Staff Technical Operations Scientist -

4 - 9 years

10 - 14 Lacs

Posted:1 day ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

  • Support the technical transfer activity for a multi-phase and multi-year project to transfer programs into a third-party contract manufacturing facility in India.
  • Provide Technical direction and support for third party manufacturing activities including coordination of activities with cross-functional roles from Quality, Regulatory, Development, Project Management, Supply Chain, Procurement and Validation.
  • Be involved in the full project life cycle - successful project completion will include full implementation from initiation to deployment for multiple products, including equipment setup validation, manufacturing process transfer and validation, Test method transfer and validation, and post launch support.
  • Support activities to ensure continuity of supply of product to the market and ensure projects are effectively set up and meet their timelines.
  • Use of DBS tools and techniques to streamline processes eg SW, TPI, VPM, Daily Management, etc.
  • Responsible for driving and implementing the Supply Chain Activities in compliance with the local and global design change process and relevant procedures.
  • Coordinate with relevant groups across the Company to ensure that procedures / specifications, raw materials, resources and facilities are in place support the contractor manufacturing activities.
  • Ensuring that all these activities are performed in a manner that ensures compliance with the relevant policy, procedures, regulatory authorities and GMP.
The essential requirements for the role include:
  • Bachelor s degree with 9+ years experience OR Master s degree with 7+ years experience.
  • Proven problem investigation and problem solving skills are essential. Demonstrated ability to effectively prioritize and lead a team to deliver on commitments and meet the needs of the business.
  • Prior experience managing strategic Supply chain projects.
  • A good working understanding of cGMP and ISO/FDA requirements.

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