• Monitoring the production process and adjusting schedules as needed.
• Supervising and checking manufacturing instructions and ensuring that these are followed.
• Supervising maintenance, premises and manufacturing equipment.
• Ensuring that necessary validation for manufacturing procedures is carried out.
• Ensuring that batch manufacturing records and batch packaging records are reviewed and signed by authorised person before they are passed on to QC /QA Department.
• Participating in audits (suppliers and subcontractors) & in self-inspection.
• Helping process complaints.
• Raising and implementing change control.
• Ensure implementation and evaluation of safety procedure.
• Ensuring reworking of any finished and semi-finished products that have been rejected and that have not been rejected.
• Ensuring that required initial and continuous training of production personnel is carried out and adapted to the need and motivate subordinates accordingly.
• Any other relevant duties assigned by higher authority as and when required.
• Ensuring the batch manufacturing records (BMR) are filled and signed properly.
• Address any deviation issues during process work and notifying to supervisor.
• Ensuring the cleaning of production area and equipment are in place.

• Festival & Annual Bonus
• Provident Fund
• Gratuity
• Group Insurance
• Lunch & Transport Facilities
• A good & healthy working environment

• Age at most 30 years
• 1-2 years experience in the similar positions in a reputed pharmaceutical company will get preference.
• Good interpersonal and communication skills.
• Ability to work under pressure.
• Self motivated and proactive in producing and delivering outputs.
• Smart, energetic and innovative.
• Computer literate.

Apply Procedure

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