Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
QMS Specialist
Eingestellt von Amoria Bond Ltd
Projektbeschreibung
For a freelance assignment with start-date ASAP, we are now urgently looking for Quality Management Systems (QMS) specialist.
The QMS specialist will be responsible to drive quality system compliance, develop and improve procedures for compliance, develop new and improve existing processes and procedures related to non-conformities, issues and CAPA's, and actively collaborate in the roll-out of changes in the QMS application.
Moreover you will organize and provide trainings of personnel in relation to management of non-conformities, issues, CAPA's, document and record control, GDP and GMP, prepare for ISO audits and FDA inspection readiness by effective interaction with other stakeholders, prepare data for Quality review meetings and Management review, and participate in audits performed by external parties.
The company itself is a major international player in niche medical devices based in the Antwerp area. For any freelancer, working there would be a great addition to his or her CV and the projects you and your colleagues will be working on are quite challenging to say the least.
Interested?
Candidates whom are interested or want to learn more about the role or position, can send an e-mail with their CV (in word-format) to Christiaan de Wit at (see below)
Key search terms: Biotechnology, biomedical, bio-technology, bio-medical, therapeutics, farma, pharma, pharmaceutical, CAPA, NC, CC, SOP, GMP, GDP, SC, QA, Quality Assurance, Quality Assurance Manager, Quality Assurance Officer, ISO, GMP, QC, Quality Control, Quality Control, Supply Chain, Medical Devices, Food Science, Cosmetic, Clinical Research Organisations, HSE, Chemical, R&D, Medical Writing & Communication, Medical Affairs, Regulatory Projects, PhD, Master, Bachelor, Freelance, Interim, zzp, contract, project, temporary,
Disclaimer:
Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age and experience, and we confirm that we are happy to accept applications from persons of any age and experience for this role.
The QMS specialist will be responsible to drive quality system compliance, develop and improve procedures for compliance, develop new and improve existing processes and procedures related to non-conformities, issues and CAPA's, and actively collaborate in the roll-out of changes in the QMS application.
Moreover you will organize and provide trainings of personnel in relation to management of non-conformities, issues, CAPA's, document and record control, GDP and GMP, prepare for ISO audits and FDA inspection readiness by effective interaction with other stakeholders, prepare data for Quality review meetings and Management review, and participate in audits performed by external parties.
The company itself is a major international player in niche medical devices based in the Antwerp area. For any freelancer, working there would be a great addition to his or her CV and the projects you and your colleagues will be working on are quite challenging to say the least.
Interested?
Candidates whom are interested or want to learn more about the role or position, can send an e-mail with their CV (in word-format) to Christiaan de Wit at (see below)
Key search terms: Biotechnology, biomedical, bio-technology, bio-medical, therapeutics, farma, pharma, pharmaceutical, CAPA, NC, CC, SOP, GMP, GDP, SC, QA, Quality Assurance, Quality Assurance Manager, Quality Assurance Officer, ISO, GMP, QC, Quality Control, Quality Control, Supply Chain, Medical Devices, Food Science, Cosmetic, Clinical Research Organisations, HSE, Chemical, R&D, Medical Writing & Communication, Medical Affairs, Regulatory Projects, PhD, Master, Bachelor, Freelance, Interim, zzp, contract, project, temporary,
Disclaimer:
Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age and experience, and we confirm that we are happy to accept applications from persons of any age and experience for this role.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges