On-Floor QA Inspector - GMP & Compliance

Piramal Pharma Limited

Sellersville (Bucks County)

On-site

USD 60,000 - 80,000

Full time

7 days ago
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Job summary

Piramal Pharma Solutions is seeking a Quality Inspector to provide on-the-floor quality oversight, ensuring GMP, GDP, and Data Integrity across manufacturing, packaging and distribution. You will support batch release, documentation control and compliance with FDA regulations.

The role requires a Bachelor of Science with at least 3 years in pharmaceutical quality assurance or GMP auditing, and the ability to travel to facilities for inspections as needed.

Qualifications

  • 3+ years of pharma quality assurance or GMP auditing experience.
  • On-the-floor quality oversight and inspections in a regulated environment.
  • Proficiency in GMP, GDP, GLP and international regulations.

Responsibilities

  • Issue batch records per production schedule and perform potency calculations.
  • Line clearance and batch readiness assessments with verification of documentation and equipment status.
  • Review Environmental Monitoring data for compliance with internal standards and regulatory requirements.
  • Review equipment logbooks and batch records to ensure adherence to GDP, GMP and Data Integrity.
  • Prepare batch records and perform first release of batches.
  • QA review and approval of non-routine workorders in SAP.
  • Draft, revise and review Quality Assurance SOPs and deviation reports to ensure clarity and regulatory alignment.
  • Conduct weekly quality surveillance activities and support audits and inspections.

Skills

GMP knowledge
GDP knowledge
GLP knowledge
Analytical skills
Communication skills
MS Office
QMS proficiency
Travel flexibility

Education

Bachelor of Science

Job description

Piramal Pharma Solutions is seeking a Quality Inspector to provide on-the-floor quality oversight, ensuring GMP, GDP, and Data Integrity across manufacturing, packaging and distribution. You will support batch release, documentation control and compliance with FDA regulations.

The role requires a Bachelor of Science with at least 3 years in pharmaceutical quality assurance or GMP auditing, and the ability to travel to facilities for inspections as needed.

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