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CHCH12 Lonza AG

(Senior) QA Qualification Specialist(m/w/x)

Visp
Full-timeOn-siteExperienced

QA qualification for pharmaceutical projects, compiling and releasing documents at a global life sciences firm. Significant pharmaceutical industry experience with cGMP regulations understanding required. Project-based work, agile career path.

Requirements

  • Academic degree in Engineering, Chemistry, Biotechnology, or related field, or vocational education with strong relevant experience
  • Significant experience in the pharmaceutical industry, ideally in a QA role
  • Good understanding of applicable cGMP regulations
  • General knowledge of engineering and manufacturing processes
  • Ability to oversee project execution to identify non-compliance from quality standards
  • Fluent German (written and verbal) required; good English language skills advantageous

Tasks

  • Represent QA Qualification in project organizations
  • Coordinate QA interests during project phases
  • Drive implementation of new qualification strategies
  • Compile, review, and release Qualification Documents
  • Support and approve quality risk analyses
  • Perform assessments and approvals of technical change requests
  • Represent qualification topics during customer audits
  • Drive CAPA and Effectiveness Checks to completion
  • Ensure deviations are investigated and recorded

Work Experience

  • approx. 1 - 4 years

Education

  • Vocational certificationOR
  • Bachelor's degree

Languages

  • GermanBusiness Fluent
  • EnglishBasic

Benefits

Bonuses & Incentives

  • Compensation programs recognizing high performance

Corporate Discounts

  • Numerous lifestyle benefits
  • Leisure benefits

Family Support

  • Family benefits

Career Advancement

  • Agile career

Informal Culture

  • Dynamic work culture
  • Inclusive workplace

Purpose-Driven Work

  • Ethical workplace

Other Benefits

  • Relocation assistance
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