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Puerto Life Sciences Announces Exciting Career Opportunities in Pharmaceutical Manufacturing
Puerto Life Sciences Pvt. Ltd., a reputed name in the pharmaceutical industry, has officially announced multiple job openings across key departments. Known for its advanced sterile manufacturing facility, Puerto specializes in SVP (Small Volume Parenterals) and LVP (Large Volume Parenterals) injectables, operating in strict adherence to global cGMP standards.
As part of its continued growth, the organization is seeking skilled, motivated, and dynamic professionals to join its expanding team.
1. Quality Control – Officers & Executives
Candidates applying for Quality Control roles will be responsible for:
Operation and calibration of analytical instruments such as HPLC, UV, and pH meters
Preparation and standardization of reagents and solutions
Maintaining documentation in compliance with cGMP and data integrity principles (ALCOA)
Supporting investigations related to OOS (Out of Specification), OOT (Out of Trend), and deviations
2. IPQA (In-Process Quality Assurance) – Officers
Key responsibilities include:
Monitoring in-process activities to ensure GMP compliance
Real-time batch record review and documentation control
Identifying deviations and ensuring proper compliance measures
Performing line clearance and in-process quality checks
3. Quality Control Microbiology – Officers & Executives
Professionals in this role will handle:
Microbiological testing for injectable products
Environmental monitoring and sterility testing (BET, MLT, etc.)
Media preparation and growth promotion test (GPT) activities
Maintaining microbiology records, trends, and data integrity (ALCOA compliance)
4. Production – 3 Piece Ophthalmic Machine
Positions available: Senior Operator & Technician
Responsible for operating and handling 3-piece ophthalmic manufacturing machines
Ensuring smooth production operations in compliance with quality standards
Candidates should have 6 to 12 years of relevant experience
Why Join Puerto Life Sciences?
Puerto offers a high-quality work environment aligned with international pharmaceutical standards. Employees benefit from:
Exposure to advanced sterile manufacturing technologies
Strong compliance-driven culture
Career growth opportunities within a globally aligned organization
How to Apply
Interested candidates are encouraged to share their updated CV along with current CTC and notice period details.
Email: hr@puerto.in
Website: www.puertolifesciences.com
FAQ
1. What analytical instruments are commonly used in Quality Control for injectable manufacturing?
Quality Control laboratories typically use instruments such as HPLC (High-Performance Liquid Chromatography), UV-Visible spectrophotometers, pH meters, and dissolution apparatus. These instruments are essential for analyzing the quality, potency, and stability of pharmaceutical products.
2. What is ALCOA and why is it important in pharmaceutical documentation?
ALCOA stands for Attributable, Legible, Contemporaneous, Original, and Accurate. It is a key principle of data integrity in the pharmaceutical industry, ensuring that all records are reliable, traceable, and compliant with regulatory requirements like cGMP.
3. What is the role of IPQA in sterile manufacturing?
In-Process Quality Assurance (IPQA) ensures that manufacturing activities comply with GMP standards during production. It involves real-time monitoring, line clearance, batch record verification, and identifying deviations to maintain product quality and regulatory compliance.
4. What microbiological tests are performed for injectable products?
Microbiology labs conduct tests such as sterility testing, Bioburden testing, Bacterial Endotoxin Test (BET), and Microbial Limit Test (MLT). Environmental monitoring and growth promotion tests (GPT) are also performed to ensure aseptic conditions.
5. What are OOS and OOT results in pharmaceutical quality control?
OOS (Out of Specification) results occur when test results fall outside predefined acceptance criteria, while OOT (Out of Trend) results indicate unexpected variations from historical data trends. Both require thorough investigation to ensure product quality and compliance.
