QA Validation Specialist 3

Uitzendbureau; Geleen; On-site; EUR 50,000 - 78,000; Full time

Benefits offered by this job

Travel allowance €0.23/km

Pension accrual

Temp contract via Manpower

Job summary

Uitzendbureau in Maastricht zoekt een QA Validation Specialist voor een GMP-omgeving en internationale life sciences context. Je reviewt en beheert validatie- en kwalificatieactiviteiten en werkt samen met QA, Engineering, Production en Technical Services om kwaliteit en naleving te waarborgen.

De rol vereist ervaring met DQ/IQ/OQ/PQ, URS, risicoanalyse en change controls. Een tijdelijke arbeidsovereenkomst via Manpower is geboden, met een fulltime 40-urige werkweek.

Qualifications

• Er is geen minimale opleiding vereist.
• Je beheerst Engels.

Responsibilities

• Reviewing and approving validation and qualification documentation (DQ, IQ, OQ, PQ).
• Assessing and approving URS (User Requirements Specifications).
• Preparing, reviewing and maintaining validation plans.
• Performing risk assessments for equipment, facilities and utilities.
• Approving FAT, SAT, commissioning and validation reports.
• Ensuring traceability throughout validation projects.
• Managing lifecycle documentation for equipment and installations.
• Conducting periodic reviews of validated GxP systems, equipment and utilities.
• Supporting production and technical services with validation activities.
• Managing deviations, change controls and CAPA processes.

Skills

Engels

Job description

Vacaturebeschrijving 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, GDP, and quality requirements
• Providing advice on quality and compliance-related matters
• Identifying and implementing improvements within validation and quality systems
• Collaborating with QA, Engineering, Production, and Technical Services to ensure compliance

What's in it for you

• Gross monthly salary between €4,500 and €7,000
• Temporary employment contract through Manpower
• Travel allowance of €0.23 per kilometer
• Pension accrual
• Full-time position of 40 hours per week
• Opportunity to work on high-level projects within the pharmaceutical and life sciences industry
• Significant responsibility within complex validation and compliance processes
• Collaboration with experienced specialists across multiple disciplines
• Room for professional and technical development
• Working environment focused on quality, knowledge sharing, and continuous improvement

Over de werkgever You will join an international organization within the pharmaceutical and life sciences sector. Every day, teams work on products, processes, and systems that must meet strict quality standards and GMP requirements. The organization invests heavily in innovation, knowledge development, and collaboration across disciplines.

Within this professional environment, you will have the opportunity to contribute to challenging validation and compliance projects while playing an important role in maintaining the quality of processes and installations.

Working hours

You will work during standard office hours.

Dienstverband:

Vaardigheden

• Er is geen minimale opleiding vereist
• Je beheerst Engels