Regulatory Jobs | Search & Apply Today

• Canonsburg
• Negotiable
• Posted 3 days ago

Director of Regulatory Affairs Advertising and Promotions Company Summary: My client, a leading global pharmaceutical company focuses on expanding access to quality treatment options for a wide variety of therapeutic areas from cardiovascular health and infectious diseases to oncology. My client ...

• Japan
• Negotiable
• Posted 5 days ago

My client is a large multinational healthcare company with its products, therapies, and digital health solutions available in more than 100 countries. They are currently looking for 2 Regulatory Leads, Pharmaceuticals and Medical Devices in Japan. Location: Tokyo Role: Regulatory Lead - Medical D...

• Trenton
• Negotiable
• Posted 10 days ago

100% REMOTE -- Hiring for a Senior Manager of Pharmaceutical Product Labeling Our client is a large, well-respected company known around the world for their family-trusted products. An ideal candidate would need at least 6 years' experience in the pharmaceutical industry OR health authority, with...

• New Haven
• Negotiable
• Posted 10 days ago

We have a current opportunity for a Scientist I, Req# 17053939 on a contract basedl in based in Boston. Scientist 1 Needed!!!!!! The duties of this role are generally conducted in both laboratory and office environments. Employees must be able, with or without accommodation to use a computer; eng...

• Switzerland
• Negotiable
• Posted 11 days ago

Partnering with a global pharmaceutical client, looking for a CTA Manager on a 12 month contract basis, starting in December. EU Regulatory Affairs - CTA Manager Provide effective operational and regulatory support for assigned regulatory submission and maintenance activities, including preparati...

• Bethesda
• Negotiable
• Posted 12 days ago

We have multiple Medical Writer positions currently open for qualified applicants. This position has WORK FROM HOME (WFH) Flexibility. For further information about this position please apply.

• United States of America
• Negotiable
• Posted 12 days ago

We have a current opportunity for a Senior Medical Writer on a permanent basis. For further information about this position please apply. Senior Medical Writer Remote Summary: My client is a full-service CRO that provides an expansive range of expertise based clinical research services to worldwi...

• Beijing
• Negotiable
• Posted 16 days ago

Title: Regulatory Operation Manager Location: Beijing, China Overview: One of the global biotech firms is currently growing and seeking a Regulatory Operation Manager to join the team. As a Regulatory Operation Manager in this biotech company, you gain the opportunity to oversee cell therapy prod...

• China
• Negotiable
• Posted 16 days ago

We have an exciting opportunity with a Global Contract Research Organisation (CRO) based in Beijing/Shanghai. Due to their recent success, they are looking for a Senior QA Auditor to be a part of their team. This is an exciting opportunity to be a part of a Global CRO with strong presence in the ...

• Lausanne
• Negotiable
• Posted 17 days ago

Our client needs the support of an experienced Regulatory Affairs Consultant working within the US Market and FDA to support two new combination products in the preparation stage for pre-submission, submission, and registration in the US. Project length: 6 - 12 months project Project start: Novem...

• New Hampshire
• Negotiable
• Posted 17 days ago

A global Biotechnology Research company is hiring for a Regulatory CMC Specialist/Manager to join their team. They are looking for motivated individuals who are accustom to working in a fast-paced work environment. Responsibilities: Prepare and review documents, ensuring compliance with Regulator...

• United States of America
• Negotiable
• Posted 17 days ago

We have a current opportunity for a Senior Manager, Medical Writing on a permanent basis. The position will be based in Menlo Park. For further information about this position please apply. Senior Manager, Medical Writing On-site - Menlo Park, CA Summary: A leading biotechnology company responsib...

• Pensacola
• Negotiable
• Posted 20 days ago

Director of Regulatory Affairs Company Summary: My client, a pharmaceutical manufacturing company focusing on animal health is looking to add a Regulatory Affairs Director to their team! This role will be based in Pensacola, Florida. The Regulatory Affairs Director will be responsible for: Design...

• Bethesda
• Negotiable
• Posted 22 days ago

HYBRID REGULATORY AFFAIRS MANAGER -- POSITION NOW OPEN Our partner client is hiring multiple Regulatory Manager Positions - The position is a hybrid role (2 days on-site in Bethesda, Maryland and 3 days working remotely) We are ideally looking for someone with previous experience in a Regulatory ...

• Beijing
• Negotiable
• Posted 23 days ago

Title: Regulatory Operation Manager Location: Beijing, China Overview: One of the global biotech firms is currently growing and seeking a Regulatory Operation Manager to join the team. As a Regulatory Operation Manager in this biotech company, you gain the opportunity to oversee cell therapy prod...

• Philadelphia
• Negotiable
• Posted 23 days ago

We have a current opportunity for a Regulatory Affairs Manager on a 4- month contract basis (likely to extend). The position will be based in Philadelphia. For further information about this position please apply. We are only able to place candidates on a W/2. The Manager, Regulatory Information ...

