiable
    • Posted 11 days ago

    Vice President of Regulatory Affairs Your tasks as the Vice President of Regulatory Affairs: Provides decisive leadership and strategic direction and serves as the point of contact for Global Regulatory Affairs for the organization both internally and externally. Actively participates as a m...

    • Boston
    • Negotiable
    • Posted 16 days ago

    Associate Director, Global Regulatory Affairs Greater Boston In this opportunity, you would have the chance to work for a world leading, global pharmaceutical company! Located just north of Boston, this company focuses on neurology & immunology, fertility, endocrinology, and oncology. Job...

    • San Diego
    • Negotiable
    • Posted 17 days ago

    Title: Associate Director, Global Regulatory Affairs Company Summary After the announcement of positive Phase 3 data, this Rare Disease Neurology biotech is looking to strengthen the Regulatory group. It is all hands-on deck to finalize yet another NDA and add to the collection of commerciali...

    • San Francisco
    • Negotiable
    • Posted 19 days ago

    Company summary: A pre-IPO biotech here in the Bay Area is looking to add a new member to their growing Regulatory team. They're working on a diverse pipeline with products in a variety of therapeutic areas, including immuno-oncology and the autoimmune space. This company has an approved product...

    • Lexington
    • Negotiable
    • Posted 23 days ago

    Sr. Development Scientist for an Exciting Specialty Pharmaceutical Company * Based in Lexington, KY * Competitive Salary + Benefits The Sr. Development Scientist will have the following Responsibilities: * Conduct quality by design studies to characterize/optimize the formulation, device an...

    • Berlin
    • £135 - £136 per hour
    • Posted 25 days ago

    The Role: Biocompatibility Specialist We are seeking a Biocompatibility & Technical Documentation Specialist as a freelancer for a company that is specialized in the development, production and distribution of medical devices for orthopaedics in the field of trauma. Location: Berlin & Home-of...

    • Baden-Württemberg Region
    • £80 - £81 per hour
    • Posted 25 days ago

    Our client is an innovation leader for osteosynthesis implants and is looking for a qualified Regulatory Affairs Consultant to support the Freiburg site immediately. Their high-tech products are developed, manufactured and globally distributed at their headquarters in Switzerland. Remote flexib...

    • Boston
    • Negotiable
    • Posted 25 days ago

    Method Development Scientist for a Leading Global Pharmaceutical Synthesis Company * Greater Boston Area * Competitive Salary + Benefits + Long Term Incentives A fast-growing Pharmaceutical Company has just secured more funding and is looking to build out their Analytical Development team t...

    • Boston
    • Negotiable
    • Posted 26 days ago

    A global, research driven pharmaceutical company in the Greater Boston Area (relocation assistance provided) is looking to hire for a Manager/Senior Manager of Regulatory Labeling. The company is among the top 10 pharmaceutical companies in the U.S. and has a global presence in over 80 countri...

    • North Carolina
    • Negotiable
    • Posted 26 days ago

    Senior Manager, Regulatory CMC Raleigh, North Carolina In this role you have a chance to work with growing global pharmaceutical company that is breaking through neurology and oncology, with a strong emphasis on research and development! They are looking for highly motivated individuals who w...

    • Tuttlingen
    • Negotiable
    • Posted 27 days ago

    Job Type: Head of Quality Management and Regulatory Affairs Location: Tuttlingen Key Responsibilities of the Head of Quality Management and Regulatory Affairs: You are responsible to provide regulatory input to new product developments and product lifecycle planning for the entire product l...