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Process Engineer (f/m)

Einsatzort: Ludwigshafen

Process Engineer (f/m)

Process Engineer (f/m)

The process scientist will work within MES Operations with the objective of providing support for all current and future


  • Contributes to process of manufacture of existing and new products, and all aspects of a product life cycle, including development, registration, clinical and commercial manufacture, especially with a focus on manufacturing process, scale-up, current and innovative new technologies, equipment, statistical analysis and mechanical / thermal process engineering
  • Support the Bulk manufacturing department and Site KPI’s
  • The role will also support all aspects of new technology introduction, plant performance, process improvements, GMP compliance and troubleshooting as part of the product support role during the commercial life span of the product.
  • Must be self-motivated and be capable of working without supervision



  • Provide the scientific support suitable for the evaluation of novel manufacturing processes
  • Generate test data to characterise trial processes and to facilitate product support according GMP requirements
  • Technology input on novel technologies on existing and future products
  • Investigation of the events that may have an impact on product quality
  • Support/generation of the annual product review for products
  • Generation or update of production batch records
  • Support the introduction of new products
  • Trending of process data and correction of product issues including statistical analysis
  • Support Plant Performance Activities on site in particular CIPs (Cost Improvement Projects)
  • Support Process Optimisation activities
  • Be familiar with the products, the manufacturing techniques and procedures.
  • Create, update or ensure Production Batch Records and SOPs are kept updated and in compliance with GMP and regulatory filing.
  • Implement and maintain manufacturing processes and associated systems in compliance with GMP and regulatory requirements

  • Engineer (Master, Dipl Ing) in Chemical, BioChemical, Pharmaceutical Specialty or equivalent experience.
  • 1-3 yrs experience in pharma environment, especially manufacturing
  • Experience with troubleshooting manufacturing processes and industrial scale equipment.
  • Experience working in a cGMP environment.
  • Previous experience in Product Development, CTS or supervisory experience in a busy production environment is a requirement.
  • Judgment, initiative, concern for excellence, providing direction, technical skill & competence, teamwork & problem analysis, driving the business, statistical analysis
  • Strong written and verbal communication skills
  • Fluency in English is requirement in order to communicate with required colleagues globally
We are looking forward to your application. Please provide information about your salary expectations and possible start date in your motivation letter.
An equal opportunity employer. AbbVie welcomes and encourages diversity in our workforce.
Learn more about AbbVie Deutschland at Visit for more information about the therapeutic areas in which we’re active.


AbbVie (NYSE:ABBV) ist ein globales, forschendes BioPharma-Unternehmen, das sich der Entwicklung innovativer Therapien für einige der komplexesten und schwerwiegendsten Erkrankungen der Welt verschrieben hat. Mission des Unternehmens ist es, mit seiner Expertise, seinen engagierten Mitarbeitern und seinem Innovationsanspruch die Behandlungsmöglichkeiten in vier Therapiegebieten deutlich zu verbessern: Immunologie, Onkologie, Virologie und Neurowissenschaften. In mehr als 75 Ländern arbeiten AbbVie-Mitarbeiter jeden Tag daran, die Gesundheitsversorgung für Menschen auf der ganzen Welt voranzutreiben. In Deutschland ist AbbVie an seinem Hauptsitz in Wiesbaden und seinem Forschungs- und Produktionsstandort in Ludwigshafen vertreten. Insgesamt beschäftigt AbbVie Deutschland rund 2.600 Mitarbeiter. Mit rund 29.000 Mitarbeitern weltweit vertreibt AbbVie Medikamente in mehr als 170 Länder.

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