TRABAJO QUALITY REGULATORY MEDICAL DEVICES BARCELONA, BARCELONA

medical strategy... regulatory compliance... medical information... medical records... collaborates productively on clinical safety tasks with colleagues from clinical...

Knowledge of the drug development and medical devices development process and launch management... )more than 5 years professional work experience in project management...

Supply chain, customer service, regulatory affairs)... quality specialist             purpose support the implementation and maintenance of the gmp/gdp quality management...

Clinical operations, pharmacovigilance, medical affairs)... educating clinical staff on regulatory requirements, quality standards and good practices...

• experience participating in regulatory inspections... • act as quality approver for quality issues and capas as assigned... • drive quality and business performance...

Coordination of medical check-ups... regarding quality management:  develop and maintain the quality management system... design and improve processes related to...

Years of gmp experience in pharma, biotech, or medical devices... join rephine barcelona: elevate quality in life sciencesat rephine, we are global experts in...

Hands-on experience with iso 9001 and iso 13485 quality systems and regulatory audits... join aurax and contribute to shaping the future of medical hardware innovation!  ...

Familiarity with import/export regulations and quality testing requirements... experience managing compliance for raw materials, single use technology and devices...

Supervise external vendors to ensure quality and on-time statistical deliverables... stay current on regulatory and methodological developments and promote best...

Authors high quality aggregate safety reports to meet regulatory and internal deadlines; ensures all safety regulatory documents are processed and submitted according...

Clinical development, medical affairs, regulatory affairs)...    experience of global regulatory submissions and interacting with major regulatory agencies...

Assess system compliance with global standards to ensure efficiency and regulatory readiness... join rephine barcelona: leading life sciences quality worldwideat...

Support and contribute to medical monitoring of trials...   p rovide expert scientific input into the preparation of regulatory documents and interactions with...

Our state-of-the-art, dog-friendly campus includes a medical center, canteen, and collaborative spaces for networking and relaxation... •    strong analytical thinking...

Cdd) provides input to development of protocols for assigned global clinical trials, scientific monitoring, and reporting of quality data...

We’re always looking towards the future, anticipating changes in medical science and technology... advance accessibility and compatibility by ensuring our solutions...