Product Development Program Manager

SPR Therapeutics

SPR Therapeutics

Product, Operations
Cleveland, OH, USA
Posted on Wednesday, September 15, 2021

Location: Cleveland, OH


  • Lead cross-functional core teams throughout the product development cycle, from concept to commercialization; help define program objectives to ensure on-time delivery of multi-generational product platforms.
  • Establish key metrics for New Product Development to improve visibility to internal stakeholders and establish confident time-to-market assessment, including budget planning, resource planning, and project financial metrics such as ROI, budget, COGS, and capital expenditures.
  • Create and proactively maintain schedules to champion delivery of on-time product launches; identify, mitigate, and proactively communicate risk while managing tradeoffs.
  • Develop and establish program management processes and best practices for a high-growth business.
  • Lead project meetings and facilitate cross-functional communication across R&D, new product development, manufacturing, purchasing, quality, regulatory, engineering, marketing, sales, clinical, external partners, and contract manufacturers; drive accountability throughout the organization.
  • Prepare and conduct regular reviews with key stakeholders, including senior leadership and executives; drive alignment with all levels of the organization on the objectives, risks, and needs for a program.
  • Champion the needs of the patient, provider, and business through an unwavering commitment to patient safety and product quality.


  • Bachelor’s degree in Engineering or related field.
  • 7+ years of progressive technical experience in R&D, Product Development, Engineering, or Quality within the medical device industry.
  • 3+ years of project management experience with electro-mechanical systems that include electrical, mechanical, firmware/software.
  • Excellent organizational, interpersonal, oral, and written communications skills.
  • PMP Certification or equivalent preferred.
  • Proficiency in MS Project or equivalent (SmartSheets preferred), MS Word, Excel, Visio, and PowerPoint.
  • Class II medical device experience required; Class III preferred.
  • Working knowledge of 21CFR820, ISO 13485, IEC 60601, IEC 62304 preferred.

Why Join Our Team?

  • Voted Top Workplaces
  • Competitive salary with company-paid medical, dental, and vision benefits
  • High growth company with game changing technology
  • A passion for improving the lives of millions of pain sufferers

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