Medical Devices Jobs in Shanghai

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees tackling some of the most important health industry challenges. Wi...

JOB DESCRIPTION:Core Job Responsibilities:Manage on-site audits for supplier and Third-party Manufacturers that provide materials/services to EPD..All activities required to plan prepare for conduct report and close the assigned audits.Ensure that all audit related information is documented into t...

JOB DESCRIPTION:Job Weighting% Main Responsibilities40% As Compliance BP provide advice solutions and review support for divisions routine transactions projects and activities.25% Conduct divisional monitoring programs perform data analytics and support corrective actions.20% Based on various audi...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all aspects of study s...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all aspects of study s...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Job TitleUsability Design InternJob DescriptionRole summaryAs a usability intern you support the MR usability to ensures that products we develop in Philips are safe effective efficient intuitive and satisfactory to use. You practice raising awareness to usability & user-centered design and advocate...

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when t...

This role is for upcoming future opportunities that may arise at Fortrea.Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when t...

JOB DESCRIPTION:MAIN PURPOSE OF ROLESummarize the main purpose of the role.Experienced professional individual contributor that works under limited supervision.Applies subject matter knowledge in the area of Regulatory Affairs.Requires capacity to apply skills/knowledge within the context of speci...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

What if the work you did every day could impact the lives of people you know Or all of humanityAt Illumina we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health t...

Job TitleChina Medical Affairs Research Program ManagerJob DescriptionJob Responsibilities: Collaborates across functions to furnish stakeholders with competitive intelligence medical and scientific insights and emerging trends fostering informed decision-making and strategic planning Translate the...

DescriptionSenior Global Quality Systems SpecialistThe Senior Global Quality Systems Specialist has the responsibility to execute to the global Quality System requirements. This position reports to the leadership of Quality Systems.Key responsibilitiesFacilitates change control review meetings and c...

DescriptionSenior Global Quality Systems SpecialistThe Senior Global Quality Systems Specialist has the responsibility to execute to the global Quality System requirements. This position reports to the leadership of Quality Systems.Key responsibilitiesFacilitates change control review meetings and c...