The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for several products. Reviews product labeling for accuracy and for other legal/regulatory requirements and communicates planned/approved changes with other functions, including but not li...
Under the direction of the appropriate level manager or administrator, the Accessibility and Compliance Instructional Support Specialist performs a variety of specialized duties involved in identifying and recommending potential solutions for accessibility barriers based on current applicable guidel...
A company is looking for a Regulatory Affairs and Compliance Director (Remote). ...
A company is looking for a Medicare Adherence Program Manager to enhance program efficiency and service levels for its members. ...
A company is looking for an IT Project Manager to oversee infrastructure projects and provide administrative support. Microsoft Project, Asana, Jira)Experience in IT infrastructure preferredProject Management Professional (PMP) certification is a plus. ...
A company is looking for a Support Services Project Manager/Specialist to provide day-to-day project management support. ...
Director, Regulatory Affairs, Immunology. A company is looking for a Director / Sr. ...
A company is looking for a Regulatory Consulting Associate responsible for preparing plan documents and providing regulatory compliance support. ...
Key Responsibilities:Develop and implement regulatory strategies for global medical device clearances and approvalsManage regulatory submissions and communications with FDA and EU notified bodiesProvide regulatory guidance to cross-functional teams throughout the product lifecycleRequired Qualificat...
A company is looking for a Privacy Program Manager to lead privacy initiatives and ensure compliance across the organization. ...
A company is looking for a Senior Ethics and Compliance Specialist to join their Corporate Compliance team. ...
A company is looking for a Compliance Specialist - Contractor to maintain its compliance programs. Key Responsibilities:Maintain the company's SOC 2 compliance programAssist in the preparation for and execution of SOC 2 auditsSupport the implementation of controls for StateRAMP complianceRequired Qu...
Manager, Regulatory Affairs III to provide strategic direction and operational support for CMC regulatory activities. ...
A company is looking for a Technical Program Manager to lead cross-functional teams in delivering complex technical projects. ...
Chemistry; advanced degree is a plus6+ years of pharmaceutical industry experience in CMC Regulatory Affairs, with a focus on small moleculesExperience in leading high-quality CMC regulatory submissions for global marketing applicationsStrong knowledge of global regulatory guidelines (FDA, EMA, ICH)...
A company is looking for a Regulatory Affairs Specialist to support US and OUS regulatory activities for Class II and III products. CFR 820, MDR)Experience in regulatory affairs, clinical affairs, Quality, or Engineering is required. ...
A company is looking for a Software Implementation Project Manager to oversee complex software implementation projects from conception to completion. ...
A company is looking for a Regulatory Compliance Specialist 4 to support and implement audit programs for cloud infrastructure. ...
A company is looking for an Associate Regulatory Operations Specialist (Remote). ...
Seniro Regulatory Affairs Specialist. Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements. Provide guidance on regulatory requirements necessary for strategic and contingency planning, including developing the preliminary regul...
The Manager Regulatory Affairs represents US regulatory affairs for device development projects. Executes US regulatory strategic plans and provides guidance to Global Regulatory Lead (GRL) and project team. Plans and prepares complex regulatory submission documents primarily for US regulatory filin...
Global Regulatory Affairs Strategy roles (U. Responsible for supporting teams & efforts around major filing activities & Regulatory Health Authority (RHA) interactions & meetings, attending & providing regulatory support to other departments, project teams & committees. Assist Re...
Director, Safety, Regulatory and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device and cosmetic portfol...
The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives for labeling activities for drugs, devices and combination products in assigned therapeutic area(s). E...
PRINCIPAL DUTIES AND RESPONSIBILITIES:Manages the operations of multiple Home Therapies programs with direct responsibility for results, including growth, patient retention, program costs, operational methods, scheduling, and staffing. Responsible for profit and loss management of the assigned progr...