Validation Engineer CSV - Flanders - Oxford Global Resources

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. · ...

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 seeking a CSV Specialist to join our team in Brabant Wallon, Belgium. As a CSV Specialist, you will play a key role in ensuring compliance and integrity of computerized systems within a leading pharmaceutical 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 ...

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

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. · ...

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

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

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. · ...

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

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 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& ...

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. · ...

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 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 ...

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 ...

We are looking for a CSV Validation Specialist to develop and execute validation strategies for CSV projects. · ...

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. · Minimum 3 years of experience in a pharmaceutical or life sciences environment within a GMP-regulate ...