Project Manager

Abbott; Minnetonka (MN); On-site; USD 99,000 - 199,000; Full time

Job summary

Abbott in Minnetonka, MN seeks a Project Manager to lead cross-functional teams delivering complex cardiovascular medical device projects from concept to commercialization, ensuring alignment with technical, regulatory, quality, schedule and business goals. The role requires 7+ years of PM experience, strong communication and stakeholder management, and familiarity with design controls.

A Bachelor’s degree is required; a Master’s or PMP is preferred.

Qualifications

• Minimum 7 years of project management experience.
• Experience managing scope, schedule, budget, resources, and risk.
• Strong communication, facilitation, and stakeholder management skills.
• Experience in medical device or regulated industry preferred.

Responsibilities

• Lead a cross-functional team responsible for a subsystem of a large-scale new product development project under the supervision of program management leader
• 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; accelerate issues to senior management with proposed options to bring to resolution.

Skills

Project management

Leadership

Communication

Stakeholder management

Education

Bachelor's degree

Master's degree

PMP certification

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Project Manager

Cardiac Rhythm Management (CRM) Delivery Systems

Main Purpose of the Role

Lead cross-functional product development teams in the planning and execution of complex cardiovascular medical device product development projects, ensuring alignment with technical, clinical, regulatory, quality, schedule, and business objectives.

Manage projects in accordance with the organization’s product development and project management methodologies. Develop, maintain, and communicate project plans, timelines, budgets, resource requirements, and risk mitigation strategies to ensure successful execution from concept through commercialization.

Drive project team alignment, facilitate decision-making, and ensure timely resolution of issues impacting project performance. Take ownership for achieving project deliverables while balancing scope, cost, schedule, quality, and regulatory requirements.

Main Responsibilities

• Lead a cross-functional team responsible for a subsystem of a large-scale new product development project under the supervision of program management leader
• 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; accelerate 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