- Locations: California, New York, New Jersey, Florida, Pennsylvania
- Related Keywords: Design, Supplements
- Regulatory Affairs
- Manpower Professional (Redwood City, CA)
- ...Class III implantable medical devices. RA delegate to project teams to assess regulatory impact/determine regulatory strategy for proposed manufacturing/ design changes; Authoring and submitting PMA Supplements (30-day notice, Real-time Reviews, 180-Day Supplements , Annual Reports);...
- Oracle Application Specialist
- The Great Atlantic & Pacific Tea Company, Inc. (Montvale, NJ)
- ...interfaces, reports, and forms. KEY ACCOUNTABILITIES . Analysis and design of technical solutions to business problems. . Work with...existing host legacy and future systems as required. . Supplements Oracle functionality by developing application extensions that address evolving...
- Regulatory Affairs
- Manpower Professional (CA)
- ...Class III implantable medical devices. RA delegate to project teams to assess regulatory impact/determine regulatory strategy for proposed manufacturing/ design changes; Authoring and submitting PMA Supplements (30-day notice, Real-time Reviews, 180-Day Supplements , Annual Reports);...
- Regulatory Affairs
- Unknown (Los Angeles County, CA)
- ...Class III implantable medical devices. RA delegate to project teams to assess regulatory impact/determine regulatory strategy for proposed manufacturing/ design changes; Authoring and submitting PMA Supplements (30-day notice, Real-time Reviews, 180-Day Supplements , Annual Reports);...
- Regulatory Affairs Associate
- Unknown (Redwood City, CA)
- ...Class III implantable medical devices.# RA delegate to project teams to assess regulatory impact/determine regulatory strategy for proposed manufacturing/ design changes;# Authoring and submitting PMA Supplements (30-day notice, Real-time Reviews, 180-Day Supplements , Annual...
- Regulatory Affairs Associate
- Collabera Inc. (Redwood City, CA)
- ...Class III implantable medical devices. RA delegate to project teams to assess regulatory impact/determine regulatory strategy for proposed manufacturing/ design changes; Authoring and submitting PMA Supplements (30-day notice, Real-time Reviews, 180-Day Supplements , Annual Reports);...
- Product Compliance Engineer
- James Hardie (Fontana, CA)
- ...and coordinate with engineers on special initiatives required to drive detailed report generation for fastener, design and install methodso Draft Technical Supplements and Technical Bulletins to address gaps in installation techniques long term Quantitative Dimensions Responsible for...
- Product Compliance Engineer
- James Hardie Building Products (San Bernardino, CA)
- ...and coordinate with engineers on special initiatives required to drive detailed report generation for fastener, design and install methodso Draft Technical Supplements and Technical Bulletins to address gaps in installation techniques long termQuantitative DimensionsResponsible for the...
- Art Director
- Staples (Overland Park, KS)
- ...Company Hiring Manager Title AI Sr Director Marketing Responsibilities Job Summary This position is responsible for the design of our Corporate Catalog, Website, Supplements and Newsletters. Responsibilities . Primary focus on the creative and technical design aspects of the...
- Art Director-Corporate Marketing
- Staples Promotional Products (Overland Park, KS)
- Job Summary This position is responsible for the design of our Corporate Catalog, Website, Supplements and Newsletters. Responsibilities * Primary focus on the creative and technical design aspects of the corporate web and catalog projects. * Determine specific graphic design ...
- Director/Sr. Manager of Regulatory Affairs
- PROVEN, Inc. (San Diego, CA)
- ...and approve regulatory submissions that meet company and regulatory agency requirements. Prepare regulatory filings and Design Dossier submissions and subsequent revisions/ supplements and amendments. Attend Project Team Meetings on a regular basis and provide assistance with regulatory...
- Director/Sr. Manager of Regulatory Affairs
- Unknown (San Diego, CA)
- ...and approve regulatory submissions that meet company and regulatory agency requirements. Prepare regulatory filings and Design Dossier submissions and subsequent revisions/ supplements and amendments.Attend Project Team Meetings on a regular basis and provide assistance with regulatory...
- Regulatory Affairs Associate
- Unknown (Redwood City, CA)
- ...Class III implantable medical devices.# RA delegate to project teams to assess regulatory impact/determine regulatory strategy for proposed manufacturing/ design changes;# Authoring and submitting PMA Supplements (30-day notice, Real-time Reviews, 180-Day Supplements , Annual...
- Contracts Manager-01
- Parsons Corporation (Washington, DC)
- ...* Proficiency in Federal Acquisition Regulations (FAR) and its Supplements , industry business practices, and the negotiation of prime contracts....We surmount the toughest logistical challenges and deliver landmark design -build projects across the globe. Our ability to plan, ...