Manager Global Supplier Qualification

RxREVU, Inc.; Mainz; Vor Ort; EUR 70.000 - 100.000; Vollzeit

Benefits dieser Stelle

Company bike

Job ticket

Deutschlandticket

Employer-funded pension

Childcare

Zusammenfassung

BioNTech in Mainz seeks a Supplier Qualification Manager to lead supplier qualifications in a GMP environment. You will manage Veeva eQMS tasks, training, and KPI dashboards while ensuring compliance and collaboration with the QA and BPO teams.

You will evaluate supplier questionnaires, support CAPA processes, and participate in audits alongside a cross‑functional, multilingual team.

Qualifikationen

• Degree in life sciences (chemistry, biology, pharmacy or equivalent).
• At least 3 years in supplier qualification in GMP/GDP environment.
• Fluent English and German, written and spoken.

Aufgaben

• Provide expertise in Veeva eQMS and guide team on system use.
• Collaborate with BPO to identify system improvements.
• Manage training overview and KPIs in Veeva eQMS.
• Conduct supplier qualifications and communicate with suppliers.
• Document supplier qualification statuses in the eQMS.
• Oversee CAPA management and risk assessments.
• Act as QA representative in Change Review Board and audits.

Kenntnisse

Veeva eQMS

Supplier qualification

GMP/GDP experience

Cross-functional collab

Bilingual English/German

Ausbildung

Bachelor's degree in life sciences

Jobbeschreibung

Mainz, Germany | full time | Job ID: 11520

This position is limited!

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

Job ID 11520 (please always specify if you have any questions)

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.