CTL Amedica is an ISO 13485 certified and FDA registered Medical Device Company with offices in Carrollton, Texas. CTL designs, manufactures and distributes medical device products and systems for spinal surgeons; specifically implants and devices.
CTL Amedica is currently seeking to fill the role of Associate Project Manager within the Research and Development department. The ideal candidate is self-motivated and detail-oriented, with strong communication skills.
Duties:
- Project management and follow up for timely execution of activities that involves all phase of product development, launch, maintenance, post market surveillance, and improvement with primary focus on generation of corresponding design control related documents
- Create and compile on-going launch(-ed) product set list and marketing collaterals (not limited to Surgical Technique, Product Overview, Patient Brochures, and other creative marketing materials)
- Creation of forecast & market intro-plan & preliminary content development for marketing/training/new letter material
- Oversee existing orthopedic product lifecycle and maintain corresponding / cohesive documentations & communication
- Communication and facilitation with other departments about product related matters that requires follow up
- Lead product knowledge communication, technical support, and training of sales team
- Assist /manage compilation of CE Technical Files
- Assist / manage compilation and submission of FDA 510(k) related documents
- Assist in liaison for product related communication with outside company
- Interact with end users and other technical personnel outside the company to support design, development, and/or improvement of product feasibility, functionality and/or manufacturability enhancements
Required Qualifications:
- Project management and follow up for timely execution of activities that involves all phase of product development, launch, maintenance, post market surveillance, and improvement with primary focus on generation of corresponding design control related documents
- Create and compile on-going launch(-ed) product set list and marketing collaterals (not limited to Surgical Technique, Product Overview, Patient Brochures, and other creative marketing materials)
- Creation of forecast & market intro-plan & preliminary content development for marketing/training/new letter material
- Oversee existing orthopedic product lifecycle and maintain corresponding / cohesive documentations & communication
- Communication and facilitation with other departments about product related matters that requires follow up
- Lead product knowledge communication, technical support, and training of sales team
- Assist /manage compilation of CE Technical Files
- Assist / manage compilation and submission of FDA 510(k) related documents
- Assist in liaison for product related communication with outside company
- Interact with end users and other technical personnel outside the company to support design, development, and/or improvement of product feasibility, functionality and/or manufacturability enhancements
Required Education Level:
- Bachelor Degree with at least 1 year of Industry Experience. (Engineering Degree, preferably Mechanical Engineer or Biomechanical Engineering)
- Please cite cumulative GPA.
Job Status
- Full Time
Location:
- CTL Amedica Headquarters – 2052 McKenzie Drive, Carrollton, TX 75006
Company Benefits:
Opportunity for advancement, 401k, Great health plans, Dental and vision coverage, Paid sick days, holiday and vacation days
Send Resume : jsuh@ctlamedica.com