Junior Supply Chain Analyst (100%) // Johnson & Johnson.

Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 120,000 people.

DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.

Main Responsibilities

The Supply Chain Analyst is responsible to analyse and support MDR Variant Supply Execution across TECA / Spine / Sports platforms, partner with cross-functional teams to ensure a smooth transition between variants. Main responsibilities include:

• Support the Eligibility Operations Team by analyzing data quality at the intersection of the regulatory and supply chain systems.
• Analyse data from multiple sources effectively track project performance versus plan and to identify risks.
• Support service issues during MDR Variant transition and drive to resolution.
• Establish proactive measures to identify relevant misconfigurations, mitigating potential supply disruptions.
• Perform ad-hoc analytics to drive day-to-day business efficiencies.
• Coordinate with Regional Planning, Supply Network Planning, Demand Requirements Planning and Regulatory Affairs to ensure MDR Variant supply execution.
• Support with the weekly/monthly cross functional team stand-up meetings, convey relevant information to broader teams and take lead to ensure timely resolution on actions assigned.
• Work closely with the Global/Regional Regulatory Affairs teams to avoid service risks associated with the MDR transition.
• Know and follow all policies, maintain the highest level of integrity, ethics, and compliance at all times.
• Support other duties and projects assigned as needed.