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Jobs (56 Matches)
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1. Regulatory Compliance Associate.   (Fulltime)0 minute(s) ago
US Welding - United States, CO, Denver - Not rated - (view employer jobs)
Categories: QA - Quality Control, Entry Level, Distribution - ShippingJob Description “Ability is what you're capable of doing. Motivation determines what you do. Attitude determines how well you do it." Lou Holtz Ability. Motivation. Attitude. The ability for this position is simple, you must be constantly willing ...
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2. Medical Device Analyst with MDR Experience   (Fulltime)1 hour(s) ago
Kelly Services - United States, CA, San Jose - Not rated - (view employer jobs)
Categories: Health Care, Nurse, OtherJob DescriptionKelly Services, Inc. is a Fortune 500 Company that is partnered with an established Medical Device Company located in San Jose, CA. We are currently seeking an experienced Medical Device Analyst with MDR knowledge. Responsibilities:- Perform detailed investigation of adverse events and generate Medical ...
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3. RA/QA Specialist   (Fulltime)2 hour(s) ago
Aerotek - United States, FL, Jacksonville - Not rated - (view employer jobs)
Categories: ScienceJob DescriptionJob Classification: Direct Hire Aerotek is seeking a qualified RA/QA Specialist for a medical device manufacturer in Jacksonville, FL. Qualified candidates must meet the following criteria: -5+ years in FDA regulated medical device industry -Strong customer service and interpersonal skills -Understanding of customer complaint and quality resolution related to ...
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4. Quality / Regulatory Affairs Associate   (Fulltime)3 hour(s) ago
BTE - United States, MD, Hanover - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob Description Quality / Regulatory Affairs Associate About BTE: BTE's expertise is human physical performance evaluation and treatment. Our Rehabilitation Equipment provides advanced evidence-based physical therapy systems for clinics, hospitals, and private practices. BTE's Workforce Solutions provides employers with superior processes and technology to enable employers to optimize productivity, ...
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5. Regulatory And Quality Affairs Analyst   (Fulltime)4 hour(s) ago
Tunnell Government Services - United States, DC, Washington - Not rated - (view employer jobs)
Categories: ResearchJob DescriptionREGULATORY AND QUALITY AFFAIRS ANALYST We have an immediate need for one of our clients in Washington, D.C. for a Regulatory and Quality Affairs Analyst. This is a long term opportunity. Responsibilities include: Providing scientific/technical/program management advice for assigned programs and projects and work ...
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Healthcare System Specialist: Compliance Officer
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6. Regulatory Specialist   (Fulltime)5 hour(s) ago
King Industries, Inc. - United States, CT, Norwalk - Not rated - (view employer jobs)
Categories: General BusinessJob Description Position:Regulatory Specialist Description: King Industries, Inc., a global supplier of high performance chemical additives for coatings, lubricants, electronics and rubber, is seeking a Regulatory Specialist with experience in the following areas: • Safety Data Sheet authoring • Hazard classification according to the requirements of various countries • ...
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7. Regulatory Affairs Associate - Westlake Village, CA   (Fulltime)6 hour(s) ago
Kelly Scientific Resources - United States, CA, Westlake Village - Not rated - (view employer jobs)
Categories: Biotech, Research, ScienceJob Description Regulatory Affairs Associate Opportunity in Westlake Village, CAKelly Scientific ResourcesMake the most of your valued expertise!Every day, Kelly Scientific Resources (KSR) connects scientific professionals with opportunities to advance their careers. We currently have an exciting contract opportunity for a Regulatory Affairs Associate in Westlake ...
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8. Quality Regulatory Reporting Specialist   (Fulltime)8 hour(s) ago
Kelly Scientific Resources - United States, FL, Miami Beach - Not rated - (view employer jobs)
Categories: Biotech, Research, ScienceJob DescriptionQUALITY-REGULATORY REPORTING SPECIALIST Position Summary: Manages, prepares, and tracks regulatory correspondences for product quality. Reviews all documents for accuracy and completeness. Processes documents and ensures they are approved and submitted to the regulatory agencies in a timely manner. Ensures that field action documentation and ...
