Senior QA Systems Officer - Environmental monitoring & Technical Support

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Date: Aug 10, 2019

Location: Braine L'alleud, Walloon Brabant, BE

Help us transform patients’ lives.

At UCB, we put our heart, soul and skills into making a difference for people living with severe
disease. Working together to push the boundaries, we blend the best of our talents to unlock
innovation. Will you join us in our pioneering adventure?


To strengthen our QA Systems, based in our hub in Braine l’Alleud, Belgium, we are looking to fill
the position of: Senior QA Systems Officer – Environmental monitoring & Technical Support.


Do you have an agile mind that enjoys being analytical? For UCB, you are an ‘agilytical’ person.
This innovative blend of talent means you are able to swiftly apply forward thinking for the good
of patients.


As a UCB 'agilytical' person and Senior QA Systems Officer – Environmental monitoring & Technical
Support you like to work in an environment where you can

•   Be involved in all technical operations related to the production and analysis of
pharmaceutical products
•   Participate in many projects to ensure the compliance regarding various operations and


As a UCB 'agilytical' person and Senior QA Systems Officer – Environmental monitoring & Technical
Support you will contribute by:


• Participating in the preparation for regulatory inspections, and lead internal audits.
• Ensuring direct follow-up of compliance audit activities, deviations, failure investigations,
change control, qualification/validation activities.
• As the internal expert in GAMP, being the QA Representative for all the local automated &
computerized system for Computerized Systems and Automation.
• Managing non-viable Environmental Monitoring & SEM support, Metrology/Calibration.
• Ensuring communication of compliance status and issues to appropriate levels of the


Interested? For this position you’ll need the following education, experience and skills:


• Master’s Degree in Chemistry, Biology or related field.
• Minimum of 5 years in a regulated pharmaceutical environment or similar, including experience in
Quality Assurance and/or Qualification & Validation.
• Experience with Quality Management System of automated systems, GAMP practical application and
Internal/External Auditing.
• Excellent organization, ability to balance multiple priorities, provide leadership and
identify problem situations.
• Fluent in French and English.


To apply please go to
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