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Associate Director: Clinical Supply Chain- Logistics and Vendor Management

Amgen

Thousand Oaks, CA; Breda, North Brabant, NetherlandsHybridPosted 15 days ago$161,560.35 - $218,581.65/year
Full TimeDirector & AboveOperations & Supply ChainPharmaceutical
Original posting ↗

Summary

In this vital role you will manage the global Logistics and Vendor Management team in Development Supply Chain. You will ensure clinical trial supplies move safely, compliantly, and reliably through a global logistics network, while building strong vendor partnerships and developing your team.

Job description

Responsibilities

  • Ensure set-up and successful operation of logistics network and logistics toolbox in assigned regions for execution of clinical trials
  • Determine distribution strategy and ensure the transportation process and vendor performance comply with Amgen quality requirements and local and regional regulations
  • Own relationships with key strategic vendors and develop the relationship in line with business needs. Drive value creation.
  • Establish effective working relationships with key partners and represents DSC in Amgen networks and cross-functional projects
  • Accountable for significant distribution budget
  • Guided by general policies and management guidance, independently determines strategy and day-to-day execution and manages assigned budget
  • Accomplishes results through coaching and advising professional team members. Is responsible for staff development and ensures team members receive the appropriate and timely training, allocates resources.
  • Owns logistics vendor portfolio and drives continuous value creation.
  • Contributes to crafting DSC strategy, long- and mid-term implementation plans and goals. Translates these into actionable departmental and individual goals.
  • Applies the MAP philosophy, defines individual goals, tracks progress of team members on projects and goals, provides feedback, prepares and performs individual performance reviews
  • Is accountable for monitoring the of the logistics network and vendor performance using appropriate key performance indicators.
  • Ensures that all processes are performed in a timely, compliant and efficient manner.
  • Ensures that processes are set-up and executed in compliance with existing regulations: GMP. GDP, Annex 13 etc.
  • Provides guidance and technical advice and becomes actively involved as required.
  • Seeks continuous improvement of processes & procedures, initiates and coordinates improvement initiatives.
  • Works closely with peers, partners and global counterparts to achieve global alignment
  • Manages the relevant interfaces between the internal and external functional groups involved in the development supply chain at various management levels
  • Support the development and execution of the clinical logistics technology roadmap, partnering with internal Digital, Technology & Innovation (DTI teams), Data Sciences and external service providers to align technology capabilities with business needs.
  • Monitors the level of satisfaction from the customers and takes appropriate action when necessary.
  • Represents the team/ department in cross-functional/ cross-site networks and projects
  • Owns and drives execution of key projects related to process improvement, new capabilities/ process requirements and other projects as assigned
  • Represents the DSC team in internal and external audits and inspections
  • Effectively manages and reports out on distribution budget and continuously seeks efficiency opportunities.
  • Willing to travel (up to 5-10% of time)

Basic Qualifications

  • Doctorate degree and 3 years of supply chain industry experience OR Master’s degree and 7 years of supply chain industry experience OR Bachelor’s degree and 9 years of supply chain industry experience OR Associate’s degree and 12 years of supply chain industry experience OR High school diploma / GED and 14 years of supply chain industry experience
  • In addition to meeting at least one of the above requirements, you must have a minimum of 3 years’ experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced above

Preferred Qualifications

  • Bachelors or Masters degree or equivalent in logistics/ Supply Chain, business administration or life science.
  • At least 6 year’s relevant working experience, preferably in the biotechnology or pharmaceutical industry, with a strong knowledge of supply chain management, logistics principles, international trade principles and clinical development principles.
  • At least 3 years of supervisory experience of Bachelor/Master level staff in a (project) management environment and in an international and regulated environment
  • Subject-matter expert knowledge of transportation, vendor management and temperature-controlled logistics
  • Working knowledge and understanding of GMP regulations, advanced understanding of GDP (Good Distribution Practices) guidelines and SOX regulations
  • Operational Excellence/ continuous improvement expertise.
  • General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
  • Experience in working in an international environment
  • Fluency in English, both in oral and written communication
  • Advanced experience in MS Office applications
  • Experience in using ERP systems, preferably SAP
  • Leadership curriculum certification
  • Project Management certification (PMP, IPMA)
  • APICS certification

