Similar posts
Regulatory CMC Associate Director
- Permanent
- Good Manufacturing Practice (GMP)
- United Kingdom
This vacancy has now expired. Please see similar roles below...
Proclinical are in partnership with a pharmaceutical company in search for a Regulatory CMC Associate Director. You will provide product support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across phases of product development from clinical to lifecycle. Support may include organising, managing and executing on regulatory CMC projects and submissions.
Skills and Requirements
- Degree in life sciences, biochemistry, or chemistry
- Must have a proven track record within Biologics (5 years+).
- Proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project;
- Ability to work both independently and as a member of a team.
- Hiring Manager is also looking for someone with experience of working on global projects.
To Apply
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
#LI-PD1
Related jobs
Highly Competitive Salary
Wilmington, USA
Proclinical is seeking a dedicated Senior Quality Specialist to provide leadership and oversight on GMP operations related to clinical manufacturing.
Highly Competitive Salary
Maidenhead, England
Proclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England.
Highly Competitive Salary
Rochester, USA
Proclinical is seeking a proactive and dedicated individual for a Customer Quality Specialist for a leading pharmaceutical company. This is a permanent position located in Rochester, NY
Highly Competitive
Brussel, België
Proclinical has been retained by a cutting edge, biopharmaceutical company to appoint a Global Head of Quality for their commercial manufacturing sites.
Highly Competitive Salary
Pearl River, USA
Proclinical is seeking a QA Manager-Site Compliance for a global mid-sized consumer healthcare and medical devices company.
US$220000 - US$250000 per annum + Highly Competitive Salary
Mountain View, USA
Proclinical Staffing is seeking a VP Quality to join a cutting-edge biotech company.
Highly Competitive Salary
Zebulon, USA
Proclinical Staffing is seeking a QC Chemist to join an ambitious pharmaceutical company.
Up to US$115000 per annum + Highly Competitive Salary
Philadelphia, USA
Proclinical Staffing is seeking a Quality Control Supervisor to join a cutting-edge biopharmaceutical company.
Highly Competitive Salary
Marietta, USA
Proclinical Staffing is seeking a QC Laboratory Technician to join a cutting-edge biopharmaceutical company.
Highly Competitive Salary
Cambridge, USA
Proclinical is seeking a QA Specialist - Equipment and Computer Systems to join a global biopharmaceutical company.