Mentor Worldwide LLC, a member of Johnson Johnson’s Family of Companies, is recruiting for aSenior Engineer, RDlocated inIrving, Texas or Raritan, NJ.

Mentor Worldwide LLC is a leading supplier of medical products for the global aesthetic market. The company develops, manufactures, and markets innovative, science-based products for surgical medical procedures that allow patients to improve their quality of life through breast, body and facial aesthetics. Learn more about Mentor at www.mentorwwllc.com

The Senior Engineer, RD will have the responsibility of leading and contributing to various cross-functional multidisciplinary project teams, such as RD, manufacturing, marketing, and regulatory and will work on designing, developing and manufacturing of Mentor products - Breast Implants, Tissue Expanders, and other related products.

Responsibilities/Duties

Lead conceptualization, design and development of new devices or elements of new devices with the intent of commercialization per Quality System RequirementsContribute to design/development of product line extensions and product improvementsHelp lead design, development, execution and analysis of results of system, device, component and material tests per laboratory best practicesAccurately and efficiently translate user and patient needs through design requirements, design specifications and into verified/validated devices and proceduresLead verification and validation activities through regulatory clearance and design transferContribute strongly in the generation of intellectual propertyCollaborate with external (e.g., clinicians) and internal customers (e.g., strategic marketing) to identify user needs and validate device and procedure designsCollaborate with clinical, regulatory, quality, manufacturing, etc., to ensure development of innovative and reliable devices that fulfill clinical needs within regulatory requirementsHelp manage development partners and other external vendors to meet project requirements and timelinesCoordinate and execute technical and peer reviews; may also include coordination and execution of design reviewsMay involve direct or indirect supervision of engineers and/or techniciansOther responsibilities as required or assigned by manager

Mentor Worldwide LLC, a member of Johnson Johnson’s Family of Companies, is recruiting for aSenior Engineer, RDlocated inIrving, Texas or Raritan, NJ.

Mentor Worldwide LLC is a leading supplier of medical products for the global aesthetic market. The company develops, manufactures, and markets innovative, science-based products for surgical medical procedures that allow patients to improve their quality of life through breast, body and facial aesthetics. Learn more about Mentor at www.mentorwwllc.com

The Senior Engineer, RD will have the responsibility of leading and contributing to various cross-functional multidisciplinary project teams, such as RD, manufacturing, marketing, and regulatory and will work on designing, developing and manufacturing of Mentor products - Breast Implants, Tissue Expanders, and other related products.

Responsibilities/Duties

Lead conceptualization, design and development of new devices or elements of new devices with the intent of commercialization per Quality System RequirementsContribute to design/development of product line extensions and product improvementsHelp lead design, development, execution and analysis of results of system, device, component and material tests per laboratory best practicesAccurately and efficiently translate user and patient needs through design requirements, design specifications and into verified/validated devices and proceduresLead verification and validation activities through regulatory clearance and design transferContribute strongly in the generation of intellectual propertyCollaborate with external (e.g., clinicians) and internal customers (e.g., strategic marketing) to identify user needs and validate device and procedure designsCollaborate with clinical, regulatory, quality, manufacturing, etc., to ensure development of innovative and reliable devices that fulfill clinical needs within regulatory requirementsHelp manage development partners and other external vendors to meet project requirements and timelinesCoordinate and execute technical and peer reviews; may also include coordination and execution of design reviewsMay involve direct or indirect supervision of engineers and/or techniciansOther responsibilities as required or assigned by manager

Qualifications:

Required:

A minimum of a Bachelor’s degree in mechanical or biomedical engineering or related field, preferably mechanical engineeringAt least 4 years medical device industry experienceFamiliar with design control requirements Good written and verbal communication skills

Preferred:

5-10 years of experience in design, development, and commercialization of Class I-III medical devices, specifically electro-mechanical, disposable, minimally invasive, handheld surgical devicesProject Management ExperienceExperience in working with cross-functional teams.Familiar with GMP GLPDesigning with 3D CAD tools, including SolidWorks and rapid prototyping, including hands-on manual prototyping, SLA and FDM Experience in test method validationExperience in executing design verification and validation

Location Travel Requirements

Location - Irving TX / Raritan NJTravel - Less than 10% travel requiredOffice and lab environment Ability to move materials and light equipment (up to 10 pounds) as needed

At Johnson Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love.

Johnson Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

This job posting is anticipated to close on July 15, 2024. The Company may however extend this time-period, in which case the posting will remain available onhttps://www.careers.jnj.comto accept additional applications.

The anticipated base pay range for this position is $88,000- $141,450

Qualifications:

Required:

A minimum of a Bachelor’s degree in mechanical or biomedical engineering or related field, preferably mechanical engineeringAt least 4 years medical device industry experienceFamiliar with design control requirements Good written and verbal communication skills

Preferred:

5-10 years of experience in design, development, and commercialization of Class I-III medical devices, specifically electro-mechanical, disposable, minimally invasive, handheld surgical devicesProject Management ExperienceExperience in working with cross-functional teams.Familiar with GMP GLPDesigning with 3D CAD tools, including SolidWorks and rapid prototyping, including hands-on manual prototyping, SLA and FDM Experience in test method validationExperience in executing design verification and validation

Location Travel Requirements

Location - Irving TX / Raritan NJTravel - Less than 10% travel requiredOffice and lab environment Ability to move materials and light equipment (up to 10 pounds) as needed

At Johnson Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love.

Johnson Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

This job posting is anticipated to close on July 15, 2024. The Company may however extend this time-period, in which case the posting will remain available onhttps://www.careers.jnj.comto accept additional applications.

The anticipated base pay range for this position is $88,000- $141,450