Senior Manager in Supplier Qualification & Audits (m/f/d)

TN Germany; Dortmund; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Senior Manager in Supplier Qualification & Audits to oversee audit preparations and ensure compliance in a GMP regulated environment. This role involves managing complex projects, coordinating with partner sites, and ensuring adherence to health authority regulations. With a focus on proactive and solution-oriented work, the ideal candidate will possess strong communication skills in both German and English. Join a dynamic team where your expertise will contribute to long-term job security and professional growth within the medical technology sector.

Leistungen

Attractive salary

Up to 30 days vacation per year

Long-term job security

Good chances of being taken on by business partners

Qualifikationen

• Several years of experience in a GMP regulated environment, preferably in quality control.
• Qualification as an auditor in a GxP regulated environment.

Aufgaben

• Preparation, sorting, and follow-up of internal and supplier audits.
• Project management for FDA readiness and audit standardization.

Kenntnisse

Audit Management

Supplier Qualification

Project Management

Communication Skills

Problem-Solving

Ausbildung

Master's degree in a scientific or technical discipline

Diploma or Doctorate in a scientific or technical discipline

Tools

MS Office

SAP

Jobbeschreibung

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Senior Manager in Supplier Qualification & Audits (m/f/d), Dortmund

Client: Boehringer Ingelheim microParts GmbH

Location: Dortmund, Germany

Job Category: Other

EU work permit required: Yes

Job Reference: c746166e32bc

Job Views: 1

Posted: 25.04.2025

Expiry Date: 09.06.2025

Job Description:

Time for a change of scenery with a new job? For our client, the medical technology company in Dortmund, we are currently looking for a Senior Manager Supplier Qualification & Supplier Audits (m/f/d). Send us your application documents online. We will take care of everything else - free of charge for you, of course. We welcome applications from people with disabilities.

Here's what we offer:

• Attractive salary and long-term job security through group affiliation
• Up to 30 days vacation per year
• Good chances of being taken on by our business partners
• Preparation, sorting, follow-up of internal audits, authority audits, TÜV audits, supplier audits, corporate audits.
• Coordination of audit preparations in the corporate association with partner sites.
• Project management FDA readiness; standardization of audit preparation/audit execution with partner sites in the corporate association.

Your profile:

• Master's degree and/or diploma and/or doctorate in a scientific or technical discipline
• Several years of professional experience in a GMP regulated environment, preferably in quality control or quality assurance
• Qualification as an auditor in a GxP regulated environment
• Several years of practical experience in the areas of audit management and supplier qualification
• Solution-oriented, proactive, independent and reliable way of working
• Assertiveness and creative drive
• Sound knowledge of the requirements/regulations of various health authorities
• Experience in managing complex projects
• Strong communication skills combined with good language skills in German and English
• Good knowledge of MS Office applications, SAP etc.