QC Analytical Project Lead (GMP)

Bachem; Vionnaz; On-site; CHF 120,000 - 160,000; Full time

Benefits offered by this job

Dynamic environment

Challenging projects

Professional development

Collaborative culture

Competitive benefits

Job summary

Bachem in Vionnaz, Switzerland, is seeking a QC Analytical Project Manager to coordinate analytical activities across the project lifecycle while upholding GMP, quality, and safety standards.

In this cross-functional role, you will lead release testing, method development, validation, and transfer activities, manage timelines and budgets, and drive continuous improvement. Fluency in French and English is required, with German a plus.

Qualifications

• GMP-regulated pharmaceutical experience.
• Experience with analytical method development and validation.
• Knowledge of regulatory requirements and quality systems.
• Ability to coordinate cross-functional projects.
• Fluent in French and English; German a plus.

Responsibilities

• Act as QC Operations representative within cross-functional project teams.
• Lead analytical activities including release testing, stability studies, method development and validation, specification setting.
• Manage analytical transfers to internal sites and external partners.
• Evaluate complex data and communicate results to customers and stakeholders.
• Define and implement QC strategies aligned with customer needs and Bachem best practices.
• Monitor timelines, budgets, resources, quality events, deviations, CAPAs, and change controls.
• Organize and facilitate project meetings with internal and external partners.
• Drive continuous improvement and ensure GMP compliance.

Skills

Project management

GMP knowledge

Stakeholder management

Analytical thinking

Communication

MS Office proficiency

Education

Analytical Chemistry / Biochemistry / Pharmaceutical Sciences degree

Tools

LIMS

CDS

MasterControl

SAP

Job description

Bachem in Vionnaz, Switzerland, is seeking a QC Analytical Project Manager to coordinate analytical activities across the project lifecycle while upholding GMP, quality, and safety standards.

In this cross-functional role, you will lead release testing, method development, validation, and transfer activities, manage timelines and budgets, and drive continuous improvement. Fluency in French and English is required, with German a plus.