Global QA Supplier Quality Lead (Pharma) in Leicester

Global QA Supplier Quality Lead (Pharma) in Leicester

Leicester Full-Time 63000 - 77000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Shape supplier qualifications and manage audits for top-notch quality in pharma.
  • Company: Join Myonex, a global leader in pharmaceutical quality assurance.
  • Benefits: Competitive salary, collaborative team, and opportunities for professional growth.
  • Other info: Work with international teams in a dynamic and supportive environment.
  • Why this job: Make a real impact on global quality standards in the pharmaceutical industry.
  • Qualifications: 5+ years in GMDP pharma, fluent English, and strong stakeholder management skills.

The predicted salary is between 63000 - 77000 Β£ per year.

Myonex is seeking a Global QA Vendor Specialist to join our Leicester (UK) team and collaborate with colleagues in Berlin, Reims and Le Haillan.

You will shape supplier qualification activities, coordinate audits, and manage technical agreements to ensure the highest standards of quality and regulatory compliance across our global network.

The role requires 5+ years in a GMDP pharmaceutical environment, fluent English and strong stakeholder management.

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Global QA Supplier Quality Lead (Pharma) in Leicester employer: Myonex

Myonex is an exceptional employer that fosters a collaborative and innovative work culture in Leicester, where you will have the opportunity to work alongside talented professionals from various locations including Berlin, Reims, and Le Haillan. With a strong emphasis on employee growth, we offer comprehensive training and development programs, ensuring that you can advance your career while contributing to our mission of maintaining the highest standards of quality and regulatory compliance in the pharmaceutical industry.

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Contact Details:

Myonex Recruitment Team

We think you need these skills to ace Global QA Supplier Quality Lead (Pharma) in Leicester

Supplier Qualification
Audit Coordination
Technical Agreement Management
Quality Standards Compliance
Regulatory Compliance
Stakeholder Management
GMDP Pharmaceutical Experience