Teva Pharmaceuticals Hiring For Clinical Research Scientist – Pharma Apply Online
Clinical Research Scientist I
Date: Jul 10, 2024
Location: Navi Mumbai, India, 400706
Company: Teva Pharmaceuticals
Job Id: 56871
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
How you’ll spend your day
- Ensure adherence to all federal, state, and local regulations regarding the handling and management of controlled substances.
- Develop, implement, and maintain SOPs related to controlled substance management.
- Oversee the inventory control processes for controlled substances, including ordering, storage, consumption, and disposal.
- Maintain and update necessary records and documentation of controlled substances to meet regulatory standards.
- Prepare and submit control substance accountability to regulatory team on a quarterly basis.
- Coordinate with the regulatory team for obtaining the import certificate (IC) and allocation of quota for controlled substances.
- Ensure all processes and procedures are compliant with regulatory requirements and best practices.
- Conduct regular audits and reconciliations of controlled substance inventory. Implement and manage tracking systems to ensure accurate inventory records.
- Collaborate with cross-functional teams to address and resolve compliance issues.
- Manage SAP system and create purchase requests (PR) as per business requirements.
- Arrange quotations for all the working standards and resources required in Bioanalytical Lab.
- Ensure adequate resources & logistics are requested to project and availability followed up to closure.
- Coordinate with the procurement team to ensure the purchase order is adequate to send to vendors.
- Ensure accurate data entry and maintenance of material inventory information within the SAP system.
- Coordinate with the procurement team for new vendor registration.
- Coordinate with HOD in preparation of Capex and Opex AOP.
- Coordinate with QA team for new vendor audit.
- Follow up with vendors for timely delivery of material.
- Timely reservation of material against the project.
Your experience and qualifications
- B.Sc, M.Sc, or M.Pharm
- 6 to 10 years of experience in SAP-related activities in Control Substance Management.
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