Commissioning and Qualification Engineer; m​/w​/d) Pharma

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• Start: ASAP
• Knowledge of automation, commissioning, qualification, or operations in a cGMP environment.
• Experience with one or more of the following industry recognized systems: MES, Programmable Logic Controllers (PLC).
• Experience in generating validation protocols and execution of protocols.
• Working knowledge, understanding and application of CSV principles, concepts, practices, and standards.
• Trouble shoot issues, track issues, build resolution plan

Profil

• Degree in mechanical, chemical, pharmaceutical, or general engineering
• Minimum of 5 years years of experience in commissioning and qualification of equipment, facilities, and utilities in the pharmaceutical industry
• Proven ability to manage/lead/coordinate
• Knowledge of cGMP, CSV, GAMP5
• Business fluent in German and English, French an advantage

Wir von der Akkodis Life Sciences besetzen Projekte deutschlandweit für renommierte Kunden in der Pharma-, Biotech-, Chemie-Branche. Von Start-Ups, Familienunternehmen, Mittelständlern, bis hin zu weltweiten Big Playern, haben wir die unterschiedlichsten Kunden und Anforderungen.

Für unsere eigene Consulting & Solutions Division suchen wir nach Menschen mit der Spezialisierung in der Prozessautomatisierung als C&Q Engineer.

• Start: ASAP
• Standort:
  Großraum Rhein Main
• Auslastung:
  Vollzeit
• Gehalt, je nach Erfahrung

Stellenbeschreibung

• Knowledge of automation, commissioning, qualification, or operations in a cGMP environment.
• Experience with one or more of the following industry recognized systems: MES, Programmable Logic Controllers (PLC).
• Experience in generating validation protocols and execution of protocols.
• Working knowledge, understanding and application of CSV principles, concepts, practices, and standards.
• Trouble shoot issues, track issues, build resolution plan

Profil

• Degree in mechanical, chemical, pharmaceutical, or general engineering
• Minimum of 5 years years of experience in commissioning and qualification of equipment, facilities, and utilities in the pharmaceutical industry
• Proven ability to manage/lead/coordinate
• Knowledge of cGMP, CSV, GAMP5
• Business fluent in German and English, French an advantage

• Seniority level Executive

• Employment type
  
  Contract

• Job function
  
  Quality Assurance
• Industries Pharmaceutical Manufacturing

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