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!
Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed OfficeJob DescriptionBusiness Job Title: Site Quality Director Swind...
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!
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