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Production Manager - Sterile - Portugal  

Company managed [?] Still accepting applications

Posted on : 15 August 2017

Project Description

Perfil da Função

  • Responsible for the implementation of aseptic processing of Pharmaceutical components and products in a cGMP manufacturing environment.
  • Participate in the design of facilities for aseptic processing and filling of pharmaceutical products.
  • Perform technology transfer of developed processes and procedures to scale up activities;
  • Engage team members to drive to true root cause of errors and seek ways to improve and optimize the process to eliminate mistakes;
  • Provide guidance on key decisions with front line leaders and junior to mid-level employees.
  • Critical, high exposure job with direct communication and face time with top site leadership 
  • Defined career path and annual performance review & feedback process

Requisitos Mínimos

  • The successful candidate will hold a degree in Pharmaceutical Sciences, Chemical Engineering or equivalent education.
  • Min 2 years related pharmaceutical industry experience in sterile manufacturing.

Competências

  • Strong leadership
  • Understand controlled environment and aseptic processing principles.
  • Understand manufacturing safety regulations and comply with current Good Manufacturing Practices.
  • Experience in implementing and maintaining clean room aseptic processing qualification.
  • Experience in performing environment monitoring.
  • Must have experience managing and developing high functioning teams
  • Must be a “go-getter” who can drive change, drive improvements, and deliver results