Global Regulatory CMC Director - Drive Therapies Forward

BioNTech; City of London; On-site; GBP 85,000 - 120,000; Full time

Job summary

A leading biotechnology company in London is seeking a Director Global Regulatory Affairs - CMC to lead the regulatory affairs for investigational medicinal products. The ideal candidate will have over 9 years of experience in regulatory CMC globally and a degree in a relevant field. You will define regulatory strategies and collaborate cross-functionally to bring innovative products to market. Competitive remuneration packages are offered.

Benefits

Competitive remuneration packages

Diverse employee support benefits

Qualifications

• More than 9 years professional working experience in Regulatory Affairs CMC globally.
• Extensive experience in preparation and revision of regulatory CMC documents.

Responsibilities

• Lead global regulatory affairs CMC for assigned products.
• Define regulatory CMC dossiers strategy for development and commercial products.

Skills

Excellent communication skills in English

Result-and goal-oriented

Knowledge of CMC drug development

Education

Degree in pharmacy, chemistry, biology, biochemistry, or equivalent

Job description

A leading biotechnology company in London is seeking a Director Global Regulatory Affairs - CMC to lead the regulatory affairs for investigational medicinal products. The ideal candidate will have over 9 years of experience in regulatory CMC globally and a degree in a relevant field. You will define regulatory strategies and collaborate cross-functionally to bring innovative products to market. Competitive remuneration packages are offered.