Regulatory Affairs Engineer
Eitan Medical
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Eitan Medical is reinventing drug delivery across the continuum of care with connected, software-based solutions from the hospital to the home. We focus on creating user-friendly, innovating patient- centered care and safe solutions; we’re looking for an excellent and experienced Regulatory Affairs Engineer to join our great team. You will join a dynamic and fast-paced environment and work with a team of talents to build and roll-out cutting-edge products that deliver the company’s innovative vision and strategy.
Job Description:
• You will Support the process of adverse events reporting to various countries worldwide
• You will Communicate with worldwide authorities
• As a Regulatory Affairs Engineer you will Conduct RA strategy and evaluation of: (i) design changes, (ii) Materials non conformities and (iii) investigations
• Field action/Recalls execution
• Leading Post Market Surveillance activities
• Participating and supporting in additional cross-department tasks
Direct manager: Regulatory Affairs Director
Requirements
· Experience: Minimum of 1 year experience as a quality/regulatory specialist
· Education: Bachelor's degree in a scientific discipline or equivalent
· Language skills: English - Mother tongue level
· Computer skills: full control in Office, SAP - advantage
· Other:
o Availability for intensive work, including unconventional hours when required
o Ability to work under pressure and in tight schedules
o Strategic thinking from planning to execution and follow up for regulatory and quality.
This job is no longer accepting applications
See open jobs at Eitan Medical.See open jobs similar to "Regulatory Affairs Engineer" LHH.