Associate Director, R&D Quality Good Pharmacovigilance Practice
Employment type
Full-time
Work setting
On-site
Location
San Mateo, CA
Schedule
Day shift
Posted
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Job overview
The Associate Director, R&D Quality Good Pharmacovigilance Practice is an onsite role based in San Mateo, CA. Compensation is not specified for this position, which supports the implementation of a global GVP Quality Assurance approach. This role exists to ensure Pharmacovigilance activities meet regulatory standards. It contributes to the company's success by shaping the GVP QA framework and ensuring inspection readiness for the oncology pipeline.
What you'll do
- Conducts QA activities
- leads PV inspection readiness
- manages quality systems and risk management
- oversees vendor audits
- maintains key QA requirements
- develops quality KPIs
- coordinates training
- collaborates with cross-functional departments.
What we're looking for
- Skills & competencies
- full-timeday shiftsan mateo cabeone medicinespharmacovigilancequality assurancegvpgcponcologyonsiteno weekendsno on-call
- Work arrangement
- Weekend coverage required
Why this role
Requires expert global knowledge of GVP and GCP requirements.
About the employer
BeOne Medicines is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.
Additional details
- Industry sector
- 54
- Industry
- Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
- Occupation code
- 11-9199.01
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Listing ID: 9a807bbe-533c-4236-b93c-daa06fa2aca8