(Sr. Manager / AGM - QA) for Oral Solid Dosage (OSD)

Location:- Jammu Exp:- 15-20 yrs Qualification:- B.Pharma/MSc Chemistry CTC: 15-18 LPA

This role involves driving a robust culture of quality, managing a team of QA professionals, and bridging quality compliance with cross-functional operations to ensure seamless product delivery.

Key Responsibilities

 Team Handling and Leadership:

o Manage, mentor, and develop a large team across sub-departments, including IPQA, Documentation, Validation, and Corporate QA. o Establish transparent performance targets, identify training gaps, and build robust succession plans for critical QA roles. o Cultivate an active culture of quality compliance and data integrity (ALCOA+) across the entire plant floor.  Inter-Departmental Coordination: o Production &

• Operations: Collaborate directly with manufacturing teams to resolve floor issues, investigate deviations in real-time, and optimize OSD lines without compromising compliance. o Supply Chain &

• Regulatory Affairs: Coordinate on vendor qualifications, raw material status,



and technical dossiers required for global regulatory submissions. o Engineering &

• Maintenance: Work together on equipment qualification (DQ/IQ/OQ/PQ), facility modifications, and preventive maintenance shutdowns.  Quality Management Systems (QMS): Maintain site systems matching global rules.  Batch Disposition &

• Audits: Make the final call to release or reject batches and lead the site during regulatory inspections.

Requirements and Skills Experience, with at least 5+ years in a senior leadership or HOD capacity.  Qualification :B.Pharma/MSc Chemistry  OSD Domain Expertise: Deep knowledge of tablets, capsules, and powder manufacturing processes.  People Management: Proven ability to manage conflict, build cohesive teams, and lead technical professionals.  Communication: Exceptional negotiation and communication skills to influence other department heads and manage external regulatory auditors.

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