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Project Lead, Innovation & Partnerships, R&D MedTech
Johnson & Johnson. Lead focused, cross-functional JJMT teams executing parallel product development projects with Johnson & Johnson Innovative Medicine .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading cross-functional teams in medical device development, ensuring compliance with GMP, ISO, and MDD standards while effectively managing project timelines and costs. Proficient in communicating complex technical information to diverse stakeholders and driving product development from concept to market.
Highest-signal resume keywords
Medical Device DevelopmentProject Management ProficiencyGMP ComplianceCross-Functional Team LeadershipData-Driven Decision Making
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Product DesignManufacturing Process DesignMarket AnalysisRisk IdentificationTechnical Direction
Soft Skills
CollaborationCommunicationTeamworkProblem Solving
Tools & Technologies
SmartsheetMS Project
Certifications & Qualifications
PMP Certification
Industry Keywords
Combination ProductsMedical ManufacturingLifecycle ManagementPerformance AgreementsTechnical Challenges
Tech Stack
Tools & technologiesPMP
About the role
Key responsibilities & impact- Lead focused, cross-functional JJMT teams executing parallel product development projects with Johnson & Johnson Innovative Medicine
- Execute market and business analysis, product design or acquisition, manufacturing process design, manufacturing pilot, and product market launch activities
- Meet performance agreement requirements for time to market, cost of goods, development costs, quality standards, and market size forecasts
- Lead external and inter-company collaboration projects from assessment and intake through execution, launch, and transfer to lifecycle management
- Lead cross-functional development teams in executing objectives under approved performance agreements
- Drive technical direction and decisions while balancing technical rigor with business needs
- Resolve technical challenges, make data-driven decisions, and escalate issues when needed
- Influence and collaborate with internal and external stakeholders to gain alignment, resources, and support
- Identify risks early and develop mitigation strategies in a regulated environment
- Ensure compliance with GMP, ISO, MDD, and company policies and procedures
- Communicate complex technical information to non-technical stakeholders
- Transfer products and manufacturing processes from development to operations and marketing
- Capture and disseminate project knowledge to improve product development processes and systems
- Develop and refine project plans, schedules, and cross-functional responsibilities
- Communicate progress, opportunities, risks, and issues to management
- Re-evaluate project validity against intake assumptions
- Foster teamwork within and across groups
Requirements
What you’ll need- A bachelor’s degree in engineering is required
- 7+ years in medical device development, with experience in combination products or related fields, is required
- Proven record of accomplishment: direct association with or leading efforts to deliver technically complex products from concept to market is required
- Project management proficiency, including PMP or similar certification, is required
- Proficiency with project management tools such as Smartsheet and MS Project is required
- Willingness to travel approximately 10%
- Experience in medical manufacturing is desirable
- A master’s or Ph.D. in biomedical engineering, mechanical engineering, electrical engineering, or a related field is strongly preferred
Benefits
Comp & perks- Retirement plan (pension)
- Savings plan (401(k))
- 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
- Inclusive interview process and disability accommodations