Qualification and Validation Specialist (The Netherlands)

Qualification & Validation Specialist

Location: Hybrid The Netherlands

Type: Full-time

Are you the kind of person who wont rest until every system process and piece of equipment runs exactly as it should and can prove it

Were looking for a Qualification & Validation Specialist whos passionate about quality precision and ensuring that life-saving products are backed by rock-solid compliance.

In this role youll play a vital part in guaranteeing that critical equipment and systems meet the highest standards from installation to performance. If you thrive on structure enjoy solving technical challenges and want to make a real impact in the pharmaceutical or life sciences world then this could be the perfect next step in your career.

Whats in it for you

Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma biotech and medical devices

Grow within a community of experts: Benefit from knowledge-sharing mentoring and exposure to diverse challenging assignments that broaden your expertise.

Build a meaningful career: As an ambitious and pioneering company we want to offer you the best possible environment to thrive within the life sciences.

A fair competitive package: We offer tailored transparent compensation aligned with your expertise preferences and local market regulations because your contribution deserves to be valued.

What youll be doing

• Bring a positive quality-first mindset to validation and qualification activities ensuring full alignment with internal policies and regulatory standards

• Collaborate closely on process validations (IQ/OQ/PQ) and test method validations turning technical precision into shared success

• Drive nonconformance and CAPA investigations with focus and ownership ensuring clear action plans and timely resolution

• Proactively share your insights to enhance our quality policies and validation procedures helping the team grow stronger together

• Represent QA as a trusted partner in cross-functional projects contributing with expertise and enthusiasm

• Empower others by delivering hands-on training coaching and support in validation quality systems and CSV

• Ensure change control processes are followed with care and discipline keeping systems validated and audit-ready throughout their lifecycle

• Keep a close eye on performance through regular system reviews ensuring compliance is maintained and improvements are made

• Put controls in place to protect data integrity and traceability making sure our quality records tell the full story

• Step up as a subject matter expert during internal and external audits including the high-stakes ones with confidence and clarity

What you bring

• You bring a solid academic foundation with a BSc degree in Life Sciences & Technology Exact Sciences Computer Science or Engineering

• You have hands-on experience in QA computer system validation (CSV) or automated processes and a practical understanding of validating products equipment processes risk management and data integrity

• Youre confident navigating regulatory landscapes with working knowledge of GMP FDA EMA and local quality guidelines. You have a good understanding of Annex 1 guidelines for validation purpose.

• Youre proactive results-oriented and flexible someone who pays attention to the details takes ownership and thrives both independently and in close collaboration with others

Who you are

Our culture is driven by values If this sounds like you youll fit right in:

• Youre resilient and tackle challenges with a positive mindset

• Youre curious and always up for learning something new

• You have a no non-sense approach honest clear respectful

• Youre innovative and bring ideas not just opinions

• And above all youre serious about your work but not too serious about yourself

About us

We support life sciences companies from idea to patient offering tailored solutions in development clinical regulatory compliance production and distribution. With 500 experts across 8 countries we help drive innovation in ATMP biotech medical devices diagnostics digital health and pharma.

We believe in JPEG:

Joy. Partnership. Going the Extra Mile. Getting Things Done.

You wont just be taking a job youll be joining a community where people grow laugh build and contribute to something bigger.

Interested Lets talk.

Send us your CV and motivation letter. You could be the next one to join the QbD family.