Principal Scientist, Preclinical R&D - MedTech

Johnson & Johnson MedTech; Cincinnati (OH); On-site; USD 117,000 - 201,000; Full time

Benefits offered by this job

Vacation –120 hours per year

Sick time – 40 hours per year

Floating Holidays – 13 days per year

Parental Leave – 480 hours

Job summary

Johnson & Johnson MedTech in Cincinnati, OH or Raritan, NJ, is seeking a Principal Scientist, Preclinical R&D – MedTech on-site five days a week. You will lead non-clinical studies to support regulatory approval and clinical adoption, collaborating with cross-functional teams to ensure safety and efficacy from concept to design.

The role requires 8+ years in non-clinical research in medical devices or pharma, plus strong leadership and regulatory knowledge. Travel up to 20% may be required.

Qualifications

• Master’s degree in biomedical engineering or related field.
• 8+ years of non-clinical research experience.
• Experience with large animal models preferred.
• Knowledge of medical device regulations.

Responsibilities

• Represent Preclinical Research on project teams.
• Develop non-clinical strategy and testing plans.
• Oversee study execution per timelines.
• Manage external CROs and vendors for non-clinical studies.
• Ensure compliance with all regulations.

Skills

Leadership

Cross-functional teamwork

Communication skills

GCP knowledge

Education

Master’s in Biomedical Engineering

Doctorate preferred

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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

Discovery & Pre-Clinical/Clinical Development

Job Sub Function

Multi-Family Pre-Clinical Development – Medtech

Job Category

People Leader

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, we’re 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 that’s 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 world’s most prevalent conditions such as obesity, cardiovascular disease, and cancer. Patients are waiting.

Our business offers a broad range of products and technologies, including surgical staplers, clip appliers, trocars and sealing devices— that are used in a wide variety of minimally invasive and open surgical procedures.

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

Johnson & Johnson MedTech is currently recruiting for a Principal Scientist, Preclinical R&D – MedTech. The position can be located in Raritan, NJ or Cincinnati, OH. This position requires the candidate to work on site 5 days a week.

Purpose

The Principal Scientist/Project Leader in the Preclinical Research department will serve as a key scientific contributor for the development and execution of strategies for preclinical evidence, necessary to competitively position products for domestic and international regulatory approval and clinical adoption. The individual will independently design, execute, analyze and interpret non-clinical studies to understand the safety and efficacy of product conceptual to final designs. The individual will work closely with cross functional groups within and external to the Preclinical Research group to meet project objectives.

You Will Be Responsible For

• Serves as key team member, representing Preclinical Research on project core teams.
• Provides scientific input on the evaluation of physical safety and efficacy for technologies and products at all stages of the product life cycle.
• Responsible for partnering and contributing to the target product profiles, evidence generation strategies, and progression through the stage gate process.
• Responsible for creating the non-clinical strategy and testing plan, as well as overseeing study execution per project timelines.
• Assess, communicate, and manage the risks associated with the non-clinical evaluation of product concepts for projects to ensure success.
• Communicates progress and milestone status to preclinical leadership, R&D partners, and others.
• Participate in experiments to develop an understanding of customer unmet needs, potential misuse situations and to help interpret customer feedback to R&D team.
• Collaborate with industrial design and human factors group to create robust usability evaluations.
• Transfer of product development models and understanding to the Professional Education department, when needed.
• Surveys the literature to identify and conduct competitive product performance assessment and safety risks.
• Responsible for development of, and modifications to, preclinical models as needed to meet product requirements.
• Serves as the preclinical subject matter expert for projects at First in Human Committee consultations and reviews.
• Performs the role as designated Study Director for all types of non-clinical studies performed internally. As Study Director:
• Is accountable and responsible for Study Protocol and Animal Use Protocol generation and approval.
• Is accountable for procedural data collection, verification, and evaluation.
• Is accountable for the quality and compliance of their assigned studies.
• Is accountable and responsible for the Final Report generation and approval.
• Performs the role of Preclinical Sponsor Oversight for all types of non-clinical studies performed at outside vendors (e.g., at CROs)
• Identify external vendors, as needed, to execute non-clinical studies. Communicates to vendor management and contract group to initiate contract and audits, if necessary.
• Provides input and reviews for study protocols and reports from external non-clinical studies.
• Partner with members of the operations team to ensure external facilities meet JnJ standards for animal use and to generate contracts for vendors.
• Responsible for communicating business related issues or opportunities to next management level.
• 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 And Requirements

• A minimum of a Master’s degree in biomedical engineering or a related discipline is required. Doctorate degree in biomedical engineering or a related discipline or veterinary medicine is preferred.
• Previous experience working in a pre-clinical lab is required.
• Experience with large animal models is strongly preferred.
• 8+ years of experience in non-clinical research in a medical device or pharmaceutical industry setting is required.
• Knowledge of medical device regulations and regulatory and notified body requirements are required.
• Demonstrated ability to work cross functionally and influence a program direction is required.
• Business acumen and experience, including skills in budgeting, resource management, and staff development are required
• Excellent communication skills – written/oral/listening
• Ability to clearly document and communicate plans and results
• Lead and work effectively in a team-oriented environment that embraces ownership and accountability for innovation, change, risk, and flexibility.
• Up to 20% travel is required, mostly domestic but can also be international.

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 https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

Required Skills

Preferred Skills:

Compliance Risk, Cross-Functional Collaboration, Design Mindset, Developing Others, Drug Discovery Development, Execution Focus, Good Clinical Practice (GCP), Health Care Regulation, Human-Computer Relationships, Inclusive Leadership, Leadership, Medical Device Regulations, Medicines and Device Development and Regulation, Preclinical Research, Quality Control Testing, Research Ethics, Scientific Research, Team Management

The anticipated base pay range for this position is :

$117,000.00 - $201,250.00

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)).

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