Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Quality Validation Consultant
Eingestellt von Berry Technical
Gesuchte Skills: Consultant, Consultants, Client, Pure
Projektbeschreibung
Quality Validation Consultant
CHF Negotiable
3-6 month contract
Solothurn, Switzerland
Our client is seeking experienced quality validation consultants to join their quality assurance team on site in Switzerland assisting with the ongoing auditing and review of previous quality assurance documentation. This is the chance to join a well established, international giant in their industry who are growing at a huge rate and expanding their teams with high calibre professionals to assist them with driving production forward. As the quality validation consultant you will execute review and propose remediation of historical validation records associated with equipments ensuring that all compliance issues and requirements of Validation Policies and Procedures are addressed.
Key experience and knowledge
*In depth knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry
*High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations
*
Medical devices progressed experience is needed, minimum of 2 - 5 years working in a regulated industry a minimum 2 of which has been spent carrying out validation
Non-Technical profile requirements:
*Pure Consultants profile will be preferred -
*Must be able to work on multiple simultaneous tasks with limited supervision;
*Excellent customer service, interpersonal, communication and team collaboration skills; -
*. Language proficiencies: -English, German a strong plus;
Please email
CHF Negotiable
3-6 month contract
Solothurn, Switzerland
Our client is seeking experienced quality validation consultants to join their quality assurance team on site in Switzerland assisting with the ongoing auditing and review of previous quality assurance documentation. This is the chance to join a well established, international giant in their industry who are growing at a huge rate and expanding their teams with high calibre professionals to assist them with driving production forward. As the quality validation consultant you will execute review and propose remediation of historical validation records associated with equipments ensuring that all compliance issues and requirements of Validation Policies and Procedures are addressed.
Key experience and knowledge
*In depth knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry
*High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations
*
Medical devices progressed experience is needed, minimum of 2 - 5 years working in a regulated industry a minimum 2 of which has been spent carrying out validation
Non-Technical profile requirements:
*Pure Consultants profile will be preferred -
*Must be able to work on multiple simultaneous tasks with limited supervision;
*Excellent customer service, interpersonal, communication and team collaboration skills; -
*. Language proficiencies: -English, German a strong plus;
Please email
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Organisation/Management