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GMP Consultant in ATMP Process Development - Remote

Posted 20 weeks ago
All others
Full Time
Worldwide

Overview

As a GMP Consultant in ATMP process development, you will contribute significantly to our business success by managing GMP projects in the biopharmaceutical industry.

In Short

  • Manage GMP projects independently in the biopharmaceutical industry.
  • Develop and conduct training sessions competently.
  • Formulate technical texts and create professional documents.
  • Demonstrate customer orientation and contribute to team success.
  • Collaborate with your team in Frankfurt and travel nationwide for client engagements.

Requirements

  • Completed university degree with a doctorate in a natural science (preferably pharmacy or biology/biotechnology) or a comparable qualification.
  • Several years of relevant professional experience in ATMP process development in a pharmaceutical or biopharmaceutical company or a university research institution.
  • Initial GMP and regulatory knowledge with a willingness to deepen this knowledge.
  • Fluency in German and English; additional language skills are a plus.
  • Good team and communication skills, with the ability to represent your expertise confidently.
  • Independent, reliable, and structured working style.

Benefits

  • Flexibility of a small company with the stability of a large parent company.
  • Industry-standard compensation with an extraordinary bonus model linked to company success.
  • Interesting tasks in a technologically exciting and new environment.
  • Opportunities for personal development and leadership roles.
  • A variety of other attractive conditions.
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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