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CH12 Lonza AG
2mo ago

Investigation Specialist(m/w/x)

Visp
Full-timeOn-siteJunior

Description

As an Investigation Specialist, you will focus on optimizing manufacturing processes and managing critical deviations. This role involves driving impactful changes and ensuring compliance with GMP standards in a sterile environment.

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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

Education

Bachelor's degree
OR
Master's degree

Work Experience

1 year

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

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
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