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 QA / IPQA
IPQA Officer
No. of Positions : 2
Experience : 1+ Year
Requirement : Sterile pharmaceutical facility experience mandatory
Key Responsibilities / Technical Requirements :
• In-process QA activities; shop-floor GMP monitoring
• Line clearance; area clearance; equipment/area readiness
• In-process checks; manufacturing process monitoring
• BMR/BPR review; verification of manufacturing activities
• Personnel/material movement compliance
• GMP/GDP; deviation reporting; investigation/CAPA support
• Change control support; batch documentation
• Coordination with Production/QC; audit readiness and inspection support
Officer – Calibration
No. of Position : 1
Experience : Relevant experience
Requirement : Pharmaceutical calibration experience preferred
Key Responsibilities / Technical Requirements :
• Calibration of manufacturing and laboratory instruments
• Calibration planning and scheduling
• Calibration tracking; review of certificates
• Calibration documentation
• Identification/reporting of calibration deviations
• Coordination with external calibration agencies
• GMP compliance; audit preparation and support
Officer – Validation
No. of Position : 1
Experience : Relevant Experience
Requirement : Pharmaceutical validation/qualification experience preferred
Key Responsibilities / Technical Requirements :
• Process Validation; Cleaning Validation
• Equipment Qualification; IQ/OQ/PQ
• Validation protocols and reports
• Validation schedules
• Change control related to validation
• Deviation/CAPA support; GMP compliance
• Validation documentation; audit readiness and support
Officer – Documentation
No. of Position : 1
Experience : Relevant Experience
Requirement : Pharmaceutical QA documentation experience preferred
Key Responsibilities / Technical Requirements :
• QA document control; SOP preparation/review/control
• Batch documentation; GDP; document issuance/release
• Controlled-document management; archival
• Training documentation; change control
• Deviation/CAPA documentation; record retention/retrieval
• Audit documentation; ensuring timely and compliant completion of QA records
Qualification : B.Pharm / M.Pharm / B.Sc / M.Sc or relevant qualification
Experience : 1+ Year / Relevant Experience
Location : Neemrana, Rajasthan
Share your CV, Current CTC & Notice Period at : hr@puerto.in
Last Date : 15th September 2026
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