...template).
Diversity & Inclusion / EEO
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
D...
...plans, estimate program effort, resource requirements using standard estimating techniques and tools, and by working with appropriate staff to understand scope and effort. Incorporate the voice of the customer into ...
About the Role
Location: Barcelona, Spain (Hybrid)
In this global role as Vigilance Process Manager, you will be responsible for the end-to-end management of assigned pharmaco- and devices vigilance processes across Nov...
...implementation experience and a passion for helping customers optimize their regulatory data and document management process. As a key member of our Professional Services team, the Senior Consultant will be responsi...
...We are looking for a Regulatory Affairs Manager- Medical Devices with experience within the medecth and/or pharmaceutical industries and team management to join us, someone who loves to take on new challenges, to wo...
...the requirements.
Perform design failure mode and effect analysis (DFMEA) on designs
Apply applicable standards and guidelines (e.g., IEC60601, ISO14971).
Create test plans to verify our electronics and emb...
...Masimo’s products, solutions and technology including OEM devices in the assigned territory
Plan and execute strategies to convert accounts (single departments and/or the whole hospital) to the use of Masimo prod...
...state, and local laws, as well as regulatory requirements
Statistical, research, and analytical purposes to understand and improve worker satisfaction, improve products & services, and performance as necessary
...
...Regulatory Affairs Analyst & VIE page is loaded Regulatory Affairs Analyst & VIE
Apply locations Barcelona time type Full time... ...mind and work is driven by our shared values: be coura...
...functions on regulatory requirements and assigned business processes.
Acting as a subject matter expert during audits and inspections (e.g. FDA and EMA), leading the preparation of responses to findings and the d...
