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Jobs (19 Matches)
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1. Associate, Regulatory Affairs   (Fulltime)4 hour(s) ago
CR Bard - United States, UT, Salt Lake City - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob Description Overview: This position implements C.R. Bard domestic and international regulatory affairs procedures. This position may also act as a liaison to Corporate Law Department, providing requested informationThe ideal candidate must be able to work in a team oriented, fast ...
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2. Agile Software Regulatory Specialist - FDA Medical Devices   (Fulltime)4 hour(s) ago
Cybercoders - United States, CA, San Carlos - Not rated - (view employer jobs)
Categories: Information Technology, Engineering, Professional ServicesJob DescriptionThis position is open as of 4/19/2015.Agile Software Regulatory Specialist - FDA Medical DeviceBased in San Carlos, CA, we are a pre-IPO biotech software company in the non-invasive prenatal diagnostics space and are making huge strides in growth for our domain. We ...
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3. Regulatory Affairs Specialist II   (Fulltime)5 hour(s) ago
CR Bard - United States, UT, Salt Lake City - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob Description Overview: This position implements C.R. Bard domestic and international regulatory affairs (RA) procedures. This position may also act as a liaison to Corporate Law Department, providing requested information. Essential Job Functions: The ...
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4. Regulatory Affairs Associate   (Fulltime)1 day ago
CR Bard - United States, AZ, Tempe - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob Description Overview: Bard Peripheral Vascular, located in Tempe, AZ – where a tradition of vascular innovation spans decades of focusing on improving the quality of patients’ lives.From C. R. Bard’s first arterial prosthesis developed in 1954, Bard and the division ...
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5. Regulatory Affairs Associate (International)   (Fulltime)1 day ago
System One - United States, IL, Vernon Hills - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob is located in Vernon Hills, IL.Regulatory Affairs Associate (International) Vernon Hills, Illinois Our client, a medical device and pharmaceutical company is seeking an experienced Regulatory Affairs Associate, International to be part of their growing team. This position is ideal for an experienced Regulatory Affairs professional who wishes to ...
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6. Compliance Specialist - Trucking   (Fulltime)1 day ago
Morgan Southern, Inc. - United States, GA, Atlanta - Not rated - (view employer jobs)
Categories: TransportationJob DescriptionCompliance Specialist - TruckingMorgan Southern, Inc. is searching for an individual with recent experience in Trucking Safety Compliance for related administrative responsibility in our Safety Department. Will be responsible for making sure that all required DOT complainace records are being maintained and procedures are being followed. Receive: Competitive pay Excellent ...
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7. Clinical/Regulatory - Safety Review Specialist   (Fulltime)2 days ago
KellyMitchell - United States, IL, Deerfield - Not rated - (view employer jobs)
Categories: Job DescriptionJob Requirements
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8. Agile Software Regulatory Specialist - FDA Medical Devices   (Fulltime)2 days ago
Cybercoders - United States, CA, San Carlos - Not rated - (view employer jobs)
Categories: Information Technology, Engineering, Professional ServicesJob DescriptionThis position is open as of 4/17/2015.Java DeveloperBased in San Carlos, CA, we are a pre-IPO biotech software company in the non-invasive prenatal diagnostics space and are making huge strides in growth for our domain. We are a team of engineers who ...
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9. Haz Comm - Regulatory Specialist   (Fulltime)2 days ago
Pace Analytical Services, Inc. - United States, OH, Maplewood - Not rated - (view employer jobs)
Categories: OtherJob DescriptionHaz Comm - Regulatory Specialist ...
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10. Senior Associate Labeling   (Fulltime)3 days ago
Kforce Technology - United States, NY, Hawthorne - Not rated - (view employer jobs)
Categories: Information TechnologyJob DescriptionRESPONSIBILITIES:One of Kforce pharmaceutical clients in the Westchester, New York (NY) area is looking for a Senior Associate Labeler.This person will be responsible for the following: Prepare, proof read and approve product labeling for new submissions Create labeling QBR section for new ANDA submissions Edit, review and ...
