About the Role

We are looking for a qualified and dedicated Production Officer to manage manufacturing activities in the dry injection sterile area. The candidate will be responsible for supervising sterile manufacturing operations, ensuring aseptic processing practices, maintaining production documentation, and complying with GMP and pharmaceutical quality standards.




Key Responsibilities

  • Handle day-to-day dry injection manufacturing activities in sterile areas.
  • Monitor aseptic processing, filling, sealing, and sterilization operations, as applicable.
  • Ensure compliance with GMP, SOPs, and sterile manufacturing guidelines.
  • Monitor production processes and maintain batch manufacturing records.
  • Ensure proper gowning, hygiene, and cleanroom practices.
  • Coordinate with QA, QC, and Engineering departments.
  • Monitor equipment cleaning, line clearance, and area cleanliness.
  • Ensure timely completion of production targets and maintain safety standards.


Requirements

  • Education: B.Pharma, M.Pharma, B.Sc., or M.Sc. in Pharmacy, Chemistry, Microbiology, or a relevant scientific discipline.
  • Male candidates required.
  • Relevant experience in dry injection or sterile pharmaceutical manufacturing preferred.
  • Knowledge of aseptic processing, cleanroom operations, and GMP guidelines.
  • Understanding of sterilization, filling, and sterile area procedures.
  • Good documentation, communication, and problem-solving skills.
  • Ability to work in controlled sterile manufacturing environments.


What We Offer

  • Competitive salary based on qualifications and experience.
  • Performance-based incentives, where applicable.
  • Career growth opportunities in pharmaceutical production.
  • Technical training and professional development.
  • Exposure to sterile manufacturing technologies and advanced production processes.


Company
KDRS Group
Vacancies
2 Openings
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