Kanthoruwa
Manufacturing & ProductionFull-timeOn-siteExecutive

Manufacturing Operations Coordinator

Assembly & Production Line·Colombo 5·Posted Jul 15, 2026

Premium International Injectable (Pvt) Ltd

Role Summary

We are a sterile Pharmaceutical Manufacturing Company looking for a young energetic individual with pristine qualifications and experience to take the lead as a Production Executive. The project is at the development stage.

Key Responsibilities

  • Maintain GMP and safety procedures in the manufacturing area.
  • Review master and executed batch records and analytical records for annual products.
  • Execute production plans to meet targets according to approved documents.
  • Ensure accurate documentation and timely qualification, calibration, and maintenance of equipment.
  • Monitor production activities, participate in equipment qualification, and enforce safety procedures.
  • Manage QMS activities including incident handling, CAPA, change control, investigations, risk assessments, deviations, market complaints, OOS, and OOT.
  • Ensure validation, qualification/requalification of equipment, and calibration/recalibration of instruments.
  • Prepare and revise BMRs, BPRs, and SOPs ensuring safety compliance.
  • Prepare URS and review all machine/equipment/instrument-related documents.
  • Participate in the execution of IQ, OQ, and PQ for machines/equipment/instruments.
  • Support Environment Health & Safety policies and statutory compliance.
  • Provide on-the-job training, monitor new processes/products, and coordinate production planning.
  • Propose process improvements, investigate production issues, and optimize resource allocation.
  • Ensure compliance with company policies, exercise inventory control, and assess production requirements.

Requirements/Qualifications

  • Bachelor of Pharmacy (B.Pharm) degree or a degree in Pharmaceutical Sciences.
  • Master of Science (MSc) degree is an added advantage.
  • Minimum 3 years of experience in sterile injectable manufacturing (vials, ampoules).
  • Strong knowledge of cGMP, WHO, and regulatory compliance for sterile products.
  • Exposure to process optimization, troubleshooting, and equipment qualification (IQ/OQ/PQ) is preferred.
  • High level of computer literacy including MS Office Packages.
  • Excellent communication skills in English (both verbal and written).

Location

BOI, Export Processing Zone, Koggala.

Salary/Benefits

The successful candidate will receive a competitive remuneration package and other benefits.