Job Title: Pharmacist – Clinical Supply Management
Location: Bangalore, Karnataka, India
Department: Biometrics / Clinical Operations
Employment Type: Full-Time, Permanent
Syngene International Ltd., established in 1993, is a global innovation-driven contract research, development, and manufacturing organization (CRDMO). We provide integrated scientific services spanning pharmaceuticals, biotechnology, nutrition, animal health, consumer goods, and specialty chemicals. Syngene partners with world-leading companies including Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife.
At Syngene, a culture of innovation and operational excellence drives our 4,240-strong team of scientists to accelerate drug discovery, clinical development, and reduce time-to-market while maintaining the highest quality standards.
The Pharmacist plays a critical role in Investigational Product (IP) management for all clinical trials, ensuring compliance with ICH-GCP, local regulatory guidelines, and company SOPs. This position involves overseeing the storage, labeling, distribution, reconciliation, and destruction of Investigational Medicinal Products (IMP) and Non-Clinical Supplies (NCS) within the Syngene Clinical Supply Unit (SCSU).
Develop protocol-specific pharmacy plans and secondary labeling strategies for IMP/NCS.
Receive, verify, and store IMP/NCS in compliance with regulatory and protocol requirements.
Perform labeling/relabeling, expiry extensions, and secondary labeling for IMP/NCS according to approved plans.
Plan, prepare, and coordinate supply and resupply of IMP/NCS to clinical investigational sites while maintaining required storage conditions.
Maintain accurate clinical supply documentation, including shipment records, inventory tracking, and reconciliation.
Arrange return, recall, and destruction of IMP/NCS following approved protocols and SOPs.
Ensure periodic maintenance and calibration of SCSU instruments.
Support internal and external audits, ensuring readiness and compliance with regulatory standards.
Perform other responsibilities as assigned by management to support clinical supply operations.
Master’s Degree in Life Sciences, Pharmacology, or related field.
Minimum 3–5 years of experience in clinical supply management or pharmacy operations within clinical trials.
Strong knowledge of ICH-GCP, Indian regulatory requirements, and clinical supply management principles.
Experience with inventory management, labeling, and investigational product handling in clinical trial settings.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Knowledge of SOP development and documentation standards.
Familiarity with handling internal and external audits.
Understanding of clinical trial documentation, safety, and compliance standards.
Strong attention to detail, integrity, and accountability.
Excellent English communication skills (verbal and written).
Ability to work collaboratively in a cross-functional, multi-disciplinary team environment.
Work with a global CRDMO renowned for scientific innovation and operational excellence.
Contribute to clinical trial success and investigational product management across multiple therapeutic areas.
Engage with cross-functional teams in a fast-paced, quality-driven environment.
Opportunities for career growth, professional development, and exposure to international regulatory standards.
Syngene is committed to providing equal employment opportunities (EEO) to all candidates, ensuring no discrimination based on age, race, gender, disability, religion, sexual orientation, veteran status, or any legally protected characteristic. Reasonable accommodations are provided to qualified individuals with disabilities.
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