Freshers Chemistry Jobs at Galentic Pharma | QC Officer Job
Freshers Chemistry Jobs at Galentic Pharma. The QC Officer position at Galentic Pharma in Mumbai offers a highly promising launchpad for postgraduates in chemistry and biochemistry who aspire to enter the pharmaceutical quality domain. This role provides extensive hands-on exposure to core analytical techniques such as HPLC, GC, and TLC, along with practical involvement in method validation, regulatory documentation, and strict GMP-compliant laboratory operations.
Working in a structured and quality-driven environment, candidates gain real-world experience in sample analysis, data interpretation, OOS investigations, and instrument handling, all of which are critical skills for long-term success in pharmaceutical quality control. For freshers seeking a technically strong, compliance-focused, and growth-oriented start to their pharma career, this opportunity offers an ideal foundation.
Company Overview:
Galentic Pharma is a leading pharmaceutical company dedicated to innovation and quality. Located in the vibrant city of Mumbai, we pride ourselves on our state-of-the-art research and development facilities. We are committed to improving health outcomes worldwide through our diverse range of pharmaceutical products.
- Job Title: QC Officer
- Location: Mumbai
- Experience: 0–1 Year (Fresher)
- Annual Package: ₹2.37 LPA
Job Responsibilities
- Perform chromatographic analyses such as HPLC, GC, and TLC on raw
materials, in-process samples, and finished products. - Prepare samples, standards, and reagents following established procedures
procedures and validated protocols. - Operate, maintain, and troubleshoot chromatography instruments; carry
Our routine calibration and preventive maintenance. - Analyse chromatographic data, interpret chromatograms, and document
results in accordance with SOPs, GLP, and GMP guidelines. - Follow laboratory safety protocols; handle and dispose of hazardous materials
chemicals and waste in accordance with regulatory requirements. - Participate in method validation, verification, and transfer activities;
assist in method development and optimization. - Conduct investigations into OOS (Out-of-Specification) results, non-conformances, and customer complaints.
- Maintain accurate documentation, including chromatograms, reports, equipment logbooks, and inventory records.
- Stay updated on advances in chromatographic techniques, regulatory changes, and quality standards; participate in training programs.
Educational Qualification:
- M.Sc. in Biochemistry
- M.Sc. Analytical Chemistry
- M.Sc. Organic Chemistry
