Eu Jobs in Georgia (NOW HIRING)

You'll manage key accounts, coordinate production across US/EU sites, and keep materials flowing smoothly through a global supply chain. What You'll Do * Manage key distributor and OEM automotive ...

S., EU, and international product registration activities. * Medical device quality systems and regulatory compliance. * Preparation and submission of FDA 510(k) premarket notifications.

Conduct the annual whistleblowing program effectiveness review, benchmarking against global regulations, including the EU Whistleblowing Directive. * Maintain the policy house for the Ethics Program ...

Maintains a continued awareness and understanding of EU and FDA regulations and guidance documents. * Prepare regulatory submissions assigned (510(k); IDE & IDE Supplements; PMA Supplements ...

As our new Engineering Manager, you will lead a talented, distributed team across US and EU time zones, acting as the critical manager bridging regional collaboration. Our Cloud Foundation team is ...

S., EU, and international product registration activities. * Medical device quality systems and regulatory compliance. * Preparation and submission of FDA 510(k) premarket notifications.

Conduct the annual whistleblowing program effectiveness review, benchmarking against global regulations, including the EU Whistleblowing Directive. * Maintain the policy house for the Ethics Program ...

Our platform, RegOS , transforms fragmented regulatory requirements (FDA SaMD, EU MDR, IMDRF) into structured, executable, and auditable workflows -- so clinical AI can be evaluated, approved, and ...

NIST AI RMF assessments, EU AI Act readiness, and emerging agentic AI governance frameworks like AIUC-1 each need the same defined scope, methodology, and client-facing materials that ISO 42001 ...

New Relic is seeking an Engineering Manager to lead a distributed team across the US and EU, shaping the future of our core platform. You will mentor engineers, promote proactive ownership, and align ...

Administer document numbering, revision history, and approval workflows for controlled documents within the QMS, in accordance with ISO 13485, 21 CFR 820, and EU MDR requirements. * Assist in ...

Preferred * Experience or strong understanding of medical device regulatory processes (FDA, EU MDR, etc.). * Knowledge of medical device project management and design/development processes.

Based in Ireland is preferred. \n \n \n EU Citizenship or Irish work permit is required \n \n \n

This role is based onsite in Dublin (Full Remote not possible) and does not offer sponsorship therefore you must have a Stamp 4 visa or EU Passport. \n \n \n \n \n

This role is responsible for clinical trial strategies within the US and EU regions for Danaher Diagnostics Neurodegenerative program. This role will specifically support Beckman Coulter Diagnostics ...

As our new Engineering Manager, you will lead a talented, distributed team across US and EU time zones, acting as the critical manager bridging regional collaboration. Our Cloud Foundation team is ...

This role is responsible for clinical trial strategies within the US and EU regions for Danaher Diagnostics. This role will specifically support Beckman Coulter Diagnostics and Life Sciences ...

... EU Passport. \n \n \n \n \n

FDA 21 CFR 820, (EU) 2017/745, Medical Device Regulation (MDR), ISO 13485, ISO 14971, and ISO 10993. * Support Device Director, Device Strategy and Device Procurement organizations on Continuous ...

This role ensures compliance with applicable regulatory requirements (e.g., EU MDR, FDA 21 CFR Part 803/806/820, ISO 13485, MDSAP) by preparing Post-Market Surveillance Reports (PMSR), Periodic ...