Pharma QA Inspector - Second Shift

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

Job summary

Cipla is seeking a QA Inspector I for the second shift in Fall River, MA. The role focuses on in-process testing, equipment checks, and strict adherence to GMP procedures to ensure product quality.

Responsibilities include conducting AQL sampling, maintaining calibration records, and reporting non-conformances. Requires a high school diploma and 2+ years in GMP pharmaceutical QA; experience with MDI is preferred. This is a full-time, on-site position with salary commensurate to experience.

Qualifications

• High school diploma required; advanced pharma training preferred.
• Minimum 2 years of QA GMP experience.
• Experience in MDI preferred.

Responsibilities

• Perform in-process testing (weight, hardness, disintegration, etc.) per batch records.
• Conduct room/equipment checks before each manufacturing stage.
• 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.
• Ensure proper isolation of rejected material and batch record accountability.
• Monitor facility environmental conditions and records.
• Review engineering records like calibration, PM, and pest control records.
• Assess online batch records for signatures, entries, and reconciliation.
• Verify equipment functionality during batch runs.
• Prepare reports for customer complaints as needed.
• Identify non-conformances and report to management.

Skills

Attention to detail

English proficiency

Teamwork

Self-starter

Organizational skills

Multitasking

Communication

Education

High school diploma

Vocational pharma training

GMP training

Tools

SAP

Microsoft Office

Job description

Cipla is seeking a QA Inspector I for the second shift in Fall River, MA. The role focuses on in-process testing, equipment checks, and strict adherence to GMP procedures to ensure product quality.

Responsibilities include conducting AQL sampling, maintaining calibration records, and reporting non-conformances. Requires a high school diploma and 2+ years in GMP pharmaceutical QA; experience with MDI is preferred. This is a full-time, on-site position with salary commensurate to experience.