Senior Manager, Regulatory Compliance

Global Regulatory and Operations Senior Director page is loaded Global Regulatory and Operations Senior Director Apply locations GB Cambridge time type Full time posted on Posted 30+ Days Ago job requisition id JR1216 Location: Cambridge (Hybrid working - On average two or three times a month in the office) Job type: Permanent At Mundipharma, we are...

Position: Sr Manager Regulatory Affairs Monday - Friday, 39 hours per week Manager of Regulatory Affairs to support one or more products from a regional regulatory perspective. As an integral member of the Global Regulatory Team (GRT), you will develop and execute regional regulatory strategies to achieve desired labelling and manage effective agency...

Position: Sr Manager Regulatory Affairs Monday - Friday, 39 hours per week Manager of Regulatory Affairs to support one or more products from a regional regulatory perspective. As an integral member of the Global Regulatory Team (GRT), you will develop and execute regional regulatory strategies to achieve desired labelling and manage effective agency...

Location: Cambridge (Hybrid working - On average two or three times a month in the office) Job type: Permanent At 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, our partners, and our employees. Role and responsibilities ...

Regulatory Affairs Labelling Associate Project Manager contract job This well-known biopharmaceutical company is looking for a Regulatory Affairs Labelling Associate Project Manager to join their Labelling team on a contracting basis. This is a 12-month contract job with scope for extension and is fully remote. As part of the Global Labelling Strategy...

Job Description Job title: Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development, execution and tracking of regulatory CMC and medical device activities. Candidates must have protein experience in addition to...

Job title: Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development, execution and tracking of regulatory CMC and medical device activities. Candidates must have protein experience in addition to medical device...

Job title: Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development, execution and tracking of regulatory CMC and medical device activities. Candidates must have protein experience in addition to medical device...

Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development, execution and tracking of regulatory CMC and medical device activities. Candidates must have protein experience in addition to medical device (auto injector)...

Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development, execution and tracking of regulatory CMC and medical device activities. Candidates must have protein experience in addition to medical device (auto injector)...

Job Description Job title: Senior Manager Regulatory Affairs Writing A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. The role will play a pivotal role in the clinical development team. You will lead a team responsible for developing the content for submissions to both US and EU...

Job title: Senior Manager Regulatory Affairs Writing A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. The role will play a pivotal role in the clinical development team. You will lead a team responsible for developing the content for submissions to both US and EU regulatory agencies. ...

Job title: Senior Manager Regulatory Affairs Writing A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. The role will play a pivotal role in the clinical development team. You will lead a team responsible for developing the content for submissions to both US and EU regulatory agencies. ...

Risk & Compliance Manager - Financal Promotions A leading tech company are looking for a Risk & Compliance Manager for the Marketing and Revenue & Trading teams with a key focus of supporting the business on regulatory and risk matters, in order to effectively manage the risk and compliance environment with a commercial lens. This role will be supporting...

Risk & Compliance Manager - Financal Promotions A leading tech company are looking for a Risk & Compliance Manager for the Marketing and Revenue & Trading teams with a key focus of supporting the business on regulatory and risk matters, in order to effectively manage the risk and compliance environment with a commercial lens. This role will be supporting...

SciPro are exclusively partnered with a global rare disease company who are on the brink of a period of phenomenal organizational change and growth. They are currently looking for an experienced individual to join their European Compliance function as Senior Manager Compliance. The ideal candidate will have experience of the UK APBI code with some...

SciPro are exclusively partnered with a global rare disease company who are on the brink of a period of phenomenal organizational change and growth. They are currently looking for an experienced individual to join their European Compliance function as Senior Manager Compliance. The ideal candidate will have experience of the UK APBI code with some...

Job Purpose The Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead a team responsible for developing the content for submissions to regulatory agencies and other external stakeholders. This role will partner closely with key internal and external stakeholders and requires critical...

Investment Risk & Compliance Analyst Please make sure you read the following details carefully before making any applications. Salary £30k Peterborough (Hybrid) This is an associate-level role for an ambitious Risk/Compliance professional, a newly-created position with a growing business in the investment and funds space. The role will directly support...

SciPro are exclusively partnered with a global rare disease company who are on the brink of a period of phenomenal organizational change and growth. They are currently looking for an experienced individual to join their European Compliance function as Senior Manager Compliance. The ideal candidate will have experience of the UK APBI code with some...