SHL RA Regulations and Standards Specialist
We at Siemens Healthineers™ are committed to helping healthcare providers globally to succeed in today's dynamic environment. We are inspired to transform the way things are done –because we want what is best for our people, our customers and ultimately the health of mankind. While we are invested in engineering excellence – leading-edge medical technologies and services, we don’t stop there. We're also deeply invested in our 46.000 people with the
hearts of pioneers and minds of engineers, highly committed and connected in this industry. And as we strive to shape the future of healthcare, our overall success will depend on our ability to continuously reinvent ourselves.
If you are ambitious and change makes you thrive, help transform Siemens Healthineers into a learning organization.
Knows who in the Regional Company is active in which of these external and internal committees and in which function (chairperson, secretary, member, etc.).
Identity standardization organizations and Healthcare business relevant technical committees, establish connection and relationship with them.
Forwards the information about relevant committees and the Regional Company’s involvement to H QT TRSM so that the position and activities could be aligned.
Cares that every person of the Regional Company active in committees knows by whom he/she is to be briefed in order to represent the agreed company’s interests and to whom the feedback report (debriefing) should be addressed.
Safeguards 3 awareness and observation of technical market access conditions such as technical law and regulation, conformity assessment and certification requirements. Responsible for active observation of relevant legislation and for providing that information into the knowledge-sharing platform in order to foster legal compliance according to the relevant technical regulation.
Supports the collaborative international Voting & Issues Management (VIM) process and acts as a contact for H QT TRSM to get the regional opinion into agreed Siemens positions on technical regulation, standardization and conformity assessment (market access) policy issues.
In consultation with units and the TRSM-O, nominates the experts to external organizations. Nominations for key positions (chairpersons and secretaries) are done in consultation with H QT TRSM.
This position may suit you best, if building learning organizations is your expertise and you have extensive experience with Top Management Learning and Leadership Development.
- Above 5 years experience in medical device regulatory affairs or standization management
- Basic skill in full understanding of regulations and medical device standards
- Excellent skill in problem solving and cooperation
- Highly verbal and written communication skills in English as well as Chinese
- Leadership experience/skill to coach and motivate team
- Able to work on international level/in an international environment
Job ID: 92794
Organisation: Siemens Healthineers
Experience Level: Experienced Professional
Job Type: Full-time