Dy. Manager - QC

Dy. Manager - QC

1 Nos.
141965
Full Time
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 8.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Pharma - Pharmacy; B.Sc - Chemistry; M.Pharma - Pharmacy
Job Description:

Position:        Dy. Manager - QC

Location:       Vapi

Experience:    6 - 8 Years

Industries:     Pharma - API

Responsibilities:

  • Manage day-to-day Quality Control activities for raw materials, intermediates, APIs, finished products, and stability samples.
  • Ensure compliance with cGMP, GLP, ICH, FDA, EU GMP, and regulatory requirements.
  • Review and approve analytical test results, COAs, SOPs, STPs, specifications, and analytical reports.
  • Supervise and guide QC analysts and senior executives to ensure timely sample analysis.
  • Oversee operation, calibration, qualification, and maintenance of laboratory instruments (HPLC, GC, UV, FTIR, KF, TOC, Dissolution, etc.).
  • Investigate OOS, OOT, laboratory deviations, incidents, and implement CAPA.
  • Coordinate analytical method validation, verification, method transfer, and cleaning validation support.
  • Ensure timely release of raw materials, intermediates, APIs, and stability samples.
  • Review laboratory documentation, logbooks, chromatograms, and data integrity compliance (ALCOA+).
  • Monitor laboratory inventory, chemicals, reagents, reference standards, and consumables.
  • Support internal, customer, and regulatory audits and ensure timely closure of observations.
  • Ensure compliance with data integrity policies and electronic systems.
  • Prepare and review trend analysis, KPI reports, and QC performance metrics.
  • Train and develop QC personnel on GMP, SOPs, safety, and analytical techniques.
  • Coordinate with Production, QA, Warehouse, and Regulatory Affairs for quality-related activities.
  • Ensure laboratory safety practices and adherence to EHS guidelines.
  • Drive continuous improvement initiatives to enhance laboratory efficiency and compliance.

Required Skills:

  • cGMP, GLP, ICH Guidelines
  • FDA / EU GMP Compliance
  • HPLC, GC, UV, FTIR, KF, TOC
  • Analytical Method Validation & Transfer
  • OOS / OOT / Deviation Investigation
  • Stability Studies
  • Data Integrity (ALCOA+)
  • CAPA Management
  • Laboratory Documentation
  • Team Leadership & People Management
  • Audit Handling
  • SAP/LIMS/Empower (preferred)
  • Root Cause Analysis
  • Risk Assessment
  • Excellent Communication & Problem-Solving Skills

Required Qualification: - B.Pham/M.Pham/B.Sc/M.Sc-Chemistry

Salary :- Upto 8.00 LPA

If you are interested for this opening please send updated resume on same mail with following details.

 

Total No. of Years Experience :-

Current CTC :-

Expected CTC :-

Notice Period :-

Company Profile

It is specializing in Active Pharmaceutical Ingredients.

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