Future Talent Program
The Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals.
Team Overview :
The Global Regulatory Affairs and Clinical Safety (GRACS) Regulatory Digital Health (RDH) team assists in bringing new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices, and solutions to the world through a highly regulated industry. We have accountability to both lead the enterprise, navigate the ever-evolving digital health regulations.
Position Overview :
Under the direction and guidance of the Regulatory Digital Health leadership team, the incumbent will assist in executing the overarching strategy for all Digital Health Modalities including, but not limited to : clinical trial tools, tools used to analyze data, and commercial innovations as well as developing processes. The responsibilities may include leading or supporting one or more projects related to Project Management, Administrative support, Digital Health related programs among others. This opportunity in our department can provide opportunities for development for your long-term goals.
Education :
- Currently enrolled in a B.S. or Graduate degree program in science or engineering field, Computer Science, Biology / Chemistry, Data Informatics, or related fields.
Required Qualifications :
Availability for in-office work based out of Upper Gwynedd, PA.Ability to start the 6-month co-op position in January 2026 and work in a hybrid model (in office 3 or more days per week)Primary Duties / Assignments :
Support the assessment, communication, and implementation of the emerging Digital Health Regulatory landscape across the company portfolio.Participate and support as appropriate, operational processes and systems to incorporate Digital Health into the company across the product portfolio.Build familiarity with Global Regulatory Affairs and Clinical Safety systems enabling departmental support for initiatives, remediation efforts, and product research (i.e., submissions, registration, regulations, risks, etc.)Candidate may be required to do research on global agency sites and participate in meetings and conversations around related to Medical Devices.Contribute to the strategic vision and planning of new digital health initiatives that establish operational processes and systems to fully incorporate device and digital health into our company's way of working across the broad product portfolio.Ensure close collaboration with cross functional and cross divisional teams (Research, Manufacturing, Commercial, IT) to align on and incorporate regulatory requirements into strategies for digital health solutions and complex combination products (with connectivity) to ensure successful product registrations.Development of best practice guidance for regulatory deliverables for digital health, diagnostics, and complex combination products to support the therapeutically aligned development teams.Salary range : $39,600.00-$105,500.00 USD