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Validation Engineer - Manufacturing - GMP
Eingestellt von Elevate Direct
Gesuchte Skills: Engineer, Engineering, Support
Projektbeschreibung
VALIDATION ENGINEER/BEERSE, BELGIUM/5 MONTHS CONTRACT/UP TO TO 42 EUR (PER HOUR)
JOHNSON & JOHNSON IS AN AMERICAN MULTINATIONAL MEDICAL DEVICES, PHARMACEUTICAL AND CONSUMER PACKAGED GOODS MANUFACTURER FOUNDED IN 1886.
Validation Engineer will:
- Be responsible for initiating business facing SDLC deliverables for a wide variety of planned and unplanned changes for systems supporting R&D activities.
- Be responsible for managing timelines and review activities related to SDLC deliverables.
- Be responsible for building training modules for select systems supporting R&D activities.
- Be responsible for planning, oversight and documentation of project deliverables.
- Be responsible for first line support and response of compliance events for select systems supporting R&D activities.
NON TECHNICAL SKILLS AND ADDITIONAL DETAILS
QUALIFICATIONS:
- A minimum of a BS in Science or Engineering is required
- Experience with SDLC workflow and documentation requirements.
- Experience working within a GMP environment, implementing and maintaining high quality standards for all aspects of the work conducted including adherence to regulatory and GMP compliance, as they pertain to data management and software development required.
- Knowledge of laboratory (lab systems) and manufacturing automation systems used in support of pharmaceutical process development and/or clinical manufacturing required.
- Project management skills are preferred.
- Dutch and English Language
IF YOU MATCH THESE REQUIREMENTS, PLEASE APPLY IN THE NORMAL WAY. ELEVATE WILL SEND YOU AN EMAIL, PLEASE OPEN, CLICK AND ACTION THAT EMAIL AND YOUR APPLICATION WILL BE VISIBLE TO THE HIRING ORGANISATION DIRECTLY.
JOHNSON & JOHNSON IS AN AMERICAN MULTINATIONAL MEDICAL DEVICES, PHARMACEUTICAL AND CONSUMER PACKAGED GOODS MANUFACTURER FOUNDED IN 1886.
Validation Engineer will:
- Be responsible for initiating business facing SDLC deliverables for a wide variety of planned and unplanned changes for systems supporting R&D activities.
- Be responsible for managing timelines and review activities related to SDLC deliverables.
- Be responsible for building training modules for select systems supporting R&D activities.
- Be responsible for planning, oversight and documentation of project deliverables.
- Be responsible for first line support and response of compliance events for select systems supporting R&D activities.
NON TECHNICAL SKILLS AND ADDITIONAL DETAILS
QUALIFICATIONS:
- A minimum of a BS in Science or Engineering is required
- Experience with SDLC workflow and documentation requirements.
- Experience working within a GMP environment, implementing and maintaining high quality standards for all aspects of the work conducted including adherence to regulatory and GMP compliance, as they pertain to data management and software development required.
- Knowledge of laboratory (lab systems) and manufacturing automation systems used in support of pharmaceutical process development and/or clinical manufacturing required.
- Project management skills are preferred.
- Dutch and English Language
IF YOU MATCH THESE REQUIREMENTS, PLEASE APPLY IN THE NORMAL WAY. ELEVATE WILL SEND YOU AN EMAIL, PLEASE OPEN, CLICK AND ACTION THAT EMAIL AND YOUR APPLICATION WILL BE VISIBLE TO THE HIRING ORGANISATION DIRECTLY.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges