Senior Global QA Specialist – Sterile Pharma Manufacturing

• Follow GXP regulations and industry trends; communicate updates to global Quality teams.
• Provide global compliance support to sites and projects; solve complex QA/Compliance issues.
• Prepare for and support regulatory inspections; manage observations and responses.
• Analyze and report audit trends.
• Write updateand review global SOPs.
• Lead internal audits.
• Improve quality processes and measure performance.
• Create and implement training materials and process documentation.
• Ensure systems remain in continuous inspectionready state.

• 10 years of pharmaceutical industry experience across multiple Quality areas (QA QC Compliance Operations).
• Experience in sterile / aseptic manufacturing environments.
• Science degree (Pharmacy Biochemistry Chemical Engineering etc.).
• Strong cGMP knowledge (FDA/EMA).
• Regulatory inspection experience is an advantage.
• Excellent communication and stakeholder management skills.
• Strong GXP mindset and independence.
• Fluency in English and Hungarian.

• Opportunity to join a global Quality team.
• Competitive seniorlevel compensation package.
• Supportive flexible company culture.
• Stable international background with development opportunities.
• Fully remote role.

Required Experience:

Senior IC