Quality Control Microbiology Job at Dr. Reddy’s in Baddi – Apply Now!
Dr. Reddy’s Laboratories is hiring a Team Member – Quality Control (Microbiology) at its Baddi, Himachal Pradesh facility. This full-time, on-site role is ideal for candidates with 2–6 years of experience in microbiology or analytical techniques within a cGMP environment. If you’re skilled in HPLC, ELISA, PCR, and committed to delivering high-quality results, this is your opportunity to contribute to one of the world’s leading pharmaceutical companies in the fast-growing biologics segment.
Company Description
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company with 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, and 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.
Job Description
Job Title: Team Member – Quality Control (Microbiology)
Location: Baddi, Himachal Pradesh
Job Type: Full-Time
Job summary
We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines.
Roles & Responsibilities
- Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures.
- Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy.
- You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process.
- Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification.
- You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques.
Qualifications
Educational qualification: An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology
Minimum work experience: 2 years
Skills & attributes
- Basic understanding of the Biologics/Biosimilar industry, including processes, regulations, and trends.
- Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques, including Size Exclusion, Reverse Phase, Ion Exchange chromatography, and Peptide mapping analysis, especially within the context of Analytics.
- Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP).
- Prioritizes effective communication and demonstrates a performance-oriented mindset.
- Effective verbal and written communication skills.
Benefits Offered
At Dr. Reddy’s, we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards.
Keywords: Dr Reddy’s Laboratories, Quality Control Microbiology, Biologics, GMP, Good Manufacturing Practices
