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Jobs (40 Matches)
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1. Regulatory Submissions Associate   (Temporary)7 hour(s) 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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2. Senior Regulatory Affairs Specialist   (Fulltime)12 hour(s) 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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3. Regulatory Affairs Specialist   (Fulltime)13 hour(s) 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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4. Sr Regulatory Affairs Specialist   (Fulltime)14 hour(s) ago
Covidien - United States, CA, East Irvine - Not rated - (view employer jobs)
Categories: Engineering, Biotech, QA - Quality ControlJob DescriptionAuthoring PMA submissions to bring medical innovations to market.Does this work inspire you?As a Senior Regulatory Affairs Specialist, you will plan and execute regulatory activities necessary to obtain and maintain regulatory approvals within the and International markets.   You will ensure compliance ...
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5. Regulatory Oerations/Publisher   (Fulltime)14 hour(s) ago
Bayside Solutions - United States, CA, Alameda - Not rated - (view employer jobs)
Categories: Biotech, PharmaceuticalJob DescriptionOur client in the Alameda/ Oakland area is looking for a Regulatory Operations/ Publisher to join their team.Regulatory Operations/PublisherDuties: - Perform submission build, compilation and publishing activities associated with generating hard copy and electronic submissions- Publish documents by creating bookmarks and hyperlinks in submission files according ...
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Art Institute of Dallas - Pittsburgh, PA
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6. Regulatory Documentation Coordinator   (Temporary)14 hour(s) ago
Experis - United States, NJ, Woodcliff Lake - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionRegulatory Documentation Coordinator You’re precision-oriented and a stickler for doing it right. You have deep expertise in pharmaceutical compliance and quality control. Your critical thinking prowess makes you a problem solver extraordinaire. You generate powerful ideas and know how to get them implemented. If this describes you, this ...
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7. Principlal Regulatory Affairs Specialist   (Fulltime)15 hour(s) ago
Covidien - United States, CA, East Irvine - Not rated - (view employer jobs)
Categories: QA - Quality Control, Engineering, BiotechJob DescriptionAuthor submissions for medical innovations within the regulatory environment.Does this work inspire you? The Principal Regulatory Affairs Specialist for our neurovascular regulatory affairs team at its Irvine, CA, has responsibility for submissions of Class II and III neurovascular medical devices. The Principal ...
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8. Regulatory Affairs Specialist   (Fulltime)16 hour(s) ago
Aerotek - United States, NJ, Bridgewater - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionObjectives:* Provide direct hands on /highly operational, administrative regulatory writing (cover letters, FDA forms etc) , and support to prepare and review content of submissions to INDs and NDAs including annual reports amendments, labeling and other non-CMC supplements correspondence, annual reports, etc.* Provide final documents to regulatory operations ...
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9. Regulatory CMC writers - Biological Compounds-Remote   (Temporary)19 hour(s) ago
MakroCare - United States, PA, Philadelphia - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionRegulatory CMC writers for Biological Compounds Sr & Jr - Contract- Remote Position Type : Contract 6 Months- can be extended to 9 months Start : Week of Nov 3 Remote workers would need to spend 1-2 weeks on-site to learn client’s systems. Resource Mix: 3-5 years – ...
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10. Regulatory Analyst (20121873)   (Fulltime)3 days ago
ARYZTA - United States, IL, West Chicago - Not rated - (view employer jobs)
Categories: OtherJob Description Position Purpose The Regulatory Analyst has the primary responsibility for ensuring regulatory compliance of formulas, labels and labeling. The Regulatory Analyst implements regulatory policies and programs to meet all regulatory, customer, and ARYZTA requirements. Scope/Complexity/Supervisory Responsibilities The Regulatory Analyst is responsible for implementing regulatory programs and ensuring labels are in ...
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11. Regulatory Affairs Coordinator   (Fulltime)3 days ago
Aerotek - United States, NY, Yonkers - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionTitle: Regulatory Affairs CoordinatorCompany Industry: OTC, Medical Devices, Cosmetics and Consumer Care ProductsReports to: Manager of Regulatory AffairsTerms: 6 Months Contract to Perm- ( the 6 months is used as a training period)Location: Mount Vernon, NYPay: $40-$45KInterview and can start immediately.The Regulatory Affairs Coordinator is responsible for assisting ...
