| 1. Regulatory Specialist (Fulltime) | 6 hour(s) ago | Wipro Limited - United States, MN, Minneapolis -  - (view employer jobs) | | Categories: DesignJob Description
Regulatory Specialist
Company Profile:
Wipro is a global provider of consulting, IT Services, and outsourced R&D, infrastructure outsourcing and business process services. We deliver technology-driven business solutions that meet the strategic objectives of Global 2000 customers. With over 25 years in the Information Technology business, Wipro is the largest outsourced ... | | View | Watch | Comment |
| 2. Regulatory Affairs-Tech Writer (Fulltime) | 14 hour(s) ago | | Aerotek - United States, MD, Germantown - - (view employer jobs) | | Categories: PharmaceuticalJob DescriptionJob Classification: Direct Hire Essential Functions:
-Coordinate all aspects of CMC regulatory submissions relevant to the assigned projects or programs and serve as the regulatory CMC representative on project teams; provide regulatory guidance during the review of change controls and deviations.
-Develop CMC submission content in eCTD format.
-Manage and ... | | View | Watch | Comment |
| 3. Manager, RA/QA - Olympus Latin America (Fulltime) | 17 hour(s) ago | | Olympus Corporation of the Americas - United States, FL, Miami Beach - - (view employer jobs) | | Categories: QA - Quality ControlJob DescriptionMiami, FL - The Manager, Regulatory Affairs/Quality Assurance will be responsible for establishing and maintaining compliance with regulatory and sanitary health laws and regulations throughout Latin America (excepting Brazil), including the management of product registrations, complaint and adverse event processing, inspections and audits, compliance, training, ... | | View | Watch | Comment |
| 4. Regulatory Specialist (Fulltime) | 18 hour(s) ago | | Confidential - United States, LA, Lafayette - - (view employer jobs) | | Categories: EngineeringJob DescriptionA Lafayette, Louisiana based Regulatory company is seeking an experienced Regulatory Specialist with a minimum of 5 years experience for a full time position. Job RequirementsExperience should include Federal/BSEE/BOEM permitting. Although State permitting experience would be beneficial, it is not required. | | View | Watch | Comment |
| 5. Regulatory Affairs Assistant (Fulltime) | 19 hour(s) ago | Kelly Scientific Resources - United States, MA, Lexington -  - (view employer jobs) | | Categories: Biotech, Research, ScienceJob DescriptionKelly Clinical research has an immediate opening for a Regulatory Operations Assistant. This is a 3 month contract in Lexington, MA at a large pharmaceutical company. The ROA will work on special projects related to archival of regulatory submissions and correspondence. They ... | | View | Watch | Comment |
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Department:Department Of Veterans Affairs
Agency:Deputy Assistant Secretary for Finance
Job ... objectives.
-Coordinate, issue, evaluate and review financial policies, systems and procedures ensuring compliance and...> | | Provided by KCBD.com |
| 6. Regulatory Affairs Specialist (Fulltime) | 1 day ago | | Becton Dickinson - United States, MD, Baltimore - - (view employer jobs) | | Categories: QA - Quality ControlJob DescriptionThe Regulatory Affairs Specialist is responsible for the preparation of regulatory submissions required to market new or modified medical devices and in vitro diagnostic devices in both domestic and international clinical markets. This responsibility entails development, execution and management of procedures and systems designed to ... | | View | Watch | Comment |
| 7. Regulatory Assistant (Fulltime) | 1 day ago | | Aerotek - United States, WA, Seattle - - (view employer jobs) | | Categories: ScienceJob DescriptionJob Classification: Direct Hire The Regulatory and Quality Control Assistant supports the International Regulatory Specialist and Quality Control Specialist on all projects for all markets throughout the products lifecycle.
Primary Responsibilities:
- Supports all international regulatory projects.
- Manages electronic database of product information and to make sure it meets pre ... | | View | Watch | Comment |
| 8. Regulatory (Temporary) | 1 day ago | | Randstad Technologies - United States, CA, Northridge - - (view employer jobs) | | Categories: Information TechnologyJob DescriptionAssignment Information12 MONTH CONTRACTPositions : 1Order Status : OpenOrder Type : Requisition for Contract LaborInterview Type : Interview Required Travel : No Travel Required Work Environment : Professional Anticipated Schedule : Typical 8 Hour/Day Required Dress Code : Business Casual Contractor Work Location : Northridge, CA USAJob ... | | View | Watch | Comment |
| 9. Documentation Specialist (Fulltime) | 1 day ago | | Aerotek - United States, IL, Downers Grove - - (view employer jobs) | | Categories: ScienceJob DescriptionJob Classification: Contract JOB SUMMARY
Responsible for performing duties associated with regulatory affairs and compliance requirements relevant to the pharmaceutical industry.
