Biomedical Engineer

Actalent; Jacksonville (FL); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Paid parental leave

In-house training

Professional development opportunities

Medical insurance

Dental insurance

401k

Job summary

Actalent in Jacksonville, FL seeks a specialist to lead Verification and Validation (V&V) activities for medical devices. You will develop protocols, test plans, and reports, and manage external labs to ensure timely, compliant V&V deliverables.

The role requires a bachelor’s degree in a scientific discipline and 1–2 years of medical device experience, with proficiency in biocompatibility, toxicology, and technical writing.

Qualifications

• Bachelor's degree in a scientific discipline.
• 1-2 years of experience in the medical device industry.
• Proficiency in biocompatibility, toxicology, and technical writing.

Responsibilities

• Lead Verification and Validation (V&V) activities for medical devices, including development of protocols, test plans, and reports.
• Manage external labs and monitors to ensure timely completion of V&V activities.
• Ensure compliance with biocompatibility, sterilization, and regulatory standards.

Skills

Biocompatibility

Medical Device Product Development

Sterilization

Technical Writing

GMP

Toxicology

FDA Regulatory Interactions

Verification and Validation

Risk Management

Design Control

Biological Safety Evaluation

Toxicological Risk Assessment

Education

Bachelor's degree in a scientific discipline

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