Quality Control Job at Dr. Reddy’s Laboratories | Apply for the Team Member Role
Dr. Reddy’s Laboratories is hiring a Team Member – Quality Control at its Baddi, Himachal Pradesh facility. This Quality Control Job involves performing routine laboratory checks, managing LIMS documentation, and executing investigations for OOS, OOT, and deviations. Ideal for candidates with a B.Sc, B.Pharma, or M.Sc, the Dr Reddy’s Job emphasizes GMP compliance, laboratory safety through JSA protocols, and timely CAPA implementation in a high-compliance pharmaceutical environment.
- Job Title: Team Member – Quality Control
- Location: Baddi, Himachal Pradesh, India
About The Company
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, and a commercial presence in 66 countries. In recent years, Dr. Reddy’s has offered many roles relevant for those pursuing a job in quality control, so this opportunity is a good fit for anyone interested in a Quality Control Job.
Job Responsibilities
- To carry out the following routine checks in the laboratory on a daily basis:
- Responsibility for investigation report writing and closure of deviation, OOS, and OOT.
- Qualification of working standards.
- Glassware verification & labelling.
- Routine calibration and verification of all instruments.
- Logbooks verification.
- To ensure that the documentation is online and error-free.
- To ensure the correctness of the document before submitting it for the review of the Group Leader/AQA reviewer.
- Column stock, inventory, indent, requirement, and routine usage verification.
- Reference/Working standard and impurities verification.
- Area upkeep and maintenance.
- Calibration schedule/document/labels routine verification.
- Carrying out the qualification of equipment and timely incorporation in system.
- Preparation and review of standard operating procedure and other GMP documents.
- Carry out an investigation related to the incident/OOS/OOT and ensure timely closure.
- Handling of change control, CAPA related to the quality control department, ensuring timely closure and effectiveness check of implemented CAPAs.
- Ensuring that all changes related to specifications/STPs/SOPs are evaluated and percolated in an effective manner to all concerned.
- Responsible for stock preparation and its inventory, i.e., chemical, standards, column, etc., in LIMS.
- Responsible for the execution of the master’s and its requirements, highlighting issues and their support for the way forward in LIMS.
- Maintain analyst qualification record and instrument registration in LIMS.
- Responsible for Lab Safety and following the JSA.
- Ensure to use the proper PPE at the workplace.
- Periodic review / SPOT check of specifications / STPs in use.
- Any other responsibility assigned by the Group Leader.
- Review the closure of audit trails.
- Verification of outside calibration and its report.
- Tracking and updating of data related to Kaizen, Near Miss, and LDM.
- Compliance Response preparation and closure support.
- Timely closure of observations related to SOI and QOI.
- Ensuring timely availability of accessories and Lab consumables for routine use (PO creation and other SAP-related activities).
- Ensuring the timely completion of all the training assigned to oneself.
- Above mentioned all activities should be performed in the presence of a buddy.
Qualifications
B.Sc/B.Pharma/M.Sc. For candidates looking for a new challenge, this role is an excellent choice if you are targeting a Quality Control position or job in the pharmaceutical industry.
