Microbiology Job at Cipla | Junior Team Member | Apply Now
Cipla, a global pharmaceutical powerhouse, is looking for a Junior Team Member – Microbiology for its manufacturing unit in Rangpo, Sikkim. This microbiology job is a core quality control position responsible for ensuring that pharmaceutical products, water systems, and manufacturing environments meet stringent microbial safety standards. Advancing a Cipla career in the North-East region offers exposure to a high-compliance GMP environment where you will execute critical testing such as sterility, bio-burden, and environmental monitoring.
- Job Position: Junior Team Member – Microbiology
- Location: Rangpo, Sikkim.
About the Company
Cipla Limited is one of the world’s leading pharmaceutical companies, with a mission encapsulated by its motto: “Caring for Life.” Founded in 1935, Cipla has grown into a global healthcare giant known for making high-quality medicines affordable and accessible to patients across the globe. It is particularly recognized for its pioneering work in providing low-cost anti-retroviral (ARV) drugs for HIV/AIDS treatment. A Cipla career offers a chance to work for an organization that operates in over 80 countries and manufactures more than 1,500 products across various therapeutic categories, including respiratory, cardiovascular, oncology, and anti-infectives.
About the Department
The Microbiology department is the frontline of defense against contamination in pharmaceutical manufacturing. In this quality job, you will work in a sterile testing environment, utilizing advanced equipment like autoclaves and dry heat sterilizers (DHS) to maintain a germ-free production cycle.
Key Accountabilities
- Analysis & Testing Dimensions
- Sterility & Bio-load: Review and release approximately 15 sterility batches weekly and 15 bio-load samples.
- Water Analysis: Conduct testing and release for 50 water samples periodically to ensure pharmaceutical-grade water quality.
- Microbial Limit Test (MLT): Daily review and release of roughly 15 MLT reports.
- Environmental Monitoring (EM)
- Monitor and release data for 200 locations daily to ensure the manufacturing area remains within predefined microbial limits.
- Execute swab analysis for equipment surfaces, documenting findings in Technical Information Sheets.
- Compliance & GLP (Good Laboratory Practices)
- Documentation: Record all raw data and findings concomitantly in relevant test data sheets to ensure no missed entries.
- GDP/cGMP: Ensure all reports comply with Good Documentation Practices and Current Good Manufacturing Practices.
- Investigation: Initiate investigations into lab errors or abnormal observations to implement CAPA (Corrective and Preventive Actions).
- Technical Requirements & Decision Making
- Inventory Management: Responsible for deciding daily media and plate requirements to ensure uninterrupted testing.
- Instrument Maintenance: Evaluate equipment breakdowns and suggest mechanisms to prevent recurring malfunctions.
- Pharmacopoeial Knowledge: Coordination with Corporate Quality Assurance (CQA) for the latest pharmacopoeial guidelines.
Job Requirements
- Education: M.Sc. (Microbiology) is mandatory.
- Experience: 1-5 years for an Analyst role; 3-7 years for a Reviewer role.
- Shift Work: Required to meet high-volume testing SLAs (Service Level Agreements).
Why Choose a Cipla Career?
- Regulatory Exposure: Gain experience in a facility that adheres to international regulatory standards.
- Professional Growth: Sikkim is a major hub for Indian pharma, providing a concentrated learning environment for quality job professionals.
- Impact: Your work ensures that life-saving medications reach patients without microbial risks.
Securing a microbiology job at Cipla’s Rangpo unit is a significant milestone for professionals dedicated to pharmaceutical quality. This quality job offers deep technical exposure to environmental monitoring and sterility testing on a massive scale. By advancing your Cipla career in the picturesque state of Sikkim, you contribute to a legacy of “Caring for Life” through scientific rigor. If you have an M.Sc. in Microbiology and a strong understanding of cGMP, apply today.
