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Jobs (53 Matches)
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1. Product Regulatory Coordinator   (Fulltime)1 hour(s) ago
AkzoNobel Inc - United States, OH, Strongsville - Not rated - (view employer jobs)
Categories: Manufacturing, OtherJob DescriptionAkzoNobel is a leading global paints and coatings company and a major producer of specialty chemicals, with leading market positions and brands in countries around the world. We operate in a number of important market segments ranging from buildings and infrastructure to transport, industrial and consumer ...
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2. Regulatory Documentation Specialist EZIJP00001823   (Temporary)2 hour(s) ago
Advanced Clinical - United States, NJ, Woodcliff Lake - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 421887Regulatory Documentation Specialist EZIJP00001823Description: Responsibilities - Review and approve daily Clinical Safety Alert Reporting (SUSAR, 6MLL, DSUR, IND Safety Alerts) - Support the distribution of Safety Alert Reports to Investigators, Ethic Committees and CRO's per US and EU/ROW country-specific requirements - Knowledge of databases (FirstDoc, ...
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3. Project Manager   (Fulltime)2 hour(s) ago
TEKsystems, Inc - United States, NJ, Jersey City - Not rated - (view employer jobs)
Categories: Information TechnologyJob DescriptionBIG PLUS- Being Fleunt in Japanese to communicate with the business overseas Target Start Date: ASAP Years of Experience: Senior (7+ yrs) Right to Hire: Yes Responsibilities: In this role, the consultant will lead small, medium, and large projects of significant scope and impact. The ability to ...
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4. Regulatory Affairs Specialist - Regulatory Affairs   (Fulltime)5 hour(s) ago
Midmark - United States, IL, Lincolnshire - Not rated - (view employer jobs)
Categories: Legal, Business Development, EngineeringJob DescriptionJob is located in Lincolnshire, IL. Regulatory Affairs Specialist - Regulatory Affairs SUMMARY - Regulatory Affairs Specialist - Regulatory Affairs: The Regulatory Affairs Specialist is responsible for implementing the global introduction and continued approval/licensure of new and revised products. They provide subject matter expertise and are ...
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5. Regulatory Affairs Specialist - Regulatory Affairs   (Fulltime)5 hour(s) ago
Midmark - United States, IL, Lincolnshire - Not rated - (view employer jobs)
Categories: Legal, Business Development, EngineeringJob DescriptionJob is located in Lincolnshire, IL. Regulatory Affairs Specialist - Regulatory Affairs SUMMARY - Regulatory Affairs Specialist - Regulatory Affairs: The Regulatory Affairs Specialist is responsible for implementing the global introduction and continued approval/licensure of new and revised products. They provide subject matter expertise and are ...
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Art Institute of Dallas - Pittsburgh, PA
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6. Regulatory Affairs Specialist - Regulatory Affairs   (Fulltime)5 hour(s) ago
Midmark - United States, IL, Lincolnshire - Not rated - (view employer jobs)
Categories: Legal, Business Development, EngineeringJob Description Regulatory Affairs Specialist - Regulatory Affairs SUMMARY - Regulatory Affairs Specialist - Regulatory Affairs: The Regulatory Affairs Specialist is responsible for implementing the global introduction and continued approval/licensure of new and revised products. They provide subject matter expertise and are responsible for advising and guiding ...
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7. Regulatory Assistant   (Fulltime)7 hour(s) ago
Adecco Engineering & Technology - United States, NC, Greensboro - Not rated - (view employer jobs)
Categories: ScienceJob Description.Adecco Engineering and Technical has a current job opportunity for a Regulatory Assistant in Greensboro, NC. This is a contract position. If you meet the qualifications listed below please apply.State Regulatory Affairs is involved in the registration and maintenance of products to State Agencies prior to ...
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8. Regulatory Affairs Associate   (Fulltime)7 hour(s) ago
The Ascent Services Group - United States, NY, Tarrytown - Not rated - (view employer jobs)
Categories: ResearchJob DescriptionAscent Pharma is seeking a Regulatory Affairs Associate in the Tarrytown, NY area***APPLY TODAY OR REFER A FRIEND! We offer a terrific referral bonus!Divna Rosenzweig/Sr. Clinical Development Recruiter(310) 933-4549WHAT:Regulatory Affairs AssociateWHERE:Tarrytown, WHAT YOU WILL BE DOING:Responsible for the project management of Regulatory submission deliverables for INDs, BLAs, MAAs, annual ...
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9. Senior Regulatory Submission Associate   (Fulltime)9 hour(s) ago
Aerotek - United States, CT, Branford - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionPURPOSE AND SCOPE OF POSITIONThe incumbent is responsible to support the preparation of electronic regulatory submissions for the US and Europe. the submission of these documents through the ATMPs Marketing Authorization Application MAA Electronic Submission Gateway (ESG) as well as traditional FDA submissions.DUTIES AND RESPONSIBILITIESPublish and submit IND ...
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10. Regulatory Affairs Consultant - Irvine, CA or Eden Prairie, MN   (Fulltime)12 hour(s) ago
United Health Group - United States, MN, Eden Prairie - Not rated - (view employer jobs)
Categories: Legal, InsuranceJob DescriptionBring us your experience, your head for strategy, your strength with relationships and your eye for opportunity. In return we offer an unmatched place to grow and develop your career among a richly diverse group of businesses driven by the power and stability of a leading ...
