Technical Product Manager Ssp Franchise - Barcelona, España - Centrient Pharmaceuticals Netherlands

Isabel García

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Isabel García

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Descripción
The Position


As a Technical Product Manager (M/F/d) you will be forming part of the Corporate - API Commercial (SSP Franchise) department reporting directly to Global Franchise Director SSP & PEN.

You will be responsible for product development for assigned APIs within the running business portfolio of Centrient, and for interface management between Technical Product Management team and internal stakeholders and external customers under the guidance of the Global Technical Product Manager.

The main activities and responsibilities

  • Lead preparation & update of product documentation (leaflets, sales material, product cards, web specifications) and internal (product) trainings for the assigned product group.
  • Lead product data trending analysis and define follow up actions for assigned APIs, in alignment with internal stakeholders.
  • Initiate and lead technical discussions with site TechOp team on product quality issues and product (market) requirements.
  • Define follow up actions & projects to address the potential product related issues and/or future opportunities based on quality and market analysis for the assigned product group.
  • Focal point for global complaint meetings for assigned sites.
  • Ensure smooth & efficient interface management with assigned production sites & maintenance of product databases.
  • Project management responsibility or assigned (sub)projects.
  • Responsible for collection and maintenance of customer information & competitive intelligence, analysis industry trends. and managing the product roadmap for assigned API.
  • Initiate and lead update of technical value proposition, for the assigned product group.
  • Support global technical product management activities and projects.
  • Support new product or grades developments in alignment with Global Tech Product Manager.
  • Responsible for adaptation of current work processes and procedures in alignment internal stakeholders.

Requirements:


  • University degree in Chemistry, Biochemistry or Pharmacy
  • Minimum of 68 years' experience in relevant pharmaceutical industry
  • Good knowledge of product and/or pharmaceutical development process
  • Good understanding of GMP practices & requirements
  • Project management experience required
  • Commercial experience is preferable
  • Fluent proficiency in English language (written and spoken)
  • Strong conceptual, analytical and communication skills
  • Ability to collaborate effectively with multiple stakeholders
  • Innovative thinking to drive improvements
  • Ability to work in a global environment
  • Independ working style

Benefits:

Terms and reward


We offer a local contract in a challenging, comprehensive, operational environment, with many opportunities for personal input and growth and plenty of discussions with other professionals.

The organization is very flat. You have a lot of freedom and responsibility in an open, direct, and informal atmosphere.

The Procedure

Reference check procedures are part of the Centrient Recruitment & Selection Process. You will be contacted when a reference check is required.

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