Skip to content
New Job?Nejo!

The AI Job Search Engine

CHCH12 Lonza AG

Investigation Specialist(m/w/x)

Visp
Full-timeOn-siteJunior

Owning investigations and CAPA implementation for critical deviations in sterile manufacturing processes at a global life sciences firm. One year sterile manufacturing experience with investigation/deviation management required. Relocation assistance provided.

Requirements

  • Bachelor's or Master's Degree in Pharmaceutical Technology, Chemistry, Pharmacy, or equivalent work experience
  • At least one year of experience in Sterile Manufacturing in operations and/or QC/QA
  • Previous experience with investigation/deviation management in TW and CAPA definition
  • Proficiency in English; German is an advantage
  • Familiarity with GMP requirements, quality procedures, and SOP execution
  • Good interpersonal skills with various interfaces within the organization and shopfloor
  • Structured, focused, proactive, and well-organized working demeanor
  • High motivation and collaboration focus; oriented towards finding solutions and driven by science

Tasks

  • Drive optimization projects for manufacturing processes
  • Own investigations and critical deviations
  • Assist in decision-making on production issues
  • Implement process changes and CAPAs
  • Conduct CAPA efficiency checks within required timelines
  • Utilize GMP systems like Trackwise, SAP, and MES
  • Perform retraining and awareness sessions as needed

Work Experience

  • 1 year

Education

  • Bachelor's degreeOR
  • Master's degree

Languages

  • EnglishBusiness Fluent
  • GermanBasic

Benefits

Bonuses & Incentives

  • Compensation programs for high performance

Corporate Discounts

  • Numerous lifestyle benefits
  • Leisure benefits

Family Support

  • Family benefits

Other Benefits

  • Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CH12 Lonza AG 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.

  • CH12 Lonza AG

    Deviation Specialist(m/w/x)

    Full-timeOn-siteNot specified
    Visp
  • Lonza

    QC Deviation & Investigation Specialist(m/w/x)

    Full-timeOn-siteExperienced
    Visp
  • CH12 Lonza AG

    GMP Ops Support(m/w/x)

    Full-timeOn-siteExperienced
    Visp
  • CH12 Lonza AG

    Manufacturing Specialist(m/w/x)

    Full-timeOn-siteJunior
    Visp
  • Lonza

    QA Specialist, Batch Record Review(m/w/x)

    Full-timeOn-siteJunior
    Visp
View all 100+ similar jobs

Nejo is an AI – results may be incomplete or contain mistakes