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IT Systems Quality Specialist
Visualizza: 155
Giorno di aggiornamento: 17-11-2025
Categoria: Garanzia di qualità / Controllo di qualità
Industria: Pharmaceutical Manufacturing
Posizione: Entry level
Tipo di lavoro: Full-time
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Contenuto del lavoro
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.About The Role
Job Description
The IT Systems Quality Specialist is in charge of the administration of the Laboratory Management Systems and the administration of analytical equipment. He/she assures the coordination of the related activities in the team
How You Will Contribute
- Assure the deployment and maintenance of the Laboratory Management Systems
- Ensure compliance of the Laboratory Management system to current regulations and requirements (cGMPs, Data Integrity, ERES, procedures and manuals)
- Manage routine Laboratory Management Systems’ maintenance through associated procedures
- Ensure SOPs and related documentation are up to date
- Coordinate interface methods Implementation (development, validation testing performing) and follow-up validated methods
- Provide Limslink/NWA/Crystal support to other services
- Communicate issues and improvement opportunities to the global team
- Provide system support to other services
- Ensure the administration access role of analytical equipment in compliance with current regulations and requirements
- assure the coordination of the activities in the team
- Ensure staff is adequately trained on the Laboratory Management Systems
- Develop innovative tools to support the team to execute and improve daily workload
- Bachelor’s or master’s degree in biochemistry / chemistry / biotechnology with strong interest for Computerized Systems (Data Management)
- At least 3 years of experience in Quality Control or related field in the pharmaceutical industry.
- Fluent in written and spoken French
- Business level in English
- Demonstrated ability to work autonomously and manage workload in a small team
- Good communication and organizational skills
- Informal working atmosphere with attention to improve your work-life balance
- Flexible ways of working
- Full time permanent contract
- Room for horizontal and vertical growth within the company
- Joining a company with strong results every year and with massive investments from the Corporate to develop further the site.
- Opportunity to interact with numerous colleagues around the globe, multinational collaboration within the Global Quality Business Unit.
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Empowering our people to shine
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, or characteristics, marital or other status. At Takeda, we embrace diversity as a whole.
#GMSGQ
Locations
BEL - Lessines
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
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Scadenza: 01-01-2026
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