Commissioning and Qualification Engineer (m/w/d) · Pharma

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Commissioning and Qualification Engineer (m/w/d) Pharma

We boost your business. On demand! Project and career opportunities for talents and professionals (m/f/d) in the Life Science / Pharma / Biotech…

• 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

Desired Skills and Experience

Programmable Logic Controller (PLC) Pharmazeutika cGMP-Praktiken MES Programmierbare Logik Computerized System Validation (CSV)

Seniority level

• Seniority level

Executive

Employment type

• Employment type

Contract

Job function

• Job function

Quality Assurance

• Industries

Pharmaceutical Manufacturing

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