QC Analyst - Overnight

Mogi I/O : OTT/Podcast/Short Video Apps for you; Boston (MA); On-site; USD 28,929 - 35,817; Full time

Job summary

A pharmaceutical manufacturing company in Fall River, MA, is seeking a QA Inspector I to ensure product quality throughout all manufacturing stages. This role requires a minimum of 3 years of QA experience in a GMP environment and a strong chemistry background. Responsibilities include conducting in-process inspections and maintaining compliance with regulatory standards. Candidates must hold a High School Diploma and possess basic computer proficiency. This position operates on third shift hours.

Qualifications

• Minimum 3 years of QA experience in a GMP pharmaceutical manufacturing environment.
• Experience performing quality checks in pharmaceutical manufacturing.
• Understanding of cGMP, QA principles, and documentation compliance.

Responsibilities

• Ensure product quality throughout all stages of pharmaceutical manufacturing.
• Perform in-process testing as per batch record instructions.
• Conduct room and equipment checks prior to each stage of manufacturing.

Skills

Attention to detail

Quality systems understanding

Regulatory adherence

Basic computer proficiency

Strong chemistry background

Education

High School Diploma

Tools

SAP

Microsoft Office

Job description

QA Inspector I

Location: USA – Fall River, MA (Onsite)

Work Type: Full Time

Experience Required: 3 – 15 Years

Compensation: USD $21 – $26 per hour

Visa Status: US Citizen / Green Card Holder

Shifts: Third Shift (11:00 PM – 07:30 AM – May vary based on business needs)

Job Overview

The QA Inspector I is responsible for ensuring product quality throughout all stages of pharmaceutical manufacturing. This role performs on-the-floor in-process inspections, AQL checks, equipment and room verifications, and documentation review in compliance with cGMP, SOPs, and batch record requirements. The position requires strong attention to detail, understanding of quality systems, and strict adherence to regulatory and safety standards. This is an onsite, 3rd-shift role supporting high-volume manufacturing operations.

Key Responsibilities

• Perform in-process testing as per batch record instructions (weight, thickness, hardness, disintegration, friability, etc.).
• Conduct room and equipment checks prior to each stage of manufacturing following established SOPs.
• Execute AQL sampling and inspections as required.
• Inspect in-process and finished product samples for the QC Lab and document results accurately.
• Maintain standard weight records and perform daily balance verification.
• Ensure proper isolation and documentation of rejected materials.
• Monitor environmental and facility operating conditions.
• Review engineering records (temperature/humidity calibration, PM data, pest control logs, contractor records).
• Assess batch records for completeness, reconciliation, signatures, and yield accuracy before releasing for next steps.

Must-Have Qualifications

• High School Diploma (minimum requirement).
• Minimum 3 years of QA experience in a GMP pharmaceutical manufacturing environment.
• Strong chemistry background (mandatory).
• Experience performing quality checks in pharmaceutical manufacturing (excluding biopharmaceutical experience).
• Understanding of cGMP, QA principles, and documentation compliance.
• Proficiency in English—written, verbal, and documentation clarity.
• Basic computer proficiency (Microsoft Office, SAP, and similar applications).
• Ability to identify quality issues, follow SOPs, and maintain accurate records.

Seniority level

• Associate

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Software Development