Senior Engineer, Intra-Company Collaborations MedTech Surgery

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

Job Function:

R&D Product Development

Job Sub Function:

R&D Mechanical Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Cincinnati Ohio United States of America Raritan New Jersey United States of America

Job Description:

About Surgery

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of surgery Ready to join a team thats reimagining how we heal Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the worlds most prevalent conditions such as obesity cardiovascular disease and cancer. Patients are waiting.

Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for a Senior Engineer Intra-Company Collaborations to support our Surgery group. This preferred location for this role is Raritan NJ however the role may also be based in Cincinnati OH. This role will work a Flex/Hybrid schedule with 3 days per week on-site. Relocation assistance is not available for this role.

Purpose: The Senior Engineer Intra-Company Collaborations conducts research directed toward discovery and/or development on a large research and development project or several small projects with many complex features under minimal supervision using established and/or novel technologies. They provide hands-on work with instruction or supervision of others secondary to own technical work have basic knowledge in a specialized area that requires a grasp of involved practices and precedents coordinates project/process management and reporting and ensures relevant project timelines are met.

You will be responsible for:

• Lead multidisciplinary project teams in the design development testing and manufacturing of wound closure devices related products and other novel medical devices and be able to function as a team member as required.
• Play a hands-on role in conducting lab-based development activities analyze and interpret performance and analytical data to guide product and process optimization document research activities in accordance with design control requirements and conduct all required research activities associated with development of new materials components raw materials and processes for wound closure devices.
• Effectively apply state-of-the-art scientific technical acumen and technical leadership capabilities to conduct research toward design of new products as well as supporting and improving (lifecycle management of) existing product offerings.
• Provide technical expertise in terms of problem solving for technical and executional problems using advanced knowledge and experience. Contribute inventions new designs new processes and techniques to solve technical problems based on customer needs.
• Identify opportunities for design and process improvements to achieve business goals.
• Ensure project timelines and all required project milestones are met.
• Conducts or manages research analysis or processes within a larger R&D activity.
• May develop procedures and processes within broader protocols.
• May develop and implement standards for reporting and operations.
• May identity and implement process level efficiencies.
• Conduct research toward new product or process development or improvement of existing products or processes.
• Interact directly with customers (surgeons) to determine and identify unmet needs.
• Contribute inventions new designs new processes and techniques to solve technical problems based on customer needs.
• Uses analytical/technical expertise to contribute to product development/testing.
• Ensures that project guidelines are followed and processes are complete.
• Executes DOEs and tests materials per protocols.
• Prepare samples as required for manufacturing testing or other evaluations and data analysis.
• Writes SOPs JSAs (Safety) and other required documentation.
• Maintenance of notebooks and batch records in compliance with GLP/GMP
• Participate in process and product transfer to operations group
• May coordinate with outside vendors and academia
• Ensures activities are completed on time and comply with industry standards and regulatory requirements.
• Follows all company guidelines related to Health Safety and Environmental practices .
• May supervise or provide instruction to professional and technical employees.
• May be responsible for operating within a budget and may provide input on budget allocation and prioritization.
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for following all Company guidelines related to Health Safety and Environmental practices as applicable.
• For those who supervise or manage a staff responsible for ensuring that subordinates follow all Company guidelines related to Health Safety and Environmental practices and that all resources needed to do so are available and in good condition if applicable.
• Responsible for ensuring personal and Company compliance with all Federal State local and Company regulations policies and procedures.
• Performs other duties assigned as needed.

Qualifications / Requirements:

• Minimum of a Bachelors Degree is required Advanced Degree strongly preferred. Mechanical Engineering background highly desired.
• At least 5-7 years of related engineering experience required (3-5 with Advanced Degree); Medical Device engineering experience strongly preferred.
• CAD (Solidworks or Creo) required PLM (Windchill) strongly preferred.
• Ability to lead complex projects.
• Effective verbal communication (large and small groups); clear and concise written communication; decision-making without supervisory input; effective team interaction with personnel or other divisions and companies.
• Must deal with abstract and complex cause and effect relationships and make sound decisions often with limited data which impact product and facilities.
• Knowledge of and experience in applying scientific principles analytical techniques and judgment to independently resolve technical issues and establish new methods controls & procedures is required.
• Knowledge of chemistry and physics with demonstrated understanding of material characterization structure-property relationships formulation development and processing and utilization towards application development is preferred.
• Must be willing to work in a laboratory environment performing hands-on experiments and be able to clearly communicate findings (oral or written) to the project team.
• Broad knowledge of medical device product development and working knowledge of biocompatible materials and their application in medical devices including familiarity with regulations and requirements for the development of implantable medical devices is preferred.
• Ability to work with minimal supervision.
• Familiarization with material and process specifications.
• Good interpersonal skills effective oral and written communication skills.
• Proficient using Microsoft Office Software.
• Must be willing to work in a laboratory environment performing hands-on experiments and be able to clearly communicate findings (oral or written) to the project team.
• Travel: Up to 20% travel may be required.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please contact us via or contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

Required Skills:

Preferred Skills:

Analytical Reasoning Auto-CAD Design Business Case Modeling Coaching Design Thinking Mechanical Engineering Problem Solving Process Oriented Product Reliability Project Management Methodology (PMM) Project Support Quality Control (QC) Research and Development Resource Allocation SAP Product Lifecycle Management Technical Credibility Technologically Savvy

The anticipated base pay range for this position is :

$92000.00 - $148350.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire employees are eligible for the following time off benefits:

Vacation 120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado 48 hours per calendar year; for employees who reside in the State of Washington 56 hours per calendar year

Holiday pay including Floating Holidays 13 days per calendar year

Work Personal and Family Time - up to 40 hours per calendar year

Parental Leave 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave 80 hours in a 52-week rolling period10 days

Volunteer Leave 32 hours per calendar year

Military Spouse Time-Off 80 hours per calendar year

For additional general information on Company benefits please go to: Experience:

Senior IC