Senior C&Q Engineer for Global GMP Projects

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Stein (AR)

Vor Ort

CHF 140.000 - 190.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden
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Zusammenfassung

Bachem is expanding with a new site in Sisslerfeld, Northwestern Switzerland, seeking an experienced Commissioning & Qualification Engineer to lead C&Q activities on global capital projects. You will shape standards, manage from concept to handover, and drive lean, agile improvements across sites.

Ideal candidate has 10+ years in pharma/biopharma, strong GMP knowledge, and proven project leadership in international settings.

Qualifikationen

  • Completed degree in engineering, natural sciences, or related field.
  • At least 10 years of professional experience in pharmaceutical/biopharmaceutical industry.
  • Proven experience in international CAPEX projects (medium to large scale).
  • Extensive C&Q expertise in biologics/drug substance, drug product, packaging, GMP infra.

Aufgaben

  • Lead C&Q activities within multidisciplinary large capital projects.
  • Coordinate C&Q deviations and changes to meet timelines and quality.
  • Manage budget, schedule, resources, and quality of C&Q execution.
  • Develop detailed C&Q schedules and execution strategies.
  • Prepare tender documents and assist in procurement; cost estimation.
  • Ensure smooth handover to Operations and Quality; risk management.
  • Lead and onboard C&Q team and external partners.
  • Train C&Q teams and ensure adherence to standards.
  • Communicate clearly with all stakeholders; collaborate globally.
  • Support supplier evaluation and coaching of local SMEs.

Kenntnisse

Leadership
Project management
Communication
Team leadership
GMP expertise

Ausbildung

Engineering degree

Tools

KNEAT Gx

Jobbeschreibung

Bachem is expanding with a new site in Sisslerfeld, Northwestern Switzerland, seeking an experienced Commissioning & Qualification Engineer to lead C&Q activities on global capital projects. You will shape standards, manage from concept to handover, and drive lean, agile improvements across sites.

Ideal candidate has 10+ years in pharma/biopharma, strong GMP knowledge, and proven project leadership in international settings.

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