Compliance Manager (United Kingdom, Germany, Ireland, Austria, Switzerland) at Jobgether

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Compliance Manager (United Kingdom, Germany, Ireland, Austria, Switzerland) at Jobgether. This position is posted by Jobgether on behalf of . TetraScience. . We are currently looking for a . Compliance Manager, EMEA. in . United Kingdom, Germany, Ireland, Austria, or Switzerland. .. Join a mission-driven organization at the forefront of the Scientific AI revolution, where you’ll play a key role in ensuring compliance with critical international standards and regulations across a rapidly expanding platform. As a Compliance Manager for the EMEA region, you'll lead efforts to support regulated pharma environments, manage internal and external audits, and influence the company’s quality strategy in collaboration with technical and customer-facing teams. If you are experienced in GxP, ISO, and EU regulatory frameworks, this is your opportunity to make a lasting impact in a high-growth, innovation-focused environment.. . Accountabilities:. . Maintain compliance across products and operations, particularly focusing on EU regulations such as GxP, ISO 9001, and Annex 11.. . Work closely with Product, Engineering, Quality, and Customer Success teams to ensure the platform meets customer validation and compliance needs.. . Own and enhance the GxP Package to support clients in achieving faster regulatory approvals and validations.. . Lead internal audits and prepare the organization for external assessments (e.g., ISO 9001, ISO 27001, SOC 2 Type II).. . Ensure the Quality Management System (QMS) is up to date and aligned with evolving industry standards.. . Act as a point of contact for compliance during sales cycles and customer engagements.. . Maintain comprehensive documentation and drive cross-functional consistency across regulatory processes.. . . 10+ years of experience in software lifecycle management and validation, with emphasis on pharma or biotech compliance.. . Solid knowledge of EU regulatory frameworks (e.g., GxP, 21 CFR Part 11, Annex 11).. . Experience preparing for and navigating ISO, SOC, and other third-party compliance audits.. . Strong documentation, project management, and cross-functional collaboration skills.. . Proven ability to influence compliance culture across multiple teams and geographies.. . Bachelor's degree in computer science, life sciences, or a related field.. . Preferred: Advanced degree in compliance or regulatory affairs; ISO 9001 Lead Auditor certification; experience working with EU-based pharmaceutical companies.. . Company Location: United Kingdom.