REGULATORY AFFAIRS MANAGER jobs in CAMBRIDGESHIRE, United Kingdom

Proclinical is seeking a Regulatory Affairs Manager. This role is pivotal in providing country-specific regulatory.... Responsibilities: Manage regulatory affairs and local regulatory strategy for a portfolio of products. Ensure timely regulatory...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Cambridge... field. Extensive experience in Regulatory Affairs across the UK market and an understanding of the local regulatory...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, UK/IE... Regulatory Affairs and Compliance particularly within pharmaceutical industry You will have a proven background working on CTA...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Cambridge... field. Extensive experience in Regulatory Affairs across the UK market and an understanding of the local regulatory...

Reference Number: JO-2404-532760 Regulatory Affairs Manager Rate: £50,000 – 55,000 Job Type: Permanent Location...: Cambridge Job Title: Regulatory Affairs Manager (Food & Beverages) Job Type: Permanent position Location: Chiswick...

Job Purpose The Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical... and other controlled documents, including for Medical and Regulatory writing activities Partners with Regulatory Affairs and cross...

Job Purpose As a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development... Senior Manager, Regulatory Affairs CMC will serve as a subject matter expert, which will involve collaborating with multiple...

areas including preclinical, clinical, regulatory affairs and manufacturing Highly collaborative, strong relationship... role of Manager, Quality, supports Quality oversight for Bicycle’s development programs, ensuring compliance...

Regulatory Affairs, CMC Supply chain…) and SPs Establish and maintain excellent professional relationships with Services...Title: Clinical Project Manager Company: Ipsen Bioscience, Inc. Job Description: Clinical Project Manager (CPM...

with clinical business teams, clinical science, clinical affairs, legal and regulatory to ensure compliance of marketing messages...Job Title Senior Product Marketing Manager for Radiology Informatics Job Description Become part of Radiology...

, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality...A market leading biotech in Cambridge are actively looking for a Business Development Manager to drive new commercial...

Affairs, Regulatory Affairs, Global Patient Safety, Clinical Operations, BioStats & Data Management, Clinical Quality...The Business Analysis & Operations Senior Manager will drive consistency across the Global Development (GD) IT team...

structure including, Regulatory Affairs, Legal, Human Resources, Finance, Public Policy, Privacy/Data Usage, Global Ethics... regulatory requirements from DORA. This position will report to the Head of 1st line Risk & Resilience in the Open Banking Team...

Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors. Complex Systems.... Although you will be leading projects in this role we are not looking for someone who is a career project manager, you will need to still be able...

. Although you will not have line manager responsibility over other engineers you will at times have project leadership responsibilities. Due..., Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory...

Design, Human Factors, Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors...., Project Manager, Medical Devices Inventor, or Mechanical Design Consultant for a newly approved role. The company is based in...

with regulatory requirements, Good Clinical Practice (GCP) guidelines and SOPs to the most rigorous standards of quality, timely... the CPM in site selection, verify timely collection of essential study documents, such as regulatory and ethics committee...