Pharm'Up 
Puerto, a specialized sterile pharmaceutical manufacturing facility focused on Small Volume Parenterals (SVP) and Large Volume Parenterals (LVP), is expanding its team. The plant operates under strict global cGMP (Current Good Manufacturing Practices) standards and is seeking motivated professionals for its production and quality divisions.
Open Positions & Responsibilities
| Department | Role | Core Responsibilities |
| Packing | Officer | Supervise SVP/LVP injectable packing; ensure line clearance and reconciliation; maintain batch records and labeling accuracy. |
| Quality Control (QC) | Officer | Operate and calibrate instruments (HPLC/GC); reagent standardization; ensure data integrity (ALCOA+); support OOS/OOT investigations. |
| QC Microbiology | Officer | Microbiological testing for injectables; Environmental Monitoring (EM); BET (Bacterial Endotoxin Test) and MLT; Media preparation. |
Technical Focus: Data Integrity & Testing
Puerto emphasizes strict adherence to ALCOA principles (Attributable, Legible, Contemporaneous, Original, and Accurate) to ensure data integrity in all laboratory and production records.
For the QC Micro role, candidates will be responsible for critical safety tests such as the Bacterial Endotoxin Test (BET), which is essential for ensuring that injectable products are pyrogen-free and safe for patient administration.
How to Apply
Interested candidates are invited to submit their updated credentials via email. Please ensure you include your Current CTC and Notice Period in the application.
- Email Address: hr@puerto.in
- Last Date to Apply: 15th February 2026
- Industry Focus: Sterile Injectables (SVP & LVP)
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