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Senior Operator Production

Cipla

India

On-site

INR 4,00,000 - 6,00,000

Full time

Today
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Job summary

A leading pharmaceutical company in India is seeking a dedicated professional to execute production operations while adhering to safety and GMP requirements. The successful candidate will optimize resources, maintain equipment for audit readiness, and conduct essential training. With a focus on documentation accuracy and compliance, this role demands a diploma in Pharmacy or Mechanical with 1-3 years’ experience in the manufacturing sector. Join us to ensure safe and efficient production processes.

Qualifications

  • 1-3 years of experience in a manufacturing organization, preferably in the pharmaceutical industry.
  • Ability to operate equipment efficiently and optimize the use of available resources.

Responsibilities

  • Execute production operations in line with safety and GMP requirements.
  • Conduct training related to cGMP and safety for workmen.
  • Maintain equipment and facility for audit readiness.
  • Perform unit operations as per SOP and batch manufacturing records.

Skills

GMP knowledge
Documentation accuracy
Resource optimization
Safety compliance
Training delivery

Education

Diploma in Pharmacy / Mechanical
Job description
Division Department Sub Department 1 Job Purpose

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

Key Accountabilities (1/6)

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 batch manufacturing record
  • Optimize the utilization of available resources for achieving production in shift
  • Maintain equipment, facility and block premises as per SOP for audit readiness
Key Accountabilities (2/6)

Provide suggestions for optimization of processes to manufacture quality product

  • Identify the deficiency in area and errors in documents and rectify them as per requirement
  • Propose and implement new idea to enhance production, optimise the use of consumable goods and maximum utilization of resources
Key Accountabilities (3/6)

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 (4/6)

Deliver training to workmen and adhere cGMP and safety guidelines in 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 usage and maintenance of PPEs by workmen during shifts
  • Report any near-miss to officer in-charge in time
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
Key Interactions (1/2)
  • 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)
Key Interactions (2/2)
  • Equipment manufacturer for troubleshooting in machine (Case Basis)
Dimensions (1/2)
  • Number of dosage forms : 2
  • Number of tech transfer supported per month : 2
  • Number of batches executed per month : 35-40
  • Achieve internal OTIF more than 90%
  • Meet percentage utilisation of plant as per the plan
  • 0% errors in documentation
  • Zero reportable accidents / incidences during manufacturing
  • Achieve 0% failures / deviations target
  • 100% compliance to SOP
Dimensions (2/2)
Key Decisions (1/2)

Scheduling house-keeping activities

Key Decisions (2/2)
  • Equipment Selection to Section Head
  • Modification in plant and equipment to Production Officer
Education Qualification

Diploma in Pharmacy / Mechanical

Relevant Work Experience

1-3 years of experience in a manufacturing organisation preferably in pharmaceutical industry

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