GMP Quality Control

MEDVACON Life Sciences; Lexington (MA); On-site; Full time

Job description

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 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.

Qualifications

MUST HAVE previous GMP experience!!

MUST HAVE authorization to work in the US. No Visa sponsorships at this time.

Additional Information

1099 CONTRACT CANDIDATES ONLY!!! NO C2C/CONSULTANTS!!!