About this role
The Quality and Regulatory Affairs Consultant will work within Emergo’s regulatory affairs team and support Emergo’s global consulting services, providing assistance with regulatory and compliance issues. May also be called upon to liaise with local consulting partners and regulatory authorities in smaller markets where needed.
- Bachelors' degree, preferably in a Medical, Engineering or Science field.
- Advanced, professional-level written and verbal English and excellent communication skills.
- Generally, 2-5 years of Quality Assurance and/or Regulatory Affairs experience working in the medical device field, in a regulatory, submissions or quality support role.
- Consulting experience a plus.
- Excellent attention to detail, research or device registrations experience a plus..
- Proficiency with Microsoft Office software.
- Strong multitasking, organization and prioritization skills.