Senior Quality Leader

2 weeks ago

Swindon, Swindon, United Kingdom Thermo Fisher Scientific Full time

Thermo Fisher Scientific is seeking a highly motivated and experienced Sr. Director of Quality for our Europe & Asia Pacific (EU&APAC) Business Unit. This critical leadership role will oversee the quality organization across five facilities, ensuring operational excellence and compliance with regulatory standards.

As the Sr. Director of Quality, you will lead a team of over 1100 professionals dedicated to maintaining the highest quality standards in our manufacturing processes. You will be responsible for developing and implementing quality strategies, driving continuous improvement initiatives, and fostering a culture of compliance throughout the region.

Key Responsibilities:
  • Provide strategic direction and leadership to the EU&APAC Quality organization, ensuring alignment with global quality standards and business objectives.
  • Develop and implement comprehensive quality management systems (QMS) that meet cGMP requirements and other relevant regulatory guidelines.
  • Lead a team of quality professionals across various disciplines, including Quality Control, Quality Operations, Quality Systems, and Compliance & Regulatory Affairs.
  • Collaborate closely with business leaders to drive operational excellence, improve product quality, and enhance customer satisfaction.
  • Establish clear performance metrics and accountability measures for the quality team, ensuring continuous improvement and adherence to key quality targets.
  • Build and maintain strong relationships with key stakeholders, including customers, vendors, regulatory agencies, and internal business partners.
  • Champion a culture of safety, compliance, and continuous learning within the EU&APAC Quality organization.
Qualifications:
  • Bachelor's degree in a scientific or technical field is required; advanced degrees (e.g., MBA, Master's) are highly desirable.
  • 15+ years of progressive experience in the pharmaceutical industry, with a strong focus on sterile injectable operations.
  • Proven leadership experience managing multiple quality units and teams within a complex matrix organization.
  • Extensive knowledge of cGMP regulations and other relevant quality standards.
  • Exceptional communication, interpersonal, and problem-solving skills.
  • Ability to travel regionally and globally (approximately 50%).

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