Quality Specialist II
As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.
Quality Specialist II
We like to hire a dedicated, adaptable and resourceful Quality Specialist to our team in Tilburg. To be responsible for the execution, management and control of quality assurance systems and operations.
You will have areas in which you will be authoritative (“SME”), but in practice you could be assisting in all mentioned areas with consult and/or as back up for your colleague, which gives the function a very wide working range. This broad range gives many opportunities to develop yourself throughout the entire Quality field within the pharmaceutical industry!
We are looking for a candidate who may already have a few years work experience or who is ready to take the first step in your career in quality assurance!
What will you do?
- Perform, maintain and continuous improvement of our quality processes
- Work with quality systems and processes such as deviation/complaint management, batch review/preparation/release, PQR, CAPA management, quality management review, supplier evaluation, management/execution of internal audits, support health authorities/client audits, quality agreements, CPV/validation / qualification (oversight),
- Change control management, documentation management / training management, food/nutritional regulations
- Performance indicators, data integrity, Risk management and Fit&Finish.
- Batch disposition (nutritional)
- Operational quality assurance trending
- Provide and communicate Available Knowledge
How will you get here?
- Bachelor’s or master’s degree preferred, with a pharmaceutical and chemical background.
- Experience in the pharmaceutical or food industry with GMP and/or GDP background.
- Consistent track record in Quality role.
- Experience with Quality computerized systems such as Documentum, Success Factors and TrackWise.
- Experience in Quality record management such as deviations, change controls and customer complaints.
- Experience with general software, such as Word, Excel and PowerPoint.
- Proficiency in Dutch and English
- Analytical capacity
- Decisiveness and integrity
- Good Quality awareness
- Enjoy working in a team
What’s in it for you?
- Competitive base salary
- Annual bonus
- Contributory Pension
- Private medical insurance
- Life Assurance
- Career Development
- Free onsite parking
- Additional optional benefits you can choose to suit you!
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
