Clinical Research Scientist I

Year    Navi Mumbai, Maharashtra, India

Job Description


Who we areTogether, 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 control substances to meet regulatory standards.
  • Prepare and submit control substance accountability to regulatory team on quarterly basis.
  • Co-ordinate with regulatory team for obtaining the import certificate (IC) and allocation of quota for control substance.
  • 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 request (PR) as per business requirements.
  • Arranged quotation 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 procurement team to ensure purchase order is adequate to send to vendors.
  • Ensure accurate data entry and maintenance of material inventory information within the SAP system.
  • Co-ordinate with procurement team for new vendor registration.
  • Co-ordinate with HOD in preparation of Capex and Opex AOP.
  • Coordinate with QA team for new vendor audit.
  • Follow up with vendor for timely delivery of material.
  • Timely reservation of material against project.
Your experience and qualifications
  • B.Sc, M.Sc OR M.Pharm
  • 6 to 10 Years of expereince into SAP related activities in Control Substance Mgmnt.
Teva\'s Equal Employment Opportunity CommitmentTeva Pharmaceuticals is committed to equal opportunity in employment. It is Teva\'s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Teva Pharmaceuticals

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Job Detail

  • Job Id
    JD3366362
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Navi Mumbai, Maharashtra, India
  • Education
    Not mentioned
  • Experience
    Year