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Quality Assurance Specialist

Job Field:
Regulatory and Drug Safety Jobs
QA Jobs
Belgium All
Contract Type:
Salary Description:
Job Ref:

Do you want to be part of an award-winning clinical research organisation who is positively working towards improving the health and lives of millions?

We have an excellent career opportunity for a determined and motivated Belgium based Quality Assurance Specialist who strives for excellence to join us on a full time, 12 month contract.

This position has regulatory impact; it is a requirement that all clinical supplies are manufactured and distributed to regulatory requirements and internal standards.

Responsibilities of the Quality Assurance Specialist: ‚Äč

Compile Qualified Person batch release dossiers
Support Packaging and Labeling activities
Provide GMP/ GDP guidance and training
Perform internal and external GMP audits
Investigating non-conformances and quality incidents


Degree educated, Master's level preferred
Minimum of 5 years' experience within the pharmaceutical or health care industry
Experience within R&D would be preferable
Knowledge of pharmaceutical processing techniques
Knowledge of regulatory and GMP standards associated with process control and validation, testing and manufacturing and packaging
Experience of SAP systems and TrackWise
Fluency in English and French languages (both written and spoken)
Willing and able to be site based in Belgium (near Brussels)

Why Work For Clintec?

At Clintec, we believe our people are our greatest asset and understand that the best performance comes from individuals who know they are part of a valued team. You can expect to receive expert training and guidance throughout your career with us, with the opportunity to develop, progress and travel globally.

We can offer you:

A competitive salary, 20 days annual leave plus 12 days RTT and 10 statutory holidays, private healthcare and hospitalisation insurance from the start of employment, meal vouchers and ECO vouchers.
Refer a Friend bonus (terms apply)
The opportunity to work with various global pharmaceutical leaders on the some of the most prestigious, ground-breaking and challenging drug development projects
Real career development opportunities and a life-long career with an innovative, forward-thinking clinical research company

Company Info

Clintec (an IQVIA company), established for 22 years, is an award-winning, full-service global clinical research organisation. Our head quarter office is based in Scotland, UK and we have operations across 50+ countries worldwide.
We differ from other players in the clinical research industry as we combine the agility and flexibility typical of smaller CROs with the global coverage and management associated with large CROs.
We provide clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries, assisting with key product development and managing clinical trials across all major therapeutic areas, with expertise in Oncology and Rare Disease studies.

Application Details

To be considered for this role, please click the APPLY NOW button. Alternatively if you want to know more about job opportunities at Clintec or our company, please visit our website or contact our internal recruitment team directly at


Quality Assurance / Regulatory/ Manufacturing / GMP / Auditing / Quality / Clinical Research / Clinical Trials / Global CRO

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