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LOLonza

Compliance Engineer DPS Growth Project(m/w/x)

Stein (AR)
Full-timeOn-siteExperienced

GMP documentation, SOPs, and audit material preparation for pharmaceutical manufacturing. Pharmaceutical GMP and engineering experience, plus project management skills, required. Relocation assistance provided.

Requirements

  • Degree in Pharmacy, Engineering, or related field
  • Experience in pharmaceutical GMP and engineering
  • Solid project management skills
  • Excellent communication and detail-oriented working style
  • Knowledge of GMP and regulatory expectations
  • Fluency in German and English
  • Stakeholder collaboration and confident GMP representation

Tasks

  • Create and review GMP documentation
  • Draft periodic reviews and qualification documents
  • Develop and update SOPs
  • Prepare presentation materials for audits
  • Organize subject matter experts for inspections
  • Coordinate with internal inspection teams
  • Support site-wide inspection readiness
  • Oversee GMP activities within CAPA processes
  • Manage change management workflows
  • Lead the full CAPA lifecycle
  • Execute and document re-qualification activities
  • Represent the Engineering Lead Team

Work Experience

  • approx. 1 - 4 years

Education

  • Bachelor's degree

Languages

  • GermanBusiness Fluent
  • EnglishBusiness Fluent

Tools & Technologies

  • GMP

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 opportunities

Informal Culture

  • Dynamic work culture

Purpose-Driven Work

  • Inclusive and ethical workplace
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