What are the responsibilities and job description for the Associate Project Engineer position at CTL Amedica?
Associate Project Engineer
CTL Amedica – Blue Bell, PA
CTL Amedica is an ISO 13485 certified, and FDA registered medical device company. CTL designs, manufactures, and distributes spinal implants and surgical systems used by spine surgeons worldwide.
CTL Amedica is seeking an Associate Project Engineer to support the Research & Development team. This role offers the opportunity to help design a variety of spine-related implants and instruments, contributing to our extensive and growing product portfolio.
The ideal candidate is organized, detail-oriented, technically curious, and able to manage multiple cross-functional activities simultaneously.
Key Responsibilities
• Design and modify implants and instruments using PTC Creo Parametric.
• Create or revise engineering drawings and inspection documentation.
• Manage maintenance, calibration, and scheduling of mechanical test equipment.
• Develop test protocols, fixtures, and reports for mechanical testing.
• Create and maintain Design History File (DHF) documentation.
• Perform design verification and validation activities to ensure designs meet specifications.
• Plan and coordinate manufacturing and/or purchasing activities as appropriate for each project.
• Support product introductions through sales training, customer calls/visits, and related activities.
• Collaborate with surgeons, consultants, and external partners to support product design improvements and feasibility evaluations.
Required Qualifications
• Bachelor’s degree in Engineering (Biomedical or Mechanical Engineering preferred).
• Strong organizational and project coordination skills.
• Excellent written and verbal communication skills.
• Ability to work with technical documentation, reports, and structured forms/templates.
• Strong analytical and problem-solving skills.
• Ability to manage multiple priorities in a fast-paced environment.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Self-motivated, dependable, and able to work both independently and collaboratively.
Preferred Qualifications
• Experience in the medical device or other regulated industry.
• Familiarity with FDA design controls, 510(k) submissions, or ISO 13485.
• Experience in design for manufacturing (DFM) or general manufacturing processes.
• Experience with FEA software (e.g., ANSYS, SolidWorks Simulation).
• Experience in product verification & validation (V&V) and/or mechanical testing.
Education
Bachelor’s degree in engineering (Biomedical or Mechanical Engineering preferred).
Job Type
Full-time
Location
Blue Bell, PA (On-site)
Start Date
June 8, 2026
Salary Range
$60,000–$80,000 (Based on qualifications and experience)
Company Benefits
• Opportunity for advancement
• 401(k)
• Health insurance
• Dental and vision coverage
• Paid holidays and vacation
Salary : $60,000 - $80,000