Director of Quality

Elevate Your Career in a Culture of Excellence in Quality and Continuous Improvement at LEO Pharma!

Are you eager to amplify your impact on global healthcare? Join us at LEO Pharma, where your contributions resonate at the highest echelons of leadership. As the Quality Director for our Dublin site, you are positioned at the heart of our operations, blending site-specific duties with a role on the global quality leadership team. Your voice not only shapes our present but also delineates our future in the dynamic field of medical dermatology.

Embark on a Transformative Journey with LEO Pharma
At LEO Pharma, our mission transcends the conventional. We're on an ambitious path to reinforce our stature as an unrivalled pioneer in medical dermatology worldwide. As the Quality Director for our Dublin facility and member of the Site Leadership Team, you are pivotal in championing revolutionary changes and driving efficiencies. Armed with a culture of continuous improvement, and supported by our cornerstones of simplification, collaboration, and accountability, your leadership is instrumental in navigating our collective aspirations towards Excellence in Quality.

Your Role: A Catalyst for Excellence in Quality

Your mandate will be to oversee all aspects of GMP Quality at a manufacturing site, steered by a relentless pursuit of excellence and continuous improvement in quality operations. You will:

• Lead the charge in fostering & improving an organizational ethos where quality permeates every facet, by leading our Quality Support, Qualification & Validation, Operational Quality, and Quality Control departments.
• Ensure GMP compliance across all production processes. 
• Establish and maintain quality systems aligned with LEO Pharma Global Standards and international GMP regulations.
• Quality oversight of manufacturing operations for GMP compliance, acting as the main contact for quality and compliance issues. 
• Develop, manage, maintain & improve procedures to ensure regulatory compliance.

This Role Offers:

• A strategic position located in Dublin  with hybrid working options and some international travel. 
• A rare opportunity to sculpt the landscape of quality in a global organization,
• An empowering environment where your initiatives and ideas can manifest into tangible improvements and stellar outcomes.
• A dual reporting line: solid to VP, Global Quality and dotted to Site VP.

Your Qualifications

To succeed in this role, we imagine that you have the following qualifications and experience: 

• Education in Life Sciences (Chemist, Chemical Engineering, or Pharm. D) 
• You will have substantial leadership experience in a Pharmaceutical Quality Assurance/Quality Control environment.
• Knowledge and experience of applicable regulatory standards and requirements for Drug Products manufacturing (EU and US FDA)
• Strong analytical skills and experience with analytical techniques such as UPLC/HPLC, GC, spectroscopy, and wet chemistry.
• Proficiency in computer applications such as SAP, Minitab, Microsoft Word, Excel, Access, and Power Point.

You will have a strong continuous improvement mindset, with curiosity and commitment to challenge the norm. 

Your New Team

You will be part of site and global quality leadership team and lead a team of dedicated professionals who are passionate about ensuring the highest quality standards in the pharmaceutical industry. Together, you will work towards driving continuous improvement and making a positive impact on patients' lives.

Your Application

You do not need to upload a cover letter, but feel free to add a few sentences in your resume or CV on why this position has your interest.