QUALIFICATION / VALIDATION ENGINEER

Accountmanager:

Locatie: Antwerpen

GENERAL INFORMATION:

Our customer is a global leading independent supplier from automation solutions in the process- and manufacturing industry.

POSITION:

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, inc. Annex 11 and 21CFR Part 11

Profile:

  • Master or equal by experience of 5 years;
  • Knowledge of 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, inc. batch, PI, OPC, ODBC, networks, database systems like Oracle;
  • Good English and Dutch proficiency speaking and writing;
  • Good attitude towards safety, health, environment.

Solliciteer

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