Cipla Recruitment 2021 II Multiple Dept. II Junior Operator-Packing/Junior Operator-Production, Junior Team Member-QA - LATEST PHARMA JOB ALERT

Saturday, April 24, 2021

Cipla Recruitment 2021 II Multiple Dept. II Junior Operator-Packing/Junior Operator-Production, Junior Team Member-QA

 




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: 

 Click here for full details and Apply Online


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