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Found 25 jobs
    • Palo Alto
    • US$75 - US$95 per hour
    • Posted about 7 hours ago

    Manager, Regulatory Affairs A specialty pharmaceutical company is currently seeking a Manager Regulatory Affairs to join their team to assist in supporting and developing regulatory strategies. This position is an onsite Contract to Hire role in Palo Alto, CA and reports to the Senior Director Re...

    • United States of America
    • Negotiable
    • Posted 3 days ago

    Director/Senior Director Regulatory Affairs A Clinical Stage biotechnology company that is focusing in tumor targeted therapies is currently seeking a Director/Senior Director regulatory affairs to join the team for a remote contract. Responsibilities: Assist in development and implementation of ...

    • Seoul
    • Negotiable
    • Posted 7 days ago

    My client is a global medical device company, headquartered in the US, specialising in Orthopaedics and General Surgery medical devices. They are looking for a RAQA expert for their Korea Team. Responsibilities: Registration of new products Review and attaining of KGMP certificates KGMP Submissio...

    • California
    • US$70 - US$85 per hour
    • Posted 14 days ago

    **Remote Role** Job opportunity with a top biopharmaceutical company that is looking for an Investigator Grants Manager to join their team on a 4-month contract. Qualifications: Experience in Academic Medical Center, clinical site operations and finance is required. Drug discovery or non-clinical...

    • Salt Lake City
    • Negotiable
    • Posted 20 days ago

    Manager Regulatory Affairs Hybrid - Salt Lake City, Utah My leading pharmaceutical client is seeking a Manager of Regulatory Affairs based in Salt Lake City, Utah. The role is hybrid and can be flexible. My client is a global leader in generic and specialty medicines with an impressive portfolio ...

    • United States of America
    • Negotiable
    • Posted 27 days ago

    Regulatory Affairs Specialist (Remote) Are you a regulatory affairs specialist with expertise in in vitro diagnostic products? Do you have experience with ISO 13485, 21 CFR 820, 510(k) submissions, and ISO 14971 risk management? We have an exciting opportunity for you to join our team as a regula...

    • New York
    • Negotiable
    • Posted 28 days ago

    Are you a seasoned regulatory affairs professional with a background in generic pharmaceuticals and a proven track record of strategic and management experience? A leading generic pharmaceutical organization is seeking a highly qualified and dynamic individual to join the team as a Senior Regulat...

    • South San Francisco
    • US$105 - US$155 per hour
    • Posted 29 days ago

    Fully-Remote: Reg. Affairs Consultant Strategist We are a clinical stage biotech that aims to lead the development of experimental allogeneic chimeric antigen receptor T cell treatments for cancer. Our team of researchers is committed to discovery and translational research, development and cell ...

    • Massachusetts
    • Negotiable
    • Posted about 1 month ago

    Title: Senior Director, Global Regulatory Affairs Summary: A world renowned leader in the pharmaceutical industry is seeking a Regulatory Affairs expert to join their team. Acting as a global lead on their vaccines team, this professional will act as a regulatory strategist for programs both in t...

    • Aachen
    • Negotiable
    • Posted about 1 month ago

    Senior Regulatory Affairs Manager (m / f / d) Medical Devices As a Regulatory Affairs Manager (m/f/d) you'll take ownership of all Regulatory topics in a very critical role to the company's future and help to fulfil relevant national and international regulatory requirements. A great opportunity ...

    • Karlsruhe
    • £90000 - £90001 per annum
    • Posted about 1 month ago

    Senior Regulatory Affairs Manager (m / f / d) Medical Devices Location: Berlin As a Regulatory Affairs Manager (m/f/d) you'll take ownership of all Regulatory topics in a very critical role to the company's future and help to fulfil relevant national and international regulatory requirements. A g...

    • Singapore
    • Negotiable
    • Posted about 1 month ago

    Title: Regulatory CMC Manager Location: Singapore Overview: One of the leading global biotech is looking to build their team for their manufacturing operations in Singapore. This is an exciting opportunity to be part of the latest biologics development and take charge of the regulatory activities...

    • Singapore
    • Negotiable
    • Posted about 1 month ago

    Title: Regulatory CMC Manager Location: Singapore Overview: One of the leading global biotech is looking to build their team for their manufacturing operations in Singapore. This is an exciting opportunity to be part of the latest biologics development and take charge of the regulatory activities...

