Assistant Vice President, Quality/Regulatory
biovectraCharlottetown, Prince Edward Island, Canada
Posted August 21, 2025
157850 - 246641 CAD year
Full Time
About the Company
BIOVECTRA is a contract drug manufacturing organization (CDMO) that partners with leading pharmaceutical and biotech companies worldwide.
Job Description
BIOVECTRA is seeking an Assistant Vice President, Quality/Regulatory to lead quality and regulatory oversight at our Charlottetown, PEI, Canada facility. The ideal candidate will have 8+ years of experience in an FDA-regulated industry and experience interfacing with regulatory bodies.
Requirements
- 8+ years working in an FDA regulated industry
- 8+ years management experience leading managers
- Strong experience with regulatory inspections in a cGMP environment
- Experience with national and international regulatory registrations
- Expert knowledge of cGMP regulations and guidance documents
- Technical knowledge/experience in: Assays utilized for the testing of biologics and small molecule drug substances and drug products
- Lean, Six Sigma training and/or certification
- Proven ability to drive cultural change across an organization
- Demonstrated track record of results using interpersonal, relationship-building skills
Benefits
- Full-time equivalent pay range: $157,850.00 - $246,641.00/yr CAD
