Manager Global Supplier Qualification (Mainz, RP, DE, 55131)

Biopharma Careers; Mainz; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

BioNTech in Mainz, Germany is seeking a Supplier Qualification Manager to support the Supplier Qualification Team in a GMP environment. You will manage supplier qualifications, oversee questionnaires, and document statuses in Veeva eQMS, ensuring system efficiency and compliance.

You will collaborate with the BPO to identify system solutions, manage training, and maintain KPIs and dashboards. Fluent English and German are required, with 3+ years in GMP/GDP environments.

Qualifikationen

• Degree in life sciences (chemistry, biology, pharmacy or equivalent).
• 3+ years of professional experience in a GMP/GDP environment.
• Strong expertise in Veeva eQMS and supplier qualification processes.
• Excellent communication skills and experience working with interdisciplinary teams.

Aufgaben

• Provide expertise in Veeva eQMS, supporting the team with system-related tasks and guiding team members to ensure correct and consistent use of the eQMS.
• Collaborate with the Business Process Owner (BPO) to identify system solutions for continuous improvement and process efficiency.
• Manage the team’s training overview, implement required trainings in the system, and maintain KPIs and dashboards within Veeva eQMS.
• Perform supplier qualifications, evaluate questionnaires, and communicate with suppliers.
• Document and maintain supplier qualification statuses in Veeva eQMS.
• Assess supplier notifications, oversee CAPA management, and manage risk assessments.
• Act as QA representative in various boards, e.g., Change Review Board, and support/conduct the annual audit plan and supplier evaluations.

Kenntnisse

Fluent English and German

Interdisciplinary collaboration

Ausbildung

Degree in life sciences

Tools

Veeva eQMS

Jobbeschreibung

Mainz, Germany | full time | Job ID: 11520

About the Role:

We are looking for a Supplier Qualification Manager to support our Supplier Qualification Team in a GMP environment. The role includes managing supplier qualifications through questionnaires, follow-up actions, and documentation, as well as providing expertise in Veeva eQMS-related topics to ensure system efficiency and compliance.

Your Contribution :

• Provide expertise in Veeva eQMS, supporting the team with system-related tasks and guiding team members to ensure correct and consistent use of the eQMS.
• Collaborate with the Business Process Owner (BPO) to identify system solutions for continuous improvement and process efficiency.
• Manage the team’s training overview, implement required trainings in the system, and maintain KPIs and dashboards within Veeva eQMS.
• Perform supplier qualifications, evaluate questionnaires, and communicate with suppliers.
• Document and maintain supplier qualification statuses in Veeva eQMS.
• Assess supplier notifications, oversee CAPA management, and manage risk assessments.
• Act as QA representative in various boards, e.g., Change Review Board, and support/conduct the annual audit plan and supplier evaluations.

A Good Match:

• A degree in life sciences, such as chemistry, biology, pharmacy, or an equivalent field.
• At least 3+ years of professional experience in a similar role, ideally within a GMP/GDP environment.
• Strong expertise in Veeva eQMS and supplier qualification processes.
• Excellent communication skills and experience working with interdisciplinary teams.
• Fluent in English and German, both written and spoken.

Your Benefits:

It's our priority to support you:

• Your flexibility: flexible hours | vacation account
• Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
• Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential
• Your health and lifestyle: Company bike
• Your mobility: Job ticket | Deutschlandticket
• Your life phases: Employer-funded pension | Childcare

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.