GMP/GDP QA Auditor

CK QLS are looking for a (Senior) GMP/GDP QA Auditor, to join our team in Allschwil, Switzerland. As a mission-driven organization, we are dedicated to ensuring GMP/GDP compliance at third party service providers and maintaining the highest quality standards in pharmaceutical operations.

Responsibilities:

• Lead in establishing external QA Audit and internal self-inspection annual Plan.
• Conduct GMP/GDP audit and self-inspections and coordinate with internal personnel and suppliers.
• Promptly report critical self-inspection findings to the Responsible Person and Management.
• Create, implement, maintain, and work with Vendors on establishing Quality Agreements.
• Interface between quality/regulatory/compliance personnel and operations to identify applicable regulatory and compliance requirements.
• Manage, review and approve change controls, deviations and CAPAs.
• Support the preparation of Regulatory Authority Inspections.
• Monitor changes in quality regulations and initiate required activities to maintain compliance.
• Promote GxP and Quality mindset at all levels within the organization.

Qualifications:

• University degree in Pharmacy, Chemistry or alternative technical/science university degree: master level minimum.
• Minimum 3 years’ experience in Auditing, 1 as Lead Auditor.
• Excellent knowledge of relevant GMP/GDP and international quality regulations.
• Ability to work on multiple projects with various disciplines and to manage complex projects.
• Strong attention to detail, excellent organizational skills, and ability to multitask effectively.
• Fluent verbal and written communication skills in English and at least basic knowledge of an additional European language.

Day-to-day:

As a (Senior) GMP/GDP QA Auditor, you will be responsible for leading external QA audits, conducting GMP/GDP audits and self-inspections, and ensuring compliance with quality regulations. You will also collaborate with cross-functional teams to obtain key performance indicators for the site and support the organization of Quality Management Review meetings.

Benefits:

• Competitive contractor rate.
• Fulltime schedule.
• Opportunity to work in a mission-driven organization dedicated to maintaining the highest quality standards in pharmaceutical operations.
• Professional development and growth opportunities.

Apply:

If you are looking for a new challenge and would like to know more them please apply and use 136 286 in all communications.

All applicants

must be an EU/EFTA Citizen or valid Swiss work Permit.