#twiceasnice Recruiting placed a Medical Device Regulatory Affairs Specialist (EU MDD/MDR; Class I & II) for a medical device manufacturer in the Mid-Atlantic. The role is in Manufacturing, specifically Medical Device Manufacturing. The client is a subsidiary company. First qualified candidate submitted in 24 days. Offer extended in 81 days from intake. Fee: 9.9% with an 18-month guarantee. #twiceasnice is a national direct-placement recruiting firm that builds every search from scratch and headhunts for every role.
Placement Record
Medical Device Regulatory Affairs Specialist (EU MDD/MDR; Class I & II)
Manufacturing · Mid-Atlantic
Legal & Compliance
Entry/Coordinator
Hybrid
Medical Device Manufacturing
Subsidiary
Medical Device Regulatory Affairs Specialist (EU MDD/MDR; Class I & II) successfully placed by #twiceasnice for a medical device manufacturer in the Mid-Atlantic.
From the completed search:
Search Details
Our client in the medical/rehabilitation device industry is looking for a Medical Device Regulatory professional to join their team in Hanover, Maryland. This position allows remote work flexibility post-acclimation. You will provide regulatory support throughout the pre and post market stages to regulatory authorities worldwide (FDA, EU, etc.), particularly for Class I & II devices. Thrive in a supportive, interactive, and casual work environment, shown by dedicated employees’ remarkable tenure. This is a fantastic opportunity for you to make a lasting impact within a globally recognized organization dedicated to making a difference.
| Role | Medical Device Regulatory Affairs Specialist (EU MDD/MDR; Class I & II) |
| Role Level | Entry/Coordinator |
| Industry | Manufacturing |
| Region | Mid-Atlantic |
| Work Model | Hybrid |
| Salary | ~$80,000 |
| Days to First Accepted Submittal | 24 |
| Intake to Offer-Extended Candidate | 81Days From Intake Call to Offer Extended Candidate |
| Our Fee | 9.9% |
| Guarantee | 18 months |