Lead - Analytical Quality Assurance - Biosimilar at Dr Reddy's Laboratories Limited

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

17 Sep, 26

Salary

0.0

Posted On

19 Jun, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Quality Assurance, cGMP, GLP, LIMS, Analytical Method Validation, Data Integrity, Quality Management Systems, Root Cause Analysis, CAPA, Stability Protocols, Technical Writing, Team Management, ICH Guidelines, Biosimilars, Audit Readiness, Cross-functional Collaboration

Industry

Pharmaceutical Manufacturing

Description

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. 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 Description The Lead – Analytical Quality Assurance is responsible for providing strategic and operational leadership to ensure the quality and compliance of all laboratory testing activities. This role oversees the review and approval of analytical documentation, ensures audit readiness, and supports cross-functional collaboration to maintain high standards of product quality and regulatory compliance. Key Responsibilities: Oversee testing and release activities for Raw Materials, Packaging Materials, In-process, and Finished Products in compliance with cGMP and regulatory requirements. Review and approve: Stability protocols and reports Standard Test Procedures (STPs) and product specifications Analytical method validation and transfer protocols/reports Internal Reference Standard qualification and re-qualification LIMS master data, ensuring alignment with approved test methods Allocate daily testing priorities based on business needs and resource availability. Provide technical guidance to QC analysts on analytical techniques and troubleshooting. Participate in cross-functional technical discussions to resolve analytical and quality issues. Ensure timely closure of QMS elements including Deviations, Change Controls, CAPAs, OOS, and OOT. Conduct audit trail reviews and ensure compliance with data integrity standards. Support batch analysis report reviews and coordinate with QA for timely batch release. Perform GEMBA walks to monitor laboratory practices and ensure GLP compliance. Collaborate with the Site Investigation Team and other departments to conduct effective root cause analysis and implement robust CAPAs. Qualifications Bachelor’s/Master’s degree in Pharmaceutical Sciences, Chemistry, or related field Minimum 12+ years of experience in Quality Control within the pharmaceutical industry Strong knowledge of ICH guidelines, cGMP, GLP, and regulatory requirements Experience with LIMS, analytical method validation, and data integrity practices Proven leadership and team management skills Excellent communication and cross-functional collaboration abilities Ability to succeed in a team-oriented environment under very dynamic conditions. Excellent communication, technical writing, organizational skills and use of Microsoft office products. Additional Information 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/#!/ Job Family: Quality Sub Job Family: Quality Assurance Business unit: Biologics

Responsibilities

Provide strategic and operational leadership to ensure the quality and compliance of all laboratory testing activities. Oversee the review and approval of analytical documentation and ensure audit readiness for raw materials and finished products.