LAVORO MEDICAL DEVICES INTERNATIONAL REGULATORY

medical compliance: ensure that software design and development practices align with relevant medical device standards and regulations... cross-functional collaboration:...

Minimum 8 years of experience in quality management within the medical device industry... support validation activities related to manufacturing processes, equipment...

Gma region and loc medical leads, ta medical heads, alliance partners, etc) and external investigators to develop us medical clinical research plans and budgets...

Experience with global cosmetic regulatory requirements...      accountabilities responsible for leading edgewell’s global regulatory organization...

regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...

As a subject matter expert, the medical strategy lead will drive thought leadership activities including presentations, publications, and interactions with the medical...

Base regulatory strategy recommendations on precedents and other regulatory    intelligence as well as regulations and guidelines...   minimum requirements/qualifications:...

What youll achieve as a quality assurance regulatory affairs (qara) specialist you will ensure the respect of the quality and regulatory standards throughout the...

Ensures that regulatory submission timelines are aligned with program level and company objectives... may serve as a regional\/local regulatory lead and point of...

Your responsibilities include some of the following: e2e management of regulatory projects ensuring timely submission and successful approval... care to join us...

Prepare site regulatory documents, reviewing for completeness and accuracy...   knowledge and ability to apply gcp/ich and applicable regulatory guidelines...

Prepare site regulatory documents reviewing for completeness and accuracy... knowledge and ability to apply gcp/ich and applicable regulatory guidelines...

Lead the technical development and optimisation of visual inspection devices and primary packaging technologies, driving continuous improvement and innovation...

regulatory affairs senior specialist... desideriamo entrare in contatto con candidat? con esperienza pluriennale nel ruolo maturata nel settore medical devices,...

Nel dettaglio si occuperà di:redazione, revisione, aggiornamento e raccolta della documentazione componente il design history file, in accordo all'mdr 2017/745 e...

Experience with quality issue resolution and regulatory inspection... represent quality in functional leadership and governance meetings for medical, safety and...

Stay informed on evolving regulatory and market trends to ensure compliant, forward-looking strategy development... translate regulatory requirements, user needs...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...     collaborate with clinical program leaders, statisticians, regulatory...

Mdn – non-active non-implantable ophthalmologic devices (e... at sgs, we have an open corporate and international culture... mdn – general non-active non-implantable...