Quality Controls Jobs at Sun Pharma | MSc Chemistry Candidates Apply
Quality Control Jobs at Sun Pharma. They are hiring skilled Quality Control professionals for its Sikkim Unit II facility, offering an exciting opportunity to work with world-class QC systems in one of India’s most respected pharmaceutical companies. This role focuses on analytical testing, laboratory documentation, GLP compliance, and the management of standards—making it ideal for candidates who want to build a strong and future-ready career in pharma quality. Interested candidates apply for the Quality Control Jobs at Sun Pharma Careers.
About Sun Pharma Laboratories Ltd
Sun Pharma Laboratories Ltd is a leading pharmaceutical company that strives to provide high-quality medications worldwide. Our commitment to excellence and innovation has made us a trusted name in the industry. We are dedicated to fostering a work environment that encourages growth, collaboration, and the well-being of our employees. Join us on our journey to enhance healthcare and improve lives globally.
Job Title: Officer – Quality Control
- Date: Nov 20, 2025
- Location: Sikkim II – Plant
- Company: Sun Pharma Laboratories Ltd
- Position Details:
- Job Title: Officer
- Business Unit: Global Quality & Compliance
- Job Grade: G12C
- Location: Sikkim, Unit II
Responsibilities:
- To prepare and maintain a tracker of working standards and qualify the working standards before the due date.
- To indent the required reference standard and impurity standard as per requirements.
- To maintain a record of working standard, reference standard, impurity standard solution, and issuance of the same.
- To perform the physical and chemical testing of the working standard.
- To maintain and follow GLP in the laboratory.
- To follow safety precautions (use of nose mask, acid-resistant hand gloves, goggles, etc.) while handling strong acids like sulphuric acid, hydrochloric acid, and poisonous chemicals.
- To make sample registration, issuance of a template, and entry of analytical data in LIMS.
- To ensure that safety practice is followed while sampling and testing of raw material in the laboratory.
- Ensure that all the critical documents, such as OOS/Events/Change control, are initiated, investigated, and closed within the stipulated time.
- Ensure audit compliance for both the external and internal audits.
- Participation in the investigation of events/OOS in the QC department.
- Sampling and analysis of raw material and documentation of the same.
- Perform any other task allotted by the quality control head.
Job Requirements:
- Educational Qualification: M.Sc./B Pharm
- Experience: 2-5 years of experience in the pharmaceutical industry.
