Senior Specialist, Supplier Quality Management (Switzerland)

CSL; Sankt Gallen; Vor Ort; CHF 100’000 - 130’000; Vollzeit

Zusammenfassung

A leading pharmaceutical company in St. Gallen is seeking a Senior Specialist, Supplier Quality Management. This role involves developing supplier qualification programs and monitoring supplier performance. Candidates should have 5-8 years in a GxP environment and a strong understanding of quality systems and regulations. Proficiency in English is required; German or French is a plus. Join a dynamic team dedicated to improving healthcare worldwide.

Qualifikationen

• Minimum of 5 to 8 years of experience in a GxP environment within the pharmaceutical industry.
• Thorough understanding of applicable regulations.
• Fluent in English (written and spoken); knowledge of German or French is an asset.

Aufgaben

• Serve as the local point of contact for the External Supplier Quality (ESQ) organization.
• Facilitate supplier enrollment and qualification processes.
• Monitor supplier performance and manage quality-related issues.

Kenntnisse

Leadership

Quality Systems

Supplier Management

Communication Skills

Regulatory Knowledge

Problem Solving

German or French

Ausbildung

Degree in a relevant business or science field

Jobbeschreibung

To strengthen our External Supply Quality team, we are looking for a dedicated and proactive individual to take on the role of Senior Specialist, Supplier Quality Management.

In this role, you will be responsible for developing and maintaining a comprehensive external supplier qualification program to assess the capabilities and quality systems of potential suppliers and service providers.

Your Responsibilities

• Serve as the local point of contact for the External Supplier Quality (ESQ) organization.
• Facilitate supplier enrollment and qualification processes.
• Revise, edit, and route Quality Agreements for signature as assigned.
• Monitor supplier performance.
• Manage quality-related supplier issues, including complaints and deviations, tracking investigations, and ensuring proper CAPA plans are implemented.
• Develop and oversee supplier improvement plans where applicable.

Your Qualifications

• Degree in a relevant business or science field, or equivalent education and experience.
• Minimum of 5 to 8 years of experience in a GxP environment within the pharmaceutical industry.
• Thorough understanding of applicable regulations.
• Demonstrated leadership and knowledge of Quality Systems and Supplier Management.
• Expertise in global cGMP regulations and ISO standards.
• Ability to work effectively in a global, matrix organization.
• Excellent communication skills with various stakeholders.
• Fluent in English (written and spoken); knowledge of German or French is an asset.

We are seeking a solution-oriented, proactive individual who enjoys continuous improvement and is eager to contribute meaningfully to our Supply Quality organization.

If this sounds like you, we look forward to receiving your online application. Please upload your CV, employment references, and copies of diplomas (in original language and/or relevant transcripts) as a single document.

About CSL Vifor

CSL Vifor is a global partner of choice for pharmaceuticals and innovative therapies in iron deficiency and nephrology. We specialize in strategic global partnerships, in-licensing, development, manufacturing, and marketing of pharmaceutical products for precision healthcare, aiming to help patients worldwide lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, headquartered in Melbourne, Australia, employs 32,000 people and delivers therapies to more than 100 countries.

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