Stellenbeschreibung:
CQ Engineer - Germany, Frankfurt - 18 Month Contract
This is a fantastic opportunity for a CQ Engineer to join our major, global pharmaceutical client on their latest new-build project based in Frankfurt, this is a large-scale greenfield capital project and investing more than $1bn.
Responsibilities
Develop and execute CQV documentation: URS, FDS, DDS, FAT, SAT, IQ, OQ, PQProgram, troubleshoot, and validate PLC systems (e.g., Siemens, Allen Bradley, Mitsubishi)Collaborate with automation engineers to integrate SCADA/HMI systemsPerform risk assessments and gap analyses for automated equipmentSupport installation and commissioning of new equipment and systemsEnsure compliance with industry standards and internal SOPsGenerate and maintain validation protocols and reportsLiaise with cross-functional teams: QA, Manufacturing, Engineering, and IT
Skills and Experience:
Bachelor’s degree in Engineering (Electrical, Automation, Computer Science, or related)Requires extensive experience in CQV within life sciences or pharmaceutical manufacturingStrong hands-on experience with PLC programming and SCADA systemsFamiliarity with GAMP 5, GMP, and FDA/EMA regulatory requirementsProficiency in technical documentation and validation lifecycle
If this role is of interest, please apply now!
NOTE / HINWEIS:
EN: Please refer to Fuchsjobs for the source of your application
DE: Bitte erwähne Fuchsjobs, als Quelle Deiner Bewerbung