Quality Assurance Specialist
SUN PHARMA · Bengaluru
- Experience0–1 yrs
- SalaryNot disclosed
- Work modeonsite
- Levelfresher
- Posted17 Sept 2026
About SUN PHARMA
SUN PHARMA is hiring in Bengaluru in pharma biotech. This role looks for around 0+ years of experience.
Skills
- Quality Assurance
- Quality Control
- Quality Management systems
- documentation control
- deviation handling
- continuous improvement
- Good Manufacturing Practice
- Quality Auditing
- regulatory requirements
- internal audits
- corrective and preventive actions
The role
A quality assurance specialist at a pharmaceutical manufacturing company applies Good Manufacturing Practice, quality auditing, and Quality Management systems to maintain compliant production and improve quality processes. The role also uses deviation handling and documentation control.
Full job description
Company Description 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.
Role Description This full-time, on-site Quality Assurance Specialist role is based in Bengaluru and focuses 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.
Qualifications
Strong foundation in Quality Assurance and Quality Control, with the ability to apply these skills in a regulated pharmaceutical environment.Experience with Quality Management systems, including documentation control, deviation handling, and continuous improvement processes.Knowledge of Good Manufacturing Practice (GMP) and related regulatory requirements applicable to pharmaceutical manufacturing.Skills in Quality Auditing, including planning and conducting internal audits and supporting external inspections.Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline.Attention to detail, strong analytical and problem-solving abilities, and proficiency in documentation and report writing.Ability to work collaboratively with cross-functional teams, with effective communication and stakeholder management skills.Prior experience in pharmaceutical or life sciences manufacturing or quality functions is an advantage.