Regulatory Affairs Expert for Global Medical Device Submissions
1 day ago
We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Collabera, a global digital solutions company.
Job Responsibilities- Collaborate with multiple business units to develop, update, and improve regulatory affairs processes.
- Assist in the implementation of regulatory affairs strategies and operations, including product registration submissions, progress reports, supplements, amendments, and periodic experience reports.
The ideal candidate will have 1-3 years of experience in Medical Device Regulatory Affairs and possess working knowledge of EU MDR and US medical device submissions. They should also have experience supporting internal and external inspections and be able to work effectively in a matrixed environment.
Requirements- BA/BS Degree
- Excellent communication and project management skills
- Ability to work independently and as part of a team
We offer a competitive salary range of $85,000 - $110,000 per year, depending on experience, and a comprehensive benefits package, including health insurance, retirement plan, and paid time off.
Collabera is a global digital solutions company providing software engineering solutions for the world's most tech-forward organizations. With roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom, and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.
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