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Lead Analytical Quality Assurance Biosimilar


Job Location:

Hyderabad - India

Monthly Salary: Not provided by the employer
Posted: 21 June 2026 (30+ days ago)
Application Deadline: 18 September 2026
Vacancies: 1 Vacancy

Job Summary

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 :

  • Bachelors/Masters 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 1015-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 900000 patients having benefited from our products till date.

Benefits Offered
At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddys 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. Reddys why they come to work every day and theyll say because Good Health Cant 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 were 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  Work :

No


Employment Type :

Full-time


About Company

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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 Wa ... View more

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