Kickstart Your Career with Cipla: Junior Operator Production role in Sikkim | Apply Now
Candidates looking to build a strong foundation in pharmaceutical manufacturing can explore this opportunity under Cipla careers for one of the most in-demand pharma operator jobs in India. This Junior Operator – Production role at Cipla’s Rangpo, Sikkim facility is ideal for diploma holders who want hands-on exposure to GMP-compliant production processes. If you are searching for stable growth-oriented roles, Cipla careers and pharma operator jobs like this offer an excellent starting point in the pharma industry.
- Job Title: Junior Operator Production
- Location: Rangpo
- Req Id: 99144
About the Company
Cipla is a leading global pharmaceutical company with a strong presence in India and international markets. The organization is known for its commitment to quality, patient-centric innovation, and compliance with global regulatory standards. Professionals exploring Cipla careers in manufacturing can benefit from structured training, GMP-driven operations, and long-term growth through stable pharma operator jobs in world-class production facilities.
Job Description
To execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift.
Key Responsibilities
- Operate the equipment efficiently without error and deviation as per SOP to meet shift targets
- Perform unit operations as per SOP and unit processes as per the batch manufacturing record
- Optimize the utilization of available resources for achieving production in a shift
- Maintain equipment, facility, and block premises as per SOP for audit readiness
- Provide suggestions for the optimization of processes to manufacture a quality product
- Identify the deficiency in the area and errors in the documents, and rectify them as per the requirement
- Propose and implement new ideas to enhance production, optimise the use of consumable goods, and maximize the utilization of resources
- Execute and update online documentation to meet cGMP requirements
- Maintain online documentation and timely entries in BMR and supporting documents
- Check documentation before submission to ensure data integrity
- Deliver training to workmen and adhere to cGMP and safety guidelines in the production process to ensure smooth operations
- Conduct training related to cGMP, equipment operation, safety, and housekeeping for workmen
- Optimize the use of resources in housekeeping
- Ensure good housekeeping and sanitisation as per the guidelines
- Ensure the usage and maintenance of PPEs by workmen during shifts
- Report any near-miss to the officer in charge in time
Education Qualification
- Diploma in Pharmacy / Mechanical
Relevant Work Experience
- 0-2 years of experience in a manufacturing organisation, preferably inthe pharmaceutical industry.
Key Interactions
- Engineering & Utility for system and equipment-related queries (Daily)
Safety for safety rounds and PPE (Weekly) - Formulation Technical Support for troubleshooting in products (Case Basis)
- Formulation Tech Transfer for support in new products (Project Basis)
- Equipment manufacturer for troubleshooting in the machine (Case Basis)
Dimensions & Performance Targets
- Number of dosage forms: 2
- Number of tech transfers supported per month: 2
- Number of batches executed per month: 35–40
- Achieve internal OTIF of more than 90%
- Meet the percentage utilisation of the plant as per the plan, 0% errors in documentation
- Zero reportable accidents/incidents during manufacturing
- Achieve 0% failures/deviations target
- 100% compliance to SOP
