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Jobs (44 Matches)
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1. Regulatory Affairs Coordinator   (Fulltime)1 hour(s) ago
Adecco Medical & Science - United States, CA, East Irvine - Not rated - (view employer jobs)
Categories: ScienceJob DescriptionA Regulatory Affairs Coordinator job in Irvine, CA needs to be filled immediately by Adecco Medical & Science. This is a four month contract opportunity. In this role, you will provide basic support for regional regulatory affairs for new registration of products and renewals of existing ...
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2. Regulatory CMC Associate   (Fulltime)1 hour(s) ago
Aerotek - United States, CA, San Francisco - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionA fast growing pharmaceutical company in the San Francisco Bay Area is seeking to hire a motivated, detail-oriented regulatory professional with exposure to CMC to join their team!RESPONSIBILITIES INCLUDE:Managing CMC aspects of an IND filing and global post-approval changes for a biologicCreating timelines and tracking deliverables to timelines ...
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3. Regulatory Affairs Labeling Specialist   (Fulltime)22 hour(s) ago
Kelly Scientific Resources - United States, MO, Saint Louis - Not rated - (view employer jobs)
Categories: Hospitality - HotelJob DescriptionKelly Scientific Resources, the premier scientific staffing provider, has an exciting opportunity available for a Regulatory Affairs Labeling Specialist with a food manufacturer in the St. Louis, MO area.  This is a direct hire opportunity and seeks the following:Key Responsibilities:•         Manage and maintain supplier documentation of ...
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4. Sr. Regulatory Affairs Specialist (IRC7722)   (Fulltime)1 day ago
Integra Life Sciences - United States, NJ, Plainsboro - Not rated - (view employer jobs)
Categories: Pharmaceutical, Biotech, Government - FederalJob DescriptionThe Sr. Regulatory Affairs Specialist is responsible to participate on manufacturing transfer projects as a Regulatory representative. This position works in partnership with operations, manufacturing, Quality Systems, Engineering and Product Development to facilitate overall regulatory compliance for transfer of manufacturing processes ...
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5. Product Compliance Associate   (Fulltime)1 day ago
Atkore - United States, IL, West Chicago - Not rated - (view employer jobs)
Categories: EngineeringJob DescriptionProduct Compliance Associate   Allied Tube & Conduit is an industry leader in the manufacture of galvanized steel tubes and pipes, electrical conduit, armored wire and cable, metal framing systems and building components; serving a wide range of construction, electrical, fire and security, mechanical and automotive applications.  Allied Tube & ...
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Supervisory Program Specialist
Veterans Administration - Houston, TX
responsibility in ChampVA coordination benefits, Decedent Affairs, Bed Control, Admissions, Registration, Veteran ... employees are given adequate information on legislative and regulatory changes; maintains responsibility for the...>
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Supervisory Financial Management Specialist
U.S. Department of Veterans Affairs - Las Vegas, NV
consolidated business entity established to enhance revenue operations throughout the Veterans Health Administration ... range of business services in support of VA Medical Center operations to include billing, collections, customer...>
Supervisory Financial Administrative Specialist (Billing Supervisor)
U.S. Department of Veterans Affairs - Leavenworth, KS
consolidated business entity established to enhance revenue operations throughout the Veterans Health Administration ... range of business services in support of VA Medical Center operations to include billing, collections, customer...>

6. Product Filing & Compliance Analyst   (Fulltime)1 day ago
Starr Companies - United States, NY, New York Mills - Not rated - (view employer jobs)
Categories: InsuranceJob DescriptionPreparation and submission of P&C filings for approval by state insurance departments via SERFF; construct filing exhibits, compose filing letters. Assist in the implementation of rates/rules/forms revisions; evaluate impact of revisions on systems as necessary. Analyze new insurance laws, regulations and bulletins to determine applicability to existing products. Track ...
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7. Regulatory Compliance Spec.   (Fulltime)1 day ago
DST - United States, CA, El Dorado Hills - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionDST Output is looking for a highly skilled HIPPA/Medicare Regulatory Compliance Specialist.  Requirements for this position include:  A minimum of 3 years’ regulatory compliance experience in a HIPPA/Medicare environment; demonstrated knowledge of how regulations impact the business and business decisions; and proficiency using a PC ...
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8. 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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9. Regulatory Affairs Operations   (Fulltime)1 day ago
Aerotek - United States, MA, Cambridge - Not rated - (view employer jobs)
Categories: PharmaceuticalJob Description* Effective coordination and prompt delivery of regulatory submissions to the US FDA as per regulatory requirements* Efficient review and approval of submissions* Coordinate and prepare submission packages ensuring compliance with defined standards and practices* Prepare regulatory submissions in electronic CTD (Common Technical Document) using publishing tools like ...
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10. Regulatory Specialist Official Title:Regulator   (Fulltime)1 day ago
MRIGlobalSearch - United States, CT, New Haven - Not rated - (view employer jobs)
Categories: ManufacturingJob DescriptionJob Classification: Full-Time RegularConnect confidentially with MRIGlobalMedDevice at: [Click Here to Email Your Resumé]Our client is a market leader in the development, production and marketing of medical devices. Our client offers great benefits, competitive salaries and on site health & wellness programs.  To be considered for this position, ...
