For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Position overview
We are currently seeking the support of a freelance/contract GMP Auditor to perform 1-2 (depending on availability) audits in Germany for us in May 2025. This project requires two vendors being audited based in Northern and Central Germany which will consist of 3 onsite days at one group and 2 onsite days at the other (preparation & write up is fully remote). The audit requires fluency in German; proven skills in GMP auditing in the life-sciences sector and the ability to offer consecutive dates in May.
Key skills required include:
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Further educated within a life-sciences discipline is a must
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Proven skills working in Quality Assurance within the life-sciences sector
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Demonstrated GMP auditing experience is critical for success
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Fluent in German and English
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Must be able to travel and perform the audit on site in Northern and Central Germany
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Thorough, quality orientated and able to deliver on key milestones
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
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What We Do
ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies. With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science
