Quality Assurance Associate

QA Manufacturing Inspector

The QA Manufacturing Inspector plays a critical role in ensuring product quality throughout all stages of the manufacturing process. This position supports compliance with established specifications, current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs).

Shift: Second Shift Monday to Friday, 3:00 PM to 11:30 PM

Experience Level: Entry Level

Reports To: QA Manager (with potential matrix reporting to other functional leaders)

Key Responsibilities

• Perform in-process testing (e.g., weight, thickness, hardness, disintegration, friability) per batch record instructions.
• Conduct room and equipment checks prior to each manufacturing stage, following detailed procedures.
• Execute Acceptable Quality Limit (AQL) sampling and inspections.
• Inspect in-process and finished product samples for the QC Lab and ensure proper documentation.
• Maintain standard weight records and verify balances daily.
• Isolate and document rejected materials during batch processing.
• Monitor environmental conditions affecting facility and product quality.
• Review engineering records (e.g., temperature/humidity logs, calibration, pest control, contractor activities).
• Assess batch records for completeness, accuracy, and reconciliation before proceeding to the next step.
• Verify equipment functionality and control systems during batch runs.
• Investigate and document customer complaints through applicable testing and reporting.
• Identify and escalate non-conformances or discrepancies to management.
• Participate in assigned projects and perform other duties as needed.

Qualifications

• Education:
  • Minimum: High school diploma
  • Preferred: Advanced vocational training or education in pharmaceutical manufacturing, industrial management, or related field from an accredited institution
• Experience:
  • Minimum of 3 years in quality assurance within a GMP pharmaceutical manufacturing environment
  • Experience with MDI (Metered Dose Inhalers) preferred
• Skills & Competencies:
  • Strong attention to detail and organizational skills
  • Effective communication (written, verbal, and presentation)
  • Ability to multitask and prioritize under strict deadlines
  • Proficient in Microsoft Office, SAP, and other business applications
  • Knowledge of cGMP standards
  • Self-starter with initiative to seek training or guidance
  • Ability to influence decisions and drive progress toward business goals
  • Strong interpersonal skills and team collaboration
  • Proficient in English (grammar, spelling, punctuation)

Pay and Benefits

The pay range for this position is $43680.00 - $54080.00/yr.

Health, Vision, 401k, Paid Holiday, Dentail

Workplace Type

This is a fully onsite position in Fall River, MA.

Application Deadline

This position is anticipated to close on Oct 20, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation, and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information, or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email acta Lentaccommodation@actalentservices.com for other accommodation options.