Quality Assurance Associate - MES

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
We are seeking an individual to verify compliance for activities in the respective counter function regularly. This role involves quality oversight of DS manufacturing facilities, reviewing real-time investigations, ensuring smooth batch manufacturing, and evaluating practices against defined standards, to ensure consistent product quality and operational compliance within the regulatory framework and global standards.

Roles & Responsibilities

• Expertise in Supporting cross functional team of MES Specialists by providing a QA perspective with regards to DS manufacturing processes, documentation requirements, and overall design of records.
• Accountable for maintaining project timelines associated with quality assurance initiatives.
• Having knowledge and hands on experience on MES application on the aspects of both designing of MBR’s and its execution in order to have a brief understanding on how the recipe (design) functions during execution.
• Reviewing and approving MES recipes, master batch records, and electronic records to meet the requirements of manufacturing and QA users.
• Identifying errors in designs and suggesting alternatives way forwards that are aligned with GMP & compliance.
• Reviewing MES change controls, MES related SOPs, work instructions, forms, Assessment reports & QRA’s.
• Collaborating in the creation, review, and approval of EBR’s with CFT’s.
• Support audits, inspections, investigations and CAPA management related to MES.
• Providing end-user support for MES usage and working closely with IT to troubleshoot problems associated with QA functions.
• Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug substance operations; where current documents are not adequate, identify path forward for establishment of procedures.
• Develop, write, review, and approve SOPs and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.
• Working with Technical Trainers to develop QA training plans for MES users.
• Provide mentorship during on-the-floor manufacturing
• DS QA/ IPQA responsibilities such as support in PCO’s, line clearances, oversight activities, shop floor visit, vial issuances

Educational qualification: M.sc (Life Science)  /M Pharm 

Minimum work experience: 4-8  years of industrial experience with specific operational experience in Quality Assurance and Manufacturing (Biosimilars)

Skills & attributes:

Technical Skills
• A solid understanding of Quality Systems and the ability to comprehend and navigate counter functions within the organization.
• In-depth knowledge and comprehension of the Bio Pharma and Pharma markets, including product knowledge, market trends, competitors, and customer needs.
• Understanding and familiarity with global cGMP (Current GMP) regulatory requirements, including those set by FDA (U.S. Food and Drug Administration), EU (European Union), and Indian regulatory authorities.
• Awareness of broader market dynamics, industry trends, and factors influencing the pharmaceutical market.
• Comprehensive knowledge of the specific products associated with the pharmaceutical organization, including their characteristics, manufacturing processes, and quality requirements.
• Ability to understand and implement organizational policies and ensuring compliance.

Behavioural skills
• Demonstrates a commitment to continuous learning.
• Strong communicating and influencing skills.
• Displays analytical and logical thinking abilities.
• Is self-motivated and takes initiative.
• Adaptability to the work environment, along with being a team player.
• Ability to go beyond boundaries, showcasing a proactive and innovative approach.

Ability to work in shifts 

About the Department
Biologics
Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon.
With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.
With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.
Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.
We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure
Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.

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/#!/