Quality Assurance Specialist NL

Quality Assurance Specialist 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 this role you will play a key part in ensuring our clients 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

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

• 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-on experience 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
• 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.