Job Summary:
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.
Key Responsibilities:
1. Production Planning & Operations:
- 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.
2. Regulatory Compliance & Quality Assurance (Crucial):
- Revised Schedule M Implementation: 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.
- Documentation: Maintain absolute data integrity in manufacturing documents. Review and approve Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and Standard Operating Procedures (SOPs).
3. QMS & Continuous Improvement:
- 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.
4. Team Leadership:
- 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.
Candidate Profile & Requirements:
Must-Haves:
- Current Location: Currently employed in HP, Punjab, or Uttarakhand.
- Facility Experience: Must have significant prior experience working in a WHO GMP approved facility.
- Regulatory Knowledge: In-depth knowledge of Revised Schedule M guidelines is a non-negotiable requirement.
- Core Competencies: Strong grip on OSD manufacturing processes (Granulation to Packing).
Preferred Qualifications:
- Audit Exposure: Proven track record of facing and successfully managing regulatory audits (e.g., WHO, or Semi-Regulated markets). Candidates with experience facing audits are highly desirable.
- Documentation Skills: Candidates with specific strength in handling Change Controls and QMS documentation will be given preference.
Note to Recruiter:
- Strict Filter: Please do not forward profiles from Gujarat or Southern India. Focus exclusively on the Baddi / Mohali / Paonta Sahib / Roorkee / Dehradun pharma belts.
- Screening Question: Ask candidates to cite specific examples of how they have adapted processes to meet Revised Schedule M norms.