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Supervisory Financial Management Specialist (Facility Revenue Manager)
U.S. Department of Veterans Affairs - St Louis, MO
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11. Regulatory Affairs Consultant - Irvine, CA or Eden Prairie, MN   (Fulltime)12 hour(s) ago
United Health Group - United States, CA, East Irvine - Not rated - (view employer jobs)
Categories: Legal, InsuranceJob DescriptionBring us your experience, your head for strategy, your strength with relationships and your eye for opportunity. In return we offer an unmatched place to grow and develop your career among a richly diverse group of businesses driven by the power and stability of a leading ...
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12. Principal Regulatory Specialist - Toxicology   (Fulltime)16 hour(s) ago
Ecolab, Inc. - United States, TN, Eagan - Not rated - (view employer jobs)
Categories: LegalJob DescriptionJoin Ecolab Regulatory Affairs as a Principal Regulatory Specialist in Toxicology. Be a recognized subject matter expert within the organization, working with product developers to get products approved in the US and working with government agencies to assure safety of products.Main Responsibilities?Act as expert level innovative technical leader ...
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13. Document Review Specialist II   (Fulltime)20 hour(s) ago
CSG, Inc - United States, NC, Raleigh - Not rated - (view employer jobs)
Categories: BiotechJob Description Effectively reviews documents created within or outside of to ensure quality of a standard that meets or exceeds client’s expectations. Documents include: regulatory submissions, integrated clinical study reports, serious adverse event narratives, study protocols and publications. Ensures integrity of data in tables against source documents. Instructs others outside ...
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14. Quality Assurance Assistant   (Fulltime)1 day ago
Novum Pharmaceutical Research Services - United States, NV, Las Vegas - Not rated - (view employer jobs)
Categories: Admin - Clerical, QA - Quality Control, ResearchJob Description A global leader in conducting clinical trials and equivalency studies, Novum Pharmaceutical Research is enjoying tremendous growth and offers exciting career opportunities. People who enjoy a fast-paced, team environment and meet our qualifications are encouraged to apply. ...
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15. Associate Regulatory Affairs Engineer (967-547)   (Fulltime)1 day ago
ZOLL - United States, PA, Pittsburgh - Not rated - (view employer jobs)
Categories: OtherJob Description ZOLL LifeVest, a Pittsburgh-based subsidiary of ZOLL Medical Corporation, develops, manufactures and markets a wearable defibrillator for persons with Sudden Cardiac Arrest (SCA) risk in the United States and Europe. The LifeVest is worn by patients at risk for sudden cardiac arrest (SCA), providing protection during their changing ...
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16. Regulatory Affairs Operations Associate   (Fulltime)1 day ago
Kelly Services - United States, IL, Lake Forest - Not rated - (view employer jobs)
Categories: Biotech, Research, ScienceJob DescriptionKelly ServicesCurrent Needs: Currently seeking a Regulatory Affairs Operations Associate in Lake Forest, IL. This is a contract opportunity.Position Description:Responsible for formatting, compiling, and electronic filing of regulatory submissions.Provides Electronic Document Publishing support (i.e., scanning, rendering, bookmarking/hyperlinking and verification)Compiles Modules 1-5 in eCTD format, ...
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17. Regulatory CMC Associate   (Fulltime)1 day ago
Valesta Clinical Research Solutions - United States, NJ, East Hanover - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionResponsibilities: - Under supervision, provide strategic and operational global CMC regulatory direction and documentation for MARKETED PRODUCT maintenance. Experience desirable. The following activities may be performed within this capacity: - Provide and/or implement global CMC regulatory strategy for products. - Lead or contribute to global CMC submission activities ...
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18. Regulatory Affairs Paralegal   (Fulltime)3 days ago
Correct Care Solutions - United States, TN, Nashville - Not rated - (view employer jobs)
Categories: QA - Quality Control, Legal, Legal Admin, Admin - ClericalJob DescriptionCCS’s Philosophy CCS’s philosophy is based on the Five H’s - qualities we value in all our team members. The5 H’s are the foundation of how we do business – with our clients, our patients, and ...
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19. Regulatory Documentation Specialist, Documentation Quality Consultant   (Temporary)3 days ago
Career Developers - United States, NJ, Woodcliff Lake - Not rated - (view employer jobs)
Categories: Pharmaceutical, ConsultantJob DescriptionRegulatory Documentation Specialist, Documentation Quality Consultant Woodcliff Lake, NJ One Year Contract Role Responsibilities: Work in the Global Regulatory Operations (GRO) team. Work across multiple GRO disciplines to drive departmental and project objectives. Review clinical and regulatory ...
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20. Regulatory Affairs Publishing Specialist   (Fulltime)4 days ago
Kelly Scientific Resources - United States, CA, Westlake Village - Not rated - (view employer jobs)
Categories: Biotech, Research, ScienceJob DescriptionKelly Clinical Research is seeking a Regulatory Affairs Publishing Specialist for a contract opportunity in Westlake Village, CA.  Under direct supervision the RA Publishing Specialist is responsible for the maintenance of systems preparation of documents supporting regulatory submissions and operational activities supporting company products.  ...
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