QA Specialist Sterile Process

NeuchatelFixe2018-11-02Master / Université
Our client, an international growing pharmaceutical company, is recruiting a

QA Specialist Sterile Process

Your Responsibilities

You will work in a small team of dedicated people to support the operations of a multisite pharmaceutical company under the supervision of the Quality Assurance Manager.
QA Activities:
  • Master Batch Records, Batch Record Reviews
  • Deviations, CAPAs, Change Controls
  • Audits and Self Inspections
  • Validation Protocols, Final Reports, SOPs
  • Personnel Trainings


Your Profile

  • Bachelor's or Master's degree in Science / Life Science related areas
  • At least 5 years of experience within a QA function or Production of a pharmaceutical company.
  • Proficient in cGMP's regulations and requirements.
  • Knowledgeable in QA related activities (Master Batch Records, Validation Protocols, Final Reports, SOP, Personnel Trainings, Batch Record Reviews, Deviations, CAPAs, Change Controls, Audits and Self Inspections.
  • Aseptic conditions knowledge,
  • Able to work within a multi-cultural complex environment
  • Strong communication and interpersonal skills in both French and English


Votre contact

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Merci de préciser la référence JN -062018-206788

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