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9. Associate Regulatory Affairs Specialist   (Parttime)1 day ago
KCS - United States, CA, Santa Ana - Not rated - (view employer jobs)
Categories: ConsultantJob DescriptionWe are currently looking for an Associate Regulatory Affairs Specialist in the Santa Ana, CA area and would love to hear from you if you meet the following criteria. **THIS IS A CONTRACT OPPORTUNITY** PART TIME 20 HOURS A WEEK The Associate Regulatory Affairs Specialist provides regulatory support for domestic and international submissions; provides responses to routine ...
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10. Regulatory Affairs Consultant - Irvine, CA or Eden Prairie, MN   (Fulltime)1 day 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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11. Regulatory Affairs Consultant - Irvine, CA or Eden Prairie, MN   (Fulltime)1 day 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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12. Drug Safety Associate   (Fulltime)1 day ago
Aerotek - United States, MA, North Waltham - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionJob Classification: Contract Aerotek is seeking a full-time, office-based Drug Safety Associate for a contract with a major client in Waltham, MA. This is a great opportunity for a CTA or other clinical professional with AE/ SAE Triage and Reconciliation experience. Responsibilities include: 1. ...
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13. Regulatory Affairs Assoc III   (Fulltime)1 day ago
Actavis - United States, UT, Salt Lake City - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionUnder limited supervision, performs 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 ...
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14. Quality Assurance Specialist - Research   (Fulltime)2 days ago
Rockwood Clinic - United States, WA, Spokane - Not rated - (view employer jobs)
Categories: Health CareJob DescriptionThe QA Specialist performs and manages the facilitation of compliance reviews and audits of internal systems, processes, clinical trial data, and functional areas as per department standard operating procedures, good clinical practices, Federal and State regulations.  Job RequirementsEducation:High School diploma or GED required.Bachelor degree in related field ...
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15. ATTN: Clinical Regulatory Affairs Experts in the West Coast   (Fulltime)2 days ago
Valesta Clinical Research Solutions - United States, WA, Tacoma - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionCALLING ALL EXPERIENCED CLINICAL REGULATORY AFFAIRS EXPERTS IN THE WEST COAST!! Create, evaluate and update Regulatory Affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced • Review labeling/promotional/advertising materials, and other documents to ensure compliance • Maintain current knowledge of relevant regulations, including proposed and ...
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16. Sr Compliance Analyst   (Fulltime)2 days ago
Alcon - United States, TX, Fort Worth - Not rated - (view employer jobs)
Categories: ManufacturingJob DescriptionThis is a universal job description meant to capture some of the primary duties of this role that are common across functions or divisions. It is not intended to represent all of the specific responsibilities of your position. Serve as a multi-functional team member, representing manufacturing for the ...
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17. Sr. Regulatory Labeling Associate   (Temporary)2 days ago
The Ascent Services Group - United States, NY, Tarrytown - Not rated - (view employer jobs)
Categories: Biotech, Pharmaceutical, ScienceJob DescriptionSr. Regulatory Labeling Associate Tarrytown, NY Contract Responsibilities: Manages the development, review, approval, and maintenance of the Company Core Data Sheets, USPI, and EU SmPC. Maintains and appropriately archives submitted and approved labeling documents and packaging component labeling Participates ...
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18. Compliance Analyst   (Fulltime)3 days ago
APS Healthcare - United States, TX, South Houston - Not rated - (view employer jobs)
Categories: Health CareJob DescriptionUniversal American is a New York Stock Exchange company with annual revenues of more than $2 billion. Through our family of healthcare companies, we provide health benefits to people covered by Medicare and/or Medicaid. We are dedicated to working collaboratively with healthcare professionals in order to ...
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19. Regulatory Affairs Assoc II   (Fulltime)3 days ago
Actavis - United States, NJ, Parsippany - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionSummary: Under general supervision, performs routine duties in the preparation, review andsubmission of pre-and post-approval submissions to the Food and Drug Administration, usinggovernmental guidelines and regulations. Essential Job Functions: This is not intended as a comprehensive list; it is intended to provide arepresentative summary of the ...
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20. Regulatory Technical Specialist 4   (Temporary)3 days ago
Viva USA, Inc. - United States, MA, Norwood - Not rated - (view employer jobs)
Categories: Information TechnologyJob Description Must have experience preparing 510(k)s in medical device industry; preferably with IVDs. Must have experience assessing design changes for impact on regulatory status, and writing Note-to-File. Must have experience reviewing advertising and promotional literature. ...
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