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Monthly
€4,167 - €5,833
Posted August 5, 2026 · 25 days agoLast seen August 30, 2026Est. expiry September 9, 2026

Quality Auditor

How this salary compares
Salary Context: Quality Auditor

Hover or tap a row for full statistics (EUR / month on this chart).

Salary analysis

Compared with the selected benchmark ("All roles in Remote - Germany"), this listing's salary midpoint is about 27% lower. The offer still falls within the benchmark range (€3,650–€10,020). The listed pay band (€4,167–€5,833) is tighter than the benchmark, which suggests lower salary variability. This benchmark is based on 15 comparable listings.

Monthly salary comparison for Quality Auditor
MarketLower bound (25th percentile)MedianUpper bound (75th percentile)
All roles in Remote - Germany€3,650/per month€5,625/per month€10,020/per month
About the role

As a Quality Auditor, you will play a key role in ensuring pharmaceutical suppliers meet the highest standards of quality and regulatory compliance. Working within the Quality team, you will independently manage and conduct audits across an international supplier network, collaborating closely with customers, suppliers, and internal stakeholders to drive quality and continuous improvement. Main Responsibilities: Prepare GxP audits, ensuring customer requirements and applicable regulations are adequately addressed. Conduct 40 remote and on-site audits of pharmaceutical providers per year. 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. Job Requirements: 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 German and English. French or Italian would be a plus. Willingness to travel for on-site audits (domestic and international). 💰 Salary At Qualifyze, our salary ranges are transparent internally, and we aim to follow a similar approach externally. For this role, we’re happy to share a reference point within the band: the expected salary range is around 50k – 70k €, centred around the median. Final compensation will depend on experience and performance during the process, with some flexibility within the range. What do we offer? 💰Competitive, annually reviewed compensation package 🌴Country vacation package that increases with your tenure 🏋🏽‍♀️Country specific benefits offering incl. private health care, fitness and meal allowances 🚀Annual personal development budget to increase your impact 🌎Hybrid working mode, plus up to 3 months of the year work from anywhere. 💻All the best kit and tools to work effectively 🎉Annual in person all company event and celebration in Europe 👫Working with an exceptional team, doing some of the best work of your career Use of AI in Our Recruitment Process: We believe in a human-led hiring process. All applications are reviewed manually by our Talent Acquisition team, and neither Talent Acquisition nor Hiring Managers use AI to screen, filter, rank, assess, or make decisions about candidates, including during interviews and assessments. During interviews, AI may be used only to support note-taking and transcription. All hiring decisions are made by people! Diversity & Inclusion at Qualifyze: At Qualifyze we actively support the power of diversity, uniting complementary talents and perspectives to address new challenges. Our collective strengths help us to find innovative solutions and turn difficulties into opportunities. We will encourage you to bring your authentic self to work, fostering an inclusive environment where everyone belongs and feels heard. We are an equal opportunity employer and we welcome applications from candidates of all backgrounds, regardless of race, ethnicity, gender identity, sexual orientation, marital status, religion, disability, or age. Our hiring practices are rooted in fairness and respect, and we strive to create a culture where everyone feels valued and empowered.

Job Details

Responsibilities

  • Prepare GxP audits, ensuring customer requirements and applicable regulations are adequately addressed
  • Conduct 40 remote and on-site audits of pharmaceutical providers per year
  • 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

  • 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 German and English
  • French or Italian would be a plus
  • Willingness to travel for on-site audits (domestic and international)

Skills & Technologies

GxP auditingauditingreport writingCAPA processesregulatory knowledgeGMP knowledge

Education Level

Bachelor
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