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Senior Principal Mechanical R&D Engineer

Kennesaw, Georgia Req ID JR-040388
Scientists wearing lab coats

Revvity | About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our diverse team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.

Find your future at Revvity.

We are seeking an experienced Senior Principal Mechanical R&D Engineer to lead our product development efforts for our homogenizer line. This key position will drive innovation and technical excellence in our life science devices.

ESSENTIAL ACCOUNTABILITIES:

  • Lead the mechanical design and development of new homogenizer products and improvements to existing lines

  • Manage R&D projects from concept to production, including prototyping and testing

  • Collaborate with cross-functional teams, including electrical engineering, manufacturing, and marketing

  • Develop technical specifications and design documentation

  • Analyze product performance and implement design improvements

  • Mentor junior engineers and provide technical leadership to the R&D team

  • Stay current with industry trends and emerging technologies in life sciences

Basic Qualifications:

  • Bachelor's Degree in Mechanical Engineering

  • 10+ years of experience in mechanical engineering, preferably in life science or medical device industries

Preferred Qualifications:

  • Master's Degree in Mechanical Engineering

  • Proven track record in product development, from concept to commercialization

  • Strong knowledge of 3D CAD software (preferably SolidWorks)

  • Experience with Design for Manufacturing (DFM) and Design for Assembly (DFA) principles

  • Excellent problem-solving and analytical skills

  • Strong leadership and communication abilities

  • Experience with FDA regulations and ISO 13485 standards is a plus

Apply Now