Medical Device Product Manager - Watertown, United States - Exergen Corporation

Exergen Corporation

Verified Company

Watertown, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

_
Exergen Corporation_ _is the recognized world leader in medical non-invasive temperature technology.

Exergen invented and manufactures non-invasive temperature measurement devices providing lower cost, higher accuracy, less invasiveness, and greater reliability than ever previously possible.

Our Temporal Scanner is the most efficacious, noninvasive thermometer ever created. Exergen holds over 100 issued and pending U.S. and foreign patents, and is the only manufacturer of retail medical thermometers in the U.S. Presently, half of hospitals and pediatricians currently use the Exergen Temporal Scanner, and well over 14 million consumers use one at home._
Founded by Harvardresearch scientist, Dr. Francesco Pompei, over three decades ago, Exergen Corporation is based in Watertown, Massachusetts, USA._

Reporting directly to the CEO, the Medical Device Product Manager will lead teams responsible for the overall execution of critical business programs from concept development through manufacturing transfer, commercialization and marketing.

Key Responsibilities and Activities:

Leadership role responsible for managing product development programs.
Lead and coach internal and external technical resources to support programs.
Work collaboratively with product marketing, development, manufacturing, engineering, operations, regulatory affairs, clinical affairs, sustaining, product specialists and quality teams to execute programs on time and on budget.
Build and implement program management tools and processes to effectively execute programs.
Timely tracking and presentation of program status.
Participates in the creation of the program objectives and overall project scope.
Ensures that projects are managed within project timeline and budget baselines.
Monitors and reports project status to the CEO.
Works independently and with the project teams to develop, maintain, and align an accurate, integrated project timeline, and resource plan.
Understands critical path activities, anticipates risks, and creates contingency plans in collaboration with project teams.
Generates analysis of timeline, and resource information that facilitate scenario planning, contingency planning, risk assessment and management, problem solving, and decision making.
Manages engagements with outside engineering partners as necessary to design, build, and test custom medical device systems, subsystems, and software.

Required Education and Experience:

8+ years of experience working in an FDA/ISO regulated medical device/medical equipment environment.
5+ years of experience preferred managing technical teams and programs.
Detail oriented with strong organizational skills.
Strong leadership and interpersonal skills.
Strong program management skills with accountability for budgets, milestones, and deliverables.
Excellent verbal and written communication skills.
Effective analytical and decisionmaking skills.
Must have a proven history of working in a fastpaced environment with a demonstrated ability to adjust to changing priorities.
Understanding of regulatory procedures/standards.
Ability to manage teams and individuals in a matrix environment, ability to track team performance against objectives, use of effective meeting management tools and techniques, and knowledge of decisionmaking and conflict resolution techniques.
An Expert or Power User level project management related software/tools to facilitate:
Scheduling
Tracking project tasks and milestones o Resource utilization
Management Reporting
Education:

BS in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or equivalent is required. Marketing, or other formal training/experience, is essential.

Job Types:
Full-time, Permanent

Pay:
$145, $150,000.00 per year

Benefits: