QA Consultant
View: 125
Update day: 16-11-2025
Location: Antwerp City Antwerp
Category: Executive management
Industry:
Job content
Are you good at multi-tasking and do you have good project management skills? Then this is the vacancy for you.
Are you interested? Then send your CV and cover letter to sam.goetschalckx@professionals.randstad.be or call +32 2 472 73 61
requirements:
- Knowledge of Quality auditing
- Knowledge of Software quality metrics
- Capacity to ‘translate’ technical information into information that can be understood at every level of the organization.
- Being able to correctly estimate the urgency, criticality and impact of decisions related to the function.
- Ability to multi-task and work on a variety of projects at one time.
- Ability to work independently and work in cross-functional team environment.
- Good communication skills.
- Good project management skills.
- Good problem solving skills.
- University degree or similar
- Fluent in English and Dutch (written and spoken)
system knowledge:
Quality Management System- Process control and IT systems used within pharmaceutical or chemical manufacturing environment
- Problem report, change request systems.
- Document Management systems
- Training Systems
- Microsoft OS, networks, virus protection
- SAP systems
- Test tools
As an answer to your high performance & flexibility, Randstad offers you an interesting salary package, with some interesting extras like:
- Meal vouchers of 7
- Net representation cost of 80
- Hospitalization insurance
- Car + unlimited fuel card OR home-work compensation
- 32 holidays
- End-of-year bonus
- Pension plan
- ECO vouchers
- Opportunities to follow trainings
And on top of this you’ll improve your skills and become an even bigger expert!
Do you believe in affordable healthcare? Are quality & safety your priority number 1? Then you’ll feel comfortable in this company, who’s one of the biggest pharmaceutical companies in the world.
Interested? Send your CV and cover letter to sam.goetschalckx@professionals.randstad.be or call +32 2 472 73 61
General activities :
- Review and approve CSV documents such as SOPs, user requirements, etc,... in order to maintain compliance to regulations, guidelines and standards.
- Be part of engineering teams and interact with other groups for the introduction of new systems and processes. To give advice and support for the preparation of CSV related activities and guard the cGMP aspects in new projects.
- Be a member of cross-functional teams to realize cross-departmental objectives
- Address and follow-up of deviations occurred during execution of qualification/validation activities. Evaluate the incidents related to CS and propose corrective actions if necessary.
- Identify possible impact on the product quality and pass the incident to QA focus if this is the case.
- Follow-up activities related to CSV resulting from audits, quality system initiatives, MAP, etc.
Deadline: 31-12-2025
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