Quality Control Jobs at Dr Reddy’s Careers – Build Your Pharma Future | Apply Now
Quality Control Jobs at Dr Reddy’s Careers offer an excellent opportunity for B.Sc, B.Pharma, and M.Sc graduates to work in a globally recognized pharmaceutical organization. Dr Reddy’s Careers are well known for strong quality systems, GMP compliance, and structured laboratory operations, making these Quality Control Jobs ideal for candidates looking to grow in pharmaceutical quality and regulatory environments.
Job Details
- Job Position: Quality Control Laboratory Professional
- Location: 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 or a commercial presence in 66 countries.
Job Description
The role involves performing routine laboratory activities, quality investigations, calibration, qualification, documentation, and compliance-related tasks as part of Quality Control Jobs at Dr Reddy’s Careers, ensuring adherence to GMP and quality system requirements.
Key Responsibilities | Quality Control Jobs
- 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 effectively to all concerned.
- Responsible for stock preparation and its inventory, i.e. chemical, standards, column,n etc., in LIMS.
- Responsible for the execution of 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 self.
- All the activities mentioned should be performed in the presence of a buddy.
Qualifications Required For Quality Control Jobs
- B.Pharma
- Basic knowledge on investigation and closure of OOS, OOT and deviation.
