... , your non-precise location, your device type, or which content you ... same Internet connection on both devices). Identify devices based on information transmitted automaticallyWith ... , your non-precise location, your device type, or which content you ...
... activities, for example:• Work in medical devices industry or closely related industries (. pharmaceutical industry) in a research and development, manufacturing, quality management or regulatory affairs capacity• Work in health services, ...
... , your non-precise location, your device type, or which content you ... same Internet connection on both devices). Identify devices based on information transmitted automaticallyWith ... , your non-precise location, your device type, or which content you ...
... 3 años de experiência como Responsable de Departamento Aduanas en un ... , your non-precise location, your device type, or which content you ... same Internet connection on both devices). Identify devices based on information transmitted automaticallyWith ...
... , your non-precise location, your device type, or which content you ... same Internet connection on both devices). Identify devices based on information transmitted automaticallyWith ... , your non-precise location, your device type, or which content you ...
... multinational environments. - Proficiency in navigating regulatory frameworks and forging strategic partnerships. - ... same Internet connection on both devices). Identify devices based on information transmitted automaticallyWith ...
... employees. Ensures adequate training of regulatory affairs group and oversees regulatory affairs practices to ensure alignment of ... and technology tools. Ensures the regulatory affairs’ activities are delivered on time, ...
... implementation details. - Familiarity with regulatory legal acts governing the companys ... non-precise location, your device type, or which content you ... Internet connection on both devices). Identify devices based on information transmitted automaticallyWith ...
... of experience in regulatory affairs, including a minimum of 5 years in a team leadership role, for IVD companies, including successful pre-market submissions. - Extensive knowledge of IVD medical device regulatory requirements and submission processes ...
... HCPs. Working closely with Global Medical Affairs and cross-functional colleagues, s he ensures that the US Medical Affairs plan is aligned with brand ... legal review and statutory or regulatory clarification, which Pfizer intends to ...