Thermo Fisher Scientific-posted 3 months ago
Full-time • Senior
Saint Louis, MO
5,001-10,000 employees
Computer and Electronic Product Manufacturing

Are you a transformative leader with experience in automation and a passion for manufacturing excellence? We are on the hunt for an experienced professional to spearhead our Manufacturing Support Automation Team within the Facilities & Engineering department. This is your chance to drive transformative projects and lead a team of dedicated individuals towards groundbreaking achievements.

  • Provide automation guidance and technical support for manufacturing equipment and is responsible for automation and automation infrastructure.
  • Effectively lead the engineering automation function at the St. Louis Biologic manufacturing facility to ensure product quality and regulatory compliance.
  • Provide technical mentorship for equipment procurement including process qualifications to cGMP requirements.
  • Communicate well with relevant departments, senior management, and clients.
  • Understand requirements of Equipment Qualification management and craft and review associated technical documents.
  • Quickly assess and evaluate multiple priorities and team resources.
  • Apply outstanding problem-solving skills in situations when manufacturing equipment breaks down.
  • Work with capital engineering team during projects to procure and install equipment and processes.
  • Actively involved in the site's Practical Process Improvement (PPI) lean activities.
  • Manage engineering risks effectively and minimize production downtime.
  • Generate, communicate, and keep up-to-date technical documents, procedures, and standards guidelines.
  • Assist with, and lead, continuous improvement initiatives within the function.
  • Serve as a role model leader, coach, and mentor.
  • Drive safety within the team.
  • Bachelor's degree in engineering field, or equivalent experience.
  • 8+ years within a GMP Environment.
  • Proficient with computers (MS Office).
  • Working knowledge of controlled documentation and data systems including SAP.
  • In-depth knowledge of cGMP regulations.
  • 8+ years of experience in pharmaceutical equipment maintenance and GMP manufacturing, preferred.
  • 2+ years of supervisory experience.
  • Experienced in Automation, GMP manufacturing, Equipment maintenance, Engineering.
  • Expert in managing changes for assessments related to equipment, systems, automation, and processes.
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