QRLP is an intensive two-year Masters-level program committed to accelerating the careers of high-potential candidates in GE’s Healthcare business. Participants with a passion for driving change, can develop their business acumen, and excel through accelerated technical coursework and three eight-month rotations working on critical business assignments within the fast-paced Quality environment.
The QRLP program involves three rotational assignments across GE Healthcare in quality assurance and regulatory affairs. Participants learn technical problem-solving skills, which are developed via quality assurance and regulatory affairs coursework. The program also includes hands-on coaching and mentoring, a variety of assignments, teamwork, ongoing reviews and defined deliverables. The program provides valuable experience in a variety of quality specialties, such as Regulatory Affairs, Production and Process Controls, Complaint Handling, Corrective and Preventative Action, Pre- and Post-Market Product Safety Surveillance, Design Controls, Supplier Quality, Quality Assurance, and Quality Management System Compliance.
Participants can look forward to exposure to senior leadership via project reviews as well as challenging and rewarding business experience in a variety of areas such as Project Management, Team Leadership, Negotiation, Regulatory Affairs, Manufacturing, Legal, Sourcing, Engineering, and Marketing. Participants’ business skills are developed via corporate leadership courses and offer the opportunity to earn certification in quality assurance and/or regulatory affairs.
Further details:
General Electric Healthcare Quality-Regulatory Leadership Program (QRLP)