Puerto Lifesciences, a rapidly growing sterile pharmaceutical manufacturing company specializing in SVP (Small Volume Parenterals) and LVP (Large Volume Parenterals) injectables, is inviting applications for the position of Quality Control (GLP) Executive. Professionals with 3–7 years of experience in sterile pharmaceutical quality control and microbiology are encouraged to apply.
If you have expertise in GLP, GMP, sterile manufacturing, microbiological analysis, environmental monitoring, laboratory documentation, and QC testing, this is an excellent opportunity to build your career with a globally compliant pharmaceutical organization.
Job Details
Company: Puerto Lifesciences
Position: Quality Control (GLP) Executive
Department: Quality Control (GLP)
Experience Required: 3–7 Years
Industry: Sterile Pharmaceutical Manufacturing
Specialization: SVP & LVP Injectable Manufacturing
Key Responsibilities
The selected candidates will be responsible for:
- Ensure compliance with GLP, GMP, and sterile pharmaceutical quality standards.
- Perform routine chemical and microbiological testing of raw materials, packaging materials, in-process samples, and finished products.
- Conduct environmental monitoring, water testing, and microbiological analysis in sterile manufacturing areas.
- Maintain laboratory documentation, logbooks, analytical records, and ensure data integrity.
- Operate, calibrate, and maintain laboratory instruments and microbiology equipment.
- Prepare, review, and update SOPs, specifications, protocols, and laboratory records.
- Investigate Out of Specification (OOS), deviations, laboratory incidents, and implement CAPA.
- Handle microbiological cultures, chemicals, media, standards, and laboratory consumables.
- Coordinate with Quality Assurance, Production, and Warehouse departments for sampling and quality activities.
- Support customer, internal, and regulatory audits.
- Maintain laboratory safety, housekeeping, and regulatory compliance.
- Demonstrate strong analytical, troubleshooting, documentation, and communication skills.
- Follow aseptic techniques and sterile pharmaceutical manufacturing practices.
Educational Qualification
Candidates should possess one of the following qualifications:
- B.Pharm
- M.Pharm
- B.Sc Chemistry
- M.Sc Chemistry
- M.Sc Microbiology
- M.Sc Pharmaceutical Sciences or other relevant Life Science qualifications.
Preferred Skills
- Strong knowledge of GLP and GMP regulations.
- Hands-on experience in sterile pharmaceutical manufacturing.
- Environmental Monitoring (EM).
- Water Testing.
- Microbiology Laboratory Practices.
- Chemical Analysis.
- OOS Investigation.
- CAPA Documentation.
- Laboratory Instrument Calibration.
- Good Documentation Practices (GDP).
- Aseptic Manufacturing Practices.
- Regulatory Audit Readiness.
Why Join Puerto Lifesciences?
- Work in a modern sterile injectable manufacturing facility.
- Exposure to SVP and LVP pharmaceutical production.
- Opportunity to work with global cGMP standards.
- Professional growth in Quality Control and Microbiology.
- Collaborative and quality-driven work environment.
- Excellent career advancement opportunities.
Salary
Estimated Salary: ₹5.5 LPA – ₹8.5 LPA (Depending on qualification, experience, and interview performance)
How to Apply
Interested candidates should email the following details:
- Updated CV/Resume
- Current CTC
- Notice Period
Email: hr@puerto.in
