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Senior CSV Consultant - Remote

Posted 11 weeks ago
All others
Full Time
Germany

Overview

Join Valicare GmbH as a Senior CSV Consultant, where you will lead projects and serve as the primary contact for clients in the field of Computer System Validation (CSV).

In Short

  • Lead and manage projects in Computer System Validation (CSV).
  • Act as the primary contact for clients regarding CSV inquiries.
  • Design tailored solutions for client requirements in CSV.
  • Contribute to the continuous development of CSV service offerings.
  • Build and maintain long-term client relationships.
  • Drive project acquisition in the CSV sector.
  • Collaborate with your team in Frankfurt and travel nationwide for client engagements.

Requirements

  • Degree in engineering or natural sciences, preferably with a doctorate.
  • Strong knowledge and practical experience in CSV-GMP regulations.
  • Relevant experience in computer system validation and GMP-regulated industries.
  • Fluency in German (C1 or better); additional languages are a plus.
  • Excellent team and communication skills with a professional demeanor.
  • Structured, proactive, and reliable work style.

Benefits

  • Flexibility of a small company with the stability of a large parent company.
  • Competitive salary with an exceptional bonus model.
  • Engaging tasks in a technologically exciting environment.
  • Opportunities for personal development and leadership roles.
  • A variety of attractive working conditions.

Translated from German

SYNTEGON logo

SYNTEGON

SYNTEGON, through its subsidiary Valicare GmbH based in Frankfurt am Main, has been providing a comprehensive range of services for the GMP environment for over 20 years, particularly for manufacturers of advanced therapy medicinal products (ATMPs). The company specializes in GMP and ISO compliance, quality management consulting, and risk-based qualification of equipment and process validation. With a focus on multidisciplinary teamwork, SYNTEGON adheres to the latest technological standards and international regulations, including FDA and GMP guidelines. The company collaborates with leading firms in the industry, offering a dynamic work environment that values expertise and innovation.

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