MEDVACON Life Sciences works with many leading pharmaceutical companies to hire FTE for projects & assignments in cGMP Quality, Compliance, Validation and CSV work.
We currently have several W2 (FTE) Quality Control positions open with our gene therapy client in Lexington, MA. We cannot work with agencies on c/c on these opportunities.
Job Description- QC Analyst - Method Validation
- QC Analyst (2nd Shift)
- QC Microbiology Tech
- QC Sample Management Tech (2nd Shift)
- QC Supervisor/Manger (2nd Shift)
- QC LIMS Admin
- QC Planner
Please apply if you think you would make a strong candidate for one of these positions.
QualificationsMUST HAVE previous GMP experience!!
MUST HAVE authorization to work in the US. No Visa sponsorships at this time.
Additional Information1099 CONTRACT CANDIDATES ONLY!!! NO C2C/CONSULTANTS!!!
Skills Required
- Previous GMP (cGMP) experience
- Authorization to work in the US; no visa sponsorships
- 1099 contract candidates only; no C2C/consultants
- No agencies; cannot work with agencies on C2C for these opportunities
What We Do
MEDVACON Life Sciences LLC is a globally recognized leader in FDA Quality, Compliance, and Technical Consulting Services. As an MBE/SBE certified firm, it helps pharmaceutical, biotech, and medical device companies navigate regulatory challenges, optimize operations, and manage compliance costs. Their comprehensive services include validation, qualification, quality systems development, and FDA audit preparation to ensure operational confidence and regulatory success.
