huMannity Medtec

Senior Program Manager

Santa Clarita, CA, US

5 days ago
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Summary

At HuMannity Medtec, we pioneer life-enhancing medical technologies for under met healthcare needs. Come join our team of engineers, scientists and medical device experts who are inspired to develop innovative solutions for tomorrow’s challenges. If you’d like to join a high-reward, truly inspiring environment with an experienced, diverse team working at their best every day, and take your career to the next level, apply today!


We truly understand the need for balance and, among other things and offer a 9/80 schedule with every other Friday off. That’s 26 long weekends a year!


Overview: The Senior Program Manager is the cross-functional leader for moderate to complex medical device programs. Program teams will include mechanical, electrical, software and systems engineering resources as well as cross- functional partners from the manufacturing, clinical, quality, and regulatory groups. The Senior Program Manager will take each program from the concept phase through the development phase including pre-clinical studies.


Work with internal and external sources, including industry key opinion leaders, business, and customer stakeholders to define product objectives and requirements.


  • Prioritize requirements and define scope to meet market needs in a timely manner.
  • Develop, maintain, and distribute standard project management deliverables for the successful launch of new products and services. These include implementation plan, project schedule, project budget and variances, issues & action items reports, meeting minutes, risks assessment and contingencies.


Ideal attributes include:

  • Bachelors degree in a technical field, preferably Engineering or Physics. Advanced Degree preferred
  • Project Management Professional (PMP) certification preferred
  • Knowledge and experience with full product development life cycle including exit strategies
  • Successful track record working with Quality Systems and the FDA (or similar regulatory body)
  • Successful track record of innovation supported by issued patents, publications, and presentations
  • 7+ years of progressive functional experience in an engineering leadership capacity
  • 7+ years experience managing and/or directing R&D and product development efforts
  • 7+ years experience working in the medical device industry and/or related or similar high technology/regulated industry

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