Pharmacist Job Opportunity at Syngene to Work in Clinical Trials | Apply Now
If you are searching for a Pharmacist Job, this opportunity through Syngene Careers could be an excellent step in your pharmaceutical career. Syngene International Ltd. is hiring a Pharmacist in Bangalore to support clinical trials and investigational product management. This Pharmacist Job at Syngene Careers offers professionals the opportunity to work in clinical supply management, regulatory compliance, labeling, and inventory handling while contributing to global pharmaceutical research and development.
- Designation: Pharmacist
- Job Location: Bangalore
About the Company
Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries around the world.
Syngene’s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240-strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation.
Key Responsibilities
- Prepare pharmacy plans and labeling plans based on the clinical trial protocol.
- Receive, verify, and store Investigational Medicinal Products (IMP) and Non-Clinical Supplies (NCS).
- Perform labeling and relabeling of clinical trial medicines as per the approved plan.
- Supply and resupply clinical trial medicines to investigational sites under the required temperature conditions.
- Prepare shipment documents and ensure enough clinical supplies are available at trial sites.
- Manage inventory and maintain proper documentation of IMP and NCS during the study.
- Handle the return, recall, and reconciliation of clinical trial supplies from sites.
- Witness the destruction of unused clinical trial medicines as per the pharmacy plan.
- Ensure all activities follow ICH-GCP guidelines, regulatory requirements, and SOPs.
- Maintain and calibrate clinical supply unit instruments as per SOPs
Qualification
- Master’s Degree in Pharmacy / Master’s in Pharmacology
Technical/Functional Skills
- Sound knowledge of ICH-GCP and Indian Regulatory guidelines
- Well-versed with Microsoft Office documents (MS Word, Excel, PowerPoint)
- Knowledge about developing SOPs
- Well versed with facing internal and external audits
Behavioral Skills
- Proficient in English (reading and writing), Integrity
