Field Modification Instruction Project Leader

Job Description Summary We are looking for one Recall Project Leader who provides program execution and leadership to the cross-functional teams and drives Field Action programs for our Consumables products in a timely and compliant manner. Our cross-functional engineering team is part of Helsinki based Monitoring Systems business. This person might be appointed to help other teams with similar field actions on a need's basis on the Helsinki site.
Job DescriptionResponsibilities

• Lead the assessment of intended Field Modification Instruction (FMI) programs for affected products, installed base size, needed data sources and resources to complete the project within the required time frame.
• Maintain the affected installed base data files to ensure accuracy and completeness, including the integration of data provided by Operations, Service, OEMs, distributors, and other suppliers.
• Develop and execute project plans according to committed timelines and within regulatory and quality guidelines and processes.
• Coordinate cross-functional work of the field action programs to drive Milestone completion.
• Coordinate tasks and deliverables to meet quality, performance, and productivity goals.
• Present complete and accurate status of all projects in review meetings.
• Participate in gathering relevant information for Regulatory reportability decisions.
• Ensure compliance to procedures and global regulatory requirements.
• Identify process weaknesses, participate work outs and activities to drive improvements in procedures.
• Collaborate with peer Project Leaders in the GEHC business to share information and harmonize/share best practices.
  

Qualifications and requirements

• Bachelor's degree in Engineering, Science or related field
• Relevant engineering work experience
• Carefulness and skills to work on documentation and large data files. Prior experience using spreadsheet and presentation software.
• Strong skills in Project Leadership and working with cross-functional global teams.
• Knowledge of hardware or software development and manufacturing
• Ability to prioritize, plan and execute to established strategic and regulatory goals.
• Strong influencing, negotiation, and communication skills both verbal and written.
• Strong presentation skills with the ability to communicate issues in English in a clear and concise manner.
• Ability to identify, influence and lead process improvements and procedural changes.
• Excellent in English and Finnish languages.

Desired skills

• Master's degree in Engineering, Science or related field
• Earlier experience in the medical device industry or working with medical product regulatory authorities.
• Knowledge of Quality Management Systems (QMS) and regulatory agencies
• Ability to mentor, motivate and inspire others.

Inclusion and Diversity
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
Behaviours
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity.
Total Rewards
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration, and support.
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Additional Job Description
Additional Information
Compensation Grade
LPB2
Relocation Assistance Provided: No