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• Hampshire
• Negotiable
• Posted about 14 hours ago

Exciting Opportunity: EMC Test Technician / Engineer About the Role Are you passionate about cutting-edge technology and innovation? Join our team of EMC specialists, where you'll play a vital role in testing the latest devices across a variety of industries. As an EMC Test Technician or Engineer...

• Jersey City
• US$140000 - US$150000 per annum
• Posted 1 day ago

EPM is partnered with an innovative global biopharmaceutical company that is looking for a Senior Medical Writer to join their US team in the NJ/NY area. Key responsibilities: Creating clinical and regulatory documents including protocols, CSRs, CSPs, IBs, ICFs, CTDs, RMPs, PIPs, INDs, NSAs, BLAs...

• New Jersey
• US$115000 - US$135000 per annum
• Posted 1 day ago

EPM is partnered with an innovative global biopharmaceutical company that is looking for a Senior Medical Writer to join their US team in the NJ/NY area. Key responsibilities: Creating clinical and regulatory documents including protocols, CSRs, CSPs, IBs, ICFs, CTDs, RMPs, PIPs, INDs, NSAs, BLAs...

• Boston
• US$240000 - US$280000 per annum
• Posted 1 day ago

Title: Senior Director Global Regulatory Lead A leading pharmaceutical company is growing their team with a Senior Director Global Regulatory Lead to develop and lead global regulatory strategies for complex projects. This is an exciting chance to join a leading company in the industry to support...

• Atlanta
• US$150000 - US$200000 per annum
• Posted 1 day ago

Title: Senior Manager Regulatory Affairs A leading global Medical Device company is seeking a Senior Manager of Regulatory Affairs to join their team on-site in their downtown Atlanta office. This new team member will be responsible for the management and leadership of the Regulatory Affairs depa...

• Copenhagen
• Negotiable
• Posted 4 days ago

We are working with a leading pharmaceutical company based in Copenhagen that are dedicated to the development, manufacturing, and commercialisation of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-o...

• Neuchâtel
• Negotiable
• Posted 4 days ago

We are currently working with a leading pharmaceutical company looking for an EHS Director to join their team. This is an exciting opportunity to build a long-term career in a dynamic and innovative environment. You will be responsible for: Overseeing all environmental, safety, and industrial hyg...

• Negotiable
• Posted 5 days ago

EPM is urgently looking for a freelance Regulatory/Clinical Affairs Specialist to support one of our key medical device clients on a 12-month assignment as soon as possible. Below is a brief overview of the role and its requirements: Regulatory Affairs / Clinical Affairs Specialist Medical Device...

• Paris
• Negotiable
• Posted 7 days ago

My client is building the first universal AI Operating System to lay the foundation for Biological Artificial Superintelligence (BASI). This OS integrates a suite of AI agents that decode complex biology, accelerate research, and dramatically increase productivity. Acting as copilots,My clients a...

• Paris
• Negotiable
• Posted 7 days ago

Job Title: Senior Regulatory Affairs Specialist Location: France (Hybrid) Start Date: Within the next month Job Type: Full-time (Consultant, Freelancer, or Contractor) Industry: Medical Devices Key Responsibilities: Documentation Specialist: Lead and manage all regulatory documentation processes,...

• Massachusetts
• Negotiable
• Posted 8 days ago

We have a current opportunity for a Regulatory Affairs Specialist on a contract basis. The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulati...

• Boston
• Negotiable
• Posted 11 days ago

Director, Regulatory Strategy - Global Biopharmaceuticals (Hybrid) A leading global biopharmaceutical company is seeking a Director of Regulatory Strategy to drive regulatory success for complex and high-impact programs. This role is responsible for defining and executing global regulatory strate...

• San Francisco
• US$250000 - US$330000 per annum
• Posted 11 days ago

Title: Senior Director Regulatory Advertising & Promotion A pioneering biopharma is looking to grow the legal team with a Senior Director Regulatory Advertising & Promotion to support their new product launch. This will be a hands-on position, serving as a high level operational and strategic lea...

• San Francisco
• US$220000 - US$280000 per annum
• Posted 11 days ago

Title: Senior Director Regulatory Affairs SUMMARY: A leading biopharmaceutical company is seeking a Sr. Director of Regulatory Affairs. This role involves developing and implementing global strategies to secure and maintain market approval for products in various regions. The position leads the r...

• Massachusetts
• US$200000 - US$230000 per annum
• Posted 11 days ago

Title: Director Global Regulatory Lead A leading pharmaceutical company is growing their team with a Director Global Regulatory Lead to develop and lead global regulatory strategies for complex projects. This is an exciting chance to join a leading company in the industry to support high-level st...

• Massachusetts
• US$200000 - US$230000 per annum
• Posted 12 days ago

Title: Director Global Regulatory Lead A leading pharmaceutical company is growing their team with a Director Global Regulatory Lead to develop and lead global regulatory strategies for complex projects. This is an exciting chance to join a leading company in the industry to support high-level st...

