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Open nowPosted 2 days ago

QA Validation Specialist 3 (240146)

EURES job mobility portal467,691 open roles

Where
Zuid-Limburg, Netherlands
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Your applicationOpen nowQA Validation Specialist 3 (240146)EURES job mobility portal · Zuid-Limburg, Netherlands

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

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The clock on this job

Early applications get read.

8.4% of postings close within 7 days. Measured by our own scanner across the market. EURES job mobility portal postings stay open a median of 6 days.

Share of postings closed within
  1. 1.8%1 day
  2. 4.0%3 days
  3. 8.4%7 days
  4. 15.4%14 days
  5. 34.3%30 days
This job: posted 2 days ago

EURES job mobility portal median: 6 days open

The posting

Would you like to play a key role within a GMP-regulated environment where quality, compliance, and validation are at the heart of every process? Do you have extensive experience with qualification and validation projects and thrive in an environment where accuracy and quality make the difference? Then this position as QA Validation Specialist in Maastricht could be the next step in your career.

In this role, you will be responsible for reviewing, approving, and overseeing validation and qualification activities within an international pharmaceutical and life sciences organization. You will work closely with colleagues from QA, Engineering, Production, and Technical Services and make a direct contribution to ensuring quality, safety, and regulatory compliance. For professionals with the right experience, this position offers a challenging environment with significant responsibility and impact.

As a QA Validation Specialist, you ensure that equipment, facilities, utilities, and processes comply with GMP guidelines, internal procedures, and applicable regulations.

Your responsibilities include:

- Reviewing and approving validation and qualification documentation (DQ, IQ, OQ, and PQ)

- Assessing and approving User Requirement Specifications (URS)

- Preparing, reviewing, and maintaining validation and qualification plans

- Performing and evaluating risk assessments for equipment, facilities, and utilities

- Approving FAT, SAT, commissioning, and validation reports

- Ensuring full traceability throughout validation projects

- Managing and reviewing lifecycle documentation for equipment and installations

- Conducting periodic reviews of validated GxP systems, equipment, and utilities

- Performing impact assessments for changes to equipment, facilities, and processes

- Supporting production and technical departments with validation activities

- Managing deviations, change controls, and CAPA processes

- Ensuring compliance with GMP, GxP, G

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