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Cipla Recruitment Junior Operator-Packing/Junior Operator-Production,Junior Team Member-QA

Cipla is Hiring for Junior Operator – Packing/Junior Operator – ProductionJunior Team Member – QA and has issued notification to accept Applications. Cipla Limited is an Indian multinational pharmaceutical company, headquartered in Mumbai, India. . Interested and eligible candidates required to fill  application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Junior Operator – Packing/Junior Operator – ProductionJunior Team Member – QA as follows.

Vacancy summary details :

  • Company Name: Cipla
  • Location : Goa
  • Post Name: Junior Operator – Packing/Junior Operator – Production Junior Team Member – QA
  • Qualification: M.Sc. / B. Pharma,diploma
  • Experience: 2 years of experience in QC department of a pharmaceutical organization
  • No of Vacancies: 01
  • Details of Salary: Not Disclosed by Recruiter
  • Closing date for online Application : Apply as soon as possible
  • Date of examination: NA
  • Time and Venue :NA
  • Mode of application : online
  • Selection Process: Shortlisted candidates may called for selection process (  Personal interview , Group discussion , etc…,)

Job Description/Skills Required: 

Accountabilities

I. Prepare the machine for packing operation as per production plan by using proper resources to ensure smooth operations
II. Operate the packing machines by using minimum resources to get quality product
III. Execute and update online documentation to meet cGMP requirements and maintain data integrity Fill Machine logs. Document entries/SOP and process simplification to meet cGMP.
IV. Perform packing machine operations safely to avoid safety incidences by appropriately handling the machines and thereby maintaining high standard of safety
V. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations

Junior Team Member – QA

Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines

Accountabilities

I. Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
II. Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
III. Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
IV. Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
V. Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
VI. Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
VII. Prepare final draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements
VIII. Collect, compile and review raw data and finalise the same for timely submission of MHRA, UK interim update document to corporate as per agency requirement by tracking interim updates at a site level, for risk based inspection planning
IX. Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP

Junior Officer – Production

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

Accountabilities

I. Execute production activities in a shift by managing available resources to achieve production target
II. Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
III. Prepare manufacturing records and update online documentation to meet production and cGMP requirements
IV. Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment
V. Execute production activities in a shift by managing available resources to achieve production target

Click here for notification and Apply

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