Quality Assurance (QA) Lead – Switzerland

Job Title: Quality Assurance (QA) Lead

Location: Zurich, Switzerland
Start Date: End of July 2025
Company: Swiss Pharmaceutical Company


Join a Leading Swiss Pharmaceutical Company

Are you ready to take the next step in your quality assurance career?
[Company Name] is looking for a Quality Assurance (QA) Lead to join our growing team in Zurich. This is your opportunity to play a critical role in ensuring product quality, regulatory compliance, and continuous improvement—while working in a forward-thinking and supportive environment.

For highly experienced candidates, a Vice President title may be considered.


Your Role and Impact

As the QA Lead, you will:

  • Lead the QA Team: Mentor and support a team of quality professionals to ensure high performance and compliance.

  • Manage the QMS: Oversee our Quality Management System (QMS), ensuring alignment with cGMP, FDA, EMA, and other regulatory requirements.

  • Ensure Audit Readiness: Prepare for and lead internal and external audits to maintain full regulatory compliance.

  • Handle Deviations and CAPAs: Lead investigations into deviations and non-conformances, implementing robust corrective and preventive actions.

  • Review Documentation: Approve batch records, SOPs, validation protocols, and other essential quality documentation.

  • Drive Continuous Improvement: Identify and implement enhancements to our quality systems and processes.

  • Support Regulatory Activities: Assist with inspections and submissions to ensure quality system readiness.

  • Train and Educate: Deliver training on GMP standards, QMS usage, and compliance best practices.

  • Assess and Manage Risk: Conduct quality risk assessments across operational areas.


What We’re Looking For

Education:

  • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or a related field.

Experience:

  • Minimum of 5 years in pharmaceutical QA.

  • Leadership or team management experience is a strong plus.

Knowledge & Skills:

  • Strong understanding of cGMP and global regulatory standards (FDA, EMA, etc.).

  • Skilled in QMS tools such as QPulse, TrackWise, or Veeva Vault.

  • Excellent communication skills—both written and verbal.

  • Fluent in English; German or French is a plus.


What You’ll Get in Return

  • Competitive salary and comprehensive benefits package.

  • A collaborative, innovative work culture focused on your growth.

  • Opportunities for career advancement in a respected pharmaceutical organization.

  • A diverse and inclusive environment that supports work-life balance.


Ready to Apply?

If you’re passionate about quality, compliance, and making a real difference in pharmaceutical care, we’d love to hear from you.

Application Deadline: July 15, 2025

Upload your CV/resume or any other relevant file. Max. file size: 100 MB.

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