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LOLonza

Senior QA Expert(m/w/x)

Stein (AR)
Full-timeOn-siteSenior

Reviewing and approving GMP documentation and material releases in biopharmaceutical manufacturing. Solid QA experience in GMP, with material management background, required. Relocation assistance provided.

Requirements

  • Solid QA experience in GMP environment
  • Experience in material management or raw materials
  • Scientific or technical education background
  • Fluency in English and German skills
  • Accurate and efficient work in regulated environment
  • Collaborative and proactive cross-functional approach

Tasks

  • Review and approve GMP documentation
  • Approve methods, protocols, and specifications
  • Oversee material testing and batch releases
  • Investigate deviations and OOS/OOE results
  • Manage change control and quality agreements
  • Drive qualification and validation activities
  • Maintain material master data in SAP
  • Support warehouse and logistics quality oversight
  • Participate in audits and inspections
  • Lead cross-functional quality projects
  • Train and mentor team members
  • Deputize for the Team Lead as needed
  • Shape new QMS platforms and systems

Education

  • Vocational certification

Languages

  • EnglishBusiness Fluent
  • GermanBasic

Tools & Technologies

  • GMP
  • CAPA

Benefits

Bonuses & Incentives

  • Performance-based compensation programs

Corporate Discounts

  • Lifestyle benefits
  • Leisure benefits

Family Support

  • Family benefits

Other Benefits

  • Relocation assistance

Career Advancement

  • Agile career

Informal Culture

  • Dynamic work culture

Purpose-Driven Work

  • Inclusive and ethical workplace
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