Engineering Program Manager/Product Development Program Manager
- 📅
- 20000GOI N° de la demande de poste
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- Wed 28 Oct 12:02 Date de publication
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About Medtronic:
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life.
We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Day in the Life section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Minimum Qualifications:
• Bachelor’s degree in Engineering or Similar related field and 5+ years of experience.
• Advanced degree in Engineering or Similar related field and 3+ years of experience.
Nice to Have
•Strong preference for those with product development experience within the medical device industry for items such as: Complex capital electrical/mechanical systems, software development and single-use disposables
•7+ years Quality System experience in medical device or other highly regulated/technical industry.
•5+ years’ experience in successfully leading projects or programs.
•Masters and/or MBA preferred.
•PMP Certification preferred.
•Design for Six Sigma (DFSS) training and/or Certification preferred.
•Ability to influence others.
•Strong analytical and problem solving skills.
•Demonstrated decision making skills.
•Ability to lead projects in a matrix structure.
•Ability to effectively communicate at all levels and across the organization.
•Good interpersonal skills.
•Performance Management Leadership and Coaching Skills.
•Good Presentation Skills.
•Good working knowledge of Word, Excel, Microsoft Project and PowerPoint.
•Must be able to handle multiple tasks/projects and manage priorities accordingly.
•Ability to manage through ambiguity.
•Experience with in-house/on-site manufacturing and working with Contract Manufacturers.
•Experience with medical device sterilization methods.
•Experience with the following standards/regulations: IEC 60601, ISO 13485, ISO 10993, ISO 14971,IEC 62366, FDA Design Controls, EU MDR
•Strong preference for those with product development experience within the medical device industry for items such as: Complex capital electrical/mechanical systems, software development and single-use disposables
•7+ years Quality System experience in medical device or other highly regulated/technical industry.
•5+ years’ experience in successfully leading projects or programs.
•Masters and/or MBA preferred.
•PMP Certification preferred.
•Design for Six Sigma (DFSS) training and/or Certification preferred.
•Ability to influence others.
•Strong analytical and problem solving skills.
•Demonstrated decision making skills.
•Ability to lead projects in a matrix structure.
•Ability to effectively communicate at all levels and across the organization.
•Good interpersonal skills.
•Performance Management Leadership and Coaching Skills.
•Good Presentation Skills.
•Good working knowledge of Word, Excel, Microsoft Project and PowerPoint.
•Must be able to handle multiple tasks/projects and manage priorities accordingly.
•Ability to manage through ambiguity.
•Experience with in-house/on-site manufacturing and working with Contract Manufacturers.
•Experience with medical device sterilization methods.
•Experience with the following standards/regulations: IEC 60601, ISO 13485, ISO 10993, ISO 14971,IEC 62366, FDA Design Controls, EU MDR
About Medtronic:
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life.
We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Day in the Life section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
