Quality Specialist II

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Job Description

At Thermo Fisher Scientific, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always on top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe.

How will you make an impact?

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!