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Reports to: Associate Director, GMP Quality Assurance
Location: Princeton, NJ, Hybrid
This role is responsible for providing GMP QA expertise, oversight and auditing support of contract manufacturing organizations supplying current investigational (and future commercial) products for PMV Pharma. Additionally, this role supports PMV’s GxP procedures program, document control, and training activities, utilizing an electronic quality management system.
To apply, please submit your cover letter and resume to recruiting@pmvpharma.com or apply through our Online Portal.
PMV Pharmaceuticals is an Equal Opportunity Employer and all applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Full Time
$123k-155k (estimate)
03/01/2024
04/28/2024
pmvpharma.com
Redwood City, NJ
25 - 50