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Manager-Production

2+ years
Not Disclosed
10 Dec. 4, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position Title: Manager – Production
Department: Operations
Company: Sun Pharmaceutical Industries Ltd
Location: Mohali

Job Summary

The Manager – Production will oversee the daily production operations and the monitoring of commercial batches to ensure they are produced as per the defined schedule and quality standards. This role is responsible for coordinating resources, managing production activities, ensuring compliance with GMP standards, and ensuring the optimal use of resources. The Manager will also handle training, implement quality systems, and manage deviations, complaints, and maintenance activities.

Key Responsibilities

  1. Production Operations

    • Monitor and manage commercial batch production as per the scheduled plan.
    • Ensure resources such as area, machinery, and manpower are available for scale-up, validation, exhibit, and commercial batches.
    • Review production records and ensure compliance with procedures.
    • Ensure efficient utilization of manpower, materials, and production areas.
  2. Resource Management

    • Ensure availability of necessary resources for smooth production activities.
    • Oversee initial and continuing training of production staff according to schedule.
    • Ensure team morale and discipline are maintained.
  3. Quality Compliance

    • Implement and monitor Current Good Manufacturing Practices (cGMP) in production.
    • Ensure adherence to SOPs and production instructions.
    • Review and approve documents such as SOPs, raw material and packaging specifications, validation protocols, and reports.
  4. Quality System Implementation

    • Implement the site’s quality system and cultivate a quality-driven culture within the production area.
    • Handle planned and unplanned deviations, investigations, and change controls.
    • Verify the effectiveness of corrective and preventive actions (CAPA).
  5. Risk Management & Maintenance

    • Perform risk assessments for changes in facilities, equipment, or processes.
    • Ensure the timely execution of preventive maintenance, calibration, and routine maintenance activities for equipment and areas.
    • Ensure equipment, area, and process validations are conducted as per the schedule.
  6. Training & Documentation

    • Organize and approve departmental training within the Learning Management System (LMS).
    • Create and release process orders for the manufacturing and packaging of commercial batches.
  7. Market Complaints & Health Safety

    • Handle market complaints received from customers.
    • Ensure adherence to environment, health, and safety norms within the production area.

Skills & Competencies

  • Strong knowledge of GMP regulations and production processes.
  • Excellent leadership skills to manage teams and ensure high performance.
  • Experience in handling production-related deviations, investigations, and change controls.
  • Proficiency in managing resources effectively and ensuring optimal productivity.
  • Strong documentation and training management skills.