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BioNTech SE

Associate Director, Audit & Inspection Management

BioNTech SE

Associate Director, Audit & Inspection Management overseeing clinical vendor audits in China and neighboring countries. Part of Global Development Quality Assurance team.

Posted 5/27/2026full-timeShanghai • 🇨🇳 ChinaSeniorWebsite

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Hard Skills
clinical auditingquality audit methodologyCAPA (Corrective and Preventative Action) PlanGCP regulationsclinical trialsclinical developmentoncology experience
Soft Skills
leadershipproject managementcommunicationinterpersonal skills
Tools & Technologies
Microsoft OfficeVeevaSharePoint
Industry Keywords
APAC regionrisk-based auditinvestigator sitesvendor audits

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Responsible for audits within the APAC region.
  • Ensuring audit objectives and scopes are risk based in alignment with the audit strategy.
  • Coordinate and oversee audits performed by contracted auditors.
  • This involves scheduling audits, selecting resources, reviewing reports, etc.
  • Execution of the audit (remote or on site) as the lead auditor when the audit is not contracted.
  • Ensure audit documentation and audit quality management system is completed according to procedures and established timelines.
  • Act as a liaison to internal BioNTech stakeholders through all phases of the audit.
  • Ensure that newly identified risks are considered for the audit strategy.
  • Support development of a robust CAPA (Corrective and Preventative Action) Plan and approve the CAPA plan.
  • Track CAPA and effectiveness checks to completion.

Requirements

What you’ll need
  • 10 years experience in clinical trials, with at least: 6 years of experience in clinical auditing in Asia Pacific region.
  • 3 years of experience managing people and/or projects.
  • Deep knowledge of quality audit methodology, with ability to execute and/or oversee clinical audits of investigator sites and/or vendor.
  • Applied knowledge of global and local GCP regulations
  • Very good understanding of Clinical Development activities, with oncology experience preferred
  • Excellent English skills, both written and verbal, in addition to Mandarin
  • Willingness to travel (at least 10% of the time)
  • Computer literate and proficient in Microsoft Office software, Veeva, and SharePoint.

Benefits

Comp & perks
  • BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base.
  • We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.
  • The availability, eligibility and design of the listed benefits may vary depending on the location.
  • The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.