A leader in the development and commercialization of Biosimilar drugs is currently hiring for a Manager/Sr. Manager Clinical QA to add to their Compliance group in the greater Bay area.
The Manager/Sr. Manager Clinical QA will be responsible for the GCP Audit Programs and Compliance oversight. This individual will be responsible for building strong relationships with CMOs as well as working cross-functionally with various groups in the organization.
This is an excellent opportunity to work in a fast-paced environment and put a stamp on the Compliance group in regards to the Clinical QA Audit program. This individual will start as an independent contributor but may have the opportunity to build out a group later on, as the team continues to grow.
Relocation assistance will be considered for the right candidate.
If you meet the requirements above and would like to learn more about this exciting opportunity, email Becky Krage at firstname.lastname@example.org or call 917-983-4441.
• B.S. Degree within a Science or Engineering related field
• Minimum 5 years in a GCP environment
• Minimum 3 years of lead auditing experience or agency inspections
• Background in large molecule