Team Member - QC (Microbiology) at Dr Reddy's Laboratories Limited

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

09 Sep, 26

Salary

0.0

Posted On

11 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Microbiological Testing, Environmental Monitoring, Sterility Testing, Endotoxin Testing, Media Preparation, Growth Promotion Testing, GLP, GDP, LIMS, Instrument Calibration, Pathogen Testing, Microbial Limit Tests

Industry

Pharmaceutical Manufacturing

Description

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description To perform routine microbiological testing of raw materials, in-process samples, finished products, and environmental monitoring samples in compliance with established SOPs, regulatory guidelines, and Good Laboratory Practices (GLP). Microbiological Testing Perform routine microbiological analysis such as: Total Viable Count (TVC) Pathogen testing (E. coli, Salmonella, etc.) Sterility testing Microbial Limit Tests (MLT) Endotoxin testing (BET/LAL) Conduct media preparation, growth promotion testing (GPT), and sterilization activities. Environmental Monitoring Perform environmental monitoring of classified areas: Air sampling (active/passive) Surface monitoring (swab/contact plates) Personnel monitoring Record and evaluate data against alert and action limits. Qualifications B.Sc / M.Sc in Microbiology Additional Information Instrument Handling Operate and maintain laboratory equipment: Autoclave Incubators Laminar Air Flow (LAF) Colony counter Particle counter (if applicable) Ensure calibration and preventive maintenance compliance. Documentation & Compliance Maintain documentation as per Good Documentation Practices (GDP). Ensure accurate recording in logbooks, worksheets, and LIMS (if applicable). Follow SOPs, STPs, and regulatory guidelines (USFDA, EU GMP, WHO). Job Family: Quality Sub Job Family: Microbiology Preferred type of working: On-Premise Business unit: GMO

Responsibilities

Perform routine microbiological testing on raw materials, in-process samples, and finished products. Conduct environmental monitoring of classified areas and maintain strict compliance with SOPs and regulatory guidelines.