Biosurgery R&D Lifecycle Intern - Lab Analytics

Johnson & Johnson Innovation; Raritan (NJ); On-site; USD 32,000 - 72,000; Full time

Benefits offered by this job

Medical benefits

Sick time benefits

Retirement plan

Job summary

Johnson & Johnson invites applications for the Biosurgery R&D Lifecycle Management Intern in Raritan, NJ. The role provides hands-on experience in laboratory testing, product documentation, and lifecycle management within a cross-functional medical device environment.

The internship runs May to August 2027, full-time (40 hours per week). It offers exposure to regulatory compliance, design history, and data-driven decision making in MedTech.

Qualifications

• Completion of Undergraduate Freshman year is required.
• Strong analytical and problem-solving skills.
• Interest in medical device development or lifecycle management.
• Excellent written and verbal communication skills.
• Experience with data analysis and laboratory environments is preferred.

Responsibilities

• Support the implementation and evaluation of laboratory test methods for device performance.
• Conduct experimental studies and analyze data to assess testing approaches and product attributes.
• Develop and document laboratory procedures and study results per quality systems.
• Review historical product and technical documentation to support lifecycle management.
• Collaborate with engineers to identify process and documentation improvements.
• Present project findings to technical stakeholders.

Skills

Analytical skills

Written and verbal communication

Data analysis experience

Laboratory experience

Minitab familiarity

Excel familiarity

Education

Undergraduate freshman year completed

Tools

Minitab

Excel

Job description

Johnson & Johnson invites applications for the Biosurgery R&D Lifecycle Management Intern in Raritan, NJ. The role provides hands-on experience in laboratory testing, product documentation, and lifecycle management within a cross-functional medical device environment.

The internship runs May to August 2027, full-time (40 hours per week). It offers exposure to regulatory compliance, design history, and data-driven decision making in MedTech.