Veranex
About Veranex
Veranex’s mission as an Innovation CRO is to improve patient outcomes by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on MedTech, we take clients’ Vision to Velocity through our comprehensive service portfolio, with expertise in human-centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role Senior Mechanical Engineer
– Lead the design and development of complex electro‑mechanical medical devices. This role is integral to our product development lifecycle, from concept through validation and manufacturing transfer. The ideal candidate brings deep technical expertise, leadership capabilities, and a passion for innovation in the medical device space.
What You’ll Do
Lead the design and development of complex electro‑mechanical medical devices and equipment.
Generate expert‑level 3D and 2D CAD data.
Develop and integrate high‑functioning design prototypes with minimal guidance.
Execute prototype testing plans and ensure compliance with safety standards.
Provide leadership, training, and mentorship to junior engineers.
Direct internal resources and manage external development partners.
Act as mechanical engineering lead on product development programs.
Ensure compliance with FDA, QSR, and ISO regulations.
Participate in business development activities, including proposal review and client engagement.
Qualifications Required
Bachelor’s degree in Mechanical Engineering.
3–6 years of relevant work experience in medical device development.
Thorough knowledge of product development and strong understanding of the medical device industry.
Excellent written and oral communication skills.
Strong analytical and conceptual skills with the ability to build functional prototypes.
Ability to solve moderate to complex technical problems.
Exercises judgment in selecting methods and techniques for obtaining solutions.
Strong ability to manage multiple tasks and projects effectively.
Familiarity with FDA, QSR, and ISO standards.
Ability to work independently with minimal guidance.
Location:
Hybrid or office‑based in Providence, RI.
Preferred
Experience leading cross‑functional teams and managing external partners.
Prior involvement in business development or input to proposals.
Advanced CAD proficiency and rapid prototyping experience.
Participation in audits and inspections for medical device projects.
Referrals increase your chances of interviewing at Veranex by 2x.
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About This Role Senior Mechanical Engineer
– Lead the design and development of complex electro‑mechanical medical devices. This role is integral to our product development lifecycle, from concept through validation and manufacturing transfer. The ideal candidate brings deep technical expertise, leadership capabilities, and a passion for innovation in the medical device space.
What You’ll Do
Lead the design and development of complex electro‑mechanical medical devices and equipment.
Generate expert‑level 3D and 2D CAD data.
Develop and integrate high‑functioning design prototypes with minimal guidance.
Execute prototype testing plans and ensure compliance with safety standards.
Provide leadership, training, and mentorship to junior engineers.
Direct internal resources and manage external development partners.
Act as mechanical engineering lead on product development programs.
Ensure compliance with FDA, QSR, and ISO regulations.
Participate in business development activities, including proposal review and client engagement.
Qualifications Required
Bachelor’s degree in Mechanical Engineering.
3–6 years of relevant work experience in medical device development.
Thorough knowledge of product development and strong understanding of the medical device industry.
Excellent written and oral communication skills.
Strong analytical and conceptual skills with the ability to build functional prototypes.
Ability to solve moderate to complex technical problems.
Exercises judgment in selecting methods and techniques for obtaining solutions.
Strong ability to manage multiple tasks and projects effectively.
Familiarity with FDA, QSR, and ISO standards.
Ability to work independently with minimal guidance.
Location:
Hybrid or office‑based in Providence, RI.
Preferred
Experience leading cross‑functional teams and managing external partners.
Prior involvement in business development or input to proposals.
Advanced CAD proficiency and rapid prototyping experience.
Participation in audits and inspections for medical device projects.
Referrals increase your chances of interviewing at Veranex by 2x.
#J-18808-Ljbffr