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Thermo Fisher Scientific

Site Quality Head Swindon

Posted 6 Days Ago
Be an Early Applicant
In-Office
9 Locations
Expert/Leader
In-Office
9 Locations
Expert/Leader
Lead the CDMO Quality and Regulatory team, ensuring quality standards and compliance in aseptic operations while fostering a culture of excellence and innovation.
The summary above was generated by AI

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office

Job Description

Business Job Title: Site Quality Director Swindon

Group/Division: Pharma Services Group / Drug Product Division - Swindon Site

This role is based in Swindon, UK, we are open to candidates from the EMEA region who are willing to relocate.

Position Summary:

As the Site Quality Director, you lead the CDMO Quality and Regulatory team, ensuring outstanding quality standards and compliance across our aseptic operations. This outstanding opportunity allows you to champion a culture of excellence and innovation, strictly adhering to regulatory guidelines and GXP compliance requirements.

Key Responsibilities:

  • Lead and manage the Site Quality and Regulatory team, establishing and maintaining flawless quality and compliance levels.
  • Maintain and continuously improve the site quality systems and processes.
  • Identify, develop, and retain top-tier talent, ensuring a strong succession plan.
  • Foster a collaborative and inclusive culture that prioritizes quality and compliance.
  • Develop and maintain proactive relationships with regulatory authorities and clients.
  • Maintain an independent authority for any decision impacting Quality
  • Act as a role model, embodying Thermo Fisher values and driving groundbreaking change.
  • Act as a member of the DPD EU & APAC QLT and partner across the organization with sister sites and global functions

How You Can Make an Impact:

  • Proven track record of 15+ years in the pharmaceutical industry including sterile drug products and aseptic operations. Preferred experience with CDMO, biotech, and vaccine production.
  • 5+ years actings a Qualified Person is preferred.
  • Extensive knowledge of quality structures and regulatory bodies.
  • 10+ years of leadership experience, successfully developing high-performing teams.
  • Outstanding communication and presentation skills, capable of engaging senior executives.
  • Strong ability to attract, hire, and develop diverse talent.
  • Proactive and strategic approach, skilled at moving between details and the “big picture.”
  • Learning agility with attention to detail
  • Demonstrated ability to make calculated, high-impact quality decisions and get results.

Join us to craft the future of our Quality function and make a tangible impact on global health initiatives!

 

 

Top Skills

Good Manufacturing Practices (Gmp)
Gxp Compliance
Quality Management Systems
Regulatory Guidelines

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