
Sun Pharma, recognized as India’s leading pharmaceutical company and a major global player in specialty medicines, has announced an opening for a Quality Control Analyst II. This crucial position is located at the company’s Billerica Plant and is geared towards ensuring the highest standards of integrity and safety for its diverse pharmaceutical portfolio.
This opportunity targets experienced analysts who are proficient in advanced laboratory techniques and possess a robust understanding of global regulatory compliance, including cGMPs and GLPs. The application deadline for this role is October 20, 2025.
The Critical Role: QC Analyst II
The QC Analyst II is responsible for executing a wide range of analytical testing protocols on all stages of product development—from raw materials to in-process samples and finished goods. The role offers the chance to work with cutting-edge instrumentation while actively contributing to the continuous improvement of Sun Pharma’s quality systems.
Core Responsibilities and Expertise
The primary functions of this role are centered on testing, compliance, and documentation:
- Analytical Testing: Performing comprehensive testing, including release, stability, validation, and complaint follow-up testing, using established USP and EP test methods.
- Instrumentation and Systems: Operating and maintaining complex laboratory equipment and systems, such as water systems and environmental chambers.
- Regulatory Compliance: Ensuring absolute adherence to cGMPs (current Good Manufacturing Practices) and GLPs (Good Laboratory Practices) in all analytical assays and laboratory procedures.
- Documentation and SOPs: Analyzing and interpreting test data, maintaining precise records according to GDPs (Good Documentation Practices), and proactively revising and updating SOPs to align with current practices.
- Laboratory Support: Preparing essential reagents and solutions, coordinating sample testing with external contract laboratories, and participating in routine equipment maintenance and cleaning schedules.
- Training: Providing training and mentorship to junior analysts in fundamental laboratory techniques and procedures.
Candidate Profile Requirements
Sun Pharma is seeking candidates who meet the following strict criteria:
- Qualification: A Bachelor’s degree in Life Sciences or a closely related field.
- Experience: 2–4 years of hands-on, verifiable experience specifically within a pharmaceutical quality control environment.
- Technical Knowledge: A strong foundational understanding of chemical principles, wet chemistry, and essential analytical techniques like titration and limit tests.
- Software Proficiency: Practical familiarity with industry-specific software such as Trackwise, Novatech, and Empower.
- Essential Skills: Must be highly detail-oriented with strong analytical, problem-solving, and excellent written and verbal communication skills.
This position represents a prime opportunity for quality-focused analysts looking to advance their careers within a leading global pharmaceutical organization at its Billerica facility.
