Regulatory Affairs Specialist

**Regulatory Affairs Specialist - Medical Device** Xplore Life Science is recruiting for a Regulatory Affairs Specialist. This role is ideal for someone who is looking to join a team that is responsible for collecting, evaluating, organising, communicating, and understanding of information relating to regulatory requirements for new and existing...

**Regulatory Affairs Specialist - Medical Device** Xplore Life Science is recruiting for a Regulatory Affairs Specialist. This role is ideal for someone who is looking to join a team that is responsible for collecting, evaluating, organising, communicating, and understanding of information relating to regulatory requirements for new and existing...

Job SummaryVectura Group plc is seeking a highly skilled Regulatory Affairs Specialist to lead our medical device regulatory activities. This role involves assuming the role of Regulatory Affairs Manager with specialized expertise in medical devices and drug-device combination products (DDCPs). About Vectura Group plcWe are a global leader in developing...

An excellent opportunity to join a well-established regulatory consultancy that is just entering a period of sustained growth. They have a large range of clients including SMEs and multi-nationals; they act as outsourced regulatory department for some clientsand have projects of all sizes with a EU wide portfolio. The roles are delivery focussed, there is no...

Job Title: Regulatory Affairs SpecialistEstimated Salary: $80,000 - $110,000 per annumAbout UsWe are a leading multinational pharmaceutical company based across global locations. Our mission is to accelerate access to affordable and innovative medicines.Job DescriptionThe successful candidate will be responsible for preparation and submission of UK MAA...

Regulatory Affairs Specialist - US Market £45k-£55k (dep on exp) Cambridge We have a brand-new vacancy for a Regulatory Affairs Specialist to join a fascinating Cambridge based R&D technology company. This business is very well established and is undergoing rapid growth due to the impact that their market disruptive technology is having on the medical...

Senior Regulatory Affairs, contract job, Emerging Markets, virology, Asia, LATAM, Africa, Middle East, EEU Senior Regulatory Affairs Associate - Emerging Markets **Your new company **This well known biopharmaceutical company are looking for an experienced Regulatory Affairs Associate for a 12 month Senior Regulatory Affairs Associate contract job, this...

Senior Regulatory Affairs SpecialistAt VCLS, we are expanding our Clinical Trial Submissions (CTS) group and seeking an experienced Regulatory Affairs professional to join our team.This role is ideal for someone with 4+ years of experience in regulatory affairs and a strong background in Clinical Trial Submissions.As part of a supportive and collaborative...

Key Role in UK Regulatory AffairsA key position has become available in our UK location for an EU Regulatory Affairs Specialist. As a vital member of our team, you will play a crucial role in supporting the preparation and submission of regulatory documentation for marketing authorization applications in the UK.Main Responsibilities:Preparation and...

Job Title: Regulatory Affairs SpecialistAbout Us:Dr. Reddy's Laboratories is a leading multinational pharmaceutical company based globally with over 24,000 employees.We accelerate access to affordable and innovative medicines for better health outcomes worldwide.Location: Dr. Reddy's (UK) Ltd, Cambridge (UK)Job Description:This role involves the preparation...

Biochrom is part of Harvard Bioscience (HBIO), a global business providing life science, laboratory apparatus worldwide. Reporting to Biochrom QRA Manager, the **Quality and Regulatory Affairs Specialist** (QRA Specialist) supports our _in-vitro_ diagnostic product registrations, timely undertaking of post market surveillance as well as monitoring...

CK Group are recruiting for a Regulatory Affairs Specialist to join a biopharmaceutical company on a remote basis, but with some occasional visits to their site based in Cambridge for a 12 month contract. **Rates**: Paying up to £28.33 PAYE or £37.67 per hour Umbrella **Company**: Our client is committed to unlocking the potential of biology for patients...

Regulatory Affairs, CMC, biologics, management, biopharmaceutical, oncology, permanent job, Your new company: Your new role: What you'll need to succeed: You will need to have had significant experience in Regulatory Affairs CMC and/or relevant pharmaceutical industry experience; experience in the preparation of CMC components of MAA or post-approval...

REGULATORY AFFAIRS | RA | INTERNATIONAL | FULL LIFECYCLE | OUT OF SCOPE This is leading biopharmaceutical company and one of the top 10 largest pharmaceutical companies across the world, with a great product portfolio across a range of therapeutic areas (Oncology and virology to name a few). They are looking to expand their internationalregulatory team by 1...

Job DescriptionWe are seeking an experienced Regulatory Affairs Consultant to join our team at LennTech Search. This is a fully remote position that requires 3-6 months of commitment with an hourly rate.Key ResponsibilitiesProvide regulatory support to the O1 Device Development (DD) team, including final review, comment, and approval of device-related...

Senior Quality Assurance & Regulatory Affairs Specialist Cambridge £45k-£55k (dep on exp) plus bonus and excellent benefits We are looking for a Senior QA & Regulatory Affairs Specialist with excellent academics and experience within a variety of different industries - a mixture of Medical and non-medical. You will be joining a high calibre,...

OverviewCpl Life Sciences is seeking a Senior Director Regulatory Affairs to join our team. This role offers the opportunity to lead client projects, provide strategic regulatory advice, and ensure compliance with UK, EU, and US health authorities.About the RoleAs Senior Director Regulatory Affairs, you will be responsible for preparing regulatory submission...

Biopharmaceutical, regulatory affairs, senior management, CMC, permanent job, oncology, hybrid. **What you'll need to succeed**You will need to have had significant experience in Regulatory Affairs CMC and/or relevant pharmaceutical industry experience; experience in the preparation of CMC components of MAA or post-approval submissions for small molecule...

Company Overview:Bicycle Therapeutics is a pioneering pharmaceutical company focused on developing innovative medicines that tackle underserved diseases. With a unique approach to target binding, the company has made significant strides in drug development, and its commitment to excellence sets it apart.The role of Senior Associate, Regulatory Affairs is...

VCLS is offering a 30-month Post-Graduate Regulatory Science Apprenticeship with TOPRA. This programme combines comprehensive Regulatory training with hands-on experience working with experienced Consultants and clients in the pharmaceutical and medical device sectors.About the ApprenticeshipThe apprenticeship is designed to provide knowledge, skills, and...