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Jobs at Zydus Group

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Assistant Manager, GLP

  • Zydus Group

    • On-site
    • Ahmedabad, GJ

Production Supervisor

  • Zydus Group

    • On-site
    • Ahmedabad, GJ

Associate Manager, QMS Central Quality

  • Zydus Group

    • On-site
    • Ahmedabad, GJ

Research Scientist, Pharmacokinetics

  • Zydus Group

    • On-site
    • Ahmedabad, GJ

Research Scientist, Packaging

  • Zydus Group

    • On-site
    • Ahmedabad, GJ

Deputy Manager, Procurement

  • Zydus Group

    • On-site
    • Ahmedabad, GJ

Executive-QC

  • Zydus Group

    • On-site
    • Ahmedabad, GJ

Deputy Manager, Central Quality

  • Zydus Group

    • On-site
    • Raiya, GJ

Shift In charge, Hydrogenation plant

  • Zydus Group

    • On-site
    • Ankleshwar, GJ

Process Engineering

  • Zydus Group

    • On-site
    • Ankleshwar, GJ

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Assistant Manager, GLP

  • Zydus Group

  • Ahmedabad, GJ
Open in New Tab

On-site

Not Disclosed

Pharma

Quality

  • Posted on:

Job Description

Summary

Assistant Manager - GLP in the Central Quality (CQ) department at Zydus Group, based at the Corporate Office in Ahmedabad, Gujarat. The role supports the QC function across Zydus Lifesciences Ltd and its subsidiaries' drug manufacturing sites, covering corporate QC procedures, global CAPA, QC investigations, laboratory practices and QC automation.

Responsibilities
  • Prepare, revise CQ documents (i.e., Policy, Standard Practices, Directive, SOP and GTPs) related to QC function, based on the identified gaps and current requirement.
  • To implement the Corporate Procedures (i.e., Policy, Standard Practices, Directive, SOP and GTPs) at Sites and verify the Site Procedures against the implemented corporate procedures for the gaps, if any, and ensure compliance on identified gaps.
  • Assessment of QC specific 483's issued to other companies and identify the Global CAPA for further prevention of same observations at Zydus Sites (whenever needed).
  • On Site/Off Site verification of Global CAPA / compliance of Quality Intelligence observations at the Drug Manufacturing Sites of Zydus Lifesciences Ltd and its Subsidiaries.
  • Trend QC investigations (e.g., OOS and Laboratory Incident) and recommend Global/Site Specific CAPA, if deemed necessary based on trend reports.
  • Perform Quality Control Laboratory walkthroughs, observe the practices and provide feedback for necessary training elements / revise the procedures etc.
  • To provide training to site personnel (QC/QA) related to QC investigation and/or other QC practices, as and when needed.
  • To review the Quality Control data as and when needed.
  • To evaluate, review and implement the automated instrument for Quality Control Laboratory.
  • To carry out the Proof of Concept (POC) for Automated instrument and QC Automation.
  • To conduct the qualification of software for QC activities automation within the scope of computer system validation (CSVMP).
  • To ensure implementation of Automation, provide training to site team and provide support for troubleshooting activities, whenever required.
Qualifications
  • Experience: 7 - 12 years
Experience:

7-12 yrs

  • Skills:
  • Quality Control
  • SOP preparation
  • CAPA
  • OOS Investigation
  • Computer System Validation
  • GLP
  • Job Type:
  • Full-time
  • Shift Type:
  • 8 hour shift
  • Monday to Friday
  • Day shift

Compensation

  • Benefits:
  • Medical, Dental, Vision
  • Additional:
  • Base Salary
  • Bonus

Job ID:

CGXP_26_28619

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