Johnson & Johnson Posted August 27, 2026

Sr Principal Clinical Engineer

Raynham, United States Full time
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Johnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

R&D Product Development

Job Sub Function:

Industrial Design & Human Factors

Job Category:

Scientific/Technology

All Job Posting Locations:

Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America

Job Description:

About Orthopaedics

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

Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for Sr Principal Clinical Engineer to be based out of Warsaw, IN and Raynham MA and Leeds, United Kingdom.

Purpose:

The Clinical Engineer will act as a Procedural Workflow Architect to define and shape end-to-end surgical procedure workflows across preoperative, intraoperative, and postoperative care. This role translates clinical, operational, economic, usability, and adoption needs into integrated procedural requirements that guide implant, instrument, enabling technology, digital, biologic, and service development. By connecting real-world surgical practice with cross-functional product development, the role helps ensure future solutions are intuitive, adoptable, clinically meaningful, economically relevant, and differentiated in the marketplace.

Job Responsibilities:

Define and design end-to-end integrated procedural workflows for prioritized surgical procedures across - preoperative planning, intraoperative execution, and postoperative follow-up including implants, instruments, technologies, digital applications, biologics, and services.

Translate surgeon, care team, patient, health system, commercial, clinical, operational, economic, usability, and adoption needs into procedural requirements, user needs, use scenarios, design inputs, and development guidance.

Map current- and future-state workflows to identify unmet needs, adoption barriers, usability challenges, economic pain points, and opportunities for meaningful differentiation.

Partner with R&D, clinical, medical education, regulatory, quality, marketing, commercial, and external clinical stakeholders to align workflow priorities, solution intent, and integrated procedural requirements.

Evaluate concepts for usability, workflow fit, clinical relevance, adoption risk, and end-user value to prioritize procedural problems and guide clinical, technical, operational, and business tradeoffs to improve efficiency, consistency, usability, and adoption.

Translate procedural needs and complex inputs into requirements, recommendations, and development guidance.

Qualifications

Required

Bachelor’s degree in engineering, biomedical engineering, life sciences, clinical discipline, health care administration, or related field required; advanced degree preferred.

Minimum 8 years of relevant experience in medical device, orthopaedics, surgical innovation, product development, clinical workflow design, human factors, systems engineering, or related health care technology environment.

Proficiency with Adobe Illustrator, Photoshop, InDesign, Figma, Miro, FigJam, Polarion native; experience with 3D visualization, CAD, KeyShot, Rhino, SolidWorks, NX or rapid prototyping methods is a plus.

Strong communication, facilitation, and stakeholder alignment skills; able to influence without authority in a matrixed environment.

Lead ambiguous, early-stage problem framing and convert insights into structured development priorities.

Familiarity with medical device development, design controls, risk management, and regulated product development.

Competencies

Visual storytelling and storyboard development

Industrial design and human-centered design methodology

Workflow mapping, journey mapping, and process visualization

Concept sketching, ideation, and rapid visual prototyping

Design communication for complex hardware, software, and procedural systems

Cross-functional collaboration and stakeholder facilitation

Ability to connect and translate user needs, clinical context, and design direction

Presentation development and executive-ready communication

Other Requirements

Will require travel to R&D sites, labs, surgeon engagement sessions, customer research activities, or project workshops.

Must comply with all applicable company policies, procedures, quality expectations, confidentiality requirements, and regulatory standards.

Role may be aligned to front-end innovation, systems engineering, human factors, or product development depending on organizational structure and project needs.

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

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, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Analytical Reasoning, Concept Testing, Consulting, Customer Intelligence, Design Mindset, Human Factor Engineering, Industry Analysis, Performance Measurement, Product Design, Product Improvements, Product Portfolio Management, Product Strategies, Research and Development, Research Documents, Risk Management, SAP Product Lifecycle Management, Standard Operating Procedure (SOP), Tactical Planning, Technical Credibility, User Research

The anticipated base pay range for this position is :

$137,000.00 - $235,750.00

Additional Description for Pay Transparency:

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

This position is eligible to participate in the Company’s long-term incentive program.

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: - https://www.careers.jnj.com/employee-benefits

Job details

Seniority
Principal
Function
Clinical Development
Therapeutic area
Not listed
Location
Raynham, United States
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 295 comparable Principal Clinical Development roles across 54 biopharma companies.

295Comparable roles tracked
286Currently active
54Companies hiring similar roles
21Countries represented

Salary context

119 of 295 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $137,000/yr – $235,750/yr
Peer group range $0 – $392,100 (median $257,050)

Where these roles are based

Top locations among the 295 comparable roles

United States186
India45
United Kingdom14
Spain9
Switzerland7
Germany5

+ 15 more countries

Seniority mix

295 of 295 peers have a known seniority level

Director183
Senior92
Principal20

Therapeutic area mix

72 of 295 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology37
Neuroscience15
Immunology6
Cardiovascular / CVRM5
Ophthalmology4
Dermatology & Aesthetics3
Respiratory1
Rare Disease1

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.