Production Planning Manager (Manufacturing)

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.