Quality Assurance Specialist at Sun Pharma in Bengaluru
Sun Pharma QA jobs offer a unique opportunity for a Quality Assurance Specialist in Bengaluru, Karnataka. This full-time role focuses on ensuring compliance with quality and regulatory standards in a leading pharmaceutical company renowned for its innovative approach and commitment to excellence.
- Position: Quality Assurance Specialist
- Location: Bengaluru, Karnataka, India
About Sun Pharma:
Sun Pharma is the world’s fourth-largest specialty generic pharmaceutical company and the leading pharmaceutical company in India, providing high-quality, affordable medicines in over 100 countries. Its global operations span more than 40 manufacturing facilities across 5 continents, supported by extensive R&D centers and a multicultural workforce representing over 50 nationalities. With around 3,000 scientists and sustained R&D investment of 6–8% of annual revenues, Sun Pharma focuses on innovation and continuous improvement. The organization emphasizes collective success, enabling team members to take charge of their growth in an environment with broad development opportunities. Through its Employee Value Proposition “Create Your Own Sunshine,” driven by the pillars Better Every Day, Take Charge, and Thrive Together, Sun Pharma supports people in achieving ambitious career goals.
Job Details:
Sun Pharma QA jobs: Job Description
This full-time, on-site Quality Assurance Specialist role is among Sun Pharma QA jobs focused on ensuring that products and processes meet Sun Pharma’s quality and regulatory standards. Day-to-day responsibilities include reviewing batch records and documentation, monitoring adherence to established procedures, and performing routine quality checks to support compliant manufacturing operations. The specialist will participate in internal audits, assist in investigations of deviations and nonconformities, and support the implementation of corrective and preventive actions. The role also involves collaborating with cross-functional teams to maintain Good Manufacturing Practice (GMP) compliance, updating standard operating procedures, and contributing to continuous improvement initiatives in quality systems.
Key Responsibilities:
- Review batch records and documentation for compliance.
- Monitor adherence to established quality procedures.
- Perform routine quality checks to support manufacturing operations.
- Participate in internal audits and assist in investigations.
- Support the implementation of corrective and preventive actions.
- Collaborate with cross-functional teams to maintain GMP compliance.
- Update standard operating procedures as necessary.
- Contribute to continuous improvement initiatives in quality systems.
Eligibility Criteria:
- Strong foundation in Quality Assurance and Quality Control.
- Experience with Quality Management systems.
- Knowledge of Good Manufacturing Practice (GMP) and regulatory requirements.
- Skills in Quality Auditing.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or related discipline.
- Attention to detail and strong analytical abilities.
- Ability to work collaboratively with effective communication skills.
- Prior experience in pharmaceutical or life sciences is an advantage.
How to Apply:
CLICK HERE FOR THE ORIGINAL NOTIFICATION
These Sun Pharma QA jobs present a significant opportunity for qualified candidates to contribute to a leading pharmaceutical organization. Interested individuals are encouraged to apply before the deadline to seize this chance to advance their careers in quality assurance.
