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We are seeking an experienced and compliance-driven Production Manager to lead our Oral Solid Dosage (OSD) manufacturing facility in Himachal Pradesh. The ideal candidate will have extensive hands-on experience in managing end-to-end production operations (Granulation, Compression, Coating, and Packing) within a WHO GMP-compliant environment. The candidate must have a strong command of regulatory documentation and Revised Schedule M guidelines, ensuring the facility is audit-ready at all times.
Job Responsibility:
Oversee daily manufacturing operations for Tablets and Capsules, ensuring production targets are met efficiently and on time
Plan and execute production schedules to align with procurement, logistics, and market demand
Manage man, machine, and material resources effectively to optimize yield and reduce wastage
Ensure smooth technical operations of key machinery (RMG, FBD, Compression machines, Auto-coaters, etc.) and coordinate with the maintenance team to minimize downtime
Lead the implementation and adherence to the Revised Schedule M guidelines within the facility
Ensure all manufacturing activities strictly comply with WHO GMP standards and company quality specifications
Champion the 'Audit Readiness' of the plant. Lead the team during regulatory inspections and customer audits
Maintain absolute data integrity in manufacturing documents. Review and approve Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and Standard Operating Procedures (SOPs)
Manage Quality Management Systems (QMS) related to production, including handling Change Controls, Deviations, and CAPA (Corrective and Preventive Actions)
Identify process gaps and drive continuous improvement initiatives to enhance product quality and operational safety
Train, supervise, and motivate the production team (Officers, Operators, and Technical Staff) to ensure a high-performance culture
Promote a culture of safety, hygiene, and discipline on the shop floor
Requirements:
Currently employed in HP, Punjab, or Uttarakhand
Must have significant prior experience working in a WHO GMP approved facility
In-depth knowledge of Revised Schedule M guidelines is a non-negotiable requirement
Strong grip on OSD manufacturing processes (Granulation to Packing)
Proven track record of facing and successfully managing regulatory audits (e.g., WHO, or Semi-Regulated markets)
Specific strength in handling Change Controls and QMS documentation
Nice to have:
Proven track record of facing and successfully managing regulatory audits (e.g., WHO, or Semi-Regulated markets)
Candidates with specific strength in handling Change Controls and QMS documentation will be given preference