A company is looking for a Regulatory Specialist in the US. ...
GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs StrategyEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group s...
A company is looking for a Global Regulatory Affairs Specialist. ...
Role: Regulatory Affairs Specialist. Follow developments before Public Utility Commission of Texas (PUCT), Texas legislative proceedings, and other regulatory or government agencies that affect gas and power marketing and trading activities and report on such developments to relevant groups within t...
A company is looking for a Regulatory & Compliance Specialist in the healthcare ecosystem. Key Responsibilities:Track state and federal legislation and regulations affecting clientsUpdate bills and rules in the online softwareMonitor Board of Pharmacy websites for relevant informationRequired Qualif...
Work with global regulatory affiliates to compile global regulatory impact for changes on commercialized medical device products. GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy. Perform regulatory assessments for US, EU, and Canada for changes on commerciali...
Deliver hands-on quality management and regulatory affairs solutions to a wide range of businesses including manufacturing, distribution, logistics, construction, health care and government. Conduct internal audits to ensure compliance with QMS and regulatory requirements. Train internal and externa...
Regulatory Affairs Specialist (R&D/QA). Provide regulatory support for products that will be transitioning from the IVDD to IVDR CE Marking. Quality Assurance, Research & Development, Marketing) to collect and coordinate information and regulatory documentation to assemble IVDR compliant technical f...
Regulatory Affairs Specialist (R&D/QA). Provide regulatory support for products that will be transitioning from the IVDD to IVDR CE Marking. Quality Assurance, Research & Development, Marketing) to collect and coordinate information and regulatory documentation to assemble IVDR compliant tec...
Review and audit of protocols, informed consents, source data, data entry, case reports forms (CRFs) and regulatory documents for accuracy and compliance. Oversee final review of regulatory and study documents prior to archiving. ...
The successful candidate will perform the full range of the Senior Intelligence Specialist duties. ...
Security Advisory Project Manager. Lead one or more large project management teams by breaking down bigger technological programs and assisting with project staffing. Communicate with the client, company and project team leadership, measuring and sharing project metrics/status; recommend program cha...
The ADA Compliance Specialist plays a vital role inensuring compliance with the Americans with Disabilities Act (ADA)within the HR operations of the organization and other relevantregulations to promote. This position focuses on implementingADA-related processes, providing operational support foracc...
The role of Government Programs Market Sales Manager is vital in achieving this commitment to our members through their focus on innovative leadership, agent support and coaching, and accountability for growth and results in all distribution channels selling UnitedHealth Group portfolio of products ...
A company is looking for a Regulatory Filing Services Associate - Second Shift Position (2-10 PM EST) - Remote. ...
Project Manager (Remote) on a Temp-To-Hire basis. ...
A company is looking for a Project Manager Associate in Regulatory Affairs. ...
Key Responsibilities:Provide federal & state compliance supportMonitor legislation and evaluate internal complianceAssist in developing and implementing compliance policiesRequired Qualifications:Bachelor's DegreePrior experience in banking/financial services industry in a compliance roleExperience ...
A company is looking for a Technical Project Manager II. Key Responsibilities:Track schedule and budget; manage and report progressPrioritize, track, and report progress in support of assembly and acceptance testingMaintain and track project plans to deliver fluids components and sub-assemblies in s...
Key Responsibilities:Assist in the development and implementation of proactive programs to support regulatory objectivesMaintain a calendar for regulatory reports and submissionsDesign and manage templates for regulatory submissionsRequired Qualifications:Bachelor's degree in Engineering, Life Scien...
A company is looking for a Regulatory Affairs Manager. ...
A company is looking for a Compliance Data Specialist in Phoenix, Arizona. ...
A company is looking for a Senior Quality Assurance Specialist. ...
A company is looking for a Regulatory Affairs Manager - Biosimilars. ...
Key Responsibilities:Craft and execute regulatory strategies for blood products aligned with business goals and global requirementsEnsure compliance with FDA, EMA, and other regulatory bodiesOversee preparation and submission of regulatory documents (IND, BLA, international submissions)Required Qual...