MEDVACON Life Sciences LLC

GMP Quality Control

Reposted 13 Days Ago

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Lexington, MA, USA

In-Office

Mid level

Professional Services • Biotech • Consulting • Pharmaceutical

The Role

Multiple GMP Quality Control roles supporting a gene therapy client in Lexington, MA, including method validation, microbiology, sample management, LIMS administration, QC planning, and supervisory positions. Candidates must have prior cGMP/QC experience and US work authorization. Roles include second-shift openings and several specialized QC functions.

Summary Generated by Built In

Company 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 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.

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!!!

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

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The Company

50 Employees

Year Founded: 2012

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.