Quality Assurance CSV Engineer - Beerse

Join a cutting-edge team dedicated to ensuring the highest standards in computerized systems validation (CSV) within the regulatory framework. · ...

We zoeken een ervaren CSV Validation Specialist met diepgaande kennis van IT-validatieprocessen binnen de farmaceutische of gezondheidszorgsector. · ...

The Advanced Therapy Quality team from Johnson & Johnson Innovative Medicine is recruiting a QA CSV engineer for the CAR-T Hub in Europe. The position will be based in Ghent Belgium. · ...

The Advanced Therapy Quality team from Johnson & Johnson Innovative Medicine is recruiting a QA CSV engineer for the CAR-T Hub in Europe. The position will be based in Ghent Belgium. · To assure that all Computer Systems Validation related regulatory requirements are fulfilled d ...

We are looking for a Quality Assurance Computer System Validation Engineer to ensure the quality and compliance of different systems on the J&J Belgian Campus. · This team belongs to the Quality organization of Johnson & Johnson Innovative Medicine Supply Chain (IMSC) and is resp ...

We are looking for a Quality Assurance Computer System Validation Engineer to ensure the quality and compliance of different systems on the J&J Belgian Campus. · Assure that all Computer System Validation related regulatory requirements are fulfilled during the complete life cycl ...

We are searching for a Quality Assurance CSV Engineer to join one of our partner companies, a large pharmaceutical company leader in the field of biomedicines. · ...

We are looking for a Quality Assurance Computer System Validation Engineer to ensure the quality and compliance of different systems on the J&J Belgian Campus. · ...

You have a passion for Quality, love well-functioning systems and you are eager to gain in-depth knowledge of the quality & compliance requirements in this field? Then this position is waiting for you · Responsibilities · Assure that all Computer System Validation related regulat ...

To support and coordinate quality and validation activities to ensure the validated status of computer systems within automation and IT/OT projects. · ...

This is a quality support project engineer position responsible for ensuring the validated status of computer systems within automation and IT/OT projects. · ...

We are looking for a dedicated professional to drive the validation processes for critical computerized systems, · You develop and implement URS SIA DQ IQ OQ PQ RV TM activities. · You generate validation documentation including protocols and reports ensuring compliance with cGMP ...

This position may be a great fit for you if you are detail-oriented, technically adept, and thrive in a compliance-focused environment. · ...

As 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 All these ...

We are seeking a Validation Engineer with hands-on experience in validating cGMP-critical computerized systems. · ...

We are looking for a Quality Assurance Computer System Validation Engineer · We as QA CSV group belong to the Quality organization of Johnson & Johnson Innovative Medicine Supply Chain (IMSC) and are responsible to ensure the quality and compliance of different systems on the J& ...

Bij Maandag kom je als CSV Validation Engineer terecht bij een projectorganisatie binnen de technische sector. · ...

Avertim is a uniquely positioned management consulting group that bridges the gap between strategy, technology and operations. We support leading Life Sciences companies in their digital transformation journey. · ...

Als CSV Validation Engineer speel je een cruciale rol in de oplevering van geautomatiseerde systemen voor de farmaceutische industrie. · ...

+Job summary · We are seeking a skilled and motivated Validation Engineer to join our team, supporting the validation of computerized systems within a cGMP-regulated pharmaceutical environment. · +QualificationsMinimum 3 years of experience in a pharmaceutical or life sciences en ...