Manager 3rd Party Plasma EU
takeda
Zurich, Switzerland
vor 4 Tg.

OBJECTIVES / PURPOSE

  • Ensure global adherence to Takeda standards for policies in scope
  • Managing sourcing of human plasma from external suppliers
  • Partner with various Takeda functions to identify and onboard new potential plasma sources
  • Cross-functional coordination across internal Takeda entities for plasma collection, testing, manufacturing, quality and regulatory
  • ACCOUNTABILITIES

  • Sourcing of human plasma in volumes & flavors according to business needs, while complying with quality requirements, applicable terms and prices
  • Identification of candidates for plasma cooperation; negotiations with existing and potential suppliers
  • Plasma supply contracts creation, management and maintenance
  • Cross-functional coordination across internal Takeda entities for plasma collection, testing, manufacturing, quality and regulatory Technical support for plasma suppliers implementation of Takeda’s technical requirements and following maintenance and control, settlement of complaints, dummy shipments, transferring of ideas and best practices
  • Observe the policies, legislation & regulatory requirements in Europe and other region countries regarding plasma
  • Support for QA Biolife EU necessary support regarding audits (appointments, translations) and Supplier Notice of Change process;
  • support of producers regarding achievement of compliance with Acceptance Criteria and GMP; basic control in plasma production facilities plasma storage conditions)

  • Plasma administration contribute to Plasma Master File-related documentation creation and update.
  • DIMENSIONS AND ASPECTS

    Technical / Functional (Line) Expertise

  • Experience in a highly regulated blood / plasma industry (min. 3 years)
  • Advanced presentation and communication skills
  • Advanced understanding of demand principles and strategies
  • Strong knowledge with Excel and PowerPoint
  • Knowledge on Good Manufacturing Practice (GMP)
  • Basic knowledge on regulations (FDA, EMA, etc.)
  • Leadership

  • Self-motivated
  • Strong communication skills (written and oral)
  • Business acumen
  • Negotiation skills
  • Teamwork & Collaboration
  • Ability to manage, prioritize and deliver on core responsibilities
  • Demonstrate strategic thinking in leading and developing the demand planning process
  • Focus on key areas and work collaboratively to ensure solutions in accordance with Takeda values
  • Decision-making and Autonomy

  • Comfortable making decisions with limited information
  • Ability to identify and resolve problems as they arise with moderate oversight
  • Ability to understand the risks and benefits surrounding decisions
  • Interaction

  • Customer ( plasma supplier) focus willing to help, respectful, prompt and accountable
  • Partners with Quality, Plasma Logistics, Plasma Laboratory, Biolife EU (incl. Sanaplasma), Manufacturing
  • Finance teams within BioLife
  • BioLife Functions in particular Operations, Quality and Logistics.
  • PDT and GMS OpU functional teams including Supply Chain leaders
  • Innovation

  • Familiar with current blood / plasma industry trends and developments
  • Open to new ideas
  • Embraces change
  • Continuous improvement.
  • Complexity

  • Ability to see the big picture and considers upstream and downstream impact of decisions
  • Ability to break down complex situations into manageable pieces
  • EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS :

  • Experience in a highly regulated blood / plasma industry (min. 3 years)
  • Master’s degree : Commercial education and / or education in natural sciences
  • Experience with Microsoft Word, Excel and PowerPoint
  • BA or Master’s Degree with a minimum 3 years of experience in life sciences (pharmaceutical, biologics, medical devices) / operations / manufacturing / product management.
  • Fluent in German, business English and further language beneficial.
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