Sr Scientist, Biomaterials R&D

Brighter Signals; West Chester (Chester County); Vor Ort; USD 109.000 - 175.000; Vollzeit

Benefits dieser Stelle

Vacation - 120 hours/year

Sick time - 40 hours/year

Holiday pay

Zusammenfassung

Johnson & Johnson’s Orthopaedics team is recruiting a Senior Scientist, Biomaterials R&D, to advance new biomaterials technologies and support in-market products through the lifecycle. Location can be Warsaw, IN or West Chester, PA.

The role requires leading experimental work, developing test methods, and collaborating across functions to drive design verification and regulatory submissions. Strong background in chemistry and materials science is essential.

Qualifikationen

• Minimum of six years in development or testing of biomaterials-based medical devices or combination products.
• MS degree in Chemistry, Materials Science, Biomedical Engineering, or equivalent; PhD preferred.
• Experience with GMP, QSR, and ISO quality requirements is preferred.
• Strong knowledge of biomaterial technologies and chemical test methods required.
• Excellent communication skills for upper management and cross‑functional teams.
• Ability to lead as a technical and project leader and manage priorities.

Aufgaben

• Act as SME in biomaterials science and chemical test methods.
• Be a technical member of a cross‑functional project core team.
• Coordinate with design, marketing, quality, supply chain, and regulatory to test new technologies.
• Develop testing protocols using laboratory instruments and standard or custom methods.
• Perform laboratory tasks safely in analytical, chemical, or biological labs.
• Develop and execute design verification/validation plans for regulatory strategy.
• Contribute to IP development for new designs or technologies.
• Collaborate with suppliers to optimize designs for manufacturability and prototypes.
• Design and execute experiments, present data with analysis, and write reports.
• Apply statistical methods for test method development and verification/validation.
• Follow New Product Development process and ensure high-quality design verifications.
• Potential budget responsibility and input on allocation/prioritization.
• Support audits, remediation projects, and regulatory compliance activities.
• Participate in the company's compliance program as required.

Kenntnisse

Biomaterials science

Chemical test methods

Project leadership

Data analysis

Regulatory knowledge

Ausbildung

MS in Chemistry

MS in Materials Science

MS in Biomedical Engineering

PhD preferred

Tools

Laboratory instruments

MS Office Suite

Jobbeschreibung

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.

All Job Posting Locations

Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America

Job Function

Discovery & Pre-Clinical/Clinical Development

Job Sub Function

Chemical Research

Job Category

Scientific/Technology

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

DePuy Synthes is recruiting for a Senior Scientist, Biomaterials R&D, located in Warsaw, IN or West Chester, PA.

Purpose

This role is for a Materials Scientist or Chemist to support the development of new biomaterials technologies and/or support in-market products through their product life-cycle within multiple cross‑functional project teams. The Scientist performs prototyping and testing of innovative materials technologies, develops new test methods and manufacturing processes, and supports regulatory submissions. This includes communication with other R&D Scientists and Engineers, Marketing and Sales consultants, and customers e.g., Health Care Professionals. The Senior R&D Scientist will be an integral resource to the R&D team, providing technical expertise on materials science, chemistry, and test methods.

Job Responsibilities

• Act as a subject matter expert in biomaterials science and chemical test methods.
• Act as a technical team member of a cross‑functional project core team (marketing, manufacturing, quality, testing, supply chain, regulatory, etc.).
• Coordinate with design engineers, marketing, quality, supply chain, manufacturing, regulatory affairs, and other functional departments to develop and test new technologies and product concepts.
• Independently develop testing protocols using laboratory instruments, following standard methods or designing custom methods.
• Perform and or coordinate laboratory tasks in a safe manner in analytical, chemical, or biological R&D labs.
• Develop and execute design verification and validation plans and activities, and test plan formation and execution to support global regulatory strategy.
• Support development of intellectual property for novel designs or technologies.
• Collaborate with supply chain, manufacturing engineering and/or suppliers to optimize designs for manufacturability and assembly to produce functioning prototypes and supporting production documentation.
• Design and execute or coordinate scientific experiments, present data and conclusions with appropriate analysis and write technical reports.
• Demonstrate proficiency in the application of statistical methods for test method development and verification and validation activities
• Understand and follow the New Product Development process accurately and maintains high quality design validation and verifications.
• May be responsible for operating within a budget and provide input on budget allocation and prioritization.
• Perform quality/compliance activities in support of audits, remediation projects, non-conformances, regulatory compliance projects.
• Diligently participate in our compliance program‑related activities as denoted by your supervisor or our Chief Compliance Officer.
• 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.
• 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/Requirement

• A minimum of six years of experience in the development or testing of biomaterials based medical devices or combination products.
• MS in Chemistry, Materials Science, Biomedical Engineering, or equivalent required. A PhD degree is preferred.
• Experience working in medical device regulations, including GMP (Good Manufacturing Practices), QSR (Quality Systems Regulations) and ISO (International Organization for Standardization) quality requirements is preferred.
• A depth of knowledge of biomaterial technologies and chemical test methods is required
• Strong communication skills - The ability to effectively communicate concepts, ideas and knowledge to upper management, other individuals, customers, e.g., Health Care Professionals and/or teams across the organization is required.
• Ability to work effectively as a technical leader and sometimes as a project leader.
• Possess strong organizational skills to support all aspects of the project management functions including scope definition, budgeting, and contingency planning.
• Excellent problem solving, decision-making, and root cause analysis skills in addition to interpersonal skills that foster conflict resolution as it relates to technical situations is required.
• Must demonstrate a strong initiative and follow through in executing project responsibilities, overcoming obstacles and balancing multiple priorities effectively through strong technical and/or project leadership experience.
• Must have the ability to effectively communicate concepts, ideas and knowledge to other individuals, Health Care Professionals, customers and/ or teams, and work effectively as a technical leader and sometimes as a project leader.
• The ability to review and critically assess patents and other forms of intellectual property is preferred.
• Proficiency utilizing the MS Office Suite (Word, Excel, PowerPoint, etc.) is required.

Preferred Skills

Chemistry, Collaboration, Critical Thinking, Data Quality, Drug Discovery Development, Emerging Technologies, Execution Focus, Industry Analysis, Innovation, Interdisciplinary Work, Pharmaceutical Trends, Pharmacognosy, Pharmacology, Quantitative Research, Research Ethics, Scientific Research, Technologically Savvy

The anticipated base pay range for this position is :

$109,000.00 - $174,800.00

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.

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