• United States of America
• Negotiable
• Posted 24 days ago

100% Remote Opportunity Summary: The Associate Director of Medical Writing will serve as the medical writing lead for the preparation of a variety of clinical documents, including but not limited to CSRs, Investigator's Brochures, and protocols, for regulatory/clinical purposes. You will also ove...

• Portsmouth
• Negotiable
• Posted 24 days ago

Regulatory Affairs CMC Project Manager Company Summary: My client, a global leading biotechnology company focused on fighting a wide range of rare diseases is looking to add a Regulatory CMC professional to their team! This role will be hybrid based in Portsmouth, New Hampshire requiring 2 days p...

• San Francisco
• Negotiable
• Posted 26 days ago

We have a current opportunity for a Director, Bioanalytical contract basis. The position will be based in San Francisco. For further information about this position please apply. A minimum of 13 years experience in the pharmaceutical A minimum of 10 years previous management experience is require...

• Japan
• Negotiable
• Posted 30 days ago

My client is a large international biopharmaceutical company with presence across more than 100 countries. They specialise in helping companies with late-stage clinical trials, clinical development, and medical affairs. They are currently looking for a Regulatory Consultant/Manager in Japan. High...

• Japan
• Negotiable
• Posted 30 days ago

My client is an international biopharmaceutical company that has more than 60k employees globally and more than 3k employees in Japan, focusing on developing and manufacturing drugs/vaccines for critical diseases. Role: Quality Assurance Specialist Location: Maibara, Shiga, Japan (Relocation pack...

• Japan
• Negotiable
• Posted about 1 month ago

My client is an international medical Equipment Manufacturing company, supporting hospitals and life science institutions with Class III and Class IIII medical devices in their most important task - saving lives. Role: QcRM/QRC, Regulatory Affairs Specialist Location: Tokyo, Japan Requirement: Ba...

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

We have a FULLY REMOTE position for a Global Labelling Product Leader (GLPL). This is an exciting position with a globally known and respected company. Perfect for a qualified candidate preferring to work from home. Ideal candidates would have: 6+ years experience in the pharmaceutical industry o...

• Bristol
• Negotiable
• Posted about 1 month ago

Looking for a Regulatory Affairs Submission Expert! This opportunity will focus on review of the submission content and assisting by developing, documenting, and submitting/filing the appropriate supplements to the FDA. Responsibilities Supporting Regulatory CMC work, including but not limited to...

• Bethesda
• Negotiable
• Posted about 1 month ago

Company Summary: My client, a full service CRO+ that is focused on providing support to global drug, vaccine, and medical device clients, is looking to add a Regulatory Manager to their team! This role will be hybrid based in Bethesda, Maryland. The Regulatory Affairs Manager will be responsible ...

• Boston
• US$180000 - US$220000 per year
• Posted about 1 month ago

We have a current opportunity for a Senior Managers to Executive Directors Regulatory CMC on a permanent basis. The position is remote with occasional meeting based in Boston. Qualifications: Experience liaising with Regulatory Agencies: led in Agency Interactions and product development meetings...

• San Diego
• US$220000 - US$240000 per year
• Posted about 1 month ago

We have a current opportunity for a (Cell Therapy) Senior Director Regulatory CMC on a permanent basis. The position will be based in San Diego. Responsibilites: Partnering with global health authorities Developing creative & innovative strategies Ensuring that CMC-related applications and/or sec...

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

Summary: The Medical Writer will support the development and creation of regulatory, clinical and scientific documents in accordance with US FDA requirements, European Medical Device Regulations and any procedures. The two main documents they will work on are Clinical Evaluation Reports (CERs) an...

• Beijing
• Negotiable
• Posted about 1 month ago

Title: Regulatory Operation Manager Location: Beijing, China Overview: One of the global biotech firms is currently growing and seeking a Regulatory Operation Manager to join the team. As a Regulatory Operation Manager in this biotech company, you gain the opportunity to oversee cell therapy prod...

• Japan
• Negotiable
• Posted about 1 month ago

My client is a global, research and development-driven pharmaceutical company headquartered in Osaka. Role: RA Manager - Oncology Location: Tokyo & Osaka Requirements: Business level Japanese, English TOEIC 730 3-5years experience in RA Oncology experience or can be from PMDA/FDA No people manage...

• Paramus
• Negotiable
• Posted about 1 month ago

Company Summary: My client, a biopharmaceutical company focusing on fighting rare diseases is looking to add a Regulatory professional to their team - they are open to hiring at the Manager level through Associate Director! This role will be hybrid based in Paramus, New Jersey requiring 2 days pe...

• Ohio
• Negotiable
• Posted about 1 month ago

An exciting Medical Device Manufacturing company is looking to bring a Senior Manager of Regulatory Affairs to their growing team. They are looking for highly motivated candidates with strong leadership experience. The Senior Manger Regulatory Affairs will be responsible for: Managing a team of R...

• Pleasanton
• US$200000 - US$240000 per year
• Posted about 1 month ago

We have a current opportunity for a Senior Director Regulatory Affairs Medical Device on a permanent basis. The position has three potential locations, two on the West Coast and one on the East Coast. There is also the opportunity for this role to be remote with occasional monthly travel to one o...

