Register
Recruit Create CV

Manager Global Regulatory Affairs Jobs

Global Regulatory Specialist Jobs
By eBay At Draper, UT, United States
2-5 Years Proven Project Management Experience.2-5 years experience with a federal government agency is preferred.
Effective and confirmed negotiation skills and have the ability to influence decisions and others.
Handle and support critical issues from regulators and monitoring authorities, media, and non-government organizations from around the world.
Support managing and further developing the eBay Regulatory Portal.
Be proficient with eBay’s customer service tools.
Conduct investigations and analysis of non-compliant/potentially criminal conduct.
Regulatory Affairs Manager Jobs
By Korn Ferry At Boston, MA, United States
5+ years of experience in regulatory affairs environment in nutrition industry.
Excellent knowledge of US and Canada Food Law - Regulations.
Korn Ferry has partnered with our client on their search for the role, Regulatory Affairs Manager.
Ensure compliance of product, ingredients, and claims.
Supply regulatory support for safety files and clinical trials/protocols in order to support R&D.
Vetting and approval of all public materials, including labelling.
Regulatory Affairs Manager Jobs
By Jobot At New York, NY, United States
Strong knowledge of OTC drug and device regulations, including labeling requirements
Significant experience with U.S. drug and/or medical device regulatory submissions and maintenance; OTC preferred
Working knowledge of U.S. clinical research and claims support
Excellent written and verbal communication skills
6+ years of experience in U.S. and/or Canada pharmaceutical or medical device Regulatory Affairs
Drug or medical device submission and/or maintenance experience
Regulatory Affairs Manager Jobs
By Brunel At Dallas-Fort Worth Metroplex, United States
5+ years of progressive regualtory affairs experience
Submissions experience - EU and International markets
Oversee the regualtory function for full product portfolio, managing a team, department and budget
Coordinate regulatory submissions in US and OUS markets
Provide regulatory input/support for audits
Regulatory strategy for product development
Regulatory Affairs Manager Jobs
By DHL At , Westerville, 43082
Presentation and project management skills
Experience with regulatory licensing, regulatory agencies and quality management/systems, practical application a plus
Advisor to Senior Management and Customers on regulatory issues/initiatives, including problem-solving, business pursuits, strategic direction, and significant issues.
Verify and analyze regulatory metrics and create executive management reporting
Coaching support for site management
Experience and working knowledge of Quality Assurance principles and methodology
Regulatory Affairs Program Manager, Us
By ZEISS Group At Dublin, CA, United States

The Regulatory Affairs Program Manager US is responsible for developing and monitoring regulatory submission timelines for a variety of US medical device submissions (such as 510(k)s, IDEs and/or ...

