Quality Assurance Quality Control (QA-QC) Inspector II

Spectraforce Technologies, Inc.; Worcester (MA); On-site; USD 34,000 - 48,000; Full time

Job summary

Spectraforce Technologies, Inc. seeks a QA-QC Inspector II in Worcester, MA for a 6‑month assignment, 2pm–10:30pm, Sunday–Thursday, onsite. The role supports data review across GMP areas, including archiving and data mining, under supervision with time‑management responsibilities.

Key duties include lab data review, archival activities in RIMS, and assisting the team with administrative tasks while maintaining GMP standards. Bachelor’s or HS with QA/QC experience is required.

Qualifications

• Bachelor's Degree or HS Diploma with 5+ years in manufacturing, QA or QC in pharma/biologics.
• Strong organizational skills and time management.
• Experience with GMP documentation and data review processes.

Responsibilities

• Archive data in the RIMS system.
• Perform routine review of lab test data (on-the-floor and off-the-floor).
• Maintain safe working environment per procedures.
• Adhere to GMP requirements for lab records and procedures.
• Complete assigned tasks and support team objectives.
• Assist with administrative tasks like logbook management and data scanning/filing.
• Participate in training of others as required.

Skills

Organizational skills

Time management

Education

Bachelor's Degree

High School Diploma + 5+ years QA/QC experience

Tools

RIMS

Empower

A280

Job description

Position Title: QA-QC Inspector II

Work Location: Worcester, MA 01604

Assignment Duration: 06 Months (Possibility of extension)

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

Work Arrangement: Onsite

Position Summary

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