Keywords: Type: Location: Industry:  
job title, keywords, or company for hire, for bid, or volunteer city, state or zip select a career focus  
Jobs (22 Matches)
Jobs By Email | Jobs By RSS
Page 1 of 2 | Next >


1. Hazard Communication Specialist   (Fulltime)2 hour(s) ago
Pace Analytical Services, Inc. - United States, MN, Minneapolis - Not rated - (view employer jobs)
Categories: OtherJob DescriptionHazard Communication Specialist ...
View | Watch | Comment
2. Regulatory Analyst   (Fulltime)4 hour(s) ago
ARYZTA - United States, IL, West Chicago - Not rated - (view employer jobs)
Categories: OtherJob Description Responsible for understanding all applicable domestic food regulations (national, state, and local) and assuring recipes, labels and labeling meet all regulations. Manages regulatory approval process for new products and contributes to maintenance of existing products Assists Marketing with New Item set up (product specifications). Assists ...
View | Watch | Comment
3. Medical Quality Assurance Specialists Needed!   (Temporary)9 hour(s) ago
OfficeTeam - United States, CA, San Francisco - Not rated - (view employer jobs)
Categories: Admin - Clerical, Customer Service, LegalJob DescriptionRef ID: 00416-9739803Classification: Administrative - MedicalCompensation: $16.00 to $16.00 per hourQuality Assurance Team is in need of 8 specialists to review Medical Records. Quality assurance team will support an innovative healthcare technology start-up in San Francisco. Quality Assurance Specialists will provide ...
View | Watch | Comment
4. Reg Affairs Specialist   (Temporary)15 hour(s) ago
US Tech Solutions, Inc - United States, IL, Warsaw - Not rated - (view employer jobs)
Categories: GovernmentJob DescriptionRegulatory Affairs Specialist  USTECH is an industry-leading, global firm providing a wide range of talent, technology and total workforce solutions to mid-market and enterprise clients, including more than 50 of the Fortune 150.  It is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce ...
View | Watch | Comment
5. Regulatory Compliance Specialist   (Fulltime)16 hour(s) ago
ALERE - United States, CA, San Diego - Not rated - (view employer jobs)
Categories: QA - Quality Control, Health Care, ManufacturingJob Description Alere has an exciting opportunity for a Regulatory Compliance Specialist. This opportunity will be based in San Diego, CA.   Responsibilities: The ideal candidate will document and evaluate complaints for USA Medical Device Reports (MDRs), EU ...
View | Watch | Comment

Matching Jobs by SimplyHired
6. International Regulatory Affairs Specialist   (Fulltime)22 hour(s) ago
GC America - United States, IL, Alsip - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionGC America Inc., winner of the prestigious Deming Award for Total Quality Management, is part of GC Corporation, a family of companies promoting oral healthcare across the globe. GCA is a leading manufacturer of dental products for dentists, hygienists and laboratory technicians throughout North ...
View | Watch | Comment
7. Regulatory Affairs Specialist I   (Fulltime)1 day ago
Merit Medical Systems, Inc. - United States, UT, South Jordan - Not rated - (view employer jobs)
Categories: ManufacturingJob DescriptionREGULATORY AFFAIRS SPECIALIST IMERIT MEDICAL SYSTEMS, INC.SOUTH JORDAN, UTAH SUMMARY OF DUTIESThis position is responsible to coordinate and help prepare document packages for regulatory submissions, internal audits, governmental inspections, recalls, Medical Device Reports and clinical trials.ESSENTIAL FUNCTIONS PERFORMED• Coordinates and prepares document packages for:• Regulatory submissions (domestic and international)• Facilitates corrective ...
View | Watch | Comment
8. Regulatory Affairs Associate   (Fulltime)1 day ago
Medpace - United States, IA, Cincinnati - Not rated - (view employer jobs)
Categories: Health Care, ResearchJob Description Regulatory Affairs Associate Prepare regulatory documents for submission to the FDA, including writing, publishing, correct placement in eCTD hierarchy; Manage IND and NDA project deliverables and timelines; Conduct meetings with internal teams, Sponsors, ...
View | Watch | Comment
9. Nutritional Label Specialists   (Fulltime)1 day ago
On Assignment - United States, WA, Seattle - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionGeneral Duties & Responsibilities Maintains an up-to-date and expert understanding of USDA labeling requirements including but not limited to the basic label setup, ingredients, nutrition panel, nutrition claims, formulas, and process methods Primary accountability and responsibility for USDA label ...
View | Watch | Comment
10. Regulatory Affairs Specialist   (Fulltime)1 day ago
Aerotek - United States, NY, Tarrytown - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionDUTIES - RESPONSIBILITIES:Regulatory Submissions project planning.Preparing regulatory submissions in electronic format and acting as liaison with electronic publishing vendor.Managing the archiving of regulatory documentation.Preparing templates, forms and drafts cover letters, collating materials and coordinating retrieval of contents for submissions from multiple departments.Management and maintenance of regulatory communications and ...
View | Watch | Comment

