(Work in Flanders) - Qualification / Validation Engineer for Pharmaceutical Automation
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 working hours 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 training on the job
Interested? - How to apply:
Please forward your motivation and resume to email@example.com mandatory mentioning the code -Work in Flanders- in the subject of the email.