Akkodis

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

Akkodis Alzey

Stellenbeschreibung:

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

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

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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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Stelleninformationen

  • Typ:

    Vollzeit
  • Arbeitsmodell:

    Vor Ort
  • Kategorie:

  • Erfahrung:

    2+ years
  • Arbeitsverhältnis:

    Angestellt
  • Veröffentlichungsdatum:

    04 Nov 2025
  • Standort:

    Alzey

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