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Johnson & Johnson

Principal Scientist, R&D – Orthopedics, Growth Factors

Johnson & Johnson

. Serve as the primary subject matter expert and technical point of contact for the CG BIO partnership .

Posted 9/15/2026full-timeWest Chester • Massachusetts • United StatesLead💰 $117,000 - $201,250 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Biomedical Engineering and advanced bone graft substitutes, with a strong focus on regulatory strategies and technical education for medical professionals. Proven ability to translate complex user needs into actionable specifications while leading cross-functional collaborations.

Highest-signal resume keywords
Ph.D. Or Master Of Science In Biomedical Engineering8+ Years R&D Or Technical Leadership ExperienceExpertise In Growth Factors And Osteoinductive MaterialsStrong Knowledge Of US Regulatory Landscape For BiologicsExperience In Spine Or Orthopedic Trauma Spaces

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Technical Point Of ContactProduct Lifecycle ManagementBiochemical And Biomechanical Data AnalysisRegulatory Submission SupportTechnical Training Module DevelopmentSurgical Workflow UnderstandingHandling Characteristics OptimizationPharmacokinetic Release Profile ImprovementCollagen Sponges And Synthetic Putties ExpertiseWhite Paper And Scientific Publication Authoring
Soft Skills
Technical CollaborationCustomer Feedback GatheringEducational Material DevelopmentEngagement With KOLs And SurgeonsPresentation Skills
Industry Keywords
Medical DeviceBiotechnologyPharmaceuticalsRegulatory LandscapeBiologicsCombination ProductsBLAPMA510(k)HCT/P

About the role

Key responsibilities & impact
  • Serve as the primary subject matter expert and technical point of contact for the CG BIO partnership
  • Lead technical activities and decisions between external R&D teams and internal DePuy Synthes teams
  • Support initial global launches and product lifecycle management
  • Optimize and improve Novosis formulations and procedural kits
  • Ensure handling characteristics, release kinetics, and bioactivity meet global spine and trauma market needs
  • Translate orthopedic and neurosurgeon user needs into actionable technical specifications
  • Lead brainstorming and technical collaborations to develop priority concepts
  • Develop pre-clinical, clinical, regulatory, and reimbursement strategies
  • Act as the primary subject matter expert on rhBMP-2 and advanced bone graft substitutes
  • Develop technical training modules and educational materials for global sales and marketing teams
  • Engage KOLs, spine surgeons, and trauma specialists through technical education and surgical training labs
  • Gather customer feedback and present at global technical conferences
  • Partner with Medical Affairs, HEMA, and Clinical teams on evidence generation strategies
  • Analyze biochemical and biomechanical data for marketing collateral
  • Author white papers, scientific publications, and technical reports

Requirements

What you’ll need
  • Advanced degree (Ph.D. or Master of Science) in Biomedical Engineering, Materials Science, Molecular Biology, or a closely related highly technical discipline
  • Minimum of 8 years of progressive R&D or technical leadership experience within the medical device, biotechnology, or pharmaceuticals sector
  • Documented expertise in growth factors and osteoinductive materials
  • Experience working directly within the spine or orthopedic trauma spaces
  • Understanding of surgical workflows, fusion criteria, and bone healing biology
  • Proven track record working with carrier materials, including collagen sponges, synthetic putties, and granules
  • Experience improving handling characteristics or pharmacokinetic release profiles
  • Demonstrated success educating and partnering with surgeons
  • Strong working knowledge of the US regulatory landscape for biologics and combination products, including BLA, PMA, 510(k), and HCT/P
  • Experience supporting regulatory submissions to the FDA

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
  • 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
  • Employee accommodation support for applicants with disabilities