\\n Does the idea of working within an international and well established company that is active in over 100 countries around the world, where you will work only with professional people and top notch products appeals to you?
Do you want to have great financial benefits and the opportunity for career progression as never before?
Then this may be the career opportunity you have been looking for!
The Role
Participate in FATs, construction walkdowns, C&Q to allow a smooth hand-over of Process Equipment\\\'s.
After Handover ensure the operation and the correct execution of all maintenance activities of the process equipment in compliance with Safety and cGMP requirements.
Carries out all activities to maintain complete and up-to-date system documentation.
Support risk analysis and establish Sops and work instructions for the new facility and equipment in the area of responsibility.
Maintaining qualification status (regarding safety and cGMP) of the assigned areas.
Consistent recording and maintaining data of functional locations, equipment and spare parts, spare part lists, instruction manuals and SOPs, etc.
Maintaining history and records in SAP and actual status of plant PIDs.
Ensures deviation and change management across its entire area of responsibility. Represents facility during inspections and audits as SME for area of responsibility.
Who are you?
Academical degree in engineering or comparable in economics with a technical focus (HF, FH, Dipl. Ing. / M. Sc. / B. Sc.).
Strong technical understanding.
Significant work experience in Engineering and Operations within Pharma Industry.
Good knowledge of SAP-PM and MS Office.
Knowledge of GMP compliance requirements preferred.
Strong analytical skills with the ability to define metrics (KPI\\\'s) and identify issues.
Fluency in English.
Express your interest by submitting an up-to-date copy of your CV and click the apply button below. You can also apply on the NonStop Consulting website, or send it to me, Claudiu Barbu, at .\\n \\n \\n \\n \\n \\n
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