Senior Director of MSAT Job at Thermo Fisher Scientific Careers, Saint Louis, MO

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  • Thermo Fisher Scientific Careers
  • Saint Louis, MO

Job Description

*Work Schedule* Standard (Mon-Fri)*Environmental Conditions* Office*Job Description* Thermo Fisher Scientific Inc. is a Fortune 100 company and a world leader in serving science, with annual revenue exceeding $40 billion. Our mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, improving patient diagnostics and therapies, or growing efficiency in their laboratories, we are here to support them. The Senior Director MSAT position involves leading a distributed team across multiple sites, encouraging effective collaboration, communication, and standard methodology sharing.

  • How you will make an impact:*
  • Lead and manage site level MSAT teams
  • Ensure the deployment of Technology Transfer and Process Validation standards.
  • Drive continuous improvement and improve manufacturing efficiency and product quality.
  • Collaborate with R&D and Quality teams for new product introductions and lifecycle management.
  • Ensure robust process control and monitoring systems including CPV deployment.
  • Lead troubleshooting efforts and implement corrective actions.
  • Build a team capable of effective Root Cause Analysis and CAPA generation.
  • Manage relationships with collaborators, including customers and regulatory agencies.
  • Foster a customer-centric attitude and ensure successful technology transfers and process validations.
  • Effectively manage the team, budget, and blocking issues.
  • Build and promote a culture of excellence within the MSAT organization.
  • Provide strong leadership and mentorship to the MSAT team, driving performance and professional development.
  • How will you get here:*
  • Education*
Advanced degree in Chemical Engineering, Biotechnology, or a related field preferred.
  • What will you do:*
  • Minimum of 15 years of experience in manufacturing science and technology within the pharmaceutical or biotechnology industry.
  • Proven track record of leading and managing global teams.
  • Extensive experience in process development, validation, and technology transfer.
  • Strong knowledge of regulatory requirements and standard methodologies in the industry.
  • Excellent problem-solving, leadership, and communication skills.
  • Customer-centric attitude with experience in a CDMO environment.
  • Experience in a CDMO environment.

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