QA Regulatory Manager (Trainee / Newly Qualified QP)Site-based with flexibility for some remote working in the long termLocation: Can be based at any UK site: Guildford, South West London, Sheffield, Preston, Stoke-on-Trent or ManchesterAre you currently working towards QP status or recently qualified and looking for an opportunity that offers genuine career development? Our client, a growing sterile pharmaceutical manufacturer, is seeking a QA Regulatory Manager to join their Quality team.This ...
Certification & Compliance SpecialistBirmingham Permanent - Hybrid (4 Days On-site / 1 Day WFH)Salary up to £55,000 + BenefitsAre you experienced in product certification and regulatory compliance within manufacturing? Looking for a role where you can shape compliance strategy, influence new product development and work across international markets?The CompanyWe are supporting a well-established manufacturer supplying innovative building services products across global markets. As the ...
Certification & Compliance SpecialistDoncaster Permanent - Hybrid (4 Days On-site / 1 Day WFH) Salary up to £42,000 + BenefitsAre you experienced in product certification and regulatory compliance within manufacturing? Looking for a role where you can shape compliance strategy, influence new product development and work across international markets?The CompanyWe are supporting a well-established manufacturer supplying innovative building services products across global markets. As the ...
Regulatory Affairs Specialist - Medical Devices - CambridgeA growing technology and product development organisation in Cambridge is looking to appoint a Regulatory Affairs Specialist to support a wide range of innovative projects. This role sits within a team that works closely with engineers, scientists and designers, helping them bring complex ideas to life while ensuring that every development pathway aligns with global regulatory expectations. The work is varied, fast‑moving and highly ...
Senior Quality Manager / Responsible PersonGenerics Pharmaceuticals | Greater London/Hertfordshire borderWorking Pattern: Hybrid (approximately three days per week in the office).A genuine opportunity to shape the future of Quality within one of the UK’s most exciting and ambitious generics pharmaceutical businesses.We’re delighted to be exclusively supporting an ambitious, privately owned pharmaceutical organisation as they continue an exciting period of sustained growth.Having significantly ...
Pharmacovigilance and Scientific Information ManagerLocation: Woking (option for up to 2 days per week remote work)A leading global manufacturer of pharmaceutical products across the UK and Europe, is seeking an experienced and dynamic Pharmacovigilance (PV) and Scientific Information (SI) Manager to join their Scientific Affairs team and lead the way in ensuring the highest standards of safety and information management.Your Impactful RoleAs the PV and SI Manager, you will be at the heart of ...
As an Insolvency Administrator in Dunfermline, you'll be responsible for managing the day-to-day administration of insolvency cases, ensuring everything runs smoothly and efficiently. This role is key in supporting the business services sector by handling cases with care and precision.Client DetailsThis company operates within the business services industry and is based in Dunfermline.DescriptionManage a portfolio of insolvency cases, including liquidations, administrations, and ...
W Talent are delighted to be partnering with an established manufacturing business to recruit a Regulatory Affairs Specialist. This is an opportunity to join a growing Technical function, supporting regulatory compliance and ensuring products meet the required standards throughout their lifecycle.Job DescriptionReporting to the Technical Manager, the Regulatory Affairs Specialist will play a key role in ensuring products meet all relevant regulatory requirements and legislation. You will take ...
Regulatory Affairs CoordinatorHertfordHybrid/Part-Time Working Available Up to £40,000An established manufacturer of regulated products is seeking a Regulatory Affairs Coordinator to support the ongoing maintenance of compliance and technical documentation across an established portfolio of products.This is a hands-on role suited to someone who enjoys practical regulatory work within an SME environment and can efficiently manage documentation and compliance activities without unnecessary ...
My client, my Pharmaceutical organisation based in Aldridge are looking for Regulatory office to join their team on a Permanent basis* Regulatory Officer* Aldridge* Full time* Permanent* Monday – Friday 8am – 4pm* £31,000 per annumThe role of the Regulatory Officer will be:Attend to all duties as requested by the Regulatory Affairs Manager, and to assist in any other area of the office, as required.To adhere to company’s Standard Operating Procedures at all times and will comply with GDP and ...
