Puerto is a sterile pharmaceutical manufacturing plant specializing in SVP and LVP injectables, operating as per global cGMP standards. We are looking for dynamic and motivated candidates 'join our growing team.
Hiring QC – ANALYTICAL
REVIEWER & GLP
Vacancy : 1 Position
Experience : 6+ Years
Qualification : B.Pharm / M.Pharm / M.Sc or relevant qualification
Mandatory / Preferred Experience : 6+ years pharmaceutical QC experience with strong Data Review & GLP exposure mandatory
Key Responsibilities
• Review of analytical raw data, chromatograms, worksheets, calculations
• System suitability, analytical reports, data integrity and ALCOA+ compliance
• GLP/GMP review, OOS/OOT review, deviation/CAPA review
• Stability data review; RM/Finished Product data review
• Method validation/verification support
• Identification of compliance gaps; audit support
• Guidance/training to QC personnel
• Ensuring laboratory documentation and GLP compliance
Technical Requirements
• Analytical raw data & chromatogram review
• GLP, GMP & Data Integrity (ALCOA+)
• Method validation / verification
• Stability studies (RM & Finished Product)
• Deviation, CAPA, OOS/OOT handling
• Audit preparation & compliance support
• Training & mentoring QC team
• Strong documentation & reporting skills
OFFICER – QC ANALYTICAL / HPLC
• Vacancy : 2 Positions
• Experience : 2+ Years
• Qualification : B. Pharm / M. Pharm / B.Sc / M.Sc or relevant qualification
• Mandatory / Preferred Experience: Hands-on pharmaceutical HPLC experience mandatory
Key Responsibilities
• HPLC operation and troubleshooting
• Assay, Related Substances / Impurity testing
• Identification; Sample and standard preparation
• Chromatographic data handling & analytical method execution
• Method validation/verification support
• Stability testing; RM and Finished Product testing
• Instrument calibration/qualification
• Analytical documentation; OOS/OOT; deviations; CAPA
• cGMP/GLP, ALCOA+ and data integrity; laboratory SOP compliance
Technical Requirements
• HPLC operation & troubleshooting
• Analytical method execution
• Assay & impurity analysis
• System suitability & chromatographic data handling
• Method validation & verification support
• Stability, RM & Finished Product testing
• Instrument calibration / qualification
• cGMP/GLP, ALCOA+ & data integrity
• Documentation & compliance (SOP, OOS/OOT, CAPA)
Share your CV, Current CTC & Notice period at : hr@puerto.in
Last Date : 15th September 2026
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