Global Clinical & Regulatory Affairs Operations Coordinator
By Orion At , $28 an hour
Experience with vendor and supplier management and engagement
Experience with contract management systems for legal agreements and contracts
May participate in continuous improvement activities related to role including supplier payment management, external agreement process, etc.
Bachelor's Degree in Business Administration, Economics, or related field preferred or a combination of education and experience.
Experience working in a fast-paced remote environment preferred as well as experience working with highly matrixed global organizations
A minimum of 3 years' experience in clinical regulatory affairs highly preferred.
Regulatory Affairs Manager Jobs
By Keystone Industries At Gibbstown, NJ, United States
Demonstrated knowledge of current Good Manufacturing Practices (cGMP) and Quality Management Systems (QMS).
Collaborate with QA to ensure the quality management system (QMS) complies with relevant regulations and standards.
Oversees the implementation of risk management processes. Work with cross-functional teams to identify and address potential risks associated with regulated products.
Assesses the impact of regulatory changes on the company's products and processes and ensures compliance with these requirements.
Advise project teams on premarket regulatory requirements.
Advise on export and labeling requirements.
Regulatory Affairs Manager Jobs
By Roche At , Carlsbad, 92008
Analyzes, monitors and provides trending of Recall and Adverse Event Reporting data for Quality Management Review Meeting (QMR).
Other duties as assigned by management.
Experience with Microsoft and Google based applications and general knowledge of PC functions necessary
Experience developing field action processes complaint with global regulatory requirements
Manages the creation and review of Standard Operating Procedures and policy guidelines for the regulatory affairs department.•
5 years of Regulatory Affairs experience. Specific experience with IVD device experience is preferred.
Regulatory Affairs Manager Jobs
By Kelly At Kansas City Metropolitan Area, United States
Prepare regulatory assessments for project teams, line management, and key stakeholders as requested. Includes support for due diligence evaluations.
Degree(s) in a relevant scientific field (BS/MS/Ph.D.) from an accredited institution with appropriate certification in Regulatory Affairs.
High-level knowledge of registration dossier preparation for US FDA/CVM. Including development, drawing conclusions, and the effect of changes.
Proactively monitor, evaluate, and communicate existing and new US regulations impacting products and projects. Assess the potential impact and/or opportunities.
Interface with regulatory authorities on new product development and registration programs, as well as industry associations.
Coordinate technical input for preparation/review of FOI summary and label language for assigned projects.
Global Customer Experience Manager (Quality & Regulatory Affairs) - Remote
By Olympus Corporation of the Americas At , Westborough, Ma $106,692 - $149,366 a year
Experience and knowledge of all call center KPI & SL metrics.
Experience in driving change via business cases for transformation.
BA/BS in Business, communications. Equivalent years of experience in the business operation field and or medical device.
Experience of managing a critical path regarding customer complaints would be advantageous
Hands-on experience with service and support workflow tools such as ServiceNow, SFDC, Veeva, Oracle Zendesk.
Strong communication skills, expresses ideas fluently and logically, is open to input and can be depended on for truthfulness.
Regulatory Affairs Manager ( Registered Nurse)
By University of Washington At , Seattle, 98195, Wa $9,000 - $12,840 a month
$ 9,000 - $12,840 per month
Who we are looking for a leader who understands:
This position serves as an expert resource and partner on:
Some of what you will do:
To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 or [email protected].
Manager, Global Communications, Public Affairs (Hybrid)
By Starbucks At Seattle, WA, United States
Experience with database management, mastery of PowerPoint and WordPress preferred.
A bachelor’s degree and 5 years or more communications experience with expertise in international or premium retail communications.
Experience managing multiple complex projects contributing to cross-functional initiatives that lead to demonstrated results.
Ability to manage multiple priorities and finding creative solutions to complex challenges.
Experience working in and across multiple geographies, across numerous time zones, with a broad range of stakeholders and influencers.
As a manager, you will…
Global Regulatory Affairs Specialist
By ICON At , , Ga
An ambitious regulatory professional with experience of working as Regulatory Specialist across multiple regions. Additional requirements include:
Provide submission strategy to the client along with all requirements and documentation requests to actualise the proposed strategy.
Become part of the supportive and extremely knowledgeable regulatory professional team who are collaborative.
Prior experience in the preparation of RA and Central IEC submissions for Clinical Trial Applications ideally across regions.
What we can offer you:
Preparation of the Core Clinical Trial Application and perform QC on the content of all central submission packages.
Global Clinical & Regulatory Affairs Coordinator
By Omni Inclusive At United States
May participate in continuous improvement activities related to role including supplier payment management, external agreement process, etc.
Maintains organizational charts for both departments and maintain email distribution lists.
Supports expense reporting for leadership in GRA and GCA.
Regulatory Affairs Manager Jobs
By DHL At Westerville, OH, United States
Presentation and project management skills
Experience with regulatory licensing, regulatory agencies and quality management/systems, practical application a plus
Advisor to Senior Management and Customers on regulatory issues/initiatives, including problem-solving, business pursuits, strategic direction, and significant issues.
Verify and analyze regulatory metrics and create executive management reporting
Coaching support for site management
Experience and working knowledge of Quality Assurance principles and methodology
Regulatory Affairs Manager Jobs
By USK Technologies At New York City Metropolitan Area, United States
You will report to the Senior Manager, Quality, Safety and Regulatory Affairs.
Product development experience strongly preferred
Skin and personal care including OTC claim review experience strongly preferred
Track record adhering to compliance requirements (i.e. FDA, Health Canada, EPA, FTC, cGMP, ISO, etc.)
Strong written communication skills, especially detail oriented and technical material
Experience communicating with cross-functional teams and customers including verbal presentations
Manager Global Regulatory Affairs
By The Fountain Group At United States
Expert knowledge of regulations, and experience with interpretation and application
Strong negotiation skills and significant experience in interacting with regulatory authorities
Experience in the development and implementation of CMC regulatory strategies throughout the lifecycle of pharmaceuticals/devices
Experience in a pharmaceutical manufacturing facility/development laboratory preferred.
Exp withGlobal responsibility for regulatory submissions and registrations preferred
Risk identification in terms of CMC regulatory strategy