(Senior) Consultant QA

Company Profile
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3D\-PharmXchange is a Dutch drug development consultancy and operational support firm located in Tilburg, Oss \& Amsterdam. We provide our clients with expert support across the development of biopharmaceuticals, including small molecules, vaccines, and ATMPs. Our team of experts covers the key areas of pre\-clinical, clinical, CMC, regulatory affairs, and project management. In addition, we provide out\-licensing, interim management support and Quality Assurance services. Our clients are innovative biotech companies, start\-ups, academia, and pharma companies.

Job description
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As a QA Consultant you will actively supporting our clients in implementing quality systems, managing compliance processes, and driving continuous improvement. Your role will ensure that clients’ QA frameworks comply with regulatory requirements while remaining practical and efficient. You will closely collaborate with our QA, CMC, Clinical and Regulatory Affairs consultants, serving as the subject matter expert (SME) for all QA\-related questions and projects. A key focus will be GMP and additionally GCP/GLP, including reviewing quality documents and guiding clients toward compliance across various stages of development and organizational maturity. You will also join or lead audits at the CDMO’s and CRO’s we work with. In addition, your role will include oversight of QMS requirements for all disciplines within 3D\-PXC.

Minimal requirements
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• BSc or MSc degree with experience in the Life Sciences sector


• 10\+ years of QA experience in the pharmaceutical or life sciences industry


• Demonstrated knowledge of GMP, GCP, and GLP regulations


• Personality skills: pro\-active, team player, solution\-oriented, can\-do mentality and the ability to put yourself in the position of our clients


• Expertise in QMS implementation, CAPA management, and audit


• A pragmatic, hands\-on approach — able to guide clients toward lean and efficient QA systems


• Strong communication and advisory skills, able to translate complex regulations into practical solutions


• Ability to engage with multiple stakeholders, from operational teams to senior management


• Train and mentor client teams on best practices in quality management


• Act as a trusted advisor, ensuring a pragmatic, risk\-based approach to compliance

• Be part of a dynamic group of experienced drug development experts


• Enjoy a company culture that prioritizes work/life balance


• Flexible remote working options


• Competitive salary


• Excellent secondary benefits, including pension


• Engage in diverse projects and work with a wide range of clients


• Work alongside with a team of friendly and supportive colleagues

Interested? Send your CV and short motivation letter to hr@3d\-pxc.com. For more information, you can also at \+31 (0\)135348272\.

Acquisition is not appreciated!

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