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

An innovative Medical Device Manufacturing company is looking to bring a Regulatory Specialist onto their team. They are seeking a highly motivated Regulatory professional who is able to work in a well established, but rapidly growing team. The Regulatory Affairs Specialist will be responsible fo...

• Japan
• Negotiable
• Posted about 1 month ago

My client is an international biotechnology company that is research-based and oncology-focused. They specialize in drug development for cancer treatment. They are currently looking for 3 positions, please refer to the below: 1. Role: Submission Operations Associate Manager (Japan/Remote Working)...

• Japan
• Negotiable
• Posted about 1 month ago

My client is an international biopharmaceutical company that has more than 60k employees globally and more than 3k employees in Japan, focusing on developing and manufacturing drugs/vaccines for critical diseases. Role: Quality Assurance Specialist Location: Maibara, Shiga, Japan (Relocation pack...

• Boston
• Negotiable
• Posted about 2 months ago

- Lead the development and strategy for clinical regulatory submission documents and other clinical documents - Experience authoring clinical study protocols and amendments, clinical study reports, investigator brochures and updates, and module 2 summaries - supporting ALL clinical project teams ...

• Hamburg
• Negotiable
• Posted about 2 months ago

Senior Regulatory Affairs Manager (m / f / d) Medical Devices Location: Multiple Locations In Germany 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 regul...

• Thüringen
• Negotiable
• Posted about 2 months ago

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 to join a leading Medical Device company in Germany with a gre...

• Lübeck
• Negotiable
• Posted about 2 months ago

Senior Regulatory Affairs Manager (m / f / d) Medical Devices Location: Lübeck,Germany 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 requireme...

• Berlin
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a Senior Regulatory Affairs Manager on a Permanent basis. The position will be based in Berlin. For further information about this position please apply. Senior Regulatory Affairs Manager (m / f / d) Medical Devices As a Regulatory Affairs Manager (m/f/d) you'll ...

• San Francisco
• Negotiable
• Posted about 2 months ago

The Associate Director of Regulatory Affairs (Strategy) will help assist in strategic and operations regulatory functions including Clinical, Non-clinical, and CMC. Key Duties: Create effective regulatory strategies and ensure regulatory compliance Work together with regulatory and cross-function...

• Japan
• Negotiable
• Posted about 2 months ago

My client is an international biotechnology company that is research-based and oncology-focused. They specialize in drug development for cancer treatment. They are currently looking for 3 positions, please refer to the below: 1. Role: Submission Operations Associate Manager (Japan/Remote Working)...

• Bethesda
• Negotiable
• Posted about 2 months ago

VP Regulatory Affairs -Fully Remote Benefits include health, dental, and vision 12-month Contract Role Passionate about Regulatory Affairs? Looking for a Regulatory Vice President to work with a Research company developing innovative strategies and groundbreaking medical advances. The company has...

• Massachusetts
• Negotiable
• Posted about 2 months ago

Title: Associate Director/Director Regulatory CMC Summary: An innovative biotech company pioneering the gene therapy space is looking to bring on an expert in Regulatory CMC this year. With a broad and deep pipeline of over 10 programs, the team is utilizing their groundbreaking platform to addre...

• Illinois
• Negotiable
• Posted about 2 months ago

Title: Regulatory Affairs Project Manager Summary: A globally established, innovative leader in the medical device industry is looking for a dynamic regulatory professional to come join their team as a Regulatory Affairs Manager. This world renowned company is looking for a regulatory leader to p...

• Japan
• Negotiable
• Posted about 2 months ago

My client is a global healthcare company that specializes in manufacturing medical devices and research for future applications in neuroscience. They are currently looking for a Regulatory & Safety Controller in Japan. Highlight: Opportunity to travel domestically in Japan and internationally Loc...

• Japan
• Negotiable
• Posted about 2 months ago

My client is a large international biopharmaceutical company with a presence across more than 100 countries. They specialize in helping companies with late-stage clinical trials, clinical development, and medical affairs. They are currently looking for a Regulatory Consultant/Manager in Japan. Hi...

• Germany
• Negotiable
• Posted about 2 months ago

Activities & Responsibilities * Evaluating quality management systems of IVD manufacturers based on current quality management standards (e.g. EN ISO 13485) and other international regulatory requirements (e.g. IVDD, IVDR, MDSAP). * Documenting and carrying out on-site audits. * Providing profess...

• South San Francisco
• Negotiable
• Posted about 2 months ago

A late-stage biopharmaceutical company that is on the forefront of muscle biology research is currently looking for a Regulatory Affairs Associate to join the team for a 6-month contract that has the potential of extension and conversion. *Hybrid Responsibilities: Reviewing and assessing submissi...

• Germany
• Negotiable
• Posted about 2 months ago

I am currently recruiting for an exciting Auditor position within one of Europe's leading Notified Bodies. If you are thinking about making the step into Notified Bodies, or already work there and would like to work for one of the largest firms in the market, then keep reading! Activities & Respo...