Site Quality Head Swindon

Thermo Fisher Scientific; Roma; In loco; EUR 103.000 - 139.000; Tempo pieno

Descrizione del lavoro

A global life sciences company is seeking a Site Quality Director to lead quality and regulatory teams in Swindon. This role requires over 15 years in pharmaceutical and sterile product operations, with strong leadership and communication skills. Candidates from the EMEA region willing to relocate are encouraged to apply. Join us to make a significant impact on global health initiatives.

Competenze

• Proven track record of 15+ years in the pharmaceutical industry.
• 5+ years acting as a Qualified Person is preferred.
• Outstanding communication and presentation skills.

Mansioni

• Lead and manage the Site Quality and Regulatory team.
• Maintain and improve site quality systems and processes.
• Develop and maintain relationships with regulatory authorities.

Conoscenze

Leadership

Quality assurance

Regulatory compliance

Communication skills

Team development

Descrizione del lavoro

Overview

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.; 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!

Job Summary

Job number: R-01328319
Date posted: 2025-09-11
Profession: Quality & Regulatory
Employment type: Full time