Biovectra is a North American CDMO that delivers end‑to‑end pharmaceutical manufacturing, spanning biologics, synthetic and fermented small molecules, highly potent APIs, bioreagents, and mRNA/pDNA/LNP therapeutics. Leveraging dual expertise in microbial fermentation and chemical synthesis, the company tackles complex molecules that few CDMOs can address. Its flexible, process‑centric approach—combining creative optimization, rigorous quality, and dedicated project management—ensures that programs advance on schedule with the highest quality outcomes. Biovectra’s commitment to bold vision and operational excellence positions it as a trusted partner for companies seeking reliable clinical‑to‑commercial scale solutions.
Open Positions
Senior Quality Assurance Associate
Bachelor of Science degree in Chemistry or Biochemistry, 5 years of relevant work experience, and 1 year of direct experience in a Quality Unit position
Assistant Vice President, Quality/Regulatory
8+ years of experience in an FDA-regulated industry, 8+ years management experience, and expert knowledge of cGMP regulations