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 and multiple R&D; centers supported by a multicultural workforce from over 50 nationalities. Sun Pharma invests 6–8% of its annual revenue in R&D;, empowering around 3,000 scientists to drive innovation and excellence.

The organization focuses on collective growth, enabling team members to take charge of their careers in an environment with extensive development opportunities. Through its Employee Value Proposition “Create Your Own Sunshine,” guided by the pillars of Better Every Day, Take Charge, and Thrive Together, Sun Pharma supports individuals in achieving ambitious professional goals.

Role Description This is a full-time, on-site role based in Halol for Qualification and Validation of Sterile Manufacturing Equipment and Utilities. The role involves planning and performing qualification activities for sterile manufacturing equipment and associated utilities, including drafting and executing protocols (IQ/OQ/PQ) in compliance with regulatory and company standards. The team member will oversee process and cleaning validation, monitor critical parameters,



and ensure data integrity throughout validation lifecycle documentation.

Responsibilities include collaborating with production, engineering, quality assurance, and quality control teams to investigate deviations, implement corrective and preventive actions, and support continuous improvement initiatives. The role also requires staying current with regulatory guidelines, participating in audits and inspections, and maintaining accurate records for equipment and utility validation.

Qualifications

- Robust expertise in equipment and utilities Validation for sterile manufacturing environments.
- Knowledge of Computer System Validation for equipment-related software, data handling, and electronic records.
- Practical experience in Quality Assurance and Quality Control within pharmaceutical manufacturing.
- Understanding of equipment and utility qualification requirements, including HVAC, purified water, and clean steam systems.
- Bachelor’s or Master’s degree in Pharmacy, Engineering, or a related scientific discipline.
- Familiarity with GMP, regulatory requirements (e.g., WHO, EU, USFDA), and data integrity principles.
- Ability to interpret technical documents, write clear protocols and reports, and manage validation documentation.
- Strong analytical, problem-solving, and communication skills, with the ability to work effectively in cross-functional teams on-site.

📌 Qualification and validation for the sterile manufacturing EQUIPMENT AND UTILITIES (Halol)
🏢 SUN PHARMA
📍 Halol