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    Pharmacy Job for Freshers at Cipla | Apply Now for the Junior Operator Production Role

    Pharmacy Job for Freshers at Cipla | Apply Now for the Junior Operator Production Role

    Cipla is hiring a Junior Operator – Production for its manufacturing facility in Rangpo, Sikkim. This Pharmacy Job is ideal for candidates with a Diploma in Pharmacy or Mechanical Engineering and 0–2 years of experience. The operator will be responsible for executing production operations in line with safety and cGMP requirements, operating specialized machinery, and maintaining Batch Manufacturing Records (BMR). Key goals include achieving an internal OTIF of over 90% and ensuring 100% compliance with SOPs and safety norms at one of India’s premier pharmaceutical sites.

    • Position: Junior Operator Production
    • Location: Rangpo
    • Req Id: 98193

    About The Company

    Cipla is a leading global pharmaceutical company dedicated to the mission of “Caring for Life”. With a robust presence in over 80 countries, the company is a world leader in high-quality, branded, and generic medicines. The Rangpo (Sikkim) facility is a critical manufacturing unit producing tablets, hard gelatin capsules, and complex dosage forms like inhalers and nasal sprays. This site operates under world-class cGMP standards, delivering life-saving medicines to millions of patients globally.

    Pharmacy Job Purpose

    Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets on a shift.

    Key Accountabilities (1/4)

    • 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.

    Key Accountabilities (2/4)

    • 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.

    Key Accountabilities (3/4)

    • 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.

    Key Accountabilities (4/4)

    • 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

    Relevant Work Experience

    0-2 years of experience in a manufacturing organisation, preferably in the pharmaceutical industry.

    APPLY ONLINE HERE

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