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11. Regulatory Affairs Specialist   (Fulltime)3 days ago
Aerotek - United States, CA, San Diego - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, genetic information or any other characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment ...
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12. Software Validation Analyst - FDA Regulations   (Fulltime)3 days ago
Cybercoders - United States, IN, Indianapolis - Not rated - (view employer jobs)
Categories: Information Technology, Engineering, Professional ServicesJob DescriptionThis position is open as of 4/16/2015.Software Validation Analyst - FDA RegulationsBased in Indianapolis, IN, we are an established and growing BioTech Company looking to hire a Software Validation Analyst with experience in an FDA regulated environment. You will be responsible ...
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13. Regulatory Affairs Intern   (Fulltime)3 days ago
CR Bard - United States, CA, East Irvine - Not rated - (view employer jobs)
Categories: QA - Quality Control, Entry LevelJob Description Overview: Bard Davol Inc., a subsidiary of C. R. Bard, Inc., is a leading developer, manufacturer, and marketer of innovative, life-enhancing medical technologies. We focus our business on key surgical specialties, including Soft Tissue Repair, Surgical ...
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14. Clinical/Regulatory - Safety Review Specialist   (Fulltime)3 days ago
KellyMitchell - United States, IL, Deerfield - Not rated - (view employer jobs)
Categories: Information TechnologyJob DescriptionThis position is a member of the Safety Operations team within Global Pharmacovigilance and serves as a case owner for adverse events to ensure timely and accurate review, processing, and reporting. This section contains a list of five to eight primary responsibilities of this role that account ...
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15. Safety Data Specialist   (Fulltime)3 days ago
Joule' Clinical - United States, NJ, Parsippany - Not rated - (view employer jobs)
Categories: PharmaceuticalJob Description Safety Data Specialist: Requirements Safety Data Specialist: MS degree in Life Sciences plus 3 years of experience in the Pharmaceutical Industry, drug safety experience is preferred. Min BA or BS degree in Life Sciences, Registered Nurse,Pharmacist or LPN with at least 4 ...
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16. Drug Safety Associate   (Temporary)3 days ago
Advanced Clinical - United States, DE, Wilmington - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 428194Drug Safety AssociateOVERVIEWThis contractor position will be responsible for reviewing, reporting and tracking of adverse drug experience reports, assisting with the preparation of aggregate (ASRs, IND annual, and ad-hoc) reports, and all aspects of Pharmacovigilance. The position will have direct impact on the work flow efficiency ...
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17. Documentation Submissions Specialist   (Temporary)3 days ago
The Ascent Services Group - United States, CA, Pleasanton - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionDocumentation Submissions SpecialistPleasanton, CADESCRIPTION Execute routine tasks required in the end-to-end regulatory submission publishing processes, including pre-production, production, processing or creation of graphics and images, e-copy development, print production, assembly, shipping, and archiving of all required submission types.RESPONSIBILITIES Under management supervision and following standard procedures, responsible for end-to-end tasks associated ...
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18. Regulatory Affairs Associate   (Fulltime)4 days ago
Aerotek - United States, MA, Beverly - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, genetic information or any other characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment ...
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19. Regulatory Assistant   (Fulltime)4 days ago
Adecco Engineering & Technology - United States, NC, Greensboro - Not rated - (view employer jobs)
Categories: ScienceJob Description.Adecco Engineering and Technical has a current job opportunity for a Regulatory Assistant in Greensboro, NC. This is a contract position. If you meet the qualifications listed below please apply.Product Labeling and Technology is responsible for insuring EPA compliant labeling for all products within the company. ...
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20. Drug Safety Associate I   (Fulltime)5 days ago
CSG, Inc - United States, NJ, Morris Plains - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionLarge pharmaceutical company in greater Morristown area has an immediate need for a Drug Safety Associate (Level I).  Onsite and initially slated for 6 months with the option to be extended.   Ideal candidate will be responsible for the following: Triage of incoming cases to ...
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