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12. Quality Associate - Medical Device   (Fulltime)3 days ago
Kelly Services - United States, CA, Menlo Park - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob Description Quality Associate Kelly Services constantly connects professionals with opportunities to advance their careers. We currently have an exciting Temporary opportunity with long term possibilities for a global leader within the Medical Device arena. The position is based in Menlo Park, CA. Quality Associate Main ResponsibilitiesConduct internal audits and Nonconformance ...
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13. Regulatory Operations Associate   (Fulltime)3 days ago
Aerotek - United States, CA, San Diego - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionJob SummaryIncumbent will be responsible for formatting documents for paper or electronic Regulatory submissions. This individual will support the regulatory team to ensure documents are consistently compiled in accordance with industry standards and company policies. Primary Duties and Responsibilities* Provides Electronic Document Publishing support (i.e., scanning, rendering, ...
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14. Regulatory Affairs/Hazard Communications Specialist New Orleans, LA   (Fulltime)3 days ago
Kelly Scientific Resources - United States, LA, Hahnville - Not rated - (view employer jobs)
Categories: Biotech, Research, ScienceJob DescriptionRegulatory Affairs/Hazard Communications Specialist New Orleans, LAKelly Services is currently seeking a Regulatory Affairs/Hazard Communications Specialist for one of our top clients in New Orleans, LA. As a Regulatory Affairs/Hazard Communications Specialist placed with Kelly Services, you will be responsible for providing subject matter expertise ...
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15. Senior Regulatory Affairs Specialist   (Fulltime)3 days ago
TerumoBCT - United States, NJ, Lakewood - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionWorking without significant direction, provides leadership to the Company in fulfilling regulatory compliance by applying a thorough understanding of regulatory/standards requirements to one or more areas of expertise such as FDA regulations, international medical device regulations, product reimbursement, product liability, and standards. ESSENTIAL DUTIES ...
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16. Regulatory Affairs Specialist, International (IRC7675)   (Fulltime)4 days ago
Integra Life Sciences - United States, NJ, Plainsboro - Not rated - (view employer jobs)
Categories: Pharmaceutical, Biotech, Government - FederalJob DescriptionThe International Regulatory Affairs Specialist is responsible for assisting with regulatory filings to market Integra’s products in International markets. Regulatory Conformity• Tracks regulatory requests from International Distributors and maintains list of product approvals ...
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17. Senior Regulatory Affairs Support Analyst   (Fulltime)4 days ago
Biotest Pharmaceuticals - United States, FL, Boca Raton - Not rated - (view employer jobs)
Categories: Professional ServicesJob DescriptionThe Senior Support Analyst will procide guidance to Plasma Centers relating to Center compliance with FDA regulations/guidances and applicable International requirements as well as coordinate communications necessary to complete government mandated tasks between Center Managers, other departments, customers and regulators to facilitate information sharing and problem resolution.  ...
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18. Regulatory Specialist   (Fulltime)4 days ago
Technical Resources International - United States, MD, Bethesda - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionFounded in 1979, Technical Resources International, Inc. (TRI) provides a unique range of support services in the areas of Communications, Health and Information Technology to both private industry and government agency clients. TRI is currently seeking a Regulatory Specialist to join our Bethesda, MD team. This position will ...
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19. Regulatory Specialist   (Fulltime)4 days ago
HornerXpress - United States, FL, Fort Lauderdale - Not rated - (view employer jobs)
Categories: Admin - Clerical, Customer Service, Legal AdminJob Description FLSA: Salary; Exempt Hours: Full-Time HornerXpress values its employees because it is through our amazing staff that we are able to provide amazing service to our ...
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20. Regulatory Affairs Specialists   (Temporary)4 days ago
Acro Service Corporation - United States, MA, Westborough - Not rated - (view employer jobs)
Categories: Professional ServicesJob DescriptionRegulatory Affairs Specialists, Westborough, MABuild and maintain knowledge and understanding of customers’ regulatory requirements related to the BioProcess business at a high levelPerform necessary investigations and prepare and deliver statements and certificatesParticipate in project teams as regulatory support expertRespond efficiently and promptly to customers’ regulatory based issues, ...
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