TM AQA reviewer

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. 

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. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).

‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.

Job Summary
 

1. 1. Review and approval of Qualification protocols and reports with respect to the Quality  Control.              
2. 1. Ensuring cGMP (current Good Manufacturing Practices), GLP (Good Laboratory Practices) and required Standard Operating Procedures are followed during manufacturing   and testing.
3. 1.  Review and approval of analytical reports of Raw materials, In-process, Finished product, Stability study, water and Hold Time study reports.
4. 1.    Initiation, evaluation, review and close out of change controls.

1. 1. Support to Investigation, root cause analysis, Corrective Action and Preventive Action for all type of notifications
2. 1. To perform specification, check and release of RM/PM/IP/FP/MICRO / water in SAP and LIMS.
3. 1. Perform periodic / random review of lab documents to verify compliance with relevant  SOP’s.
4. 1. Monitor and ensure cGLP (current Good Laboratory Practices) in Quality control and Micro Lab and implementation of standard operating procedures.
5. 1. To participate and support continuous improvement projects.
   2. To review and close out of investigations arising from incidents, out of specifications, out of trends, system failures, market complaints to identify the root cause and implement         appropriate corrective and preventive actions

Educational qualification: M.Sc.

Minimum work experience: 5-7 years of experience in, Quality control analysis or review of QC related documents 

Skills & attributes:
Technical Skills
• All analytical instrument related activity.
• Good knowledge of Labware LIMS, Empower, Review of audit trails. 
• Ability to review monthly audit rail, and experience in handling Out-of-Specification (OOS) incidents.
• Knowledge of analytical techniques used in the pharmaceutical industry.
• Understanding of electronic data management in line with 21 CFR Part 11.
• Skill in conducting and managing investigations related to QC
• Understanding and adherence to regulatory compliance standards.
Behavioural skills
• Strong communication skills for liaising with SCM, Cross-Functional Teams, and addressing queries.
• Analytical thinking for assessing vendor qualification documents and audit reports.

 

About the Department
Global Manufacturing Organisation (GMO)
At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry.
We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities.
Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future.

Benefits Offered
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.

Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
For more details, please visit our career website at https://careers.drreddys.com/#!/