GMP Quality Control

MEDVACON Life Sciences

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Lexington, MA, us on site Until 8/22/2026 First posted March 27, 2025 Last posted March 27, 2025
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.

  1. QC Analyst - Method Validation
  2. QC Analyst (2nd Shift)
  3. QC Microbiology Tech
  4. QC Sample Management Tech (2nd Shift)
  5. QC Supervisor/Manger (2nd Shift)
  6. QC LIMS Admin
  7. QC Planner

Please apply if you think you would make a strong candidate for one of these positions.

MUST HAVE previous GMP experience!!

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

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

About this role

Summary

perform quality control, validation, compliance, and CSV tasks in a GMP environment

Job title

GMP Quality Control

Experience level

not specified

Industry

pharmaceutical

Location requirements

on-site in lexington, ma, no remote work allowed

Salary

Not specified

Management role

No

Skills & keywords

Required skills

gmp experienceauthorization to work in us

Preferred skills

None specified

Specializations

gmpquality controlvalidationcsv
Locations

Structured locations inferred from the posting.

Lexington, MA, USA

On-site City
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