2nd Shift QA Inspector – GMP Pharmaceutical

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

Job summary

Cipla USA Inc. in Fall River, MA seeks a QA Inspector I for the 2nd shift to monitor product quality across manufacturing stages in a GMP environment. The role involves in-process testing, equipment and room checks, and strict documentation.

Requirements include a high school diploma, with 2+ years in QA within GMP pharma; preferred MDI experience. Proficiency in MS Office and SAP is expected, along with strong attention to detail and teamwork.

Qualifications

• Minimum high school diploma.
• Advanced vocational training or education in pharmaceutical manufacturing preferred.
• Minimum of two (2) years’ experience in quality assurance in a GMP pharmaceutical manufacturing operation.
• Experience in MDI preferred.

Responsibilities

• Perform in-process testing (weight, thickness, hardness, disintegration, friability, etc.).
• Conduct room and equipment checks prior to each manufacturing stage.
• Execute AQL sampling and inspections as required.
• Inspect in-process and finished product samples for QC Lab and document results.
• Maintain records of standard weights and daily balance verification.
• Ensure proper isolation of rejected material and accountability in batch records.
• Monitor facility and product environmental conditions.
• Review engineering records (temperature, humidity, calibration, PM, pest control).
• Assess batch records for completeness before next step.
• Verify equipment functionality during batch run.
• Prepare reports for customer complaints.
• Identify and report non-conformances to management.

Skills

MS Office

SAP

Attention to detail

Communication skills

Education

High school diploma

Technical training in pharma manufacturing preferred

Tools

Microsoft Office

SAP

Job description

Cipla USA Inc. in Fall River, MA seeks a QA Inspector I for the 2nd shift to monitor product quality across manufacturing stages in a GMP environment. The role involves in-process testing, equipment and room checks, and strict documentation.

Requirements include a high school diploma, with 2+ years in QA within GMP pharma; preferred MDI experience. Proficiency in MS Office and SAP is expected, along with strong attention to detail and teamwork.