Career Category
Supply ChainJob Description
Job Description
The Sr. Manager Supply Chain will be responsible for device supplier(s) and accountable for the device production/delivery, project timelines, deliverables prioritization, supplier strategy and setting supplier/Amgen goals annually. Staff will lead a cross-functional Supplier Relationship Engagement (SRE) team to ensure delivery of clinical and commercial supply, support device launches, and deliver supplier projects aligned to Amgen’s goals. The role requires networking across key Operations’ functions, FPT, Quality, Supply Chain, GSS, Finance, and Commercial to ensure all aspects of the device and supplier are carefully considered.
Responsibilities:
Actively manage and maintain excellent relationship and communication with supplier and internal partners.
Identify, establish and monitor key performance measures that will ensure supply and quality of our combination products.
Ensure supplier sites are monitored and corrective actions are implemented in a timely fashion.
Identify strategic objectives utilizing the SRE framework and partnering with the Executive Sponsor to drive shared strategic goals
Analyze, consolidate, and report demand and supply plans at the component / supplier level and provide supplier forecasts
Analyze company raw material inventory plans including inventory levels, scrap, inventory purchases, category spend and consumption and determine areas for improvement
Leverage and utilize Operational Excellence tools and resources to institutionalize continuous improvement mindset
Identify issues, escalate appropriately and work closely with key executives on resolution
Facilitate Operational and Executive reviews
Identify critical device subcomponents and understand the subcomponent supply chain to actively manage and mitigate risks
Develop and implement short and long range supply risk mitigation strategies (technical, supply, innovation, etc.)
Drive Continuous Improvement efforts between supply chains (I.e. Lead time reduction, flexibility, supplier responsiveness, forecast accuracy, on time delivery, etc.)
Domestic and International travel up to 20%
Basic Qualifications
- Doctorate degree and 2 years of experience OR
- Master’s degree and 4 years of experience OR
- Bachelor’s degree and 6 years of experience OR
- Associate’s degree and 10 years of experience OR
- High school diploma / GED and 12 years of experience
Preferred Qualifications
Experience in a regulated device and/or drug product environment
Experience in managing a supplier, CMO, third party in a regulated industry
Experience running biotech, pharma or deviceExtensive experience in the biotechnology/pharmaceutical industry including leadership roles (e.g. team or cross functional roles) in key Operations’ functions
Strong leadership skills (cross functional team leadership, executive presence)
Project management leading the development, approval milestone management and executive communications
Experience managing external suppliers
Device and/or combination product development, supply chain or manufacturing experience
GMP knowledge and background
Diverse assignments in Operations or supporting functions (Regulatory Affairs, Clinical Development, etc.)
Supplier negotiations and contract review experience
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