Open Positions
Our focus is on Philadelphia-based positions
Director of Clinical Studies
- Min 10 years in clinical research, medical device
- 3 years Clinical Project Mgt.
- BS or MS in life science or related
- IRB, FDA, ISO 13485, 21 CFR 820
Product Manager, Medical Devices; lead the team in global introduction!
- Min. 5+ years’ experience in complex medical device commercialization
- Market data and analytics
- KOL contact, surveys and demonstrated technical product leadership
- Financial acumen & skills to determine trends, costs, forecasts
- BS/BA or higher in marketing, analysis, business admin., life sciences or similar
Communications and Marketing Manager: Highly visible position coordinating and leading a global life-saving technology
- BA/BS in related field
- 7+ years leading company-wide efforts to launch technical medical devices or combo products.
- Media preparation, production, scripts and staff education, news outlets and PR
- Experience Lead associations, medical and patient advocacy groups, clinical societies and KOL
- Content experience: Social media, articles, blogs, marketing materials, activity reporting
R&D Systems and Electrical Engineer: fascinating new medical device commercialization and next gen development
- BS in EE. Computer or systems a plus, MS a plus
- 3+ years complex medical device experience
- PCB, embedded microcontrollers, bus protocols, sensors, EN60601-1 standards and related FDA documentation
- Key role in leading development effort
Fall 2020 – expansion hiring!
- RA/QA Department Software QMS Management; fascinating neonatal device.
- R&D engineers medical devices
- Clinical researchers/technicians medical device experience
- Field Service engineer, top notch with electro-mechanical expertise and medical device knowledge
Recently Filled
Vice President R&D:
15 years min. in Medical Device development, and team leadership. Understanding the path to commercialization.
15 years min. in Medical Device development, and team leadership. Understanding the path to commercialization.
Director of Quality Systems/Documentation:
Lead the effort in a breakthrough neonatal medical device firm.
10+ years in QMS, 21 FCR 820, ISO 13485. Create a best in class QMS program.
R&D Engineers: Medical Devices. Director and Manager level opportunities:
Join breakthrough med device organization commercializing a life-saving product for infants
Electrical engineers, Mechanical Engineers, Materials Engineers, Bio-Engineers with medical device, PMA, 510K, or FDA process and 3+ years’ experience or more. Senior opportunities for experienced engineers too.
Join breakthrough med device organization commercializing a life-saving product for infants
Electrical engineers, Mechanical Engineers, Materials Engineers, Bio-Engineers with medical device, PMA, 510K, or FDA process and 3+ years’ experience or more. Senior opportunities for experienced engineers too.
Program Manager:
BSME, BSEE, BSBE or similar with ISO13485 experience, product development and supplier skills
BSME, BSEE, BSBE or similar with ISO13485 experience, product development and supplier skills
Pre-Clinical Director:
7 or more years’ experience managing the Pre-clinical trial team for Medical Device introduction.
7 or more years’ experience managing the Pre-clinical trial team for Medical Device introduction.
Software Engineer, Medical Device:
Creative experience in new product development, data capture and regulatory approval.
Creative experience in new product development, data capture and regulatory approval.