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Site QA Lead

Reference: BBBH29512
Date posted: 18/08/2026
Job details
Specialism
Quality Assurance
Expertise
QP
Location
Visp, Visp, Switzerland
Job type
Permanent
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Description

Passionate about aseptic manufacturing, contamination control, and building high-performing QA teams? This could be your next leadership challenge.

R&D Partners is seeking a Site QA Lead to join a leading pharmaceutical company in Switzerland. This role offers the opportunity to lead and evolve Quality Management Systems (QMS) while ensuring compliance with global GMP regulations. The ideal candidate will be a seasoned quality leader with expertise in aseptic processing, contamination control, and cultural transformation within a fast-paced manufacturing environment.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Lead the development, optimization, and remediation of robust QMS in alignment with FDA, EMA, and ICH regulations.
  • Manage core quality processes, including deviations, CAPAs, change control, document management, and audit readiness.
  • Apply expertise in aseptic processing, environmental monitoring, cleanroom behaviors, and contamination control strategies.
  • Drive cultural and operational transformation initiatives within the quality function and across the organization.
  • Build and foster a strong quality culture in a dynamic environment.
  • Ensure accountability for quality and compliance across cross-functional teams.
  • Align compliance goals with broader business objectives.
  • Mentor and develop Quality Assurance professionals to build a high-performing team.
  • Collaborate effectively with manufacturing, technical operations, and supply chain teams.
  • Communicate and influence at all organizational levels, from floor staff to executive leadership.
  • Simplify and streamline QA processes without compromising compliance or effectiveness.
  • Make data-driven decisions and apply sound risk management principles.

Key Skills and Requirements:

  • Proven experience in a GMP-regulated environment.
  • Expertise in building, optimizing, or remediating QMS in line with global GMP regulations (FDA, EMA, ICH).
  • Strong track record in managing quality processes, including deviations, CAPAs, and audit readiness.
  • Deep understanding of aseptic processing, environmental monitoring, and contamination control strategies.
  • Exceptional leadership skills with experience driving cultural and operational transformation.
  • Collaborative mindset with experience working closely with manufacturing, tech ops, and supply chain teams.
  • Excellent communication, negotiation, and influencing skills.
  • Strategic thinker with a pragmatic approach to problem-solving and process improvement.
  • Strong analytical skills and ability to make data-driven decisions.

For more information, please contact Frankie Cunningham.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

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

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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