Product Development Lead

About the role

Phillips Medisize, a Molex company, is seeking a Product Development Lead for Medical and Drug Delivery Devices to join our team at our Hudson, WI site. In this role, you will spearhead the design, development and launch for cutting-edge medical device and drug delivery solutions. This role offers the opportunity to guide technical direction, oversee system architecture and ensure compliance with industry standards, while working closely with customers and cross-functional teams.

At Phillips Medisize, we aspire to be the preferred partner of choice for leading global customers, to create innovative products that help people around the world live healthier, more productive lives. We are an end-to-end provider of innovation, development, and manufacturing solutions to the medical, regulated products, automotive, consumer and defense markets. As a contract design and manufacturing organization (CDMO), we work closely with our customers to deliver proven, highly engineered products.

Responsibilities

• Lead the technical direction and execution of medical device and drug delivery projects from concept through launch.
• Collaborate with customers and cross-functional teams (R&D, Quality, Regulatory, Manufacturing) to ensure seamless product development and compliance with FDA, ISO 13485, IEC 60601, and related standards.
• Oversee system architecture, design specifications, risk management, and verification/validation plans, while managing and mentoring engineering teams to foster innovation and technical excellence.
• Drive technical decision-making, risk mitigation, and documentation (DHF, DMR, technical files).
• Lead root cause analysis and support CAPA for device issues.
• Stay current on emerging technologies and regulatory changes.
• Communicate project status and challenges to internal and external stakeholders.
• Guide system-level integration across technical domains (mechanics, electronics/software, molding/assembly, usability, etc.), and define development strategy with strong engineering and data traceability, especially in customer-driven programs.

Requirements

• Bachelor’s Degree or higher in Biomedical, Electrical, Mechanical, or Biological Engineering.
• 5+ years’ experience in medical device design/development, with 3+ years in technical leadership.
• Experience with FDA Class II/III devices, design controls, risk management (ISO 14971), and validation.
• Familiarity with FDA 21 CFR Part 820, ISO 13485, IEC 62304, IEC 60601.
• Experience supporting development of regulatory submission documentation packages.
• Experience working with multiple, diverse quality management systems.

Qualifications

• Experience in Drug Delivery, MedTech or Diagnostics.
• Strong leadership experience facilitating risk-based decision-making.
• Excellent project management, communication, and problem-solving skills across complex team and project structures.

Benefits

• Medical, dental, vision
• Flexible spending and health savings accounts
• Life insurance, accidental death & dismemberment (ADD), disability
• Retirement plan
• Paid vacation/time off
• Educational assistance
• May also include infertility assistance, paid parental leave, and adoption assistance

Specific eligibility criteria is set by the applicable Summary Plan Description, policy or guideline and benefits may vary by geographic region.

Additional information

This position does not qualify for VISA sponsorship.