Piramal Pharma Ltd

Manager - QA (Vendor Qualification)

Piramal Pharma Ltd · Mumbai, Maharashtra, India

Pharmaceutical Manufacturing · 1,001-5,000 employees

4 d ago
Senior (5-10 yrs) Full-time India
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About the role

The role involves managing vendor qualification activities and maintaining approved vendor records to ensure regulatory compliance. Additionally, the manager will oversee QMS activities and support process and cleaning validation through protocol execution.

What they look for

Vendor Management Vendor Qualification Quality Management Systems Deviations CAPA Change Controls Investigations Document Management Regulatory Compliance Process Validation Cleaning Validation Validation Protocols Validation Reports Process Control

Requirements

The candidate is expected to have experience in vendor management, quality management systems, and validation processes. Strong knowledge of regulatory compliance and documentation standards is required for this position.

Full description

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Division

Piramal Pharma SolutionsPiramal 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

Manager - QA (Vendor Qualification)Job Description

The role involves supporting Vendor Management activities, including vendor qualification, documentation review, and maintenance of approved vendor records. The candidate will also support QMS activities such as deviations, CAPA, change controls, investigations, and document management to ensure regulatory compliance.

Additionally, the position will support Process Validation and Cleaning Validation activities through preparation, review, and execution of validation protocols and reports to ensure compliance and effective process control.• Vendor Management

  • QMS
  • Process validation
  • Cleaning validation