Puerto Life Sciences Pvt. Ltd., a leading sterile pharmaceutical manufacturer specializing in Small Volume Parenterals (SVP) and Large Volume Parenterals (LVP) injectables, is actively expanding its team. Operating a state-of-the-art facility compliant with global cGMP standards, the company focuses on high-quality parenteral products including IV fluids and respules. Located in the RIICO Industrial Area at Ghiloth, Neemrana, Rajasthan, Puerto Life Sciences is seeking dynamic, motivated professionals for key quality roles in its growing organization.
This is an excellent opportunity for candidates experienced in sterile manufacturing and quality assurance/control to join a forward-thinking pharma company committed to excellence and data integrity.
Available Positions and Key Responsibilities
IPQA Officer In-Process Quality Assurance officers play a critical role in ensuring manufacturing compliance.
- In-process line monitoring and GMP compliance verification.
- Real-time batch record review and documentation control.
- Deviation identification, investigation, and compliance verification.
- Line clearance and in-process quality checks.
Quality Control Officer QC professionals handle analytical testing and instrument management in a cGMP environment.
- Operation and calibration of QC instruments (HPLC, UV, pH meters, etc.).
- Preparation and standardization of reagents and solutions.
- Documentation as per cGMP and data integrity principles (ALCOA+).
- Support for OOS, OOT, and deviation investigations.
Quality Control Microbiology Officer Microbiology specialists focus on testing for injectable products.
- Performing microbiological testing for injectable products.
- Conducting environmental monitoring, BET, MLT, and sterility testing.
- Managing media preparation and growth promotion tests (GPT).
- Maintaining microbiology records, trends, and data integrity (ALCOA+).
These positions suit candidates passionate about quality in sterile pharmaceuticals and ready to contribute to a compliant, high-standard production environment.
Required Qualifications and Experience
Candidates should hold relevant qualifications such as B.Sc./M.Sc. in Microbiology, Biotechnology, Chemistry, or B.Pharm/M.Pharm in Pharmaceutical Sciences or Quality Assurance. Prior experience in sterile injectable manufacturing (SVP/LVP) is highly preferred, along with knowledge of cGMP, data integrity (ALCOA+), and instruments like HPLC/UV. Freshers with strong academic backgrounds may be considered for entry-level support roles, but experienced professionals are prioritized.
Salary, Benefits, and How to Apply
Competitive salary packages are offered based on experience and role (realistic range for these officer-level positions in Rajasthan pharma plants: ₹3.5 – 6.5 LPA, negotiable for candidates with relevant sterile pharma expertise). Benefits typically include performance incentives, health coverage, and professional development opportunities in a modern facility.
To apply, email your updated CV, current CTC, and notice period to hr@puerto.in. Mention the position applied for in the subject line. Alternatively, reach out via the company’s official channels.
