Regulatory Affairs Specialist

Social network you want to login/join with:Regulatory Affairs Specialist, CambridgeClient:Cure TalentLocation:CambridgeJob Category:OtherEU work permit required:YesJob Views:1Posted:30.03.2025Expiry Date:14.05.2025Job Description:Cure Talent are delighted to be partnered with an exciting Diagnostics company, specialising in Gastrointestinal Cancer, who, due...

About the job In the context of our growing activities, we are looking for a Regulatory Affairs Specialist to join our teams in the United Kingdom. You will integrate a team of dedicated Regulatory Affairs professionals and will have the mission to develop PLG's local UK Regulatory Affairs presence, taking responsibility for new regulatory activities...

Regulatory Affairs ManagerLocation: Cambridge, Hybrid - Open to remote workingDepartment: Regulatory AffairsJob type: PermanentJoin us and make a difference when it matters mostAt Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals,...

Regulatory Affairs ManagerLocation: Cambridge, Hybrid - Open to remote workingDepartment: Regulatory AffairsJob type: PermanentJoin us and make a difference when it matters mostAt Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals,...

Job Title: Regulatory Affairs AssistantContract Duration: 12 MonthsLocation: United Kingdom, CambridgeKey Responsibilities:Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.Work collaboratively to support the team by executing routine data entry, such as the input of submission related dates and...

Job Description Regulatory Affairs and Quality Assurance Assistant - Medical Devices - CambridgeDue to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company's Quality Assurance and Regulatory Affairs Manager. The team provide quality...

Regulatory Affairs and Quality Assurance Assistant - Medical Devices - CambridgeDue to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company's Quality Assurance and Regulatory Affairs Manager. The team provide quality assurance and regulatory...

Job Title: Regulatory Affairs AssistantContract Duration: 12 MonthsLocation: United Kingdom, CambridgeKey Responsibilities:Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.Work collaboratively to support the team by executing routine data entry, such as the input of submission related dates,...

Job Title: Regulatory Affairs AssistantContract Duration: 12 MonthsLocation: United Kingdom, CambridgeKey Responsibilities:Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.Work collaboratively to support the team by executing routine data entry, such as the input of submission related dates,...

Social network you want to login/join with:Responsibilities:Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.Work collaboratively to support the team by executing routine data entry, such as the input of submission related dates, regulatory assessment comments.Ensure completeness, correctness and...

Overview Job Title: Senior Director, Regulatory Affairs Job Type: Full-time, permanent position Location: Cambridge, UK – Hybrid Remuneration: £130,000 + Benefits Cpl Life Sciences is collaborating with a prestigious global drug development consultancy business that specialises in supporting pharma, biotechs, spin-outs, and academic...

Job DescriptionKite, a Gilead company, is grounded by one common goal - curing cancer. We are at the forefront of immunotherapy and engineered T cell therapy. Our personalized approach is what sets us apart. Unlike traditional pharmaceutical manufacturing, our therapies are not created on an assembly line. With CAR T-cell therapy, we are reengineering a...

CK Group are working with a very well backed biotechnology company, with a strong pipeline who are looking for an Associate Director, Regulatory Affairs, for a six-month contract. The role will be in support of their expanding Oncology portfolio; extensive Oncology experience is an absolute must, radiopharmaceuticals experience would be highly advantageous....

The Director Regulatory Affairs CMC will be responsible for the development strategy and tracking of CMC regulatory activities for assigned BicycleTx programs or projects.The Director Regulatory Affairs CMC will be responsible for supporting the delivery of CMC regulatory strategy and submissions for their assigned BicycleTx programs or projects working...

Description   The CMC (Chemistry, Manufacturing, and Controls) Regulatory Affairs International Affiliate Team is seeking a motivated, curious, flexible, and culturally aware experienced Regulatory professional to assume a full-time employment position in Gilead's office in Cambridge, United Kingdom in the capacity of  CMC   Regulatory Affairs Senior...

Description   FUNCTION: Regulatory Affairs (RA) Labeling POSITION OVERVIEW: Regulatory Affairs Labeling is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams. Regulatory Affairs Labeling creates, updates, and maintains product information and labeling...

Description   We are looking for an experienced Regulatory professional to join our global team. Location: Cambridge or Uxbridge. In this role, you will be responsible for acting as one of the EU Regulatory leads for Kite's existing commercial and/or clinical programs. Your duties will include defining the regulatory strategy, plans, and objectives...

Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company with global operations.Location: Dr. Reddy's (UK) Ltd, Cambridge, UKMain Responsibilities:Coordinate and submit MAA procedures for UK national and IRP modules.Prepare, submit, and coordinate UK national variations and renewal procedures, including response documents to deficiency...

Social network you want to login/join with:Associate Director, Regulatory Affairs CMC, CambridgeshireClient:Gilead Sciences International, Ltd.Location:Cambridgeshire, United KingdomJob Category:OtherEU work permit required:YesJob Reference:0014f5d00087Job Views:7Posted:03.03.2025Expiry Date:17.04.2025Job Description:DescriptionWe are looking for an...

Social network you want to login/join with:Senior Manager, Regulatory Affairs CMC, CambridgeshireClient: Gilead Sciences International, Ltd.Location: Cambridgeshire, United KingdomJob Category: OtherEU work permit required: YesJob Reference: d2e44a447d37Job Views: 7Posted: 03.03.2025Expiry Date: 17.04.2025Job Description:The CMC (Chemistry, Manufacturing,...