Matching Jobs by SimplyHired
11. Dynamic & Experienced Drug Safety Experts Needed   (Fulltime)1 day ago
On Assignment - United States, CA, San Francisco - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionDynamic & Experienced Drug Safety Expert Needed ( call me directly to discuss) Demonstrated knowledge of safety concepts, per ICH and FDA guidelines per drug safety reporting requirements. • Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case ...
View | Watch | Comment
12. Regulatory Affairs   (Fulltime)2 days ago
Aerotek - United States, CA, Pomona - Not rated - (view employer jobs)
Categories: ScienceJob DescriptionJOB DESCRIPTIONResponsible for developing and implementing US and International regulatory strategies for company (GHS, OSHA, CPSC, Europa, etc.). Accountable for preparing Technical files and documents as necessary for the global market.Looking for experience with the following:-MSDS, 21CFR, GHS, and Reach DocumentationAbility to effectively negotiate and influence peers as ...
View | Watch | Comment
13. Regulatory Operations Associate I or II   (Fulltime)2 days ago
Aerotek - United States, WA, Seattle - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionEssential Duties and Job Functions : -As a member of the Regulatory Operations team, performs routine and non-routine submission publishing activities associated with sending information and data to health authorities.-As a member of the Regulatory Operations team, prepares basic to complex eCTD submission publishing using specialized software such ...
View | Watch | Comment
14. Hazard Communication Specialist   (Fulltime)3 days ago
Pace Analytical Services, Inc. - United States, PA, Pittsburgh - Not rated - (view employer jobs)
Categories: OtherJob DescriptionHazard Communication Specialist ...
View | Watch | Comment
15. Regulatory Affairs Specialist   (Fulltime)3 days ago
Aerotek - United States, CA, San Diego - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionResponsible for preparation and maintenance of both U.S. and foreign regulatory pre-market submissions and other premarket filings to acquire appropriate commercial distribution clearances in an expeditious manner.Determine/document appropriate regulatory strategy for proposed new products and initiate necessary activities by working with Regulatory management as needed.Ability to determine and ...
View | Watch | Comment
16. Drug Safety Associate   (Temporary)3 days ago
Advanced Clinical - United States, DE, Wilmington - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 426584Drug 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 ...
View | Watch | Comment
17. Sr. PV Associate   (Temporary)3 days ago
Advanced Clinical - United States, NJ, Far Hills - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 426613Sr. PV AssociateOVERVIEWSenior level Individual contributor for PV safety unit responsible for collection, collation and evaluation of global productSafety reporting with expanded responsibilities for support of PV applications/tools, generation of aggregate reports and training/mentoring of new safety specialists.Business System Administrator of electronic adverse event database (Argus) ...
View | Watch | Comment
18. - QA/RA Specialist - Medical   (Temporary)3 days ago
Belcan Corp - United States, IA, Cincinnati - Not rated - (view employer jobs)
Categories: EngineeringJob DescriptionJob Description • Completes assigned activities for site operational and compliance projects. The activities may include developing, drafting, reviewing, editing, compiling and/or obtaining internal approval for project related documentation, executing software and spreadsheet validations and/or verifications, and preparing project related documentation for ...
View | Watch | Comment
19. Regulatory Affairs Associate   (Fulltime)3 days ago
Arthrex - United States, FL, Naples - Not rated - (view employer jobs)
Categories: BankingJob DescriptionRequisition ID: 10601 Title: Regulatory Affairs Associate Division: Arthrex, Inc. (US01) Location: INC- Naples, FL (US08) Main Objective: Supports regulatory and compliance activities for Arthrex, Inc. Essential Duties and Responsibilities: Under direct supervision, prepares and submits regulatory filings with FDA, Notified Bodies, Canada, and other ...
View | Watch | Comment
20. Regulatory Affairs Specialist   (Fulltime)3 days ago
Arthrex - United States, FL, Naples - Not rated - (view employer jobs)
Categories: Information TechnologyJob DescriptionRequisition ID: 11801 Title: Regulatory Affairs Specialist Division: Arthrex, Inc. (US01) Location: INC- Naples, FL (US08) Main Objective: Supports Regulatory Affairs activities for Arthrex, Inc. Essential Duties and Responsibilities: With minimal supervision, prepares and submits regulatory applications to secure worldwide product approvals. Develops regulatory ...
View | Watch | Comment



Jobs By Email | Jobs By RSS Page 1 of 2 | Next >