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Senior Associate Process Engineer(m/w/x)
Subject Matter Expert for fermentation, lyophilization, aseptic filling, and packaging. Pharmaceutical GMP manufacturing experience required. Company fitness program, meal allowance.
Requirements
- Bachelor's or Master's degree in Process, Chemical, Bioprocess, or Mechanical Engineering
- Experience in pharmaceutical or biopharmaceutical manufacturing within GMP regulated environment
- Excellent communication and cross-functional collaboration skills
- 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
Tasks
- Provide technical engineering support
- Act as Subject Matter Expert for fermentation, lyophilization, aseptic filling, utilities, and packaging
- Lead process improvement initiatives
- Lead technology transfers
- Lead scale-up projects
- Manage deviations within a GMP environment
- Manage CAPAs within a GMP environment
- Manage change controls within a GMP environment
- Manage equipment qualification activities (IQ/OQ/PQ) within a GMP environment
- Resolve complex process issues
- Resolve complex equipment issues
- Lead root cause investigations
- Lead cross-functional taskforces
- Drive operational excellence
- Provide technical leadership to operational teams
- Provide mentorship to operational teams
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Purpose-Driven Work
- Room for initiative
Flexible Working
- Flexibility
Learning & Development
- Development opportunities
Healthcare & Fitness
- Company fitness program
Additional Allowances
- Meal allowance
Team Events
- Team events
More Vacation Days
- Up to 30 days holiday
- Special leave days
Bonuses & Incentives
- Christmas bonus
- Holiday bonus
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Senior Associate Process Engineer(m/w/x)
Subject Matter Expert for fermentation, lyophilization, aseptic filling, and packaging. Pharmaceutical GMP manufacturing experience required. Company fitness program, meal allowance.
Requirements
- Bachelor's or Master's degree in Process, Chemical, Bioprocess, or Mechanical Engineering
- Experience in pharmaceutical or biopharmaceutical manufacturing within GMP regulated environment
- Excellent communication and cross-functional collaboration skills
- 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
Tasks
- Provide technical engineering support
- Act as Subject Matter Expert for fermentation, lyophilization, aseptic filling, utilities, and packaging
- Lead process improvement initiatives
- Lead technology transfers
- Lead scale-up projects
- Manage deviations within a GMP environment
- Manage CAPAs within a GMP environment
- Manage change controls within a GMP environment
- Manage equipment qualification activities (IQ/OQ/PQ) within a GMP environment
- Resolve complex process issues
- Resolve complex equipment issues
- Lead root cause investigations
- Lead cross-functional taskforces
- Drive operational excellence
- Provide technical leadership to operational teams
- Provide mentorship to operational teams
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Purpose-Driven Work
- Room for initiative
Flexible Working
- Flexibility
Learning & Development
- Development opportunities
Healthcare & Fitness
- Company fitness program
Additional Allowances
- Meal allowance
Team Events
- Team events
More Vacation Days
- Up to 30 days holiday
- Special leave days
Bonuses & Incentives
- Christmas bonus
- Holiday bonus
About the Company
Elanco
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer im Bereich Tiergesundheit, der sich der Innovation und der Bereitstellung von Produkten und Dienstleistungen zur Prävention und Behandlung von Krankheiten bei Nutztieren und Haustieren widmet.
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QA Representative (QA Associate)(m/w/x)
Full-timeOn-siteJuniorCuxhaven - DE02 Lohmann Animal Health Gmb
Director Production / Produktionsleiter(m/w/x)
Full-timeOn-siteSeniorCuxhaven - Vibalogics GmbH
Operator(m/w/x)
Full-timeOn-siteExperiencedCuxhaven