Assistant Manager - GLP

Zydus Group

Ahmedabad District

On-site

INR 1,200,000 - 2,100,000

Full time

14 days+

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Job summary

Zydus Lifesciences seeks a QC professional at Corporate Office, Ahmedabad, Gujarat, India, to drive QA/QC documentation, CAPA and automation initiatives. You will align site procedures with corporate standards, oversee CAPA trends, and train site personnel in QC investigations and practices.

With 7–12 years in QC quality assurance, you will implement automated QC instruments and CSVMP-compliant software qualifications, ensuring rigorous quality control across sites.

Responsibilities

  • Prepare and revise CQDocuments (Policy, SOPs, directives and GTPs) for QC based on identified gaps and current requirements.
  • Implement corporate procedures at sites and verify site procedures against the corporate guidelines to close gaps and ensure compliance.
  • Assess QC-specific 483s issued to other companies and identify global CAPA to prevent recurrence at Zydus sites.
  • On-site/off-site verification of Global CAPA/compliance at Drug Manufacturing Sites of Zydus Lifesciences Ltd and subsidiaries.
  • Trend QC investigations (e.g., OOS, Laboratory Incidents) and propose Global/Site CAPA as needed.
  • Conduct QC Laboratory walkthroughs, observe practices and provide training recommendations and update procedures.
  • Provide training to site personnel (QC/QA) on QC investigations and related practices.
  • Review Quality Control data as required to support QA processes.
  • Evaluate, review and implement automated instruments for QC laboratories.
  • Carry out Proof of Concept (POC) for automated instruments and QC automation.
  • Qualify software for QC activities automation under CSVMP scope.
  • Ensure automation implementation, train site teams and support troubleshooting as required.

Job description

Corporate Office|Corp. Office, Ahmedabad, Gujarat, India

7 - 12 Years

Job Description
  • 1 Prepare, Revise CQDocuments (i.e., Policy, Standard Practices, Directive, SOP and GTPs) relatedto QC function, based on the identified GAPs and current requirement.
  • 2 To Implement theCorporate Procedures (i.e., Policy, Standard Practices, Directive, SOP andGTPs) at Sites and Verify the Site Procedures against the implementedcorporate procedures for the gaps, if any and ensure compliance on identifiedgaps.
  • 3 Assessment of QC Specific483’s issued to other companies and identify the Global CAPA for furtherprevention of same observations at Zydus Sites (whenever needed).
  • 4 On Site/Off SiteVerification of Global CAPA / Compliance of Quality Intelligence observationsat the Drug Manufacturing Sites of Zydus Lifesciences Ltd and itsSubsidiaries.
  • 5 Trend QC Investigations(e.g., OOS and Laboratory Incident) and recommend Global/Site Specific CAPA,if deemed necessary based on trend reports.
  • 6 Perform Quality ControlLaboratory Walkthroughs, observe the practices and provide feedback fornecessary training elements / revise the procedures etc.
  • 7 To provide training tosite personnel (QC/QA) related to QC investigation and/or other QC practices,as when as needed.
  • 8 To review the QualityControl data as when as needed.
  • 9 To evaluate, review andimplement the automated instrument for Quality Control Laboratory
  • 10 To carry out the Proof ofConcept (POC) for Automated instrument and QC Automation
  • 11 To conduct thequalification of software for QC activities automation within the scope ofcomputer system validation (CSVMP)
  • 12 To ensure implementationof Automation, provide training to site team and provide support fortroubleshooting activities, whenever required.
Job Snapshot

Updated Date

08-10-2026

Job ID

JOB10875

Department

CENTRAL QUALITY

Location

Location Corporate Office|Corp. Office, Ahmedabad, Gujarat, India

At Zydus Lifesciences, w e nurture a culture of innovation, excellence, and inclusivity , driving meaningful advancement in the pharmaceutical and healthcare industries. Fueled by creativity , we constantly exploring new ways to improve patient care and expand healthcare accessibility.

Our commitment to a positive and empowering work environment has earned us recognition as one of India's Best Workplaces in Biotechnology & Pharmaceuticals.

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