A company is looking for a Regulatory Affairs Specialist I to manage regulatory documentation and submissions.Key ResponsibilitiesCompile and maintain regulatory documentation databasesCoordinate the preparation of regulatory documents and submissionsCommunicate with regulatory agencies regarding compliance and submission strategiesRequired QualificationsBachelor's Degree in any fieldExperience in Regulatory Affairs or U.
S. SubmissionsKnowledge of regulatory rules and changesAbility to conduct employee regulatory trainingFamiliarity with international regulations and standards
Principal Regulatory Affairs Specialist
A company is looking for a Principal Regulatory Affairs Specialist, US Regulatory Policy. FDA regulatory requirements and policyRegulatory experience within the medical device industry or a regulatory agencyExperience in advocacy related to healthcare policy and regulationsStrong research and analyt...
Regulatory Affairs Specialist
Yoh is seeking a Regulatory Affairs Specialist for our Pharmaceutical client here in St. Plan/author/compile/submit/manage variations for marketed products outside the United States Respond to health authority information requests and comments to achieve approval Review and assess CMC regulatory imp...
Regulatory Affairs Specialist
A company is looking for a Regulatory Affairs Specialist I to manage regulatory documentation and submissions. ...
Sr. Regulatory Affairs Specialist - Pet Food
As the Senior Regulatory Specialist, you will work with cross functional teams, providing guidance and direction to ensure regulatory compliance across the organization. The Senior Regulatory Specialistutilizes people skills, regulatory knowledge and experience gained to support internal cross-funct...
Regulatory Affairs Specialist
Yoh is seeking a Regulatory Affairs Specialist for our Pharmaceutical client here in St. Plan/author/compile/submit/manage variations for marketed products outside the United States Respond to health authority information requests and comments to achieve approval Review and assess CMC regulatory imp...
Regulatory Affairs Specialist
The Regulatory Affairs Specialist responsibilities encompass the support of international drug product applications. Review and assess CMC regulatory impact and provide regulatory strategy for post-approval changes proposed at the manufacturing site. Self-starter who takes initiative to learn, grow ...
Compliance Nurse Specialist (RN)
Assists in education of clinicians and billing staff to support compliance with third party documentation and billing standards. Works on joint projects with other internal compliance staff to resolve billing and documentation issues. ...
Environmental Project Manager
As an Environmental Project Manager with Civil & Environmental Consultants, Inc. CEC), you'll be involved with environmental projects and provide client-focused customer service in the manufacturing, energy, mining, and real-estate markets. You'll interact with clients, contractors, and local govern...
Revenue Enablement Program Manager
A company is looking for a Revenue Enablement Program Manager to drive the execution of enablement programs and support the revenue organization. Key Responsibilities:Design, execute, and continuously improve enablement programsFacilitate training for internal and external new hires and provide team...
CyberSecurity Program Manager
We are looking for 8-10 years of Program/Project Management with good CyberSecurity project experience. Years in a Program/Project management position. Keen understanding of project dependencies and program interdependencies. ...