QC Data Reviewer - 2nd Shift

Summary: 

Advance your QA/QC career with a Top-Tier Global Biopharmaceutical Leader in Worcester, MA! We are seeking an organized Associate Data Reviewer (VMS Title: QA-QC Inspector II) to join a fast-paced GMP laboratory environment. This is a 6-month contract role operating on a stable second-shift schedule (Monday–Friday, 2:00 PM – 10:30 PM), focused on supporting the data review team with high-quality review, archival, and administrative tracking.

Responsibilities: 

Perform routine on-the-floor and off-the-floor review of low-complexity laboratory test data for raw materials, in-process samples, or stability testing.

Archive critical GMP laboratory testing data accurately within the RIMS system.

Support the data review team with essential administrative tasks, including logbook management and the scanning/filing of analytical data.

Maintain strict adherence to GMP compliance guidelines regarding laboratory records, procedures, and data integrity systems.

Collaborate effectively with team members to ensure testing milestones and documentation deadlines are met.

Qualifications: 

Required:

Bachelor’s Degree OR a High School Diploma with 5+ years of combined experience in manufacturing, QA, or QC within the pharmaceutical or biologics industry.

Strong organizational and time-management skills within a regulated environment.

Ability to work the required second shift schedule: Monday–Friday, 2:00 PM – 10:30 PM onsite in Worcester, MA.

Preferred:

Direct experience utilizing RIMS, Empower software, or A280 testing methods.

Prior experience working inside a fast-paced GMP laboratory.