Zentiva is a leading pharmaceutical company committed to delivering high-quality, affordable medicines to improve patients’ lives worldwide. With a strong focus on innovation, compliance, and operational excellence, Zentiva provides a dynamic work environment for professionals in the pharmaceutical industry.
Job Overview
As an Executive – QC, Microbiology, you will play a crucial role in ensuring the quality and safety of pharmaceutical products by performing microbiological testing, environmental monitoring, and compliance with GMP/GLP standards. This position offers an excellent opportunity to work in a GMP/GLP-compliant environment and contribute to maintaining high-quality standards in pharmaceutical manufacturing.
Key Responsibilities
1. Microbiological Analysis
- Conduct microbial analysis of raw materials, finished products, and water systems (Potable, Process, and Purified Water).
- Perform Bacterial Endotoxin (LAL) Testing.
- Monitor Environmental Monitoring (EM) in controlled areas and maintain documentation as per regulatory guidelines.
2. Laboratory Compliance & Maintenance
- Ensure adherence to Good Laboratory Practices (GLP).
- Perform calibration and maintenance of lab equipment (e.g., autoclave, incubator, balances).
- Handle microbial cultures, media preparation, and lab reagents.
3. Data Management & Compliance
- Maintain accurate microbiology testing records and raw data.
- Participate in OOS (Out of Specification) investigations and retesting procedures.
- Assist in analytical method validation and cleaning validation as per protocols.
4. Coordination & Safety Compliance
- Coordinate with production teams for EM and water sampling activities.
- Follow HSE (Health, Safety, and Environment) guidelines for lab operations.
- Identify and report unsafe conditions to ensure a safe working environment.
Qualifications & Requirements
- Education: M.Sc. (Microbiology/Biotechnology) or B.Pharm
- Experience: 2-4 years in microbiology within the pharmaceutical industry
- Technical Skills:
- Knowledge of GMP, GLP, LIMS, and QMS
- Experience in microbial testing, environmental monitoring, and endotoxin testing
- Proficiency in data trending and lab equipment handling
- Soft Skills: Strong analytical, communication, and coordination skills
Why Join Zentiva?
✅ Work in a GMP/GLP-compliant environment with global quality standards.
✅ Opportunity to contribute to life-saving pharmaceutical products.
✅ Career growth in a reputable pharmaceutical company.
✅ Exposure to advanced microbiological testing and validation processes.
How to Apply
