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 Production Team
Assistant Manager – Production
Vacancies : 1 Position
Experience : 7+ years
Mandatory / Preferred Experience : Sterile injectable pharmaceutical manufacturing experience — Mandatory
Key Responsibilities :
• Overall production supervision
• Production planning & schedule execution
• Manpower planning & batch manufacturing
• BMR/BPR & SOP compliance
• Manufacturing process monitoring
• Area/equipment readiness & yield monitoring
• Material reconciliation & deviation investigation
• CAPA & change control
• Coordination with QA/QC/Engineering/Warehouse
• Shop-floor discipline, training & development
• Audit/inspection readiness & continuous improvement
• Achievement of production targets
Key Technical Requirements :
• Sterile injectable manufacturing
• BMR/BPR & SOP compliance
• Process monitoring & yield monitoring
• Material reconciliation
• Deviation investigation / CAPA
• Change control
• QA/QC coordination
• Audit readiness
• Leadership & team management
Officer – Production
Vacancies : 2 Positions
Experience : 3+ years
Mandatory / Preferred Experience: Pharmaceutical production experience; sterile injectable production experience required/preferred depending on assigned area
Key Responsibilities :
• Day-to-day production operations
• Execution of manufacturing activities
• BMR/BPR documentation
• Process monitoring & GMP compliance
• Manpower coordination
• Production reporting & yield monitoring
• Material reconciliation & deviation reporting
• Area/equipment readiness
• Cleaning & line-clearance coordination
• Coordination with QA/QC/Engineering/Warehouse
• Audit support
Key Technical Requirements :
• GMP compliance
• BMR/BPR documentation
• Process monitoring
• Material reconciliation
• Deviation reporting
• Area/equipment readiness
• Line clearance & cleaning coordination
• QA/QC coordination
• Audit support
Mixing Operator
Vacancies : 2 Positions
Experience : Relevant experience
Mandatory / Preferred Experience: Pharmaceutical sterile/liquid manufacturing experience — Preferred / Required
Key Responsibilities :
• Mixing/manufacturing operations
• Operation of mixing equipment
• Material issuance as per batch documents
• Following manufacturing instructions / SOPs
• Equipment cleaning
• Operational checks
• Manufacturing documentation
• GMP & safety compliance
• Coordination with Production/QA
• Maintaining area cleanliness & discipline
Key Technical Requirements :
• Operation of mixing equipment
• Material changeover
• Following SOPs
• Equipment cleaning
• Operational checks
• Manufacturing documentation
• GMP & safety compliance
• Area cleanliness & discipline
Officer – Sterile Injectable Production
Vacancies : 2 Positions
Experience : 2+ years
Mandatory / Preferred Experience: Sterile injectable pharmaceutical manufacturing experience — Mandatory
Note : Only relevant candidates will be considered.
Key Responsibilities :
• Sterile injectable manufacturing operations
• Process monitoring
• Approved SOP/BMR/BPR compliance
• GMP & aseptic practices
• Area/equipment readiness
• Coordination with QA/IPQA
• Deviation reporting/investigation support
• Cleaning & sanitization
• Yield/reconciliation
• Production documentation
• Audit & inspection support
Key Technical Requirements :
• Sterile injectable operations
• SOP/BMR/BPR compliance
• GMP & aseptic practices
• Process monitoring
• QA/IPQA coordination
• Deviation reporting
• Cleaning & sanitization
• Yield/reconciliation
• Production documentation
• Audit support
Additional Information
Experience : 2-7+ years
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Location : Neemrana, Rajasthan
Industry Type : Pharma
End Date : 30th September 2026
Share your CV, Current CTC & Notice period at : hr@puerto.in
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