Are you an experienced Quality, Supplier, or Process Validation Engineer looking to make a meaningful impact in the medical device industry?
Develop efficient, risk-based validation strategies that balance quality, compliance, and business timelines.
Support and challenge external supplier validations and ensure alignment with internal standards and regulatory expectations.
Collaborate cross-functionally with R&D, Regulatory Affairs, and Manufacturing to support product industrialization.
Serve as a project lead on validation and supplier-related initiatives, managing external partners with appropriate oversight and escalation.
Several years of experience in the medical device industry, ideally in Supplier Engineering, Process Validation, Quality Engineering, or Project Management roles.
Proven ability to lead projects and work effectively with external partners and suppliers.
Strong communication skills in English; German is a plus.
Work in a cross-functional, international environment where your input directly impacts patient lives.
Be part of a high-growth organization with opportunities for personal and professional development.
If you’re passionate about ensuring quality and process excellence in the medical device space, apply now and/or contact Hollie Dear at Adaptive Life Science for more information!