Head - Quality Assurance - Oral Solid Dosage Manufacturing - Pharma

Job Summary:

We are looking for an experienced Quality Assurance Head to lead the Quality Assurance function for an Oral Solid Dosage (OSD) manufacturing facility. The ideal candidate should possess extensive experience across all Quality Assurance functions and have a proven track record of leading QA teams in a regulated pharmaceutical manufacturing environment. The role is responsible for ensuring compliance with cGMP, regulatory requirements, and organizational quality standards while driving continuous quality improvement initiatives.

Key Responsibilities:

- Lead the overall Quality Assurance function for the OSD manufacturing facility.

- Oversee all QA functions, including Analytical Quality Assurance (AQA), In-Process Quality Assurance (IPQA), Documentation, Quality Management Systems (QMS), Validation, and Regulatory Compliance.

- Ensure compliance with cGMP, regulatory requirements, and internal quality standards.

- Drive continuous quality improvement initiatives across manufacturing operations.

- Lead and mentor Quality Assurance teams in a regulated pharmaceutical manufacturing environment.

- Ensure effective implementation and maintenance of quality systems and documentation practices.

- Support regulatory inspections and ensure audit readiness of the facility.

- Collaborate with cross-functional teams to maintain product quality and compliance throughout the manufacturing lifecycle.

Required Skills & Experience:

- 20-25 years of relevant experience in the pharmaceutical industry.

- Mandatory: End-to-end experience in Oral Solid Dosage (OSD) manufacturing.

- Strong experience across AQA, IPQA, Documentation, QMS, Validation, and Regulatory Compliance.

- Proven experience leading Quality Assurance teams in a regulated manufacturing environment.

- Strong understanding of cGMP and pharmaceutical quality systems.