Regulatory CMC Dossier Manager

At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients. The CMC Dossier Manager plays a crucial role in developing the...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science....

Walker Cole International are looking for a CMC Regulatory Affairs Director to join an established Pharmaceutical Business in the UK. In this role you will be responsible for the development and execution of CMC regulatory strategy for the business. As the CMC Regulatory Affairs Director, you will be responsible for: * The development and creation of the...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their...

Job Description Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science....

Job DescriptionContribute to dossier strategy and complex product development plans at a compound level, demonstrating autonomy and accountability.Lead and supervise dossier authoring activities for early and late-stage projects with limited guidance from the manager.Identify areas for business improvement and support the implementation of enhancements under...

Proclinical are recruiting a Regulatory CMC Consultant for a pharmaceutical organisation. This role is on a contract basis and is located in West London. **Responsibilities**: - Accountable for highlighting possible delaying factors promptly to line management as well as share knowledge of regulatory documentation and processes with others. - You will...

CK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in Uxbridge 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 human...

**Salary**: Highly Competitive Job type: ContractDiscipline: CMC**Location**: United Kingdom- London, England - Posting date: 14 Mar 2024 Reference: 59472 Proclinical is seeking a Regulatory CMC Associate for a 12-month contract role. This position will provide support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for...

Walker Cole International are looking for a CMC Regulatory Affairs Director to join an established Pharmaceutical Business in the UK. In this role you will be responsible for the development and execution of CMC regulatory strategy for the business. As the CMC Regulatory Affairs Director, you will be responsible for: * The development and creation of the...

CK Group are recruiting for a Regulatory Affairs Manager CMC to join a biopharmaceutical company who are based in Uxbridge 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 human...

**Description Overview**: As a major player in consumer health and cosmetics, Perrigo is an American pharmaceutical company committed to supporting the health and well-being of consumers through a unique portfolio of market-leading brands such as EllaOne® or Norlevo® (Women’s Health), Compeed® or Mederma® (Skincare), XLS Medical® (Weight Management)...

We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. The CMC Dossier Manager plays a crucial role in developing the technical eCTD sections to support Regulatory CMC dossier applications. Additionally, they coordinate timelines, virtual documents, and the generation of the Quality...

Regulatory Affairs CMC Manager - International markets Your new company This well-known biotech is looking for an experienced Regulatory Affairs CMC Manager to join their well-established team on a contract basis. This role will mostly be managed from home with one quarter travel to the office based. This is a 12-month contract job with scope for...

Your new company A global biopharmaceutical company focusing on rare diseases is looking for a CMC consultant to come in to cover maternity leave for 12 months.Your new role You will be responsible for Regulatory CMC support for post-approval submissions for commercial biological products, and new international MAA fillings for the EU.What you'll need to...

Are you an experienced Regulatory Affairs professional with a background in Chemistry, Manufacturing and Controls and experience working in the Biopharmaceutical/Biotechnology industry, and are you looking for a new opportunity? We have your next role, we are recruiting for a Regulatory Affairs CMC Manager with Post Approval Submissions and who has...

Job Description Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science....

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science....