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Executive - Quality Assurance, Pharma

External
zentiva logoZentiva · India
Full-timeOn-siteToday
ComplianceCross-functional CollaborationDocumentationSAP
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Responsibilities

  • Quality Management/Continuous Improvement
  • a. Line Clearance and shop floor compliance
  • b. Carry out in-process checks and calibration of IPQC instruments.
  • c. Handle e tools i.e. SAP Hana, LIMS, eDMS, Track Wise system.
  • d. Assisting in Complaint Investigation system at site
  • e. Assisting in Qualification and validation system, change control system, deviations
  • f. Preparing & review the Annual Product Quality Review
  • g. Review of Batch Manufacturing & Packing Records
  • h. Coordination of cGMP Training activity.
  • Compliance
  • Ensure adherence to company Quality Standards, Local FDA MHRA regulations, by
  • i. Understanding the requirements
  • ii. Performing the Gap analysis to find out the gaps in existing system
  • iii. Preparing a compliance plan for closure of gaps
  • iv. Execution of compliance plans
  • v. Review of completion for compliance activity
  • Validations & Qualifications:
  • a. Ensure validated status of all equipment's, manufacturing processes, and cleaning processes
  • b. Review of protocols for qualification and validation of facility/ equipment / product / process
  • c. Review of validation reports after execution of validation of facility /equipment / product / process
  • Documentation Control:
  • a. Preparation and Review of SOPs
  • b. Controlled distribution and archival of documents & record
  • c. Control of master documents
  • Assuring quality of products by :
  • a. Ensuring SOP compliance
  • b. Review of Batch Manufacturing & Packing Records
  • c. Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints
  • d. Ensuring the effectiveness review of the implemented CAPA
  • cGMP Training:
  • a. To prepare training modules and organize training in GMP
  • b. Execute the training program in coordination with all concerned departments
  • Other:
  • a. Review of maintenance and calibration program.

Requirements

  • 1-5 years of relevant experience in Pharma Quality Assurance / Documentation
  • Skills & Competencies
  • Strong knowledge of cGMP, GDP, and Quality Systems
  • Hands-on experience with batch documentation and document control systems
  • Good understanding of APQR preparation and regulatory expectations
  • Strong analytical, organizational, and coordination skills
  • Effective communication and cross-functional collaboration abilities
  • Attention to detail and commitment to data integrity

Additional Information

Position Title: Executive I - Quality Assurance, Pharma Qualifications & Experience Educational Qualification Bachelor's or master's degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline.


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