Quality Assurance Specialist - NL

TRIUM Clinical Consulting NV; Zuid-Holland; Hybrid; EUR 55,000 - 75,000; Full time

Job summary

TRIUM Clinical Consulting NV is seeking a Quality Assurance Specialist to join the Hybrid, NL team. You will generate and maintain quality records, prepare reports, conduct risk assessments, and investigate deviations with CAPA to ensure product and process quality.

The role involves collaboration across functions, audits, and continuous improvement in GMP environments. Fluency in Dutch and English is essential.

Qualifications

• Bachelor or Master degree in pharmacy, bioengineering, biomedical sciences, or applied sciences.
• Hands-on experience in QA in a GMP environment, preferably in a commercial GMP manufacturing setting.
• Eye for detail and product quality; structured, flexible and stress resistant.
• Proactive, results-oriented, and team-oriented.
• Fluent Dutch and English verbally and in writing.

Responsibilities

• Generate, and maintain Quality records in support of the Quality Systems.
• Prepare detailed reports and present data-driven recommendations to management and stakeholder.
• Conduct risk assessments and proactively identify critical process parameters and potential failure points.
• Investigate deviations, non-conformities, and customer complaints using root cause analysis and CAPA.
• QA batch record review, support materials release and support batch release process.
• Support regular audits and inspections to verify processes comply with internal standards and external regulations.
• Collaborate cross-functionally to design, validate, and optimize processes that meet quality attributes.
• Ensure quality requirements are incorporated from development through production, supporting lifecycle management.
• Keep knowledge up to date with latest guidelines, methodologies, and trends.

Skills

GMP QA experience

Quality systems

Data analysis

Cross-functional

Dutch & English

Education

Bachelor/Master in Pharmacy

Job description

Quality AssuranceSpecialist NL

Location: Hybrid, NL

Type: Full-time

Are you passionate about delivering exceptional quality and driving continuous improvement? We are looking for a detail-oriented and proactive Quality Assurance Specialist to join our team. In this role, you will play a key part in ensuring our client's products and processes consistently meet the highest standards. If you thrive in a collaborative environment, have a keen eye for detail, and are committed to excellence, this could be the next step in your career

What's 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 you’ll be doing

• Generate, and maintain Quality records in support of the Quality Systems
• Prepare detailed reports and present data-driven recommendations to management and stakeholder
• Conduct risk assessments and proactively identify critical process parameters and potential failure points
• Investigate deviations, non-conformities, and customer complaints using root cause analysis and risk-based corrective and preventive actions (CAPA)
• QA batch record review, support materials release and support batch release process.
• Support regular audits and inspections to verify that processes consistently operate within defined design spaces and comply with internal standards and external regulations
• Collaborate cross-functionally to design, validate, and optimize processes that consistently deliver products meeting quality attributes
• Ensure quality requirements are incorporated from development through production, supporting lifecycle management.
• You keep your knowledge within your expertise up to date with the latest guidelines, methodologies, and trends.

What you bring

• You bring a solid academic foundation with a Bachelor or Master degree in pharmacy, bioengineering, biomedical sciences, or applied sciences.
• Hands-onexperience in QA in a GMP environment, preferably in a commercial GMP manufacturing setting
• A keen eye for detail and product quality is your main concern. You think and act in a structured way, are flexible and stress resistant
• You’re proactive, results-oriented, and flexible — someone who pays attention to the details, takes ownership, and thrives both independently and in close collaboration with others
• You have an excellent command of both Dutch and English, with strong written and verbal communication skills.

Who you are

Our culture is driven by values If this sounds like you, you’ll fit right in:

• You’re resilient and tackle challenges with a positive mindset
• You’re curious and always up for learning something new
• You have a no non-sense approach honest, clear, respectful
• You’re innovative and bring ideas, not just opinions
• And above all, you’re 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 won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.