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Contract Specialist
U.S. Department of Veterans Affairs - Cincinnati, OH
reporting (i.e. Federal Procurement Data System (FPDS), financial management (i.e. Integrated Funds Control, ... in any combination of the following fields: accounting, business, finance, law, contracts, purchasing, economics,...>

11. Sr. RA Specialist   (Fulltime)1 day ago
MRIGlobalSearch - United States, CT, Bridgeport - Not rated - (view employer jobs)
Categories: ManufacturingJob DescriptionJob Classification: Full-Time RegularConnect confidentially with MRIGlobalMedDevice at: [Click Here to Email Your Resumé]This emerging, profitable company is not only focused on finding the best people, but also on challenging these people to achieve rigorous program milestones and ultimately, to realize their personal and professional potential. Their employees ...
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12. RA Specialist/Sr. RA Specialist   (Fulltime)1 day ago
MRIGlobalSearch - United States, NC, Charlotte - Not rated - (view employer jobs)
Categories: ManufacturingJob DescriptionJob Classification: Full-Time RegularConnect confidentially with MRIGlobalMedDevice at: [Click Here to Email Your Resumé]With the use of state-of-the-art technology, this dynamic company is emerging as one of the market leaders in the development of innovative medical devices. In addition to abundant career growth and development opportunities, they offer ...
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13. RA Specialist/Principal RA Specialist   (Fulltime)1 day ago
MRIGlobalSearch - United States, MN, Minneapolis - Not rated - (view employer jobs)
Categories: Science, BiotechJob DescriptionJob Classification: Contract Full-TimeConnect confidentially with MRIGlobalMedDevice at: [Click Here to Email Your Resumé]Our client has an immeadiate need for a RA Specialist/Principal RA Specialist.  This is a contract position with the possibilty of converting to perm.  You will be part of a team that bases ...
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14. Regulatory Document Specialist   (Temporary)1 day ago
Joule' Clinical - United States, NY, Tarrytown - Not rated - (view employer jobs)
Categories: Biotech, PharmaceuticalJob DescriptionJob is located in Tarrytown, NY.Responsible for independently formatting and publishing electronic documents for Regulatory submissions. Integrates and applies strong knowledge of US electronic regulatory submission requirements in support of ongoing drug development programs. Requires some guidance from direct manager. ...
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15. Regulatory Document Specialist   (Temporary)2 days ago
Joule' Clinical - United States, NY, Tarrytown - Not rated - (view employer jobs)
Categories: Biotech, PharmaceuticalJob DescriptionResponsible for independently formatting and publishing electronic documents for Regulatory submissions. Integrates and applies strong knowledge of US electronic regulatory submission requirements in support of ongoing drug development programs. Requires some guidance from direct manager. Independently formats ...
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16. Regulatory Affairs Specialist, Flavors Group   (Fulltime)2 days ago
Sensient Technologies Corporation - United States, IL, Hoffman Estates - Not rated - (view employer jobs)
Categories: BankingJob DescriptionJob Summary: To assure compliance of Sensient Technologies products with appropriate regulations and to serve as a regulatory resource to internal and external customers.  To maintain technical databases related to raw materials, formulas, and finished products.  To understand, respect, and act ethically when dealing with matters related ...
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17. Senior Clinical Quality Analyst - HEDIS - Las Vegas, NV   (Fulltime)2 days ago
United Health Group - United States, NV, Las Vegas - Not rated - (view employer jobs)
Categories: Management, Health Care, InsuranceJob DescriptionTalk about meaningful work. Talk about an important role. Let's talk about your next career move. Delivering quality care starts with ensuring our processes and documentation standards are being met and kept at the highest level possible. This means working behind the scenes ...
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18. Regulatory Submissions Associate   (Temporary)2 days ago
pharmascent - United States, NY, Tarrytown - Not rated - (view employer jobs)
Categories: Biotech, PharmaceuticalJob DescriptionRegulatory Submissions AssociateTarrytown, NYContract Description: Responsible for building Regulatory submissions such as INDs, IND amendments, BLAs, BLA supplements, MAAs, MAA variations and/or CTAs in accordance with applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH, etc) Performs submission build activities, including, but not limited to, ensuring submissions ...
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19. Senior Regulatory Affairs Specialist   (Fulltime)2 days ago
Adecco Engineering & Technology - United States, FL, Jacksonville - Not rated - (view employer jobs)
Categories: Engineering, ScienceJob Description.Sr. Regulatory Affairs Specialist needed for a direct hire opportunity inJacksonville,Florida! Only candidates with a medical device or pharmaceutical background will be considered. Job Summary: Position is responsible for securingU.S.and international regulatory clearance or approval for orthopedic products/accessories, including developing regulatory submissions and ...
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20. Regulatory Affairs Specialist   (Fulltime)3 days ago
Kelly Scientific Resources - United States, KY, Erlanger - Not rated - (view employer jobs)
Categories: Biotech, Research, ScienceJob DescriptionRegulatory Affairs Specialist- Erlanger, KYKelly Services is currently seeking a Regulatory Affairs Specialist for one of our top clients in Erlanger, KY.  This is a direct hire position! PURPOSE: Provides Regulatory support and expertise to ensure customer satisfaction and success of the overall business strategy ...
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