    • Hampton
    • Negotiable
    • Posted about 1 month ago

    Associate Director, Regulatory CMC Company Summary: My client, a global industry leading pharmaceutical company focuses on providing innovative solutions for underserved patient populations in a variety of therapeutic areas. My client is looking to add a Regulatory CMC Associate Director to their...

    • Parsippany-Troy Hills Township
    • Negotiable
    • Posted about 1 month ago

    Regulatory Affairs Specialist Company Summary: My client, a rapidly growing medical device company focuses on delivering personalized solutions for cancer patients using 3D printing and personalized surgical planning. My client is looking to add a Regulatory Affairs Specialist to their team! This...

    • Switzerland
    • Negotiable
    • Posted about 1 month ago

    EPM Scientific have partnered with a Swiss consultancy with a global client portfolio who is in need of a Junior or Senior Consultant Cleaning, Sterilization, Reprocessing, Microbiology. The Junior or Senior Consultant Cleaning, Sterilization, Reprocessing, Microbiology role will perform the foll...

    • Switzerland
    • Negotiable
    • Posted about 1 month ago

    EPM Scientific have partnered with a Swiss consultancy with a global client portfolio who is in need of a Senior SME Cleaning, Sterilization, Reprocessing, Biocompatibility & Toxicology. Personnel responsibility: During periods when supporting the Head of Department (Deputy Head position) Budgeta...

    • Switzerland
    • Negotiable
    • Posted about 1 month ago

    EPM Scientific have partnered with a Swiss consultancy with a global client portfolio who is in need of a Head of Department Cleaning, Sterilization, Reprocessing, Biocompatibility & Toxicology. The Head of Department Cleaning, Sterilization, Reprocessing, Biocompatibility and Toxicology assumes ...

    • Cincinnati
    • Negotiable
    • Posted about 2 months ago

    Senior Manager Regulatory Affairs On-site - Cincinnati, Ohio (Relocation provided) My client is a leading medical device life science company that develops, manufactures, markets, and distributes a broad range of innovative diagnostic products. The Senior Manager Regulatory Affairs, Pre-Market an...

    • Switzerland
    • Negotiable
    • Posted about 2 months ago

    We have a current opportunity for a Regulatory Affairs Consultant on a 0.5 FTE 6 month contract basis. Regulatory Affairs Consultant: Prepare regulatory documentation for submissions Responsible for submissions to Swiss and EU regulatory requirements Communication and Collaboration with Contract ...

    • Singapore
    • Negotiable
    • Posted about 2 months ago

    Title: Regulatory CMC Manager Location: Singapore Overview: One of the leading global biotech is looking to build their team for their manufacturing operations in Singapore. This is an exciting opportunity to be part of the latest biologics development and take charge of the regulatory activities...

    • England
    • Negotiable
    • Posted about 2 months ago

    *Freelance Regulatory Medical Writing Opportunity* EPM Scientific are currently partnered with a global CRO who are looking for multiple freelance medical writers to join their rapidly-expanding team. In this role you will be working on regulatory submission documentation such as CSR's, IB's and ...

    • Nederland
    • €70 - €105 per hour
    • Posted about 2 months ago

    Regulatory Affairs Submissions Contractor EPM Scientific are seeking a freelancer based in the Netherlands to support a large medical device manufacturer on their MDR compliance activities and general regulatory activities to ensure compliance for their product portfolio. Responsibilities Identif...

    • France
    • Negotiable
    • Posted about 2 months ago

    Draft regulatory registration files and ensure coordination with international Notify bodies Participate in marketing declarations and draft technical files (CE marking) Advise and assist the departments concerned on regulatory aspects (R&D, production, quality, marketing, sales, etc.); provide t...

    • Cleveland
    • US$135000 - US$140000 per year + 15- 20% annual bonus target
    • Posted about 2 months ago

    Title: Nuclear Pharmacy Manager Location: Greater Cleveland, Ohio Area Company: Global Radiopharmaceutical Company If you are interested in joining an industry leading Pharma company with a leading portfolio in multiple therapeutic areas, then look no further! My client is a growing nuclear pharm...

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