4 beste vacatures voor de functie van senior quality assurance consultant in hoogeloon (nieuwe medewerkers gezocht)

(Senior) Consultant QA
3D-PharmXchange —Tilburg
- E-mail
- Bediening
- Master
- Bachelor
Senior Quality Assurance Consultant
Mérieux Nutrisciences | Expert Partners —Tilburg
- € 3.800 - € 6.000 per maand
- Parttime
- Reiskostenvergoeding
- Tankpas
WMS Solutions Architect
Rhenus SE & Co. KG —Tilburg
- Online sollicitatie
- ERP systemen
- Master
- Bachelor
- Budget voor professionele ontwikkeling
Tax Advisor Global Mobility en Loonheffingen
Forvis Mazars —Eindhoven
- Parttime
- Hybride werken
- Kantoor
- Bachelor
- Reiskostenvergoeding
- Tankpas

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(Senior) Consultant QA
3D-PharmXchange —Tilburg
Ability to engage with multiple stakeholders, from operational teams to senior management. You will closely collaborate with our QA, CMC, Clinical and…
Senior Quality Assurance Consultant
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€ 3.800 - € 6.000 per maand

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(Senior) Consultant QA

3D-PharmXchange
Tilburg

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Vacaturegegevens

Kwalificaties

Bediening
Master
Kwaliteitsborging
Bachelor

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Company Profile

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

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

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

Our offer:

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?

Interested? Send your CV and short motivation letter to [email protected]. For more information, you can also at +31 (0)135348272.

Acquisition is not appreciated!

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senior quality assurance consultant vacatures in hoogeloon

(Senior) Consultant QA

Senior Quality Assurance Consultant

WMS Solutions Architect

Tax Advisor Global Mobility en Loonheffingen

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