Lead key sustaining programs to maintain business supply continuity, such as supplier changes, market-released product component changes, and obsolescence.
Track and trend component supply for key product development programs and manage ongoing relationships with external suppliers so that the organization receives satisfactory standards of service.
Develop and maintain integrated project plans, schedules, budgets, resource forecasts, and key performance metrics.
Monitor project progress and performance against established objectives, identifying and proactively addressing risks, issues, and barriers to execution. Identify and resolve operational problems and minimize delays; escalate issues to senior management with proposed options to bring to resolution.
Partner with R&D, Quality, Regulatory Affairs, Clinical, Manufacturing, Supply Chain, and Marketing teams to ensure project deliverables are completed on schedule and in compliance with applicable regulatory and quality requirements.
Prepare and present project status, financial performance, key risks, and recommended actions to functional or executive leadership.
Promote a culture of accountability, collaboration, continuous improvement, and execution excellence across project teams.
Education
Required
Education Level: Bachelor's degree in Engineering, Life Sciences, Business, or related technical field (± 8 years)
Preferred
Master's degree in Engineering, Life Sciences, Business Administration, or related discipline (± 6 years)
PMP certification or equivalent project management certification.
Experience / Background
Required
Minimum 7 years of project management experience.
Experience managing project scope, schedule, budget, resources, and risk.
Strong communication, facilitation, and stakeholder management skills.
Preferred
Experience within the medical device, biotechnology, pharmaceutical, or other regulated industry.
Experience managing projects involving cardiovascular catheters or associated cardiovascular delivery system products.
Demonstrated success leading complex cross-functional projects through product development to global commercial release.
Working knowledge of design controls, risk management, and quality system requirements.
- The base pay for this position is
- $99,300.00 – $198,700.00
- In specific locations, the pay range may vary from the range posted.
JOB FAMILY
Project Management
DIVISION
CRM Cardiac Rhythm Management
LOCATION
United States > Minnesota > Minnetonka : 14900 Minnetonka Industrial Road
ADDITIONAL LOCATIONS
WORK SHIFT
Standard
TRAVEL
No
MEDICAL SURVEILLANCE
Yes
SIGNIFICANT WORK ACTIVITIES
Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Work in a clean room environment
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
