Quality Assurance Quality Control (QA-QC) Inspector II

Virtual Company; Worcester (MA); On-site; USD 37,000 - 40,000; Full time

Job summary

The Fountain Group is seeking a QA/QC Inspector II for a 6-month contract in Worcester, MA. The role focuses on data review, GMP documentation, and ensuring laboratory records meet compliance standards.

The candidate will support the data review team across raw materials, environmental monitoring, in-process testing, stability, and validation in a fast-paced GMP environment.

Qualifications

• Bachelor's degree or 5+ years pharma/QC experience.
• Experience with GMP data review and documentation.
• Familiarity with RIMS/Empower/A280 systems.

Responsibilities

• Perform routine reviews of laboratory data, including on-the-floor and off-the-floor reviews for low-complexity test methods.
• Archive laboratory data and documentation within the RIMS system.
• Review assays and support data mining projects.
• Maintain GMP compliance with laboratory records, procedures, and electronic systems.
• Support administrative activities, including logbook management, scanning, and filing of laboratory data.
• Assist with demonstrating procedures and training activities for other employees.

Skills

Data review

Time management

GMP compliance

Independent work

Education

Bachelor's degree or equivalent experience

Tools

RIMS

Empower

A280

Job description

We are currently seeking a QA/QC Inspector II for a 6-month contract opportunity with a prominent pharmaceutical company in Worcester, MA.

Job Details:

• Position: QA/QC Inspector II
• Pay: $27–$29/hr
• Duration: 6 months
• Location: Worcester, MA (100% onsite)
• Schedule: Sunday–Thursday, 2:00 PM–10:30 PM

About the Role:

The QA/QC Inspector II will support the data review team in a fast-paced GMP environment, ensuring laboratory data and records are accurately reviewed, maintained, and archived. This position will support various areas, including raw materials, environmental monitoring, in-process testing, stability, and validation.

Responsibilities:

• Perform routine reviews of laboratory test data, including on-the-floor and off-the-floor reviews for low-complexity test methods.
• Archive laboratory data and documentation within the RIMS system.
• Review assays and support data mining projects.
• Maintain GMP compliance with laboratory records, procedures, and electronic systems.
• Support administrative activities, including logbook management, scanning, and filing of laboratory data.
• Assist with demonstrating procedures and training activities for other employees.

Qualifications:

• Bachelor's degree or equivalent experience; alternatively, a high school diploma with 5+ years of combined pharmaceutical or biologics manufacturing, QA, or QC experience.
• Experience with RIMS, Empower, and/or A280.
• Strong organizational and time management skills.
• Ability to work independently, manage multiple assignments, and meet deadlines in a fast-paced GMP environment.