You manage project timelines and deliverables while ensuring product compliance. Your role includes creating detailed documentation and promoting a culture of improvement through mentorship and expertise in engineering practices.
Anforderungen
- •Bachelor's in Engineering preferred
- •Master's Degree preferred
- •PhD preferred
- •MBA preferred
- •7+ years of experience in medical device design
- •Minimum 3 years of experience in people management
- •Experience with FDA, ISO, GMP regulations
- •Experience with manufacturing process equipment
- •Previous project leadership experience
- •Experience executing in vitro and in vivo tests
Deine Aufgaben
- •Maintain international product approvals and make necessary adjustments.
- •Communicate project schedules and health reports.
- •Lead programs and projects to meet objectives and deliverables.
- •Create comprehensive technical documentation for engineering efforts.
- •Act as a subject matter expert in project management and data analytics.
- •Promote a culture of ownership and continuous improvement through guidance and mentoring.
Deine Vorteile
Dynamic international work environment
Diverse challenging projects
Career growth opportunities
Flexible working conditions
Attractive employee benefits
Original Beschreibung
# Manager Engineering (m/f/d)
* Hechingen
* Forschung, Entwicklung, Lehre
* Publiziert: 01.04.2025
!Manager Engineering (m/f/d), 1. Bild
It’s a good feeling to know you're doing your best with purpose every day.
We are hiring a
**Manager Sustaining Engineering (m/f/d)**
## Your Strength
* BS in Engineering (Medical Engineering or Biomedical preferred), MS, PhD, MBA preferred
* 7+ years of experience working in medical device design, development and production of tissue and medical devices (capital equipment, disposables, and implantable devices).
* Minimum of 3 years of experience in people management
* Experience with FDA, ISO, GMP and design control regulations
* Experience with development, acquisition and improvement of manufacturing process equipment
* Previous project leadership of complex product change activities, including managing external engineering and testing resources
* Experience developing and executing in vitro, in situ, in vivo, and ex vivo tests and experiments for medical devices
## Your Contribution
* Maintaining the international approvals of our products on the market, carrying out all necessary changes and adjustments
* Communicate credible project schedules and project health reports
* Leadership of programs and projects to completion of objectives and generation of all deliverables within timeline and budget constraints following design control requirements
* Construct robust comprehensive technical documentation for all sustaining engineering efforts
* Acknowledgement as a subject matter expert in best practices for project management, data analytics, and engineering analysis
* Foster a team culture of ownership, accountability, continuous evaluation, and improvement by providing team guidance, regular feedback, education, coaching and mentoring
## Our Strength
* A dynamic, international work environment with opportunities for innovation and leadership.
* Diverse and challenging projects with significant global impact.
* Opportunities for career growth and specialized training programs.
* Flexible working conditions, including hybrid
* Attractive employee benefits, such as pension plans, EGYM Wellpass