Regulatory Operations Senior Manager

Senior Director, Regulatory CMC Policy & Intelligence Superb senior role in Regulatory CMC Policy & Intelligence and a key hire for a dynamic and fast-growing Biopharma. Leadership, influencing and advising skills both internally and externally. This outstanding role requires the candidate to provide EU Regulatory Intelligence expertise in order to steer the...

Cambridge (Hybrid working - On average two or three times a month in the office)PermanentWe challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.The Global Regulatory & Operations Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory...

Job title: Senior Regulatory Affairs Manager CMCFor a complete understanding of this opportunity, and what will be required to be a successful applicant, read on.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...

Job Description CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in Uxbridge or Cambridge on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and...

Regulatory Affairs Manager Monday - Friday, 37.Contract Length: 12 months (Inside IR35) Our client, a multinational pharmaceuticals company, are seeking a Regulatory Affairs Manager The successful candidate will provide country regulatory expertise for the development, registration, and life-cycle management of all molecules within our client's portfolio ...

For Current Gilead Employees and Contractors:Please log onto your Internal Career Site $) to apply for this job.At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access...

Senior Manager Regulatory Affairs Vendor Governance page is loaded Senior Manager Regulatory Affairs Vendor Governance Apply locations United Kingdom - Cambridge time type Full time posted on Posted 6 Days Ago job requisition id R For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. At Gilead,...

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in Uxbridge or Cambridge on a contract basis for 12 months.Company:Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative...

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

HOW MIGHT YOU DEFY IMAGINATION? At Amgen, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission—to serve patients—has driven our status as one of the world's preeminent biotechnology companies, reaching over 10 million patients worldwide. Leverage your high-level expertise to lead and forge...

HOW MIGHT YOU DEFY IMAGINATION?At Amgen, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission—to serve patients—has driven our status as one of the world's preeminent biotechnology companies, reaching over 10 million patients worldwide. Leverage your high-level expertise to lead and forge...

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

Proclinical is seeking a Regulatory Affairs Manager. This role is pivotal in providing country-specific regulatory expertise and execution for the management of biotechnology products. The successful candidate will be responsible for coordinating and carrying out regulatory submissions in compliance with national regulatory requirements as well as the...

Proclinical is seeking a Regulatory Affairs Manager. This role is pivotal in providing country-specific regulatory expertise and execution for the management of biotechnology products. The successful candidate will be responsible for coordinating and carrying out regulatory submissions in compliance with national regulatory requirements as well as the...

Proclinical is seeking a Regulatory Affairs Manager. This role is pivotal in providing country-specific regulatory expertise and execution for the management of biotechnology products. The successful candidate will be responsible for coordinating and carrying out regulatory submissions in compliance with national regulatory requirements as well as the...

It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. REGULATORY AFFAIRS MANAGER In this vital role you will support one or more oncology products from a European regional...

Senior QA Officer required for a cell therapy CDMO who have a state-of-the-art facility based near Cambridge for multiproduct GMP production. This site allows scale up of current commercial production and the provision of contract manufacturing services to meet the growing demand for such services in the UK. The Senior QA Officer will be working within the...

CMC Regulatory Affairs Senior Associate/Executive | EU/USYour new companyWithin a globally emerging pharmaceutical company based in Cambridge, you will be a part of a small, tight-knit, team-orientated, innovative team, playing an active part in developing drugs and services for patients with rare diseases to improve their qualityof life and improve their...

Regulatory Affairs and Quality Assurance Assistant - Medical Devices - Cambridge Due 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...

Based in North Cambridge, my client is a global innovative company who are currently seeking an experienced Quality Assurance and Regulatory Affairs Manager looking for the next step-up in their career, to join their team on a full-time, permanent basis.Main duties will include: Providing global companywide support across multiple projects Focussing...