Role & responsibilities Implement and maintain EHS policies and procedures. Conduct risk assessments and hazard analysis. Manage EHS documentation and records. Ensure compliance with updated EHS regulations. Lead and support EHS audits Preferred candidate profile Strong communication, interpersonal, and leadership skills. Certification in NEBOSH, OSHA, or ILO standards is mandatory. Experience in a similar role within the manufacturing or pharmaceutical industry is preferred. Ability to work independently and collaboratively in cross-functional teams. Proactive and detail-oriented with strong analytical and problem-solving abilities.
Key Responsibilities: Organize and supervise daily production activities to achieve defined output targets. Ensure all products comply with Pharmacopoeial standards and specified physical parameters. Supervise packing and other production-related departments as required. Ensure compliance with all regulatory and GMP documentation requirements. Manage QMS documentation related to production activities. Effectively handle manpower and ensure optimal shop floor productivity. Be audit-ready and experienced in facing regulatory, client, and internal audits. Requirements: 58 years of relevant experience in pharmaceutical production (OSD preferred). FDA approved for Tablets and Capsules . Strong knowledge of GMP, QMS, and audit preparedness. Hands-on experience in manpower management and production documentation. Qualification : M.Pharm / B.Pharm Location : Palghar Plant