About this role
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.
Job Description
0 Responsibilities:
- To carry out the following routine checks in the laboratory on 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 done is online and error free.
- To ensure the correctness of the document before submitting it for the review of 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 qualification of equipment and timely incorporation in system.
- Preparation and review of standard operating procedure and other GMP documents.
- Carry out investigation related to incident/OOS/OOT and ensuring timely closure.
- Handling of change control, CAPA related to 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 execution of masters and its requirements, highlighting issues and their support for way forward in LIMS.
- Maintain analyst qualification record and instrument registration in LIMS.
- Responsible for Lab Safety and follow the JSA.
- Ensure to use the proper PPE at workplace.
- Periodic review / SPOT check of specifications / STPs in use.
- Any other responsibility assigned by Group Leader.
- Review closure of audit trails.
- Verification of outside calibration and their report.
- Tracking and updation of data related to Kaizen, Near Miss, 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 timely completion of all the training assigned to self.
- Above mentioned all activities should be performed in the presence of buddy.
Qualifications
B.Sc/B.Pharma/M.Sc.
Additional Information
About the Department
Basic knowledge on investigation and closure of OOS,OOT and deviation
Other facts
About Dr Reddy's Laboratories Limited
Established in 1984, we are a global pharmaceutical company headquartered in Hyderabad, India. Driven by our purpose of ‘Good Health Can’t Wait’, we work to provide access to affordable and innovative medicines. We offer a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC. Our major markets include USA, India, Russia & CIS countries, China, Brazil and Europe. As a company with a history of deep science that has led to several industry firsts, we continue to plan ahead and invest in future growth drivers such as access to novel molecules, digital therapeutics and consumer healthcare. As an early adopter of sustainability and ESG actions, we released our first Sustainability Report in 2004. Our current ESG goals aim to set the bar high in environmental stewardship; access and affordability for patients; diversity; and governance. For more information, log on to: www.drreddys.com.
Caution Notice: Dr. Reddy's has been made aware of candidates receiving fraudulent job opportunities from unauthorised recruiting agencies or people impersonating Dr. Reddy's leaders. These fraudulent jobs may be advertised on employment sites or mimic our careers site and company email addresses. Please know that Dr. Reddy's Laboratories has no affiliation or connection to these situations. Dr. Reddy's (and its associated/group companies) follows a formal recruitment process through its own HR department. Please report immediately in case you suspect a fraudulent job. You may raise your concern by:
Accessing https://drreddys.ethicspoint.com.
Calling on the hotline number. List of hotline numbers are available in https://drreddys.ethicspoint.com. The hotline is available 24x7 in multiple languages.
Writing to [email protected] or [email protected].
For our community guidelines on LinkedIn, please visit: https://shorturl.at/LTvNZ
What you'll do
- The Team Member in Quality Control is responsible for conducting routine laboratory checks, writing investigation reports, and ensuring compliance with documentation standards. They also handle calibration, inventory management, and maintain lab safety protocols.
Ready to join Dr Reddy's Laboratories Limited?
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