Executive-QA

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.

Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Executive-QA

Job Description

Responsible for managing QA documentation, ensuring GMP compliance, and supporting quality systems through effective handling of SOPs, BMR/BECR review, validation and qualification activities. Oversees document control, vendor qualification, calibration and maintenance coordination, and ensures timely closure of deviations, change controls, and CAPAs while maintaining data integrity and audit readiness across all QA operations.

• Issuance, archival and retrieval of documents.
• Issuance of Control coples to respective dept.
• Destruction of the GMP documents once the retention term has passed and controlled coples of the obsolete GMP documents.
• Tracking of all QA documents. 5. Maintaining backup of QA softcoples.
• Maintaining SOP/s with proper indexing.
• Preparation and review of SOPs
• Management of QA Stationary (Controlled Coples and logbooks)
• Dispatch and line clearance activity.
• Review of BMR/BECR
• Perform Qualification for new Equipments/Existing Equipments
• Ensure & Co-ordination of area validations.
• Reviewing of calibration /PM Schedules.
• Preparation of VMP &validation Documents
• Handling of Vendor Qualification Activities.
• Any other work assigned by HOD/Second line.
• Involving in handling Deviations, Change Control and related CAPAS.
• To ensure data integrity compliances while performing activities