Junior Executive- Quality Assurance

1 - 3 years

3 - 5 Lacs

Posted:None| Platform: Naukri logo

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Work Mode

Work from Office

Job Type

Full Time

Job Description

Job Responsibilities:

  1. To ensure implementation of cGMP norms in manufacturing areas
  2. To give line clearance in dispensing, manufacturing and packaging
  3. To monitor dispensing, manufacturing and packaging
  4. Sampling of In-process, finished stage and process validation batches and forwarding the same to Quality Control department for analysis
  5. To ensure that gowning and entry/ exit procedures are followed as per standard procedures
  6. Monitoring of environmental conditions (temperature, humidity & pressure differential) in manufacturing areas
  7. To carry out IPQA checks in manufacturing and packaging areas
  8. To ensure online documentation
  9. To verify that the appropriate qualification, calibration and preventive maintenance of instruments/equipment are done as per frequency during line clearance
  10. To ensure the destruction of used Stereo, semi finished and finished product left over
  11. Responsible for withdrawal of control sample and stability samples of finished product
  12. Review of BMR, BPR etc
  13. Responsible for AQL of Finished goods (tablets and capsules)
  14. Maintain the continue process verification for all products
  15. Fulfill the regulatory requirements of RA department
  16. To verify the assigned batch number, Mfg date, Exp date to finished products for in house and loan license products
  17. Monitoring of training activity in entire plant as per scheduler
  18. Maintenance of Approved Vendor files, Product dossier files
  19. Responsible for investigation of market complaint, deviation, change control, incidence, returned goods, product recall.
  20. Supervise all QMS documentation issuance/ distribution, retrieval and destruction
  21. Preparation of Self- inspection plan, Site master file, Validation master plan, Safety Manual, Quality manual, water manual
  22. Prepare and review Annual Product Quality Report (APQR)
  23. Prepare and check SOPs
  24. Monitoring of training activity in entire plant as per scheduler.

Pedigree

B.Pharm/ M.Pharm with minimum 1-3 years of relevant experience in QA department

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Pelltech Healthcare

Healthcare Technology

San Francisco

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