Key Responsibilities :

• Provide QA oversight of day-to-day operational activities (manufacturing, packaging, tech transfer, etc.)
• Manage quality documentation (SOPs, protocols, reports, etc.)
• Support in the management of Quality Records (Change Request, CAPAs, Deviations/Investigations)
• Perform batch record review
• Drive continuous improvement initiatives and ensure best practices are applied
• Support regulatory inspections and client audits
• Collaborate with multidisciplinary teams (operations, validation, regulatory, etc.)

About you:

• Experience of minimum 3 years in Quality Assurance / Quality Control in a pharma or biotech company.
• Master Degree (or equivalent) in Life Sciences or a related discipline.
• Thorough understanding of cGMPs, Eudralex, GLP and FDA 21 CFR regulatory requirements.
• Excellent written & oral communication skills.
• You have good analytical, organizational, time management and problem-solving skills.
• French with good knowledge of English. German is a plu

About us :

• Human-sized company with great colleagues from a large diversity of cultural and professional backgrounds
• We do care about our people, communicate openly and value feedback
• Work as a team where every member is valued and appreciated
• Opportunity to contribute to ambitious projects within an international and multicultural environment that fosters innovation, collaboration, and professional growth.
• Continuous learning and development opportunities via internal or external training and workshops
• Competitive salary package in line with industry practice together with exceptional employment benefits

At GXP Consulting Switzerland everyone contributes to our joint success and grows individually!

If you also share the same passion and values, we will be glad to hear from you! Please send us your application.