Job Description

Job Brief :

The Quality Assurance (QA) Associate/Manager plays a crucial role in ensuring the

compliance, safety, and quality of pharmaceutical products within our company. This position

involves implementing and maintaining quality systems, performing quality checks, audits,

and providing guidance to various teams to ensure adherence to regulatory standards and

company policies.

Roles and Responsibilities

• Develop, implement, and oversee a comprehensive documentation system in line with WHO GMP guidelines and applicable regulations.
• Implement and manage robust IPQA procedures to monitor critical manufacturing processes in real-time.
• Review and verify in-process batch records to ensure accuracy, completeness, and adherence to Standard Operating Procedures (SOPs)
• Create, review, and approve a wide range of quality documents, including SOPs,batch records, validation protocols, technical reports, and quality agreements.
• Manage the document control process, including version control, distribution, and archival of controlled documents.
• Lead the review process for critical documents, ensuring accuracy, completeness and compliance before approval.
• Plan, execute, and report internal audits to assess documentation practices,identifying gaps and opportunities for improvement.
• Manage, mentor, and lead the QA team, providing guidance, training, and support to ensure professional growth and high-performance outcomes.
• Foster a collaborative and empowered team culture that places a premium on quality,compliance, and continuous improvement.

Skill Sets * Should have complete knowledge of documentation as per WHO GMP guidelines. Can

create and review all the documents. * Should have knowledge of IPQA

• Can manage team of QA

Office Time - 9am to 5:45pm

• Week off - Monday

Benefits:

• Transportation
• Mediclaim for self, spouse and children.
• Canteen Facility with charges of 10 rs. per meal

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