Overnight Pharma QA Inspector I – QC & GMP Focus

Cipla; Fall River (MA); On-site; USD 32,000 - 41,000; Full time

Job summary

Cipla is seeking a QA Inspector I for the third shift in Fall River, MA. This role supports the quality assurance team in monitoring and ensuring product quality across manufacturing steps in GMP-compliant processes.

Responsibilities include in-process testing, equipment checks, documentation, and batch record reconciliation, with a focus on adherence to SOPs and quality standards. Requires high school diploma and 2+ years QA GMP pharma experience.

Qualifications

• Requires minimum high school diploma; advanced training preferred.
• Minimum 2 years' QA experience in GMP pharma manufacturing environment.
• Strong attention to detail and ability to work in a team.

Responsibilities

• Perform in-process testing (weight, thickness, hardness, disintegration, friability) per batch records.
• Conduct room and equipment checks before each manufacturing stage following procedures.
• Execute AQL sampling and inspections as required.
• Inspect in-process and finished product samples for QC and document results.
• Maintain records of standard weights and daily balance verifications.
• Monitor facility and product environmental conditions; manage non-conformances.

Skills

SAP

English proficiency

cGMP knowledge

Education

High school diploma

Advanced vocational training in pharma manufacturing

GMP pharmaceutical experience

Tools

Microsoft Office

Job description

Cipla is seeking a QA Inspector I for the third shift in Fall River, MA. This role supports the quality assurance team in monitoring and ensuring product quality across manufacturing steps in GMP-compliant processes.

Responsibilities include in-process testing, equipment checks, documentation, and batch record reconciliation, with a focus on adherence to SOPs and quality standards. Requires high school diploma and 2+ years QA GMP pharma experience.