Qualification / Validation Engineer for Pharmaceutical Automation

HR Globally Published: 20th November 2017
Job Type
Category

Description

Qualification / Validation Engineer for Pharmaceutical Automation

Description:

  • Review, adaptation and creation of local procedures based on global SOP’s
  • Organize or contribute to GAP assessments, Risk assessments, Remediation plans
  • Organize or contribute to Change control execution during full project cycle
  • Training of people on the newest procedure updates
  • Documentation compliant to cGMP regulation, incl Annex 11 and 21CFR Part 11

Your profile:

  • Master or equal by experience of 5 years
  • Knowledge of the requirements and evolution of cGMP and motivation to master this field
  • People skills in terms of information gathering, training and managing contractors
  • Solid technical background knowledge on automation systems like: DCS, incl. batch, PI, OPC, ODBC, networks, database systems like Oracle
  • Good English and Dutch proficiency speaking and writing
  • Good attitude towards safety, health, environment

We offer:

  • The space to work independently
  • Flexible workinghours
  • Attractive secondary salary (company car, food vouchers, medical- and group assurance)
  • A non-hierarchically company structure with direct communication lines
  • The opportunity to develop your personal- skills and career
  • Courses and traning on the job
Apply
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