Manager, Regulatory Affairs III to provide strategic direction and operational support for CMC regulatory activities. ...
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...
A company is looking for a Regulatory Affairs Manager responsible for establishing strategies for worldwide product approval submission activities. ...
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 Regulatory Staff by identifying & gathering...
We are seeking a Regulatory Affairs - CMC professional to join our team as Senior Manager, Regulatory Affairs - CMC. Regulatory professional with 5+ years of industry experience in pharmaceutical, biotechnology or related industry in CMC, Regulatory, Quality, R&D, and Manufacturing or related, with ...
General Description:The Senior Manager, Regulatory Affairs CMC, is responsible for developing and implementing global regulatory CMC strategies to secure and maintain market access for assigned product(s) in line with business objectives, and in coordination with key internal stakeholders. Provides ...
Manager in Regulatory Affairs is responsible for developing and managing regulatory strategies to remain compliant with U. Extensive knowledge of regulatory requirements, including ICH and regional requirements and an understanding of current global and regional trends in regulatory affairs. FDA and...
Regulatory Affairs Manager – APAC. Regulatory Affairs Manager – APAC. You will be responsible for managing a small team overseeing the Diabetes Care product portfolio in the APAC region, creating robust global regulatory strategies, working with cross-functional teams as the regulatory SME, provide ...
In this role as a Regulatory Affairs Specialist, you will have responsibility for developing and influencing regulatory policy and determining and pursuing courses of action necessary to obtain and expand regulatory approval of Hinge Health’s medical device portfolio. This Specialist will work with ...
Experience in California or other state or federal regulatory and government affairs. Representing and advocating for Verizon's interests before state regulatory commissions and relevant state legislative policy committees in California and other states. Testifying before state regulatory commission...
Experience in California or other state or federal regulatory and government affairs. Representing and advocating for Verizon’s interests before state regulatory commissions and relevant state legislative policy committees in California and other states. Testifying before state regulatory commission...
Liaise with colleagues in Regulatory Affairs therapeutics teams, company local Affiliates, Regulatory Operations, Regulatory Project Management and third-party local agents to develop filing plans and deliver submissions to agreed priorities and timelines. Senior Manager, Regulatory Affairs III. Sen...
We are seeking a Manager, Global Regulatory Affairs to work closely with the Global Regulatory Lead (GRL) for a given program(s). Combination of the following can be considered: PhD or PharmD with 2+ years of pharmaceutical industry experience in regulatory affairs; MS with 4+ years; BS with 5+...
We are seeking a Manager, Global Regulatory Affairs to work closely with the Global Regulatory Lead (GRL) for a given program(s). You will be responsible for interfacing with Regulatory Operations and CROs to support various submissions to Health Authorities, in support of investigational applicatio...
Closely monitor, analyse, develop regulatory priorities and coordinate positions and strategies for regulatory and market affairs in MISO and other priority markets. Communicate regularly and effectively in a cross-functional matrix with development, origination, fundamentals, finance, and political...
Identifies growth and areas of opportunity to enhance Regulatory Affairs and AHS initiatives. Assists in all accreditation and regulatory activities, including surveys, survey preparation and readiness assessments. Finalizes corrective action responses to The Joint Commission and other regulatory ag...
Regulatory Affairs Manager – Digital Health Technology. Regulatory Affairs Manager – Digital Health Technology. Remains current on developments in field(s) of expertise, regulatory requirements, as well as industry trends and trains staff regarding changing regulations that affect regulatory submiss...
Biogen company, is seeking a Manager, Global Regulatory Affairs to work closely with the Global Regulatory Lead (GRL) for a given program(s). Combination of the following can be considered: PhD or PharmD with 2+ years of pharmaceutical industry experience in regulatory affairs; MS with 4+ years; BS ...
The Ambulatory Regulatory Compliance Specialist has a pivotal role within the organization and is responsible for ensuring adherence to regulatory standards across diverse areas. The Ambulatory Regulatory Compliance Specialist will play a crucial role in ensuring ongoing compliance with The Joint Co...
Under the guidance of the Campus Risk Manager, the ERM Analyst 3 will perform a broad range of tasks in connection with the review of insurance, indemnification and limitation of liability provisions in complex contractual agreements for compliance with Regents Standing Orders. The ERM Analyst 3 wil...
A company is looking for a Compliance Corrections Specialist to oversee corporate ethics and compliance programs. ...
A company is looking for a Senior Localization Technical Project Manager to oversee projects in the digital space. Python, SQL)Experience with project management tools such as Asana or Jira. ...
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 Project and Program Management - Program Manager Tech 3. ...
A company is looking for a Manager I, Data Projects to lead data analytics initiatives for government clients. ...