Sr. Project Leader

Job Detail

Job-ID 396048

Job-Beschreibung

Johnson & Johnson is currently seeking Sr. Project Leader join our TEAM. The role is based in Zuchwil.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 atAbout J&J MedTechAt Johnson & Johnson MedTech, we unleash diverse healthcare expertise, purposeful technology, and a passion for people to transform the future of medical intervention and empower everyone to live their best life possible. For more than a century, we have driven breakthrough scientific innovation to address unmet needs and reimagine health. In surgery, orthopedics, vision, and interventional solutions, we continue to help save lives and create a future where healthcare solutions are smarter, less invasive, and more personalized.OverviewOur Sr. Project Lead is responsible to lead projects, issues, strategic programs, and drive operational excellence between DePuy Synthes and our external manufacturing partners. This supply chain-based role will lead multi-functional teams to ensure that all projects relating to Patient Safety, Quality, Compliance, Service, Growth, and Value are executed to exceed business metrics. This exciting role will be responsible for creation of a project business case, developing transformational projects and ensuringKey Responsibilities

Lead/Execute projects in line with standard project management guidelines
Lead issues which relate to Reliability, Quality and Compliance improvements
Instill and maintain a sense of urgency and customer focus within the Supply Chain team in collaboration with external manufacturing partners
Successfully integrate and improve lifecycle management process to achieve wider business objectives to deliver successful performance metrics to meet the needs of our customers
Ensure that projects are performed in compliance with the Quality System and drives efforts to improve a culture of quality and compliance
Develop strong business partner relationships throughout the organization to drive alignment on strategic priorities
Develop in-depth understanding of various business processes, governances and supporting systems and the tools/templates used for project & portfolio management
Demonstrate strong project management skills, including accurate and effective project planning, creation of shared team goals, delivering project in line with established milestone dates, resource management, capital/expense management, developing and executing communication plans, leading resolution of risks & issues, risk management and balancing multiple activities to accomplish goals.

QualificationsEducation:

Minimum Bachelor’s degree required; Engineering, Science, or a related Field required
Master’s degree or higher in Engineering, Science, or a related Field is preferred
Project management methodology certification (e.g., PMP/PMI, FPX) is preferred

Required:

Minimum 6+ years of relevant work experience (4+ years of relevant experience with Master’s degree, 2+ years of relevant experience with Ph.D)
Work experience within the healthcare (i.e. Medical Technology or Pharmaceuticals) industry
Project Management experience, including developing and implementing processes for new or existing products/process and/or new technologies
Demonstrated ability applying project management methodologies and tools, resource management practices and organizational change techniques
Outstanding communication and interpersonal skills (written, presentation, meeting management, documentation) to effectively persuade and work across segments and functions at all levels of the organization

Preferred:

Supply Chain, Operations, and/or Manufacturing experience
Familiarity with such functions as R&D, Regulatory Affairs, and/or Quality
Medical Device industry experience is a plus
Knowledge of and experience in applying Six Sigma and Lean methodologies; certification is a plus

Other:

Minimum language required: English (mandatory)
Requires up to 10% domestic and international travel

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.Don’t miss this exceptional opportunity to join a world-class company and make a lasting impact. Apply now and be part of our ambitious team!