QA-QC Inspector II

Spectraforce Technologies; Worcester (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

Spectraforce Technologies in Worcester, MA is seeking a QA-QC Inspector II to support GMP‑compliant data review across raw materials, environmental monitoring, in‑process, final bulk, stability, or validation. The associate reviewer will complete assay reviews, data mining projects, and data archiving under supervision, balancing time to meet deadlines.

Candidates should have a bachelor's degree or equivalent experience, strong organizational and time‑management skills, and familiarity with

Qualifications

• Bachelor's Degree or HS Diploma with 5+ years in manufacturing, QA/QC in pharma or biologics.
• Strong organizational and time-management capabilities.
• Experience with RIMS, Empower, A280 is preferred.

Responsibilities

• Archive data in the RIMS system.
• Perform routine review of lab test data including on-the-floor and off-the-floor review for low complexity methods.
• Maintain a safe work environment in accordance with procedural requirements.
• Understand and maintain GMP compliance for lab records, procedures and systems.
• Complete assigned tasks and support team objectives.
• Assist with logbook management and data scanning/filing; participate in training as needed.

Education

Bachelor's Degree OR High School Diploma with 5+ years of combined experience in manufacturing, QA, QC in pharmaceutical or biologics industry

Tools

RIMS

Empower

A280

Job description

Position Title: QA-QC Inspector II

Work Location: Worcester, MA 01604

Assignment Duration: 06 Months (Possible Extension)

Work Schedule: Sunday-Thursday, 2pm-10:30pm

The Associate Data Reviewer supports the data review team within a fast paced GMP environment in support of one or more of the following areas; raw material, environmental monitoring, in-process, final bulk, stability or validation. The coordinator will complete review of assays, data mining projects, and archiving of data. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties

Key Responsibilities:

• Archiving data in the RIMS system
• Performs Routine Review of Lab test data including On-the-Floor Review, and Off-the-Floor Review for low complexity test methods.
• Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements
• Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements
• Accepts responsibility to complete assigned tasks as committed. Works with other to maintain a positive atmosphere to accomplish business objectives
• Supports the review team with administrative tasks such as logbook management and scanning/filing of data.
• Participates in training of other employees, but focused on demonstration and not management of training delivery

Qualifications & Experience:

• Bachelor's Degree OR High School Diploma with 5+ years of combined experience in manufacturing, QA, QC in pharmaceutical or biologics industry
• Organizational skills
• Time management
• Experience with RIMS, Empower, A280