TRABAJO REGULATORY QUALITY SPECIALIST MEDICAL
(+1000 ofertas de trabajo)
Listado de trabajos de Regulatory quality specialist medical
Quality and regulatory manager (software as a medical device)
Required qualificationsminimum 5 years of experience in quality management and in regulatory affairs specifically within the medical device industry...
Supply chain, customer service, regulatory affairs)... quality specialist purpose support the implementation and maintenance of the gmp/gdp quality management...
Specialist external quality assurance
Job description a fantastic opportunity has arisen for a specialist external quality assurance... relevant experience in the pharmaceutical industry and/or biotechnology...
quality data management:track, analyze and report quality metrics e... work closely with regulatory affairs, r&d;, laboratory, and external partners to ensure quality...
regulatory information associate, regulatory operations & systems management
Position: regulatory information associate, regulatory operations & systems managementlocation: madrid (on site)experience: 3 to 5 years’ experience in regulatory...
Medical safety lead / sr medical safety lead (crm)
medical strategy... regulatory compliance... medical information... medical records... collaborates productively on clinical safety tasks with colleagues from clinical...
Associate director, quality assurance - third party quality management - hybrid
Serves as a quality spokesperson on a variety of quality or compliance-related issues... interprets complex regulatory requirements for various audiences, reviews...
Regulatory affairs specialist (flavors)
In food science, regulatory affairs, or a related field... evaluate raw materials and supplier documentation for regulatory compliance... eu, fda, codex, efsa)...
Quality and regulatory manager for health ai products
Spotlab has built a solid foundation in quality and regulatory affairs, including: the in vitro medical device manufacturer license granted by the spanish medicines...
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Medical information specialist - (spanish & english speaking), us hours
Human science, experience and/or training: call center, medical information, pharmaceutical industry, and clinical experiences including medical writing...
Regulatory affairs, admin specialist
While part of the regulatory affairs organization, this role is not technical or strategic, but rather centered on routine administrative support to help ensure...
Medical information specialist - (spanish & english speaking), us hours
medical writingon-call responsibilities on an as assigned basis... human science, experience and/or training: call center, medical information, pharmaceutical industry...
Assist the quality manager and project quality lead in document control processes and quality records management... support quality audits by providing required...
Colaborar con el regulatory affairs manager y con el regulatory affairs head, aportando la información necesaria para realizar el seguimiento del presupuesto asociado...
Quality assurance operations specialist
Summary the qa operations specialist manages quality aspects and projects within area of responsibility... review and approve standard operating procedures (sops)...
Medical information specialist with latvian and english and additional foreign language
Responsibilities provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product...
Quality and operation specialist
Manage risk identification, resolution and rectification in the region, organize investigations and analysis and promote major quality anomalies, regularly organize...
Quality and regulatory affair (qara) manager
Knowledge and/or expertise in quality (iso 13485) and regulatory (mdr and fda) processes... our new team member will support the implementation and documentation...
Data quality technical specialist – kpi implementation
Job title: data quality technical specialist – kpi implementationlocation: remote from spainlanguages required: english (minimum c1)candidates must possess a valid...
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