探花合集

Manager Deviation & QMS Deployment (70%)

Highly Competitive
  1. Contract
  2. Good Manufacturing Practice (GMP)
  3. Switzerland
Bern, Switzerland
Posting date: 19 Aug 2026
70564

Do you thrive on solving complex quality challenges and turning investigations into lasting improvements?

探花合集 is seeking a Manager Deviation & QMS Deployment (70%) to join a dynamic team in Switzerland. In this role, you will take ownership of the local deviation management system and contribute to the continuous improvement of the Quality Management System (QMS). Collaborating with both local and global stakeholders, you will ensure quality processes are harmonized, regulatory requirements are met, and sustainable improvements are implemented.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

  • Oversee the local Deviation Management System and act as the Local Process Champion for the Bern site.
  • Continuously develop processes, SOPs, and work instructions related to deviation management, ensuring regulatory compliance.
  • Support change management, complaint management, and other global QMS processes in close collaboration with local and global quality teams.
  • Coordinate and manage complex deviations, assist with root cause analyses, and promote the use of effective investigation methods.
  • Lead or support improvement projects aimed at harmonizing and optimizing quality processes and standards.
  • Prepare for audits and regulatory inspections, present your areas of responsibility to auditors, and assist in addressing audit observations.
  • Generate KPI and trending reports, derive improvement measures, and present relevant quality metrics to stakeholders.
  • Conduct training sessions and requalifications within your area of responsibility, supporting team members in applying QMS processes effectively.

Key Skills and Requirements:

  • Degree in pharmacy, chemistry, biology, or a related scientific field.
  • Professional experience in a GMP-regulated environment, ideally in Quality Assurance, Compliance, or Quality Management Systems.
  • Familiarity with deviation management, investigations, and root cause analysis is advantageous.
  • Experience in creating and maintaining SOPs, as well as conducting training and requalifications.
  • Strong analytical, structured, and solution-oriented approach with the ability to communicate complex topics clearly.
  • Excellent communication and stakeholder management skills, with a collaborative mindset.
  • Proficiency in German and English, both written and spoken.

If you are having difficulty in applying or if you have any questions, please contact Ria Tailor at r.tailor@proclinical.com.



Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

探花合集 is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. 探花合集 is acting as an Employment Agency in relation to this vacancy.

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