Sun Pharma Hiring Chemistry Graduates | Apply for Senior Officer Quality Control Position
Sun Pharma Hiring! Join Sun Pharmaceutical Industries Ltd as a Senior Officer in Quality Control at our Dadra facility. This role offers a hands-on opportunity to ensure the highest standards of pharmaceutical quality and compliance with US FDA regulations and current Good Manufacturing Practice (cGMP) practices. If you have expertise in analytical testing and a passion for precision, this is your chance to make a tangible impact in the pharmaceutical industry.
- Job Position: Senior Officer – Quality Control
- Location: Dadra – Quality Control Department
About the Company
Sun Pharmaceutical Industries Ltd. is a global leader in pharmaceutical manufacturing, committed to delivering high-quality medicines worldwide. With a focus on innovation and compliance, Sun Pharma provides a dynamic work environment for professionals passionate about healthcare and quality assurance.
Job Description
The Senior Officer – Quality Control Job is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products. The role ensures compliance with US FDA regulations, cGMP standards, and internal specifications, thereby maintaining product quality, safety, and efficacy.
Key Responsibilities
- Analytical Testing:
- Conduct chemical, physical, and microbiological tests using HPLC, GC, UV-Vis, FTIR, titration, and dissolution techniques.
- Conduct stability studies and method validation in accordance with regulatory guidelines.
- Documentation & Compliance:
- Maintain accurate and complete records of all testing activities in compliance with GDP.
- Document and investigate Out-of-Specification (OOS) results.
- Ensure adherence to cGMP, GLP, and USFDA regulations.
- Equipment Handling:
- Calibrate, maintain, and troubleshoot laboratory instruments.
- Ensure proper usage and upkeep of analytical equipment.
- Cross-Functional Collaboration:
- Coordinate with Production, QA, and R&D teams to resolve quality issues.
- Participate in internal and external audits.
- Continuous Improvement:
- Assist in developing and validating new analytical methods.
- Recommend improvements to testing procedures and quality systems.
Educational Qualifications
Bachelor’s or Master’s degree in Chemistry
Experience and Skills
- 2–5 years of experience in a pharmaceutical QC laboratory, preferably in a USFDA-approved facility.
- Hands-on experience with analytical instruments and techniques.
- Knowledge of regulatory guidelines (USFDA, ICH, WHO).
- Strong attention to detail and analytical skills.
- Certified Quality Analyst (CQA)
- Training in cGMP, GLP, and data integrity
- Excellent communication and documentation skills
- Ability to work independently and in a team
- Problem-solving and critical thinking abilities
