Quality Auditor

Qualifyze

Quality Auditor conducting GxP audits for pharmaceutical providers, supporting regulatory compliance and continuous improvement. Collaborating with cross-functional teams to ensure quality standards across Europe.

Posted 7/2/2026full-timeRemote • 🇵🇱 PolandMid-LevelSenior💰 PLN 130,000 - PLN 210,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in GxP auditing, ensuring compliance with international GMP regulations and quality systems. Proficient in preparing audit reports and collaborating with cross-functional teams to enhance auditing methodologies and quality processes.

Highest-signal resume keywords

GMP Auditing ExperienceGxP Regulations KnowledgeAudit Report PreparationProfessional Proficiency in Polish and EnglishBachelor’s or Master’s Degree in Life Sciences

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

GMP AuditingGxP Compliance AssessmentAudit Report WritingSupplier CAPA ReviewQuality Systems Knowledge

Soft Skills

Effective CommunicationOrganizational SkillsCollaboration

Certifications & Qualifications

Accredited Auditor Training

Industry Keywords

Pharmaceutical IndustryQuality ProcessesContinuous ImprovementInternal ProceduresAudit Lifecycle

About the role

Key responsibilities & impact

Prepare GxP audits, ensuring customer requirements and applicable regulations are adequately addressed.
Conduct remote and on-site audits of pharmaceutical providers.
Assess compliance against applicable GxP regulations, guidelines, and internal procedures.
Prepare clear, accurate, and timely audit reports in accordance with internal quality standards.
Participate in the audit report review process, collaborating with cross-functional teams to ensure consistency and quality.
Review and assess supplier CAPA responses to ensure audit findings are appropriately addressed.
Communicate effectively with suppliers, customers, and internal stakeholders throughout the audit lifecycle.
Maintain up-to-date knowledge of applicable GxP regulations and industry best practices.
Support continuous improvement initiatives related to auditing methodologies, procedures, and quality processes.

Requirements

What you’ll need

Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotech, Life Sciences, or related field.
Minimum 5 years of GMP auditing experience in the pharmaceutical industry.
Evidence of relevant and accredited auditor training or justified experience in auditing with experienced inspectors.
Strong knowledge of international GMP regulations and quality systems.
Excellent organizational, communication, and report-writing skills.
Professional proficiency in both Polish and English.
Czech or German would be a plus.
Willingness to travel for on-site audits (domestic and international).

Benefits

Comp & perks

Competitive, annually reviewed compensation package.
Country vacation package that increases with your tenure.
Flexible schedules throughout the year.
The option to work from abroad for up to 45 days per year.
All necessary work equipment (laptop, headphones, etc.).
Two official company events per year to celebrate success.
Individual coaching and mentoring on your development roadmap within Qualifyze.
Working with an exceptional team, doing some of the best work of your career.