Minimum 1-4 years industrial experience in sustainability, eco-design and/or product related environmental regulations applicable for engineering products. • Good knowledge of applicable environmental regulatory requirements and industry standards, including WEEE, RoHS, REACH, animal origin, country of origin, Low voltage directive, Machinery directive, Battery directive and other eco-design and energy efficiency requirements. • Proven expertise in developing hardware substance (metals, non-metals, plastics, semiconductor devices) compliance matrix with respect to above mentioned regulatory requirements. • Ability to communicate with suppliers on regulations and possess strong rigor in material data collection. • Familiarity with product life cycle thinking and use of product life cycle assessment software or tools to evaluate the eco-profile of products. • Ability to pull relevant information from engineering, standards bodies, industry standards, and other technical resources to develop an overall GE Healthcare life sciences environmental strategy and drive change. • Good in development of processes and SOPs. • Experience in design documentation to comply with ISO and European standards. • Ability to develop standards and run projects remotely, such as in other geographies within the Europe and US. Essential Responsibilities • Ensure Compliance/Regulatory requirements for products across Life sciences. • Assessment of the substances used in engineering Hardware (both Electrical and Mechanical). • Change management of substances as per restrictions and regulatory needs and sustainability for the same. • Ensure data on regulations up to date to drive competitive advantage and increase responsiveness to customer tenders.