A company is looking for a Regulatory Compliance Specialist 4 to support and implement audit programs for cloud infrastructure.
Key ResponsibilitiesPlan, manage, and execute multiple audit programs, focusing on PCI assessmentsCollaborate with subject matter experts to enhance audit processes and compliance effortsCommunicate audit status and findings to executive leadership and drive remediation effortsRequired Qualifications8+ years of audit program management experience, preferably in IT or CloudKnowledge of regulatory frameworks such as PCI DSS, SOC 1 & SOC 2, and HIPAAHands-on experience with enterprise-level cybersecurity solutionsBachelor's degree or equivalent experienceRelevant certifications such as PMP, CISA, or PCI Professional Certification preferred
Regulatory Compliance Specialist
A company is looking for a Regulatory Compliance Specialist 4 to support and implement audit programs for cloud infrastructure. ...
Regulatory & Compliance Specialist
The Quality and Regulatory Compliance Specialist is responsible for ensuring that development processes for all in vitro diagnostic (IVD) products comply with applicable regulatory requirements and quality standards. Job Title: Regulatory & Compliance Specialist. Ensure compliance with regulator...
Regulatory & Compliance Specialist
The Quality and Regulatory Compliance Specialist is responsible for ensuring that development processes for all in vitro diagnostic (IVD) products comply with applicable regulatory requirements and quality standards. Job Title: Regulatory & Compliance Specialist. Ensure compliance with regulator...
Regulatory Affairs Program Manager
A company is looking for a Regulatory Affairs Program Manager to lead program and operations management for regulatory affairs. ...
Senior Regulatory Affairs Specialist (IVD)
A leading provider in the health care and digital health space is seeking a Senior Regulatory Affairs Specialist to join their regulatory team. As a key player in regulatory oversight, you will help ensure product compliance with global regulatory standards, including ISO 13485 and FDA regulations. ...
Associate Director Regulatory Affairs
Associate Director Regulatory Affairs (Temp to Perm). Oversee regulatory submissions and approvals, ensuring alignment with global regulatory standards. Regulatory Affairs, including. Lead regulatory strategy development and execution for both U. ...
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This Associate Director of Regulatory CMC will directly report to the Senior Director of Regulatory Affairs, CMC, and will be responsible for representing regulatory CMC on cell therapy pipeline + products. Associate Director, Regulatory Affairs CMC. Regulatory Affairs CMC experience in a pharma/bio...
Senior Associate, Regulatory Affairs
As a Senior Associate of Regulatory Affairs, you will support Regulatory Affairs management in the day-to-day operational aspect of the department and support interactions with global regulatory authorities. Senior Associate, Regulatory Affairs. Represent Regulatory Affairs on project teams and clos...
Sr. Regulatory Affairs Specialist (Locals only with experience composing submissions)
The Regulatory Affairs Specialist will coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. Senior Regulatory Affairs Specialist (Locals Only with experience composing submissions...
Senior Regulatory Affairs Specialist for Medical Devices (Full Remote)
An international medical devices manufacturer is seeking a Senior Regulatory Affairs Specialist to join their US team. Keep abreast of legislation, guidelines, and regulations relating to regulatory affairs in the US; inform and advise the team in Japan. Participate in medical, industrial activities...