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Summary
About the Role
About You
- Bachelor’s degree in a life sciences field (Chemistry, Pharmaceutical Sciences); advanced degree a plus.
- 9+ years of experience in FDA-regulated pharmaceutical or biotech environments.
- Strong working knowledge of cGMPs, 21 CFR Parts 11, 210, 211, 820, and international standards (ISO 13485, ICH, WHO, PIC/S).
- Proven leadership in regulatory inspection preparedness and eQMS implementation.
- Hands-on experience with combination products, sterile manufacturing, and contract manufacturing oversight.
- Strong communicator and collaborator who thrives in fast-paced, high-growth settings.
The global Life Sciences industry is dominant in today’s world. Drug development processes are progressing faster than ever before. The need for vaccines, treatments and medical devices continues to grow at an exponential rate to ensure treatment for disease reaches those it needs to. That means for Barrington James, we grow at the same speed. With 14 global offices specialising in niche areas of the Life Science industry, we are ready to support our growing group of clients in sourcing the most, senior, specialist and rare candidates to join them. ‘We Invest In Our People’ through training and development, through meritocratic progression, and through unrivalled commission structures, shareholder and bonus schemes. Barrington James Board & Executive Partners Barrington James is your global and award- winning Life Science Executive recruitment partner. With combined experience of over 100 years, our Executive Search team has access to the deepest pharmaceutical networks. Our primary focus is to understand and address the business challenges and hiring needs of our clients through a range of bespoke services, including Executive Search, Project Management, Market Research, Mapping Practice and Reference Check Insights.