Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries. Driven by a commitment to innovation, we continuously strive to enhance access to medicines and improve patient care, creating better health outcomes for millions around the world.
Post : QC Analyst II
Job Description
Job Summary
As a Quality Control Analyst II, you will play a critical role in ensuring the integrity and safety of our pharmaceutical products. You’ll conduct analytical testing on raw materials, in-process samples, and finished goods, adhering to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs). This position offers the opportunity to work with cutting-edge laboratory equipment and contribute to the continuous improvement of our quality systems.
Areas of Responsibility
• Perform release, stability, validation, and complaint follow-up testing on raw materials and finished products.
• Execute analytical assays using USP and EP test methods, ensuring compliance with GLPs.
• Operate and maintain complex laboratory instrumentation and systems (e.g., water systems, environmental chambers).
• Analyze and interpret test data; maintain accurate records in accordance with Good Documentation Practices (GDPs).
• Revise and update SOPs to reflect current practices and regulatory requirements.
• Coordinate with contract laboratories for sample testing and data collection.
• Prepare reagents, solutions, and equipment for chemical testing; clean and maintain lab glassware.
• Train junior analysts in laboratory techniques and procedures.
• Participate in monthly equipment maintenance and cleaning schedules.
• Support visual inspection qualification training and other assigned duties.
Candidate Profile
• Bachelor’s degree in Life Sciences or a related field.
• 2–4 years of hands-on experience in a pharmaceutical quality control environment.
• Strong understanding of chemical principles, wet chemistry, and analytical techniques (e.g., titration, limit tests).
• Proficiency in operating and troubleshooting laboratory instruments.
• Familiarity with Trackwise, Novatech, and Empower software.
• Excellent written and verbal communication skills.
• Detail-oriented with strong analytical and problem-solving abilities.
• Knowledge of cGMPs, GLPs, and regulatory compliance standards.
Additional Information
Experience : 2–4 years
Qualification : Bachelor’s degree in Life Sciences
Location : Billerica - Plant
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : QC
End Date : 20th October 2025
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