Main Accountabilities Coordinate product certification activities for all APTIV CS product lines. Act as the main interface for certification and regulatory compliance topics towards customers, authorities, and certification bodies. Coordinate certification requirements with Engineering, Quality, Manufacturing,
Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people
ZEISS Semiconductor Manufacturing Technology Enabler for smaller, more powerful, and more energy-efficient microchips Working for tomorrow today. Around 80 percent of all microchips worldwide are produced using ZEISS technologies. As the centerpiece of
Mission Brief We deliver the half of the rocket that stays on the ground. As Senior Specialist, you will be responsible for end-to-end safety & compliance of the company’s ground infrastructure systems according to location and
We exist to create positive change for people and the planet. Join us and make a difference too!Job title: Technical Specialist & Scheme Manager - Active DevicesLocation: Global HomebasedBSI is seeking experienced medical device professionals to
We exist to create positive change for people and the planet. Join us and make a difference too!Job Title-Technical Specialist- IVD (In Vitro Diagnostic)Location: EMEA/UK- HomebasedBSI is seeking R&D Scientists and Production Scientists to join our
Step out of your comfort zone, excel and redefine the limits of what is possible. Thats just what our employees are doing every single day – in order to set the pace through our innovations and
Overview In this role you will support CE marking for IVD devices by managing schemes, delivering expert technical reviews, and guiding QMS and regulatory activities. You’ll mentor healthcare personnel and collaborate with the commercial team to enable compliant,
Overview As Technical Specialist & Scheme Manager, you will support the certification of active medical devices for the European market. You will review technical and clinical documentation, manage certification activities, and provide regulatory guidance across CE marking schemes.