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Jobs at Cipla Limited

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Junior Officer, Production

  • Cipla Limited

    • On-site
    • Rangpo, SK

Team Member, Asset Integrity & Reliability

  • Cipla Limited

    • On-site
    • Rangpo, SK

Junior Operator, Packing

  • Cipla Limited

    • On-site
    • Rangpo, SK

Junior Operator, Packing

  • Cipla Limited

    • On-site
    • Rangpo, SK

Electrical Engineer

  • Cipla Limited

    • On-site
    • Rangpo, SK

Junior Team Member, Microbiology

  • Cipla Limited

    • On-site
    • Rangpo, SK

Junior Operator, Packing

  • Cipla Limited

    • On-site
    • Rangpo, SK

Senior Factory Finance Accountant

  • Cipla Limited

    • On-site
    • Bengaluru, KA

Junior Officer, Packing

  • Cipla Limited

    • On-site
    • Rangpo, SK

Junior Operator, Production

  • Cipla Limited

    • On-site
    • Rangpo, SK

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Junior Officer, Production

  • Cipla Limited

  • Rangpo, SK
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On-site

Not Disclosed

Pharma

Manufacturing

  • Posted on:

Job Description

Summary

Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets

Responsibilities

Execute production activities in a shift by managing available resources to achieve production target

  • Execute assigned tasks as per planned production activity to meet production targets for a shift
  • Regulate usage of consumables in the production process at optimum levels to save costs
  • Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area


Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality

  • Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance
  • Ensure equipment, facility and block premises are maintained as per regulatory compliance
  • Maintain system integrity by updating documentations and deviations on CipDox while performing operations
  • Perform validation, qualification and calibration as per schedule and update output of all activities in the systems
  • Prepare new documents and update existing documents as per GMP requirement


Prepare manufacturing records and update online documentation to meet production and cGMP requirements

  • Maintain online documentation and timely entries in BMR and supporting documents
  • Prepare new documents and update existing documents as per GMP requirement
  • Operate software such as SAP, CipDox and QMS


Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment

  • Ensure safety systems and procedures followed by the operators in the shift
  • Ensure availability and usage of PPEs in the shift by coordinating with HSE department for requirements and shift schedule


Execute production activities in a shift by managing available resources to achieve production target

  • Execute assigned tasks as per planned production activity to meet production targets for a shift
  • Regulate usage of consumables in the production process at optimum levels to save costs
  • Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area


Major Challenges

  • Meeting shift targets due to unavailability of adequate resources. Overcome by efficient work load distribution and resource optimisation
  • Meeting production targets due to lapses in knowledge transfer between shifts. Overcome by bridging gaps between inter-shift communication
  • Maintaining cGMP requirements during system downtime. Overcome by coordinating with the engineering team and technical support team
Qualifications

Education Qualification

  • Bachelor in Pharmacy


Relevant Work Experience

  • 3-4 years of experience with 2 years of experience in pharmaceutical manufacturing
  • Knowledge of cGMP practices, equipment operations required for Formulation Production
Education

Degree

Bachelor

Specialization

Pharmacy
Experience:

3-4 yrs

  • Skills:
  • Pharmaceutical Manufacturing Knowledge
  • Formulation Production
  • Production operations
  • BMR & Manufacturing Documentation
  • Equipment operations
  • GMP & Safety Compliance
  • Job Type:
  • Full-time
  • Shift Type:
  • 8 hour shift
  • Monday to Friday
  • Day shift

Compensation

  • Benefits:
  • Medical, Dental, Vision
  • Additional:
  • Base Salary
  • Bonus

Job ID:

CGXP_26_27816

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