Location: Rewari, Haryana, India (Hybrid)
We are seeking a Microbiologist to support the Quality Control (QC) Microbiology Laboratory by performing microbiological testing, environmental monitoring, data review, and quality system activities to ensure compliance with GMP, GLP, regulatory, and company requirements. The role is responsible for ensuring timely testing and release support for raw materials, finished products, water systems, and packaging materials while maintaining laboratory excellence and audit readiness.
Working at the intersection of quality, compliance, and laboratory operations, you will collaborate with Manufacturing, Quality Assurance, Engineering, EHS, and Supply Chain teams to ensure product quality, data integrity, and continuous improvement across microbiological processes.
What you will get
Opportunity to contribute to the production of high-quality healthcare products through robust microbiological quality control practices.
Hands-on experience with microbiological testing, environmental monitoring, microbial identification, and laboratory investigations.
Exposure to GMP-compliant quality systems including deviations, OOS/OOT investigations, change controls, CAPAs, and audits.
Cross-functional collaboration with Manufacturing, Quality Assurance, Engineering, EHS, and Supply Chain teams.
Career growth within a highly regulated pharmaceutical and healthcare manufacturing environment.
What you will do
Perform microbiological analysis of raw materials, finished products, water samples, and packaging materials in accordance with approved procedures and specifications.
Execute environmental monitoring activities for manufacturing areas and microbiology laboratories, including trend analysis and reporting.
Prepare microbiological media and perform Growth Promotion Testing (GPT) to support laboratory testing activities.
Review, interpret, and document microbiological test results while ensuring data integrity and compliance with GMP/GLP requirements.
Support laboratory investigations including deviations, OOS/OOT events, change controls, CAPAs, and annual product quality reviews.
Conduct microbial identification activities and support investigation of environmental and product-related microbiological excursions.
Participate in qualification, validation, calibration, and routine verification of microbiology laboratory equipment, methods, AHUs, and LAF systems.
What we are looking for
Bachelor’s or Master’s degree in Microbiology, Biotechnology, Life Sciences, Pharmaceutical Sciences, or a related scientific discipline.
Experience in a Quality Control Microbiology laboratory within the pharmaceutical, healthcare, life sciences, or regulated manufacturing industry.
Strong knowledge of microbiological testing techniques, environmental monitoring, water testing, microbial identification, and aseptic laboratory practices.
Understanding of GMP, GLP, data integrity requirements, and applicable regulatory guidelines.
Experience handling laboratory quality systems including deviations, CAPAs, change controls, OOS/OOT investigations, and audit support.
Familiarity with qualification, validation, calibration, and maintenance of microbiology laboratory equipment and systems.
Strong analytical, problem-solving, documentation, and data review capabilities.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
