Cipla Recruitment 2021 II Multiple Dept. II Junior Operator-Packing/Junior Operator-Production, Junior Team Member - QA
• Department: Packing, Production, QA
• Job role: Junior Operator – Packing/Junior Operator – ProductionJunior Team Member – QA
• Education: M.Sc. /B. Pharma, Diploma
• Experience: 02 Yrs of experience in QA Dept.
• Location: Goa
Job Description:
Junior Operator – Packing
Job Purpose
Operate & maintain packing machines to achieve quality product & shift wise targeted output with maximum utilisation
Accountabilities
Prepare the machine for packing operation as per production plan by using proper resources to ensure smooth operations
Operate the packing machines by using minimum resources to get quality product.
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.
Perform packing machine operations safely to avoid safety incidences by appropriately handling the machines and thereby maintaining high standard of safety.
Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations
Junior Team Member – QA
Evaluate the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines
Accountabilities
Collate, Evaluate and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
Evaluate Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
Evaluate annual product quality Evaluate report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
Evaluate, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
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
Assemble, compile and Evaluate 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
Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP
Execute on time and errorless submissions by Evaluateing product license, all certificates for product registration and tender , staff approvals and other applications to adhere to legal requirements
Support in CDSCO and state FDA inspection to be GMP compliant and getting product licence, FDA stall approvals by ensuring cross functional interaction
Junior Officer – Production
Monitor and execute the production duties in an area during the shift by maintaining cGMP and safety norms to achieve production targets
Accountabilities
Execute production duties in a shift by managing available resources to achieve production target
Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
Prepare manufacturing records and update online documentation to meet production and cGMP requirements
Follow safe work processes and ensure safety appliances are utilised during production duties in shifts to create a safe working environment
Execute production duties in a shift by managing available resources to achieve production target
Selection Process: The selection will be based on interview.
How to Apply:
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