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...
A company is looking for a Marketing Program Manager to oversee training and enablement for customer-facing teams in the technology sector. ...
A company is looking for a Regulatory Affairs and Compliance Director (Remote). ...
Manager, Regulatory Affairs III to provide strategic direction and operational support for CMC regulatory activities. ...
A company is looking for a Project Manager for Cloud Modernization. ...
A company is looking for an Associate Director, Global Regulatory Project Management and Strategic Planning - GI. ...
Director, Regulatory Affairs, Immunology. A company is looking for a Director / Sr. ...
A company is looking for a Senior Regulatory Compliance Specialist to assist with the implementation and maintenance of its Compliance Software Program. ...
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 Sustainability Project Manager to oversee complex programs focused on carbon reduction and decarbonization initiatives. ...
A company is looking for a Certifications Program Manager to oversee customer and end-user software certifications. ...
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 Senior Medicare Communications Compliance Specialist to support regulatory requirements associated with Medicare materials and sales compliance. ...
A company is looking for a Compliance Corrections Specialist to oversee corporate ethics and compliance programs. ...
A company is looking for a Senior Ethics and Compliance Specialist to join their Corporate Compliance team. ...
At Attic Projects, we are at the forefront of our industry, driving innovation and growth across our locations in San Diego, Orange County, and North & South Seattle. Our Operations Managers play a pivotal role in ensuring seamless day-to-day operations, optimizing efficiency, and upholding our ...
Carbon Zero Buildings is seeking a dynamic Project Manager to oversee the installation of electrification technologies (heat pump water heaters and HVAC systems), as well as other energy efficiency upgrades, in large multifamily housing complexes. Project Management: Develop and execute comprehensiv...
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 Sr Manager Regulatory Affairs represents US regulatory affairs for device development projects. Plans and prepares (or oversees) complex regulatory submission documents primarily for US regulatory filings, ensures technical accuracy, and regulatory compliance. Responsible for development, commun...
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...
The Program Manager - Clinical Quality Assurance is primarily responsible for leading the management of GCP quality activities in support of studies and projects across one or more clinical programs to drive proactive quality management, and ensure compliance with corporate policies and functional p...
PURPOSE AND SCOPE:Responsible for the day-to-day program operations and supporting the growth of the assigned single site Home Therapies program in coordination with the Business Unit management, in-center staff and other support functions. Responsible for profit and loss management of the assigned ...