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Senior Scientist, Biomaterials R&D
Johnson & Johnson. Support development of new biomaterials technologies and in-market products through their product life cycle .
Posted 10/16/2026full-timeWarsaw • Pennsylvania • United StatesSenior💰 $109,000 - $174,800 per yearWebsite
Tech Stack
Tools & technologiesAssembly
About the role
Key responsibilities & impact- Support development of new biomaterials technologies and in-market products through their product life cycle
- Perform prototyping and testing of innovative materials technologies
- Develop new test methods and manufacturing processes
- Support regulatory submissions
- Provide technical expertise in materials science, chemistry, and test methods
- Support design and development of complex medical devices and projects through all product life-cycle phases
- Organize, plan, execute, and oversee development of new biomaterials technologies
- Support product development, regulatory filing, product launch, and commercialization
- Act as a subject matter expert in biomaterials science and chemical test methods
- Participate as a technical team member on cross-functional project core teams
- Coordinate with design engineering, marketing, quality, supply chain, manufacturing, regulatory affairs, and other departments
- Develop testing protocols using laboratory instruments and standard or custom methods
- Perform or coordinate laboratory tasks safely in analytical, chemical, or biological R&D labs
- Develop and execute design verification and validation plans and test activities
- Support development of intellectual property for novel designs or technologies
- Collaborate with supply chain, manufacturing engineering, and suppliers to optimize designs for manufacturability and assembly
- Design and execute or coordinate scientific experiments; present analyzed data and conclusions; write technical reports
- Apply statistical methods for test method development and verification and validation
- Follow the New Product Development process and maintain high-quality design validation and verification
- Provide input on budget allocation and prioritization when responsible for a budget
- Perform quality/compliance activities supporting audits, remediation projects, non-conformances, and regulatory compliance projects
- Communicate business-related issues or opportunities to the next management level
- Follow Health, Safety and Environmental practices and applicable regulations, policies, and procedures
- Perform other assigned duties as needed
Requirements
What you’ll need- 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
- Experience in medical device regulations, including GMP, QSR, and ISO quality requirements is preferred
- Depth of knowledge of biomaterial technologies and chemical test methods required
- Strong communication skills required
- Ability to work effectively as a technical leader and sometimes as a project leader
- Strong organizational skills supporting scope definition, budgeting, and contingency planning
- Excellent problem solving, decision-making, root cause analysis, interpersonal, and conflict resolution skills required
- Strong initiative and follow-through in executing project responsibilities and balancing multiple priorities
- Ability to communicate concepts, ideas, and knowledge to individuals, Health Care Professionals, customers, and teams
- Ability to review and critically assess patents and other intellectual property is preferred
- Proficiency utilizing the MS Office Suite (Word, Excel, PowerPoint, etc.) required
Benefits
Comp & perks- Consolidated retirement plan (pension)
- Savings plan (401(k))
- Long-term incentive program
- Vacation – 120 hours per calendar year
- Sick time – 40 hours per calendar year; 48 hours for employees residing in Colorado; 56 hours for employees residing in Washington
- 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 period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year