Biomedical Engineer

Job Description

The specialist will lead Verification and Validation (V&V) activities for medical devices, including the development of protocols, test plans, and reports. They will manage external labs and ensure compliance with biocompatibility, sterilization, and regulatory standards.

Requirements: Candidates must have a bachelor's degree in a scientific discipline and 1-2 years of experience in the medical device industry. Proficiency in biocompatibility, toxicology, and technical writing is required.

Key Skills: Biocompatibility, Medical Device Product Development, Sterilization, Technical Writing, GMP, Toxicology, FDA Regulatory Interactions, Verification and Validation (V&V), Risk Management, Design Control, Biological Safety Evaluation, Toxicological Risk Assessment

Benefits: Paid parental leave, In-house training, Professional development opportunities, Medical insurance, Dental insurance, 401k