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The Quality Engineer collaborates closely with the engineering team to identify and understand critical-to-quality design attributes and specifications. This role involves reviewing and releasing custom hardware, sub-project, and project DHF documentation to ensure compliance with all applicable regulatory requirements. The individual will contribu...

As a Quality Assurance Specialist with a focus on CAPA (Corrective and Preventive Actions), you will be a key contributor to maintaining and improving our quality management system. This role goes beyond investigations-you will ensure that CAPA processes are integrated into our overall QA strategy, supporting compliance, risk mitigation, and contin...

Head of Regulatory AffairsPosition OverviewA commercial-stage biotech focused on neurodegenerative diseases, is seeking a seasoned regulatory leader to drive global regulatory strategies for approved products, ensuring compliance and supporting lifecycle management activities. This role will primarily focus on post-approval regulatory work, includi...

Quality Assurance Specialist - Medical Device Manufacturing (Poland 🇵🇱)Join a global innovator in medical technology on a critical manufacturing project in Poland! We're seeking Quality Assurance Specialists to uphold product integrity, compliance, and patient safety across the entire device lifecycle.📍 Location: Poland (Hybrid) 📅 Duration: 12-...

Title: Senior Validation EngineerLocation: Boston, MA (on-site) About the Role:A growing biotech company working on regenerative medicine is looking for a Senior Validation Engineer to join their team. If you're experienced in GMP environments and enjoy hands-on work with equipment, processes, and documentation, this could be a great fit. You'll be...