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Cipla Recruitment-Send Resume TO Hr mail

Job Summary

  • Position: Junior Operator, API Production
  • Company: Cipla
  • Location: Bangalore
  • Experience Required: 1 to 3 years in a manufacturing environment
  • Education: B.Sc. (Chemistry, Botany, Zoology, Physics, Mathematics) or Diploma in Chemical Engineering
  • Employment Type: Full-time, Shift-based

About the Role

Cipla is looking for a dedicated and detail-oriented Junior Operator to join our Active Pharmaceutical Ingredient (API) production team in Bangalore. In this role, you will be responsible for executing daily production activities while adhering to stringent safety and Current Good Manufacturing Practice (cGMP) standards. The ideal candidate will be focused on operational efficiency, ensuring that manufacturing targets are met without compromising on quality or compliance. You will play a vital role in our production floor, managing equipment, documentation, and team collaboration to ensure seamless manufacturing processes.

Key Responsibilities

Production Execution and Operational Efficiency

  • Execute daily production operations according to established Standard Operating Procedures (SOPs) and batch manufacturing records.
  • Operate complex manufacturing equipment with high precision, ensuring error-free performance and minimizing deviations from production plans.
  • Optimize the utilization of available materials and resources to ensure all shift manufacturing targets are met efficiently.
  • Maintain the production facility, equipment, and general workspace in an audit-ready state at all times by following strict sanitation and maintenance protocols.

Quality Assurance and Process Improvement

  • Actively identify any deficiencies within the production area or errors in manufacturing documentation and take prompt corrective action.
  • Propose and implement innovative ideas to enhance production output, minimize waste, and improve the efficiency of consumable goods.
  • Provide proactive suggestions for process optimization to ensure the highest quality of pharmaceutical products.

Documentation and cGMP Compliance

  • Maintain accurate and timely online documentation, ensuring all entries in Batch Manufacturing Records (BMR) and related documents are complete.
  • Conduct thorough reviews of documentation before submission to ensure total data integrity and compliance with cGMP requirements.
  • Follow all regulatory guidelines to ensure that all documentation reflects the actual manufacturing process accurately.

Safety, Training, and Leadership

  • Provide essential training to junior workmen regarding cGMP standards, equipment operation, safety protocols, and housekeeping practices.
  • Ensure all team members correctly use and maintain Personal Protective Equipment (PPE) throughout their shifts.
  • Maintain an organized, clean, and sanitized work environment, overseeing the efficient use of cleaning resources.
  • Report any safety incidents or near-misses to the officer in-charge immediately to ensure a safe working culture.
  • Bridge communication gaps between shifts to ensure continuity in production and resolve potential lapses in knowledge transfer.
  • Manage workload distribution effectively to overcome challenges related to resource availability.

Preferred Candidate Profile

We are seeking a motivated professional who thrives in a fast-paced manufacturing environment. The successful candidate should possess:

  • Education: A Bachelor of Science degree (with a specialization in Chemistry, Botany, Zoology, Physics, or Mathematics) or a Diploma in Chemical Engineering.
  • Experience: 1 to 3 years of hands-on experience in a manufacturing organization, preferably within the pharmaceutical or API industry.
  • Technical Skills: A strong understanding of API manufacturing unit operations and a clear grasp of cGMP and safety regulations.
  • Soft Skills: Excellent attention to detail, strong problem-solving abilities, and the capacity to work effectively within a team structure.
  • Communication: Ability to communicate clearly with shift supervisors and team members to ensure operational transparency and productivity.

Why Join Cipla?

At Cipla, we are committed to providing “Caring for Life.” By joining our production team, you will be part of a mission-driven organization that prioritizes global health and innovation. We offer a structured work environment, opportunities for professional development, and the chance to contribute to the manufacturing of life-saving medicines. You will work alongside industry experts in a facility that values safety, integrity, and operational excellence.

How to Apply

If you are interested in this position and meet the specified criteria, please submit your updated resume for consideration. We look forward to reviewing your application and discussing how your skills and experience can contribute to our production objectives in Bangalore.

Please send your resume to: [email protected]

Note: Please ensure that your subject line clearly states your name and the position you are applying for to ensure your application is processed promptly.