Job Description
Job Description
(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 clear 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.