Team Member – Quality Control at Dr. Reddy’s Laboratories
This Dr. Reddy’s Baddi vacancy is a rare chance for aspiring Quality Control Analysts to join Dr. Reddy’s Laboratories in Baddi, Himachal Pradesh. The organization seeks a competent and detail-oriented individual to support Quality Control activities for Oral Solid Dosage formulations. Interested candidates should apply promptly.
About The Company
Dr. Reddy’s Laboratories is a global pharmaceutical company based in India, dedicated to providing affordable and innovative medicines to patients. The company operates in various segments, including pharmaceuticals, biotechnology, and over-the-counter products. With a commitment to quality and compliance, Dr. Reddy’s Laboratories aims to enhance the quality of life for people worldwide.
Job Details
- Company: Dr. Reddy’s Laboratories
- Position: Team Member – Quality Control
- Location: Baddi, Himachal Pradesh, India
- Posted On: 19 hours ago
- Applicants: 60
Job Description
For this Dr Reddy Baddi vacancy, the QC Analyst will be responsible for sampling, testing, and release of Raw Materials, Packing Materials, and Finished Products in accordance with approved specifications, cGMP requirements, and internal quality standards. This role requires expertise in analytical instrumentation, laboratory documentation, data integrity practices, and adherence to regulatory requirements.
Key Responsibilities
- Perform sampling and analysis of Raw Materials and Packing Materials as per approved specifications, STPs, and pharmacopoeial requirements.
- Execute routine quality control testing and ensure timely reporting of results.
- Prepare and review analytical records, worksheets, and test reports.
- Operate, maintain, and troubleshoot analytical instruments, including HPLC, GC, Auto Titrator, Karl Fischer Titrator, UV-Visible Spectrophotometer, and FTIR Spectrophotometer.
- Maintain accurate and complete analytical records in compliance with cGMP, GLP, and ALCOA+ data integrity principles.
- Support investigations related to OOS, OOT, deviations, and laboratory incidents.
- Manage the handling and storage of chemicals, solvents, reference standards, and laboratory consumables.
- Adhere to laboratory safety requirements, JSA, and EHS guidelines.
Eligibility Criteria
- Educational Qualification: M.Sc. in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or related discipline.
- Experience: 4–6 years of experience in Quality Control within the pharmaceutical industry, preferably in Oral Solid Dosage manufacturing.
Required Skills
- Strong knowledge of analytical testing techniques for Raw Materials and Packing Materials.
- Hands-on experience with HPLC, GC, KF, UV-Visible Spectrophotometer, FTIR, and Auto Titrator.
- Knowledge of cGMP, GLP, data integrity, and regulatory compliance requirements.
- Familiarity with SAP/LIMS and laboratory documentation systems.
- Experience in calibration, verification, and maintenance of laboratory instruments.
- Understanding of OOS, OOT, deviations, CAPA, and investigation processes.
- Proficiency in preparation and standardization of reagents and volumetric solutions.
How to Apply for This Dr Reddy Baddi Vacancy
Interested candidates can apply through the following link:
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This Dr Reddy Baddi vacancy is an excellent opportunity for qualified candidates to join Dr. Reddy’s Laboratories as a Quality Control Analyst. Interested individuals are encouraged to apply before the deadline to secure their chance to contribute to the pharmaceutical industry.
