Site Quality Head Swindon

Experteer Italy; Swindon; On-site; GBP 90,000 - 120,000; Full time

Job summary

A leading pharmaceutical company is seeking a Site Quality Director in Swindon to lead the CDMO Quality and Regulatory team. The ideal candidate has over 15 years in the pharmaceutical industry, extensive experience in regulatory compliance, and a strong focus on developing high-performing teams. This role offers a chance to impact global health initiatives while fostering a culture of excellence and innovation.

Qualifications

• 15+ years in the pharmaceutical industry, especially sterile drug products.
• Experience as a Qualified Person preferred.
• 10+ years of leadership experience.

Responsibilities

• Lead and manage the Site Quality and Regulatory team.
• Improve site quality systems and processes.
• Maintain proactive relationships with authorities.

Skills

Leadership

Regulatory compliance

Communication

Team development

Quality systems

Job description

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 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 acting as 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