Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.
Get past ATS filters
Benefits offered by this job
Bonus
Equity
Comprehensive benefits
Job summary
A leading biotech firm in San Diego is seeking a professional for technical oversight in biologics development and manufacturing. The candidate will manage CMO partnerships, ensuring compliance with cGMP and regulatory guidelines. Required qualifications include a Master’s or PhD, experience in biotech or pharma sectors, and a strong understanding of technology transfer. This role offers a competitive salary range of $140,000 - $175,000, along with bonus and benefits.
Qualifications
8 years of experience in biotech or pharma industry required.
Experience with diverse project activities and third-party facilities.
Strong understanding of technology transfer and regulatory submissions.
Responsibilities
Oversee all operational aspects of the manufacture of drug substances.
Support regulatory filings and provide technical oversight.
Implement a data management framework for cGMP manufacturing data.
Skills
Project management
Cross-functional communication
cGMP knowledge
Data management
Education
Master’s degree in Biology, Biochemistry, Chemical Engineering or related discipline
PhD degree preferred
Job description
A leading biotech firm in San Diego is seeking a professional for technical oversight in biologics development and manufacturing. The candidate will manage CMO partnerships, ensuring compliance with cGMP and regulatory guidelines. Required qualifications include a Master’s or PhD, experience in biotech or pharma sectors, and a strong understanding of technology transfer. This role offers a competitive salary range of $140,000 - $175,000, along with bonus and benefits.