TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE

Previous medical device submission experience preferred... demonstrated expertise in medical device regulatory requirements and processes... experience with u...

Minimum 3+ years related regulatory affairs experience, preferably within medical devices (2+ years with advanced degree)... medical device business services, part...

Position: regulatory affairs management director (rad), regulatory science & execution, global regulatory affairs location: barcelona - spain (3 days working from...

Documentation preparation: prepare comprehensive regulatory documentation for medical devices, including ivds and medical device software, ensuring compliance with...

We are looking for a medical writer expert– regulatory affairs for our team of development, strategy and scientific writing expert unit... why working at asphalion??️permanent...

Johnson & johnson is recruiting for an associate director, cmc regulatory affairs... escalates issues to cmc regulatory affairs management that affect registration...

Minimum 5 years of pharmaceutical or medical device regulatory affairs or related experience... collaborate with global cross-functional teams and the global regulatory...

Represents regulatory affairs on cross-functional project teams... provide regulatory affairs support during internal and external audits...

External core interactions with: regulatory authorities, cros, consultants, partners... champions use of expedited regulatory pathways globally to accelerate patients’...

As a regulatory affairs lead ukraine, you are part of the turgan cluster and report to a regulatory affairs head... you will also be in charge of planning of regulatory...

With our expertise, we interpret, anticipate, and shape global health authority expectations to build insightful cmc and device regulatory strategies...

The director, global medical affairs strategy & execution is responsible for leading the strategic development and implementation of cross-therapeutic area (ta)...

Due to our constant growth, we are looking for a regulatory affairs specialist to support our projects in our office in madrid (spain)you will be responsible for:execution...

Run regulatory local projects meeting timelines and costs understand relevant legislative and regulatory guidance applicable to activities prepare risk benefit analysis...

Extensive experience in quality assurance, with a strong preference for experience within the medical device industry... direct training programs for quality and...

The new assets medical advisor will report to the medical director... position summary the new assets medical advisor is an office-based position within spain &...

At least 2 years of experience in regulatory affairs within the medical device industry... maintain an in-depth understanding of global medical device regulations...

Summary the global medical affairs team acts as enterprise medical voice across the asset lifecycle and leads the medical strategy for the therapeutic area...

You will have previous in field experience as an msl or medical affairs and a track record of high performance in driving kol engagement and successful medical activities...

Medtech business analyst - connected regulatory intelligence the iqvia connected regulatory intelligence (cri) is a groundbreaking innovative solution that simplifies...