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Quality Assurance Analyst
Quality Assurance AnalystElvis Eckardt Recruitment & Sales Solutions Limited • Providence, United States
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Quality Assurance Analyst

Quality Assurance Analyst

Elvis Eckardt Recruitment & Sales Solutions Limited • Providence, United States
[job_card.30_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

The Role :

Role : Quality Assurance Analyst

Industry :  Pharmaceuticals / Biotechnology / Clinical Research

Location :  Fall River, Massachusetts, USA, 100% onsite

Employment Type :  Full-Time

Experience Required :  3 Years minimum

Work Authorisation :  US Citizen or Green Card Holder

Work Hours :  General :  8 : 30 AM – 5 : 00 PM ( May vary depending on business needs )

About The Job :

We are seeking a diligent and detail-oriented Quality Assurance (QA) Analyst I to join a pharmaceutical manufacturing company based in Fall River, MA.

This role ensures quality is built into every step of the manufacturing process through real-time monitoring, in-process checks, and compliance oversight — not by performing laboratory testing, but by preventing issues before they occur.

You will report to the Quality Assurance Manager and be an essential part of maintaining strict compliance with regulatory standards, including Good Manufacturing Practices (GMP) — a system designed to ensure products are consistently produced and controlled according to quality standards.

Key Responsibilities :

  • Conduct in-process testing (e.g. weight, thickness, hardness, disintegration, friability) in accordance with manufacturing batch record instructions.
  • Perform room and equipment checks prior to each manufacturing stage, following written SOPs.
  • Execute Acceptable Quality Limit (AQL) sampling and inspections.
  • Inspect in-process and finished product samples for Quality Control (QC) lab handoff and document results precisely.
  • Maintain daily verification of balances and calibration standards.
  • Ensure proper isolation and documentation of rejected materials during batch production.
  • Monitor and record environmental operating conditions during production.
  • Review batch documentation, temperature logs, humidity data, calibration and pest control records.
  • Verify equipment readiness and proper function throughout the production cycle.
  • Support investigations into customer complaints through applicable quality testing and reporting.
  • Identify and escalate non-conformances, deviations, or documentation errors as appropriate.
  • Contribute to process improvement initiatives and assist with quality-related projects.

Ideal Profile :

MUST HAVE Qualifications :

  • Bachelor’s degree (BS or BA) in Chemistry or a Physical Science discipline.
  • Minimum 3 years' experience in quality assurance within a GMP-regulated pharmaceutical manufacturing environment.
  • Experience with MDI (Metered Dose Inhalers) or parenterals preferred (solid dosage, liquids, tablets, and capsules also acceptable).
  • Vocational training or degree in pharmaceutical manufacturing, industrial management, or a related field preferred.
  • Required Skills :

  • Working knowledge of Good Manufacturing Practices (GMP) – the industry standard for ensuring product quality and regulatory compliance.
  • Working knowledge of Good Manufacturing Practices (GMP) – the industry standard for ensuring product quality and regulatory compliance.
  • Strong attention to detail and commitment to documentation accuracy.
  • Proficient in Microsoft Office (Excel, Word, Outlook); SAP or similar systems a plus.
  • Excellent communication skills (verbal, written, and presentation).
  • Highly organised, self-motivated, and capable of handling multiple tasks under deadlines.
  • Team-oriented with strong interpersonal relationship-building skills.
  • Strong attention to detail and commitment to documentation accuracy.Proficient in Microsoft Office (Excel, Word, Outlook); SAP or similar systems a plus.
  • Excellent communication skills (verbal, written, and presentation).
  • Highly organised, self-motivated, and capable of handling multiple tasks under deadlines.
  • Team-oriented with strong interpersonal relationship-building skills.
  • What's on Offer?

  • Work in a company with a solid track record of performance
  • Leadership Role
  • Fantastic work culture
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