What are the responsibilities and job description for the Sr. Manager, Systems Verification position at Abbott?
The Opportunity
Leading an active lifestyle is important to the many people we serve. In Abbott’s Electrophysiology division, we’re advancing the treatment of heart disease through breakthrough medical technologies, allowing people to restore their health and get on with their lives.
The Senior Manager, Systems Verification at our Little Canada / St. Paul, MN location, will play a key role in this fast growing, highly visible group, designing and developing electromechanical medical devices in Abbott’s Electrophysiology medical device division. In this role, you will provide functional and technical leadership for system verification team. The team is responsible for the product development of new products and subsystems for our market-leading Electrophysiology (EP) mapping, diagnostic, and ablation devices.
What You’ll Work On
- Building and coaching a team through identifying career development opportunities, providing constructive feedback when necessary, and increasing the technical proficiency across all team members.
- Working with program managers and cross-functional leaders to guide and scope program planning, schedules, and budget. Ensuring the team is aligned with meeting program timelines and milestones. Participation in formal design reviews.
- Managing the development of goals, objectives and strategies for system verification team.
- Developing and maintaining system level expertise and continually working to improve system level test methods and strategy.
- Drive ownership of V&V plans and execution. Work cross-functionally with other areas of R&D, regulatory, and quality to ensure comprehensive design characterization and V&V strategies.
- Support Systems Engineering requirements development and tracing.
- Identify opportunities to develop data for claims substantiation.
- Communicating to senior management as required including technical presentations, status updates, and program reviews as required.
- Remains current on developments in field(s) of expertise, system engineering best practices, regulatory requirements, as well as industry trends.
- Promoting and supporting the development of intellectual property and clinical relevance of test methods.
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Required Qualifications
Preferred Qualifications
The base pay for this position is $127,300.00 – $254,700.00. In specific locations, the pay range may vary from the range posted.
Salary : $127,300 - $254,700
