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Senior Process Engineer; m​/w​/d- Pharma

in 27474, Cuxhaven, Niedersachsen, Deutschland
Unternehmen: Elanco
Vollzeit position
Verfasst am 2026-08-30
Berufliche Spezialisierung:
  • Fertigung/Herstellung
    Qualitätsingenieur, Fertigungsingenieur, Validierungsingenieur
  • Ingenieur
    Qualitätsingenieur, Prozessingenieur, Fertigungsingenieur, Validierungsingenieur
Gehalts-/Lohnspanne oder Branchenbenchmark: 70000 - 90000 EUR pro Jahr EUR 70000.00 90000.00 YEAR
Stellenbeschreibung
Stellenbezeichnung: Senior Process Engineer (m/w/d)- Pharma
Location: Cuxhaven

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Lohmann Animal Health GmbH – a global leader specializing in the production of poultry vaccines – has been part of Elanco since 2014. With our innovative products and services, we strive to take responsibility for the community and enrich the lives of both people and animals. Our vaccines are exported to more than 70 countries worldwide. With more than 180 employees and a long-standing company history, Lohmann Animal Health GmbH offers an exciting, international, and impactful working environment.

Your Role:
Process Engineer

As a Process Engineer, you will be part of the manufacturing operations team to deliver technical expertise across vaccine production facilities. In this role, you’ll be responsible for optimizing performance in key areas such as utilities, fermentation, freeze drying (lyophilization), aseptic filling, and packaging to ensure operational excellence.

Your Responsibilities:
  • Provide technical engineering support and act as a Subject Matter Expert (SME) for fermentation, lyophilization, aseptic filling, utilities, and packaging.
  • Lead process improvement initiatives, technology transfers, and scale-up projects to enhance reliability, efficiency, and product quality.
  • Manage deviations, CAPAs, change controls, and equipment qualification activities (IQ/OQ/PQ) within a GMP environment.
  • Resolve complex process or equipment issues by leading root cause investigations and cross-functional taskforces.
  • Drive operational excellence while providing technical leadership and mentorship to operational teams.
What You Need to Succeed (minimum qualifications):
  • Bachelor’s or Master’s degree in Process Engineering, Chemical Engineering, Bioprocess Engineering, Mechanical Engineering, or related discipline
  • Experience in pharmaceutical or biopharmaceutical manufacturing within a GMP regulated environment
  • Excellent communication skills with the ability to collaborate across functions and leadership levels
What will give you a competitive edge (preferred qualifications):
  • Fluency in English and German
  • Experience with GMP manufacturing unit operations
  • Proven experience with equipment qualification (IQ/OQ/PQ) and process validation
  • Experience leading engineering projects or continuous improvement initiatives
WHAT WE OFFER YOU
  • Interesting and varied working environment in a modern and growing global company in the pharmaceutical industry
  • Room for initiative and flexibility
  • Exciting development opportunities
  • Company fitness program
  • Meal allowance
  • Corporation benefits
  • Team events
  • Up to 30 days holiday
  • Special leave days (wedding, work anniversaries etc.)
  • Attractive remuneration according to the company collective agreement incl. Christmas and holiday bonus
  • 38 hours/week

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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10+ Jahre Berufserfahrung
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