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WEWest Pharmaceutical Services

Working Student Engineering(m/w/x)

Stolberg
Part-timeWorking StudentOn-site

Supporting qualification and validation of medical device manufacturing equipment. Technical studies in Mechanical Engineering or comparable field preferred. On-site work with rotating project tasks.

Requirements

  • Ongoing technical studies in Mechanical Engineering or comparable field
  • Completed technical vocational training
  • Previous intern or apprentice experience preferred
  • Good knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook)
  • Strong written and verbal communication skills
  • Organizational skills with careful, detail-oriented working style
  • Knowledge of Lean principles
  • Good English skills
  • Satisfactory post-offer background screening

Tasks

  • Support engineering in qualification and validation
  • Prepare qualification and validation activities
  • Execute qualification and validation activities
  • Document qualification and validation activities
  • Work on project-specific tasks
  • Ensure GMP-compliant process implementation
  • Ensure GMP-compliant process modification
  • Ensure GMP-compliant process optimization
  • Create technical documentation
  • Maintain technical documentation
  • Revise technical documentation
  • Participate in planning qualification activities
  • Participate in executing qualification activities
  • Participate in planning testing activities
  • Participate in executing testing activities
  • Analyze project-related data
  • Prepare project-related data
  • Support project management with research
  • Prepare for meetings
  • Take meeting minutes
  • Coordinate smaller work packages
  • Gain insights into regulatory requirements
  • Gain insights into technical operations
  • Contribute to production process analysis
  • Contribute to production process optimization
  • Participate in feasibility studies
  • Support continuous improvement initiatives
  • Assist in creating technical documentation
  • Assist in updating technical documentation
  • Collect production data
  • Analyze production data
  • Collaborate with Maintenance
  • Collaborate with Quality
  • Resolve process-related issues
  • Conduct tests to verify process efficiency
  • Conduct measurements to verify process efficiency
  • Support validation processes of tools
  • Support validation processes of machines
  • Monitor validation processes of tools
  • Monitor validation processes of machines
  • Observe equipment performance
  • Observe tool performance
  • Observe product quality
  • Observe compliance with global protocols
  • Participate in continuous improvement projects
  • Assist with administrative tasks

Education

  • Vocational certificationOR
  • Currently in higher education

Languages

  • EnglishAdvanced

Tools & Technologies

  • Microsoft Office
  • Word
  • Excel
  • PowerPoint
  • Outlook
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of West Pharmaceutical Services and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

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