Production Executive
About the Employer
Job Description
Career Opportunity
We are a sterile Pharmaceutical Manufacturing Company looking for a young energetic individual with pristine qualifications and experience to take the lead in the following position. The project is at the development stage and is located in BOI, Export Processing Zone, Koggala.
Production Executive
Roles and Responsibilities
- To maintain GMP and safety procedure in manufacturing area.
- Online review master and executed batch record, analytical records annual products.
- Execute production plans to meet targets and manufacture products 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.
- Responsible for QMS activities like: Handling and review of incident, CAPA, change control, Investigation, Risk Assessment, deviation, market complaint, OOS and OOT etc. and to ensure validation, qualification / requalification of equipment, calibration / recalibration of Instrument activities.
- Prepare and revise BMRs, BPRs, and SOPs, ensuring compliance with safety procedures.
- To prepare URS and review of all machine / equipment’s / instruments related documents.
- To actively participate in execution of IQ, OQ, PQ of all machine / equipment’s / instruments.
- Support Environment Health & Safety policies and statutory compliance.
- Provide on-the-job training, monitor new processes/products, and coordinate with departments for production planning.
- Propose process improvements, investigate production issues, and optimize resource allocation for efficient operations.
- Ensure compliance with company policies and standards, exercise control over inventory, and assess production and resource requirements.
Qualifications & Requirement
- Bachelor of Pharmacy (B.Pharm) degree, or a degree in Pharmaceutical Sciences (Pharma)
- Master of Science (MSc) degree would be 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
- Should possess excellent communication skills in English (both Verbal and written)
The successful candidate would receive a competitive remuneration package and other benefits. If you meet these required criteria, please e-mail your CV, including contact details of two non-related referees to reach us within 07 days of this advertisement.
Email: - [email protected]
