As a Global Clinical Supply Chain Leader (CSCL) you will be responsible for the clinical study supply chain of Investigational Medicinal Products (IMP) and have the technical expertise to collaboratively establish an effective, efficient, and cost conscious clinical supply chain. As a Global Clinical Supply Chain Leader you will play a variety of roles according to your experience, knowledge, and the general business/team requirements, such as: Demand and Supply Planning and inventory management... more details
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Genentech, a member of the Roche Group.
The Global Clinical Supply Chain Organization’s mission is to ensure that no patient goes without treatment and no clinical trial is delayed. Our vision is to enable an adaptive Supply Chain delivering innovative and sustainable clinical supply solutions anytime, anywhere, to anyone. As a part of our team, you will directly contribute to the success of Roche’s robust and diverse pipeline of biopharmaceuticals as our team is accountable for the Clinical Supply of more than 100 molecules in 600+ clinical trials across 7 disease areas. We believe our people are our greatest strength, and only by empowering and developing them will we realize Roche’s life-saving purpose!
The Opportunity
As a Global Clinical Supply Chain Leader (CSCL) you will be responsible for the clinical study supply chain of Investigational Medicinal Products (IMP) and have the technical expertise to collaboratively establish an effective, efficient, and cost conscious clinical supply chain.
As a Global Clinical Supply Chain Leader you will play a variety of roles according to your experience, knowledge, and the general business/team requirements, such as:
Demand and Supply Planning and inventory management in ERP system (i.e. SAP) for aggregate and long range IMP program planning
Ensuring alignment of key activities & timelines of cross-functional team to successfully set up and supply each clinical trial, including maintaining oversight on performance and issues to ensure study supplies are provided in line with the agreed scope of work and timelines
Forecast, plan, communicate, and initiate procurement of Other Study Drug / comparator drug as required
Consider and incorporate all regulatory & quality relevant requirements and changes for clinical trial material into supply plan
Ownership of various Clinical Supply Chain business processes and/or related systems; leading cross-functional teams as required driving business improvement, influencing change, and ensuring global process integration
You will work with the broader Demand and Supply Planning team as well as colleagues in other Clinical Supply Chain functions to deliver project and foundational work.
Who you are
Required Experience & Education:
5+ years of related experience in Clinical Supply Chain, Clinical Operations, Planning, Manufacturing, Quality, Regulatory, or other Supply Chain discipline, preferably in the Biotechnology / Pharmaceutical industry; minimum of 4 years with a Master’s Degree
Work experience in the GMP environment (e.g. pharmaceutical or food industry) or in equivalent supply chain functions
Experience in global supply chain or related project team environment
Preferred:
Your previous experience may include roles or responsibilities such as Clinical Supply Manager, Demand Planner, Supply Planner, Project Management, Global Sourcing Manager, and Supply Chain Analytics.
Academic degree or equivalent diploma, preferably in Life Sciences, Business (Economics, Operations Management, Supply Chain Management) or Engineering
ERP system experience, e.g. SAP, OMP or APO and IRT preferred
Experience in cross-functional / cross-cultural and agile organizational models and leadership styles is preferred
Supply chain certification is a plus (e.g. APICS, CPIM, CSCP)
Operational Excellence/Six Sigma/Lean training a plus
Relocation benefits are available for this job posting.
The expected salary range for this position based on the primary location of South San Francisco, CA is $117,600 to $218,400. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.