ESSENTIAL JOB FUNCTIONS
1. Administers and maintains the Company’s Change Control System for compliance documentation.
2. Reviews and evaluates product labeling to ensure compliance with all regulations and requirements.
3. Uses ... | | View | Watch | Comment |
| 10. Packaging Specialist (Fulltime) | 1 day ago | | Eddy Packing - United States, TX, Yoakum - - (view employer jobs) | | Categories: ManufacturingJob Description
Reviews, updates and approves corporate labeling designs. Develops Nutrition Facts Panels for assigned products, ensuring compliance with all label related health and wellness claims. Develops ingredient statements and ensures products meet appropriate FDA/USDA standard of identities. Works across functions and communicates with all functional and operating groups on ... | | View | Watch | Comment |
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| 11. Associate Regulatory Affairs Engineer (240-547) (Fulltime) | 2 days ago | | ZOLL Medical Corporation - United States, PA, Pittsburgh - - (view employer jobs) | | Categories: QA - Quality ControlJob 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 ... | | View | Watch | Comment |
| 12. REGULATORY AFFAIRS COORDINATOR (Fulltime) | 2 days ago | | Innovative Dialysis Systems - United States, NY, Long Beach - - (view employer jobs) | | Categories: NurseJob DescriptionInnovative Dialysis Systems, (IDS) is looking for a motivated candidate for fill the position of Regulatory Affairs Coordinator. This candidate will be responsible for performance reviews for IDS and our managed dialysis operations in the areas of licensing & Medicare certification. Also responsible for semi-revision of manuals, provision ... | | View | Watch | Comment |
| 13. Post Market Clinical Specialist (Fulltime) | 2 days ago | | Fresenius Medical Care - Corporate - United States, MA, North Waltham - - (view employer jobs) | | Categories: EducationJob DescriptionPURPOSE AND SCOPE: The Post Market Clinical Investigation Specialist is responsible for clinical evaluations, clinical investigations, and complaint review/reportability decisions to include timely submission of applicable adverse event reports (MDRs/ADEs). This individual will also be responsible for receiving, reviewing, and investigating adverse events. Requires basic understanding ... | | View | Watch | Comment |
| 14. Regulatory Affairs Specialist (Temporary) | 2 days ago | | Comrise - United States, NJ, Mahwah - - (view employer jobs) | | Categories: Pharmaceutical, QA - Quality Control, BiotechJob Description
Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines.
Ensure compliance with all US, EU and SO international requirements and corporate policies and procedures regarding ... | | View | Watch | Comment |
| 15. Regulatory Compl Analyst Sr (Fulltime) | 2 days ago | | Lockheed Martin - United States, TX, Altair - - (view employer jobs) | | Req ID264213BRIndustry Job TitleRegulatory Compl Analyst SrJob Code/TitleE5053:Regulatory Compl Analyst SrJob DescriptionProvides guidance to company personnel pertaining to U.S. Export/Import laws and regulations, including the International Traffic In Arms Regulations (ITAR), Export Administration Regulations (EAR), Customs and Border Protection (CBP) regulations, Bureau of Alcohol Tobacco and Firearms (BATF) regulations, and ... | | View | Watch | Comment |
| 16. Regulatory Affairs Assoc II (Fulltime) | 2 days ago | | Actavis - United States, UT, Salt Lake City - - (view employer jobs) | | Categories: QA - Quality ControlJob DescriptionUnder general supervision, performs routine dutiesin the preparation, review and submission of pre-and post-approval submissions to the Food and Drug Administration, using governmental guidelines and regulations. Essential functions include: *Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws.*Prepares timely original ... | | View | Watch | Comment |
| 17. Drug Safety Associate (Fulltime) | 2 days ago | | Actavis - United States, NJ, Morristown - - (view employer jobs) | | Categories: QA - Quality Control, Science, PharmaceuticalJob DescriptionAssist the Director, Medical Affairs in managing the mandatory safety reporting requirements and other functions of the Drug Safety Group. Included in these functions are: Triaging, Data entry; Case processing; Creation of case reports; Submission of case reports; Compilation of aggregated reports; ... | | View | Watch | Comment |
| 18. Drug Safety Associate (Fulltime) | 2 days ago | | Actavis - United States, NJ, Morristown - - (view employer jobs) | | Categories: QA - Quality Control, Science, PharmaceuticalJob DescriptionAssist the Director, Medical Affairs in managing the mandatory safety reporting requirements and other functions of the Drug Safety Group. Included in these functions are: Triaging, Data entry; Case processing; Creation of case reports; Submission of case reports; Compilation of aggregated reports; ... | | View | Watch | Comment |
| 19. Sr. Regulatory Specialist (Fulltime) | 2 days ago | | MRI - The Boston Group - United States, MD, Southern Md Facility - - (view employer jobs) | | Categories: ManufacturingJob DescriptionMRINetwork™ is the world's largest executive search and recruitment organization. We have a global network of more than 1,000 offices. Management Recruiters - The Boston Group is our 5 office organization, established in 1966 to provide executive and management level staffing services to a wide variety of industries. ... | | View | Watch | Comment |
| 20. Regulatory Affairs Fellowship (Fulltime) | 3 days ago | | Kelly Scientific Resources - United States, MO, Hazelwood - - (view employer jobs) | | Categories: Biotech, Research, ScienceJob DescriptionREGULATORY AFFAIRS FELLOWSHIP PROGRAM - 2013 The Department of Regulatory Affairs has established a one-year Industry Fellowship Program to provide candidates with the opportunity to apply their scientific training while learning about careers within regulatory in the pharmaceutical industry. The goal of the program ... | | View | Watch | Comment |
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