hirly

Da Vinci Engineering GmbH

Senior Auditor / R&D Quality Manager (m/f/d)

Frankfurt am Main, Hessen, Germany

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Da Vinci Engineering GmbH first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Role family
Engineering
Seniority
Lead / management
Country
DE
Work mode
On-site / unstated
First seen by hirly
1 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Nothing provides more motivation than success. Da Vinci Engineering is highly committed to ensuring the own employees' success. Become a part of us!

Senior Auditor / R&D Quality Manager (m/f/d)

  • Stellen-ID: 22169
  • Standort: Frankfurt am Main

We are searching intelligent and innovative employees. If you are interested in working for a dynamic company with flat hierarchy, we look forward to receiving your application.

  • Your tasks:
  • Plan and conduct clinical project audits, process audits, and supplier/vendor audits in accordance with GxP and regulatory requirements.
  • Develop and maintain risk-based audit plans and study assessment strategies
  • Evaluate audit findings, ensure proper documentation, and support CAPA development and follow-up
  • Lead and manage quality escalations arising from clinical study activities
  • Contribute to the development and maintenance of the Quality Management System, including SOPs, CAPA, deviations, and document control
  • Provide quality consultation to Clinical Operations teams on study processes and quality-related topics
  • Support qualification and evaluation of clinical service providers such as CROs, laboratories, couriers, and archiving services
  • Deliver training on GCP, Good Clinical Laboratory Practice, and other quality-related topics
  • Your profile:
  • University degree in a scientific or technical field such as Life Sciences, Pharmacy, or Medical Technology
  • Several years of experience in Quality Management, Clinical Research, or auditing within a GxP/GCP-regulated environment
  • Strong knowledge of regulatory requirements for medical devices and pharmaceuticals
  • Proven experience in planning, conducting, and following up on internal and external audits
  • Solid understanding of CAPA processes, deviation management, and document control systems
  • Strong analytical skills and a structured, risk-based approach to quality oversight
  • Excellent communication and advisory skills when working with cross-functional teams and external partners
  • Very good command of English (written and spoken)
  • You can expect ...
  • Experience in exciting and international projects
  • Continuous salary development
  • Da Vinci Corporate Benefits
  • On-the-job training and language courses
  • Appreciation, motivation and commitment
  • Kontaktdaten für Stellenanzeige
  • Frau Andrea Cindric
  • Da Vinci Engineering GmbH
  • Hauptstätter Straße 149
  • 70178 Stuttgart
  • +49 711 72240 107
  • [email protected]
Original posting on Da Vinci Engineering GmbH's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job