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Work Mode

On-site

Job Type

Full Time

Job Description

About the Role:

Production Officer/Executive


Key Responsibilities:

Production Planning and Scheduling

  • Assist in creating and managing daily and weekly production schedules for OSD manufacturing to ensure timely execution of batch orders.
  • Monitor production progress and adjust timelines as required based on operational priorities or customer requirements.

Resource Management and Stock Control

  • Ensure availability of required raw materials, packaging materials, and equipment for planned production.

Quality Standards and Compliance

  • Ensure adherence to cGMP, GDP, and internal SOPs during all stages of production.
  • Support in maintaining product quality standards as per specifications and regulatory requirements.
  • Assist in implementing in-process checks and quality monitoring during manufacturing.

Production Process Monitoring

  • Supervise and monitor OSD manufacturing processes such as granulation, compression, coating, and packing.
  • Identify bottlenecks and take corrective actions to ensure smooth workflow and improved efficiency.

Cross-Functional Coordination

  • Collaborate with QA, QC, Maintenance, and Supply Chain teams to ensure uninterrupted operations.
  • Support in resolving issues impacting production timelines or quality.

Health and Safety Compliance

  • Ensure compliance with health, safety, and environmental guidelines in the production area.
  • Promote safe work practices and report unsafe conditions promptly.

Customer Order Fulfillment

  • Ensure production is aligned with customer delivery schedules and quality expectations.
  • Coordinate with logistics to support timely dispatch of finished products.

QMS Activities

  • Participate in Quality Management System (QMS) activities, including documentation, deviation handling, and CAPA implementation.
  • Support in preparation for internal and external audits and regulatory inspections.


Requirements:

  • B.Pharm / M.Pharm / B.Sc / M.Sc.
  • 1–5 years’ experience in pharmaceutical production.
  • Knowledge of cGMP, documentation, and regulatory requirements.
  • Strong problem-solving, communication, and teamwork skills.

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