EU / UK Transportation Analyst Key Responsibilities: Shipment Scheduling - Inbound and Outbound: using internal...
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specific compliance requirements; Assist the Legal team with the interpretation of various US and EU laws and technical...
in surveillance programs (e.g., EU/UK-style regimes such as MAR/MiFID II referenced in surveillance team practice). Comfort working...
for development within this role? Exposure to global regulatory frameworks (FDA, EU MDR, ISO standards), Opportunities..., with a proven track record of successful submissions. 2. Skills: USFDA 510k submission, CE certification, EU MDR, ISO 13485, ISO...
working with agile teams. Strong intercultural skills and experienced in working with US/UK/EU based companies Exceptional...
between requirements, test protocols, and results to support FDA, EU MDR, and ISO 13485 submissions. Project Support: Provide input...
/Technical File. Develop Regulatory Compliance Declarations (RCDs) for EU MDR/IVDR, FDA, UKCA aligned to IEC 60601, IEC 62304...' experience in Design/Development Quality in the medical device industry. Strong understanding of ISO 13485, ISO 14971, EU MDR...
, and be part of delivering sustainable change. Worley takes personal data protection seriously and respects EU and local data...
. Worley takes personal data protection seriously and respects EU and local data protection laws. You can read our full...
Do: Serve as a trusted advisor to USA & EU-based mid-market and enterprise customers. Own and drive customer retention... & written English with a professional, modern communication style. Deep experience working with USA & EU customers...
14971, EU MDR, and FDA QSR. Experience in DHF review, risk management, and design control compliance. Excellent..., EU MD, FDA QSR Years Of Exp: Above 7 Years Designation: Associate...
, you should have below skills: Excellent understanding of OFAC, OFSI, EU, and UN sanctions laws, regulations, regulatory expectations, and industry...
with global teams across EU, APAC, and US. Occasional travel to R\&D or manufacturing sites depending on business needs....
Description Normal Office Environment. This role will be for APAC/EU/NA Work during Holidays as may... queries. About the team Normal Office Environment. This role can be reporting on a APAC/EU/NA shift Work...
imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive...
with applicable global regulations and standards (i.e., ISO 9001, FDA 21 CFR Part 11, EU Annex 11, FDA guidance documents, GAMP5... Pharmaceutical, Medical Device, or Life Sciences industry (e.g., US FDA 21 CFR 11, EU Annex 11, ISO 9001, ISO 27001, FDA Computer...
with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality...
of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment...
with the EU team and with the global squad Contribute to code reviews, quality control, and backlog grooming. Core Skills...