• San Francisco
• US$250000 - US$330000 per annum
• Posted 14 days ago

Title: Senior Director Regulatory Advertising & Promotion A pioneering biopharma is looking to grow the legal team with a Senior Director Regulatory Advertising & Promotion to support their new product launch. This will be a hands-on position, serving as a high level operational and strategic lea...

• San Francisco
• US$220000 - US$280000 per annum
• Posted 18 days ago

Title: Senior Director Regulatory Affairs SUMMARY: A pharmaceutical company is seeking a Director/Sr. Director of Regulatory Affairs. This role involves developing and implementing global strategies to secure and maintain market approval for products in various regions. The position leads the reg...

• Northern Ireland
• Negotiable
• Posted 19 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clinical trials. GAP Asse...

• Northern Ireland
• Negotiable
• Posted 19 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clini...

• Irvine
• Negotiable
• Posted 19 days ago

Title: Regulatory Affairs Senior Manager Summary: Our client is seeking an experienced Senior Manager of Regulatory Affairs to lead the preparation and submission of global regulatory filings, ensuring compliance with clinical, pre-, and post-market requirements. This role involves cross-function...

• Kuala Lumpur
• Negotiable
• Posted 21 days ago

Job Title: Regulatory Affairs Quality Assurance (RAQA) Executive Location: Kuala Lumpur, Malaysia About Us: Our client is a leading medical device company dedicated to improving healthcare through innovative medical devices. Our commitment to quality and regulatory compliance ensures that our pro...

• Tokyo
• Negotiable
• Posted 23 days ago

Job Title: Associate Director, Regulatory Affairs Location: Japan Company Overview: Our client is a leading pharmaceutical company dedicated to developing and delivering innovative therapies to improve patient outcomes. Position Overview: The Associate Director of Regulatory Affairs will be respo...

• Tokyo
• Negotiable
• Posted 23 days ago

Job Title: Associate Director, Regulatory Affairs Location: Tokyo, Japan Company Overview: Our client is a leading pharmaceutical company dedicated to developing and delivering innovative therapies to improve patient outcomes. Their commitment to excellence and patient care drives its mission to ...

• Malaysia
• Negotiable
• Posted 23 days ago

Job Title: Regulatory Affairs Quality Assurance Executive Location: Malaysia About Us: Our client is a leading medical device company dedicated to improving healthcare through innovative medical devices. Their commitment to quality and regulatory compliance ensures that our products meet the high...

• Negotiable
• Posted 23 days ago

Job Title: Regulatory Affairs Quality Assurance Executive Location: Malaysia About Us: Our client is a leading medical device company dedicated to improving healthcare through innovative medical devices. Their commitment to quality and regulatory compliance ensures that our products meet the high...

• Northern Ireland
• Negotiable
• Posted 25 days ago

We have a current opportunity for a Senior Clinical Project Manager working with IVDs on a contract basis. 6 months contract (possible extension) Clinical protocols, risk management plans, knowledge of IVD regulation within Europe Client-facing position (face-to-face) Remote with occasional site ...

• New Jersey
• US$75000 - US$90000 per annum
• Posted 26 days ago

Title: Senior Associate of Regulatory Affairs Summary: A leading, global pharmaceutical client of ours is looking to hire a Senior Associate of Regulatory Affairs, based out of their New Jersey office. This rapidly growing client has drug products spanning generics, branded prescriptions, and inj...

• New Jersey
• Negotiable
• Posted 26 days ago

Title: Senior Associate of Regulatory Operations/CMC Summary: A leading, global pharmaceutical client of ours is looking to hire a Senior Associate of Regulatory Operations and CMC, based out of their New Jersey office. This rapidly growing client has drug products spanning generics, branded pres...

• Morristown
• Negotiable
• Posted 27 days ago

Job Title: Senior Associate, Regulatory Affairs Location: Morristown, New Jersey About the Role: We are seeking a highly motivated and detail-oriented Senior Associate, Regulatory Affairs to join our team. In this role, you will help author, compile, review, and submit high-quality regulatory sub...

• Freiburg im Breisgau
• Negotiable
• Posted 28 days ago

We are looking for ambitious and motivated individuals who enjoy working in a dynamic and fast-growing environment. Together we want to further expand our customer and product portfolio and actively shape the future of medical technology. Regulatory Affairs Specialist (m/w/d) Your tasks: Internal...

• Mountain View
• Negotiable
• Posted 28 days ago

Summary: My Client is seeking an Associate Director of Regulatory Affairs - US Lead to support the department head for developing and implementing global strategies to secure and maintain market approval for product(s) globally (US, EMA, Japan, Australia, Canada). The Associate Director serves as...

• San Francisco
• US$220000 - US$280000 per annum
• Posted 29 days ago

Title: Senior Director Regulatory Affairs SUMMARY: A pharmaceutical company is seeking a Director/Sr. Director of Regulatory Affairs. This role involves developing and implementing global strategies to secure and maintain market approval for products in various regions. The position leads the reg...

