Emplois actuels liés à Quality Projects Associate - Puurs - Arcadis
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il y a 2 semaines
Puurs, Belgique Select Projects Temps pleinSelect Projects is op zoek naar een nieuwe collega die aan de slag wil gaan als **Quality Associate** ter versterking van ons team bij een farmaceutisch bedrijf in Puurs. Als **Quality Associate** zal je instaan voor: - Kwaliteitsbeoordeling van validatiedocumentatie, change records en procedures - Beoordelen van impact assessments - Coördineren van...
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Quality Associate
il y a 2 semaines
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Quality Projects Associate
il y a 2 semaines
Puurs, Belgique Pfizer Temps pleinFunctie omschrijving Als Quality Projects Associate ben je verantwoordelijk voor het bewaken van de product-gerelateerde validatie en registratie aanpak binnen de Pfizer Puurs productiesite. Je bent het aanspreekpunt en de quality authority voor validatie en compliance met de huidige Pfizer-normen, de wettelijke voorschriften (cGMP, ICH, GDP...) en de...
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Quality Projects Associate
il y a 4 semaines
2870 Puurs, Belgique Arcadis Temps pleinThe Quality Project Associate focuses on quality oversight and project support where you will primarily deliver essential quality oversight and comprehensive project support for pharmaceutical processes and products within Belgian sites, specifically the aseptic manufacturing plant. You act as an independent quality authority for product-related...
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Quality Projects Associate
il y a 2 semaines
Puurs, Belgique Pfizer Temps pleinFunctiebeschrijving In deze rol ben je verantwoordelijk voor het bewaken van de validatie en registratie aanpak voor alle equipment (vullijnen, autoclaven, inspectie machines, HVAC, computer systemen, labo systemen,) van een volledige productie eenheid. Je bent het aanspreekpunt en de quality authority voor validatie en compliance binnen deze productie...
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Site Quality Head
il y a 2 semaines
Puurs, Belgique Novartis Temps plein220 that’s the number associates working in our Quality department. As a QA head, you will run and direct all Quality Assurance and Quality Control activities for the 4 plants (solutions, visco-elastics, ointments and biologicals) as well as all the distribution activities where the Puurs plant is involved. - Your responsibilities: - Your responsibilities...
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Project Quality Engineer
il y a 3 semaines
Puurs, Belgique Arcadis Temps pleinAs a Quality support project engineer within the ICS department, you will execute different support tasks which results a validated state of computer systems. These tasks are:Operational support by giving advise based on knowledge and experience of procedures so solutions for software and infrastructural problems can be implemented correctly.Responsible for...
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Project Quality Engineer
il y a 3 semaines
Puurs, Belgique Arcadis Temps pleinAs a Quality support project engineer within the ICS department, you will execute different support tasks which results a validated state of computer systems. These tasks are: Operational support by giving advise based on knowledge and experience of procedures so solutions for software and infrastructural problems can be implemented correctly. Responsible...
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Project Quality Engineer
il y a 3 semaines
2870 Puurs, Belgique Arcadis Temps pleinAs a Quality support project engineer within the ICS department, you will execute different support tasks which results a validated state of computer systems. These tasks are: Operational support by giving advise based on knowledge and experience of procedures so solutions for software and infrastructural problems can be implemented correctly. Responsible...
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Quality Support Project Engineer
il y a 2 jours
Puurs, Belgique Arcadis Temps pleinDepartmentAs a center of excellence in technology, innovation and project management, the engineering department of our client in Puurs is working on the future of the site. The ICS team within Puurs is working actively on the automation and integration of systems and data flows. Thanks to the expertise and the use of new technologies, we can build robust...
Quality Projects Associate
il y a 2 semaines
The Quality Project Associate focuses on quality oversight and project support where you will primarily deliver essential quality oversight and comprehensive project support for pharmaceutical processes and products within Belgian sites, specifically the aseptic manufacturing plant. You act as an independent quality authority for product-related qualifications and validations, ensuring regulatory CMC compliance of plant processes with regulatory filings, and contributing to compliant and right first-time product launches. Key responsibilities include:Performing quality reviews of validation documentation, change records, and proceduresCoordinating regulatory submissionsProviding crucial support for Quality Management Systems, including validation, Quality Risk Management (QRM), and change managementConducting end-to-end validations of new products (covering formulation, filling, and packaging), which involves preparing validation documents, monitoring production batches, analyzing results, and performing root cause investigations for deviations with proposed corrective and preventive actionsSupporting the creation and maintenance of Master Batch RecordsActively contributing to continuous improvement initiativesQualifications:Master's degree in a relevant scientific or engineering discipline, such as Industrial Engineering, Civil Engineering, Bio-engineering, or (Industrial) Pharmacy, or equivalent experience in fields like Biochemistry or BiotechnologyKnow-how of project management within the pharmaceutical or related industries, with a strong focus on GMP-regulated and aseptic environmentsStrong analytical and problem-solving abilities, excellent organizational skills, and a meticulous, accurate, and quality-conscious work approachStrong communication, interpersonal, and technical writing skills to effectively collaborate with cross-functional teams and external stakeholdersA perfect command of Dutch and good knowledge of English (written and oral) are required
