Regulatory Documents Jobs in Bothell, WA

Job Description Summary Senior Regulatory Affairs professional with 8 years of experience in medical devices specializing in US FDA EU MDR and APAC regulations. Proven track record in leading 510(k) PMA and EU Technical Documentation submissions managing audits and inspections and driving end-to-end...

POSITION SUMMARYYou will be responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio. Additionally you will be responsible for leading a team of clinical development scientists in...

POSITION SUMMARYYou will be responsible for scientific oversight data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.KEY RESPONSIBILITIESClinical development expert for assigned studies maintaining current scien...

ROLE SUMMARYThe Chemical Process and Analytical Development (CPAD) group in Bothell WA develops innovative and phaseappropriate synthetic routes and scalable chemical processes for novel small molecule targeted therapeutics. Our process chemists analytical scientists and chemical engineers collabora...

SummaryThis position reports to the Head of Oncology Early Stage Development and is involved in strategic oversight of a substantial proportion of the early pipeline. Manages multiple Global Development Product Leads and lead the direction planning execution and interpretation of clinical trials or...

Job TitleClinical Development ScientistJob DescriptionClinical Development Scientist Oral HealthcareThe Clinical Development Scientist will manage the direction and evidence collection of Philips Oral Healthcare products working with a highly skilled clinical affairs team responsible for driving saf...