TRABAJO ASSOCIATE REGULATORY SUBMISSIONS BARCELONA, BARCELONA

Organizes regulatory information, logs and tracking... maintains regulatory files/database and chronologies in good order... participate in the product development...

• lead clinical-regulatory authoring teams during the regulatory response period up through approval... job description role holders expertly drive strategic communications...

Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...

Strong cmc technical knowledge with a strategic regulatory mindset... preferred knowledge: regulatory frameworks for medical devices and food supplements...

Job title – regulatory affaire documentation specialist, perfumery&beauty () location – barcelona, spain job model – hybrid do you enjoy being surrounded by regulatory...

Coordinate and prepare regulatory documentation, including technical files, for submission to global regulatory authorities... handle regulatory documentation for...

Oversee regulatory risk, change management, and assurance activities, including sample auditing and feedback/escalation on compliance...

regulatory reports, health authority responses and the safety content of marketing authorisation applications... we are looking for an experienced associate director...

For associate director role, experience of program design knowledge of the technical and regulatory requirements related to the role leadership capabilities to be...

Sustainability, origin) with main focus on regulatory inquires... provide where used data for regulatory assessment, alternate vendors qualification or raw materials...

Experience in managing external service providers and knowledge of quality standards and regulatory requirements... monitor implementation of the quality plan and...

Support regulatory team in preparing documents for study submissions... job description as a clinical research associate i you will work on the frontline of communication...

About the opportunity the associate financial control and reconciliation acts as a subject matter expert in the financial control and reconciliation team within...

The global study associate director (gsad) is responsible for the delivery of clinical studies, including quality, timelines, budgets, resources, investigational...

Senior analyst / associate director, model validation... • develop a solid knowledge of model governance practices and the regulatory environment...

The individual will also be responsible to the ideation of new methods and applications of rwe for new clinical development challenges and will be responsible for...

Submit the raw material documentation to the regulatory and sustainability groups for review... the raw material specialist works in cooperation with the regulatory...

• ensure data quality regular checks and ensure the timely provision of all information required for regulatory reporting 2... ensure fluent and effective information...

Other: based on areas of expertise, supports development of individuals within the team, including secondees and graduates via a buddy system operates in compliance...

Pbrers, psurs, or dsurs) and renewal documentation submitted to regulatory agencies and the patient safety contribution to global regulatory submissions (nda, bla...