Key Competencies

  • Strong coaching and management skills
  • Strong communication, presentation and facilitation skills
  • Effective influencing and leadership skills.
  • Sound relationship management and organizational skills
  • Skilled negotiator, understanding of resource management
  • Results- and process- oriented, strong adherence to timelines
  • Ability to handle multiple responsibilities and priorities simultaneously in a fluid environment with time pressures.
  • Initiator with analytical, problem solving and decision making skills
  • Ability to operate in a team or matrix environment
  • Self-leadership & motivation
  • Thinks strategically, has a general understanding of company priorities and direction and translates these into actionable plans
  • Team player in cross-functional and international setting
  • Provides guidance in the design and implementation of organization-wide projects and systems
  • Considers financial implications of decisions and sets priorities to meet business needs
  • Able to distill complex information into a logical concise manner for senior management
  • Experience in dealing in changing and ambiguous environment
  • Able to act on operational, tactical and strategic level
  • Role model for Amgen’s values and Leadership Attributes

Requirements

  • Doctorate degree and 3 years of supply chain industry experience OR Master’s degree and 7 years of supply chain industry experience OR Bachelor’s degree and 9 years of supply chain industry experience OR Associate’s degree and 12 years of supply chain industry experience OR High school diploma / GED and 14 years of supply chain industry experience
  • Minimum of 3 years’ experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
  • Bachelors or Masters degree or equivalent in logistics/ Supply Chain, business administration or life science
  • At least 6 year’s relevant working experience, preferably in the biotechnology or pharmaceutical industry
  • Strong knowledge of supply chain management, logistics principles, international trade principles and clinical development principles
  • At least 3 years of supervisory experience of Bachelor/Master level staff in a (project) management environment and in an international and regulated environment
  • Subject-matter expert knowledge of transportation, vendor management and temperature-controlled logistics
  • Working knowledge and understanding of GMP regulations, advanced understanding of GDP (Good Distribution Practices) guidelines and SOX regulations
  • Operational Excellence/ continuous improvement expertise
  • General understanding of regulatory guidelines impacting clinical supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive)
  • Experience in working in an international environment
  • Fluency in English, both in oral and written communication
  • Advanced experience in MS Office applications
  • Experience in using ERP systems, preferably SAP
  • Leadership curriculum certification
  • Project Management certification (PMP, IPMA)
  • APICS certification
  • Strong coaching and management skills
  • Strong communication, presentation and facilitation skills
  • Effective influencing and leadership skills
  • Sound relationship management and organizational skills
  • Skilled negotiator, understanding of resource management
  • Results- and process- oriented, strong adherence to timelines
  • Ability to handle multiple responsibilities and priorities simultaneously in a fluid environment with time pressures
  • Initiator with analytical, problem solving and decision making skills
  • Ability to operate in a team or matrix environment
  • Self-leadership & motivation
  • Thinks strategically, has a general understanding of company priorities and direction and translates these into actionable plans
  • Team player in cross-functional and international setting
  • Provides guidance in the design and implementation of organization-wide projects and systems
  • Considers financial implications of decisions and sets priorities to meet business needs
  • Able to distill complex information into a logical concise manner for senior management
  • Experience in dealing in changing and ambiguous environment
  • Able to act on operational, tactical and strategic level
  • Role model for Amgen’s values and Leadership Attributes

Benefits

  • Retirement and Savings Plan
  • Medical, Dental & Vision
  • Life and Disability Insurance
  • Flexible Spending Accounts
  • Discretionary Annual Bonus
  • Stock-based Long-term Incentives
  • Paid Time-off
  • Flexible Work Models

Company overview

Amgen Inc. is a leading American multinational biopharmaceutical company headquartered in Thousand Oaks, California, founded in 1980. As one of the world's largest independent biotechnology companies, Amgen specializes in discovering, developing, manufacturing, and delivering innovative human therapeutics. The company focuses on six key therapeutic areas: inflammation, oncology/hematology, bone health, cardiovascular disease, nephrology, and neuroscience. Amgen's portfolio includes blockbuster drugs such as Enbrel for autoimmune diseases, Prolia and XGEVA for osteoporosis, Repatha for cholesterol management, Otezla for psoriasis, and Neulasta for chemotherapy-induced neutropenia. With approximately 28,000 employees worldwide, Amgen operates as a component of both the Dow Jones Industrial Average and Nasdaq-100 indices. The company maintains a robust research and development pipeline with numerous clinical programs across various stages, leveraging cutting-edge biotechnology and human genetic data to address some of the world's most challenging diseases. Amgen's manufacturing capabilities span multiple global locations, and it distributes products through pharmaceutical wholesale distributors and direct-to-consumer channels.

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