Life Cycle Management Specialist

Job Description

Our client is a leading international company within the medical device industry, specializing in the manufacturing of high‑quality products for aesthetic and reconstructive procedures. The organization operates in a highly regulated environment and utilizes advanced technologies for product design, material processing, and sterile manufacturing.

In this role, you will be responsible for managing product and component changes across the full lifecycle of implantable medical devices. You will ensure that design updates, labeling modifications, documentation revisions, and BOM changes are executed in accordance with GMP, ISO 13485, and design control requirements.

Responsibilities

• Lead and coordinate product design changes from initiation through release, ensuring full compliance with design control, GMP, and ISO 13485 requirements.
• Support material introductions and phase-outs with sourcing teams an...