Regulatory CMC Associate – Pharma – Regulatory or Document Management exp required – Remote (must be
Hydrogen Group
This is a Full-time position in las vegas, nv posted May 9, 2022.
A leading biopharma company in San Diego is hiring for a Regulatory CMC Associate to support tracking and planning of regulatory submissions for marketed products or products in development. This is a fully remote, 12 months + w2 contract role paying a competitive hourly rate with high probability for conversion to FTE/permanent hire. You would be eligible for a premium hourly rate, health/dental/vision/life insurance and a 401k vehicle.
You will meet the following requirements:
1-2+ years experience in regulatory CMC or quality Chemistry, Manufacturing and Controls (CMC) for drug development or medical devices (pharma, biotech, CRO, CMO or Med Device arena is fine)
Bachelor’s Degree in a scientific discipline is required
Experience using Oracle Veeva preferred – using styles or starting point templates- preferred – publishing, formatting, version control processes
If you meet the above requirements and are interested in this role, please apply with your latest resume for immediate consideration.