Title : Regulatory Affairs Coordinator III
Location : Irvine, CA (Hybrid) – Position is open to Fully Remote candidates
Note : This is a W2 contract role – C2C & 3 rd party candidates WILL NOT be considered
The Regulatory Affairs Coordinator will support US and EU regulatory submissions, exercising judgment to protect proprietary information, and track timelines and document milestone achievements. Additionally, they will;
- Participate in assessing and collating regulatory impact and developing regulatory strategy
- Collaborate and approve change requests / change notifications
- Participate in providing guidance and feedback to business unit regulatory teams on registration requirements for new and renewal registrations, product and process changes, and labeling content
- Handle other incidental duties, as assigned by leadership
Position Qualifications :
5-7 years of regulatory affairs experience, with a strong understanding of global regulations for new products or changes to relevant to medical devices, Class II, and / or Class III devicesAbility to interact professionally with all organizational levels, and manage competing priorities in a fast paced environmentAbility to work in a team environment, including inter-departmental teams, while representing the organization on specific projects; ability to build productive internal / external working relationshipsProven expertise in Microsoft Office Suite, including Word, PowerPoint and ExcelStrong written and verbal communication skills, and interpersonal relationship management skillsGood problem-solving, organizational, analytical, and critical thinking skills; strict attention to detailBachelor's Degree in Biology, Microbiology, Chemistry, Engineering, or other related field, including coursework, seminars, and / or other formal government and / or trade association trainingNote : This is a W2 contract role – C2C & 3 rd party candidates WILL NOT be considered