• San Francisco
• US$100000 - US$170000 per annum
• Posted 29 days ago

Title: Principal Regulatory Affairs Specialist A leading medical device company is seeking a Principal Regulatory Affairs Specialist to support their growing product portfolio. This is an exciting opportunity to join an innovative company working on breakthrough products. Responsibilities: Develo...

• United States of America
• Negotiable
• Posted about 1 month ago

* Authoring high-quality CMC documentation for US/ EU / UK countries, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle. * P...

• Nottingham
• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.

• Atlanta
• US$150000 - US$200000 per annum
• Posted about 1 month ago

A leading global Medical Device company is seeking a Senior Manager of Regulatory Affairs to join their team on-site in their downtown Atlanta office. This is an exciting opportunity to support high risk innovative products and join a high performing team to achieve global approvals. What You'll ...

• United States of America
• Negotiable
• Posted about 1 month ago

A leading organization in the pharmaceutical and regulatory affairs industry, dedicated to increasing project efficiency and establishing project management standards; are looking for a talented and experienced Project Manager to join the Project Management Office (PMO) team. Key Responsibilities...

• Seattle
• Negotiable
• Posted about 1 month ago

Title: Head of Regulatory and Quality Summary: Join a pioneering leader in medical technology dedicated to advancing patient care and safety. Our client is at the forefront of developing innovative solutions that address critical gaps in diagnostic accuracy and infection prevention. As the Head o...

• New Jersey
• Negotiable
• Posted about 1 month ago

Title: Regulatory Affairs Senior Manager Summary: A leading, global pharmaceutical client of ours is looking to hire a Senior Manager of Regulatory Affairs at their prescription drug specific subsidiary, based out of New Jersey. This rapidly growing client has drugs spanning many different therap...

• Massachusetts
• US$175000 - US$195000 per annum
• Posted about 1 month ago

Title: Associate Director Regulatory Affairs A small but growing clinical stage company is seeking an Associate Director Regulatory Affairs to join the team in a remote capacity. They are seeking a well-rounded RA professional to lead the Regulatory Strategy for their pipeline of phase III produc...

• Tokyo
• Negotiable
• Posted about 1 month ago

Job Title: Regulatory Affairs Specialist Location: Tokyo, Japan Job Type: Full-time (permanent) Our client, a leading pharmaceutical company dedicated to improving global health through innovative medicines. They are committed to excellence in research, development, and regulatory compliance. Job...

• United States of America
• US$140000 - US$190000 per annum
• Posted about 2 months ago

Job Title: Senior Medical Writer OR Associate Director, Medical Writing (Regulatory) Location: Hybrid schedule in San Francisco, New Jersey, or New York Position Overview: A bio-pharmaceutical company is seeking a highly skilled and experienced Senior Medical Writer or Associate Director, Medical...

• Oberhonnefeld-Gierend
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a Head of QA/RA on a permanent basis. The position will be based in Oberhonnefeld-Gierend. For further information about this position please apply. Job Summary: The Head of Quality and Regulatory Affairs will oversee and manage all quality and regulatory functio...

• Germany
• Negotiable
• Posted about 2 months ago

Job Description: Integrated Clinician - Medical Devices (Active & Non-Active) Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct clinical evaluations and assessments of active and no...

• Barcelona
• Negotiable
• Posted about 2 months ago

I am working with a highly innovative biotech company based in Barcelona, specializing in the development of groundbreaking medical devices. We are looking for a Regulatory Affairs & Quality Assurance Specialist to join their team. Ideal Profile: Experience in regulatory strategies and documentat...

• New York
• Negotiable
• Posted about 2 months ago

Regulatory Affairs Manager - Pharma (Remote - East Coast Preferred) A global leader in drug delivery systems is seeking a Regulatory Affairs Manager to support U.S. regulatory activities across multiple business divisions. This role will be instrumental in defining regulatory strategies, ensuring...

• Massachusetts
• Negotiable
• Posted about 2 months ago

Senior International Regulatory Affairs Specialist - Orthopedic Medical Device Location: Greater Boston, MA We are seeking a Senior International Regulatory Affairs Specialist to join a leading orthopedic medical device company in the Greater Boston area. This role will be responsible for develop...

• Cincinnati
• US$90000 - US$120000 per annum
• Posted about 2 months ago

Title: Senior Regulatory Affairs and Quality Systems Specialist The Regulatory Affairs and Quality Systems Specialist is responsible for supporting regulatory and quality assurance processes related to in vitro diagnostic (IVD) medical devices. This organization offers a dynamic and collaborative...

• Philadelphia
• Up to US$225000 per annum
• Posted about 2 months ago

Director of Regulatory Affairs Strategy This position is with a rapidly growing pharmaceutical company known for its commitment to advancing transformative therapies. In this role you will have a unique opportunity to lead regulatory strategies for innovative pharmaceutical products, making a mea...

• Connecticut
• Negotiable
• Posted 2 months ago

Quality Control Supervisor Are you a dedicated Quality Control professional looking for an opportunity to lead and make a significant impact within the biopharma industry? As QC Supervisor, your responsibilities will include: - Overseeing daily operations within the Quality Control department - E...