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Senior Manager - Block Head Production (OSD)

18 - 20 years

20 - 27 Lacs

Posted:1 hour ago| Platform: Naukri logo

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Work Mode

Work from Office

Job Type

Full Time

Job Description

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This role is responsible for overseeing the operations of a specific block within the manufacturing facility, ensuring efficient production processes, compliance with quality and safety standards, and meeting production targets.
  • To meet the production targets
  • To ensure the implementation of current Good Manufacturing Practices and SOPs at work place
  • To maintain and improve the product quality as per standard
  • To ensure Accuracy, Reliability, validity, integrity and completeness of the cGxP data/records
  • To plan the department activities as per weekly delivery schedule for OSD and Liquid orals
  • To ensure the effective control on man, machine and material in the department
  • To participate and coordinate various on-going qualification and validation activities
  • Collaborate with the site quality head, QA & QC head in ensuring that the production is aligned to the quality standards and regulatory requirements
  • To ensure the completeness of all the trainings (Sops, Technical, Developmental and Regulatory etc.) assigned to block personnel s
  • To organize and implement the on-job training activities in the department
  • To ensure the implementation of EHS practices during work
  • To ensure the maintenance of equipment and upkeep of department constantly
  • To control the rejection during manufacturing and packing operations
  • To do counseling and grievance handling of the subordinates
  • To prepare, review and approve the Standard Operating Procedures
  • To evaluate deviations, change controls and other quality documents for appropriate conclusion
  • To ensure the market compliant investigations as per the track wise module and its timely closure and awareness training to all the concerned persons
  • Handling of QMS related activities of Block
  • To carry out the batch failure investigation for root cause identification and accordingly appropriate corrective action and preventive action taken
  • To review and approve the equipment qualification protocols, process validation protocols, reports, specifications and master formulae

Job Requirements

Educational Qualification

M.Sc. /B Pharma / M.Pharm

Experience

Tenure
: 18-20 years

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