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Jobs (44 Matches)
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1. Regulatory Affairs Specialist III   (Fulltime)6 hour(s) ago
Apple & Associates - United States, FL, Sarasota - Not rated - (view employer jobs)
Categories: Science, Pharmaceutical, BiotechJob DescriptionOur client is a leading manufacturer of Medical Devices, seeking a Regulatory Affairs Specialist III for their growing team in Sarasota, Florida. The Regulatory Affairs Specialist III will be responsible for coordinating, preparing and maintaining regulatory submissions and documents globally. The Regulatory Affairs Specialist ...
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2. Regulatory Affairs Publisher   (Fulltime)16 hour(s) ago
Pharmalink Consulting - United States, NJ, Short Hills - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionThe Regulatory Affairs Publisher will aid in ensuring delivery on all regulatory submission milestones and maintains compliance with applicable regulatory obligations. Role Description: Deliver project specific paper and electronic submissions. ...
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3. Specialist, Product Complaints IRC7686   (Fulltime)18 hour(s) ago
Integra Life Sciences - United States, NJ, Plainsboro - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionProvides clinical and safety data assessment of individual reports from post marketing events involving Integra LifeSciences products. Coordinates assessment and documentation associated with adverse reactions, product technical complaints and/or serious individual adverse events leading to medical device reports or adverse event reports as well ...
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4. Haz Comm - Regulatory Specialist   (Fulltime)19 hour(s) ago
Pace Analytical Services, Inc. - United States, OH, Maplewood - Not rated - (view employer jobs)
Categories: OtherJob DescriptionCategory : Biotech/R&D/ScienceLocation/City : MN - MaplewoodId : 911Candidate will provide product Hazard Communication and Product Regulatory Support to our customers. If you are a scientist who enjoys working with people and projects, this is an excellent career opportunity. Responsibilities: Generate SDS's (formerly MSDS's) and ...
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5. Hazard Communication Specialist   (Fulltime)19 hour(s) ago
Pace Analytical Services, Inc. - United States, TX, South Houston - Not rated - (view employer jobs)
Categories: OtherJob DescriptionCategory : Biotech/R&D/ScienceLocation/City : TX - HoustonId : 961Candidate will author OSHA and GHS compliant Safety Data Sheets (SDS's) in support of our customer's regulatory program.Responsibilities: Author SDS's to provide correct and up to date information to customers SDS tasks include: authoring new and ...
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Art Institute of Dallas - Pittsburgh, PA
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6. Regulatory Compliance Analyst   (Fulltime)20 hour(s) ago
DST - United States, AL, Birmingham - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionRegulatory Compliance Analysts monitor, research, analyze, and interpret federal and state regulations and proposed regulations to determine applicability and risk to both technical and operational aspects for the company and its products and services. Associates possess knowledge of HIPAA, Graham Leach-Bliley, Medicare and Medicaid regulations, ...
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7. Regulatory Submissions Publishing Associate   (Fulltime)1 day ago
GeniusPool - United States, MD, Rockville - Not rated - (view employer jobs)
Categories: Biotech, PharmaceuticalJob DescriptionRegulatory Submissions Publishing Associate Our client is seeking a Regulatory Submissions Publishing Associate to work out of their Rockville, MD location. This role is critical to the company's continued success. Major duties and responsibilities: Under direct supervision, perform Word and PDF publishing and formatting of regulatory submission documents ...
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8. Site Start-Up & Regulatory Specialist II   (Temporary)1 day ago
Advanced Clinical - United States, IA, Cincinnati - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 423131Site Start-Up & Regulatory Specialist IISummary: Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory ...
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9. Regulatory Affairs Coordinator   (Fulltime)1 day 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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10. Regulatory CMC Associate   (Fulltime)1 day 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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11. Regulatory Affairs Labeling Specialist   (Fulltime)2 days 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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12. Sr. Regulatory Affairs Specialist (IRC7722)   (Fulltime)2 days 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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13. Product Compliance Associate   (Fulltime)2 days 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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14. Product Filing & Compliance Analyst   (Fulltime)2 days 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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15. Regulatory Compliance Spec.   (Fulltime)2 days 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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16. Associate Regulatory Affairs Engineer (967-547)   (Fulltime)3 days 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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17. Regulatory Affairs Operations   (Fulltime)3 days 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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18. Regulatory Specialist Official Title:Regulator   (Fulltime)3 days 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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19. Sr. RA Specialist   (Fulltime)3 days 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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20. RA Specialist/Sr. RA Specialist   (Fulltime)3 days 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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