TRABAJO REGULATORY AFFAIRS MEDICAL DEVICES

Experience regulatory affairs submission for clinical trials in one or more countries...   to provide strategic regulatory guidance and information to projects;...

Multinacional medical devices|regulatory affairs - temporary contract (6 months min)multinational company specialised in medical devices...

The manager regulatory affairs is responsible for regulatory leadership in project teams by providing regulatory guidance throughout the full product development...

Experience in the registration and post-market surveillance of in vitro diagnostic medical devices (ivdr) and/or medical devices (mdr)... we are looking for an experienced...

Site name: gsk tres cantos, madrid posted date: apr job purpose the purpose of this role is to support the delivery of medical affairs excellence and provide dynamic...

Gsk tres cantos, madrid 发布日期: apr job purpose the purpose of this role is to support the delivery of medical affairs excellence and provide dynamic leadership within...

• experience in medicinal product and medical device regulatory affairs... • ensures training for the regulatory affairs staff... • develops budgets for the regulatory...

To provide strategic regulatory guidance and information to projects; to acquire pertinent regulatory information from agencies and organizations; to support regulatory...

The associate director/director, regulatory affairs leads the submission-related activities associated with the us filings for the approved product lines in collaboration...

Providing strategic input, regulatory support and guidance... we have extensive functional expertise including: regulatory affairs, pharmacovigilance, qa, qc, submissions...

Consultant, regulatory affairs, quality assurance... candidate should have minimum 1 - 2 years of experience doing regulatory affairs, product registration and...

Contact for regulatory affairs manager, project manager, quality assurance department and training department of linical... act as liaison with regulatory agencies...

Must have medical devices and medical device technology experience... 2+ years working in the medical industry... experience working within a qms medical directive...

At least 5 years of experience in regulatory affairs within the medical devices industry, working in cross-functional teams... we seek to incorporate a regulatory...

The phase ii-iv medical writing group, includes writers who prepare documents in support of clinical trials and who assist regulatory affairs professionals with...

In-depth understanding regulatory requirements under the medical devices directive, 93/42/eec and mdr 2017/745... oversee regulatory and quality activities needed...