Quality Assurance at FUTRUE GmbH
Germany, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

05 Jan, 27

Salary

50000.0

Posted On

07 Oct, 26

Experience

7 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Biotechnology

Description

We are a leading global biopharmaceutical company specializing in the development and distribution of innovative medicines for the treatment of chronic pain. Our vision is clear: a world free of chronic pain! With VER-01, we have developed a unique cannabinoid-based medicine for the treatment of chronic pain, which was approved in Germany and Austria in June 2026 under the name Exilby. This marks a significant milestone after more than eight years of intensive research and development.


Approval in the USA is planned for 2029. Our goal is to establish Exilby as the leading therapy for the treatment of chronic pain by 2030, setting new standards in pain management. Does


this sound exciting to you? Then apply now! We look forward to getting to know you.

Your mission with us

You ensure that the quality of our pharmaceuticals and active ingredients isn't just a factor during audits. As Team Lead / Director of Quality Assurance, you shape the quality assurance process for the products marketed by VERTANICAL. With an effective quality system, you identify risks early and support the specialist departments as a sparring partner in pragmatically and sustainably embedding compliance in everyday practice.

 


Your tasks

  • You will develop, operate and improve the quality system for our pharmaceuticals and active ingredients, including relevant processes, SOPs, training, change management, deviation management and CAPA.
  • You coordinate the release of batches, packaging materials, marketing materials and responses to external inquiries in close coordination with CMC, Operations, Product Management and Medical.
  • You are the contact person for existing and new regulations in the pharmaceutical sector at both national and international levels, in particular AMG, GDP, GMP, HWG, SGB, AM-RL.
  • You assess quality events, deviations and trends, support root cause analyses and ensure that appropriate corrective and preventive actions are implemented and their effectiveness is tested.

Responsibilities
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