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Jobs (18 Matches)
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1. Regulatory Affairs Associate Director +   (Fulltime)7 hour(s) ago
Accenture - United States, PA, Berwyn - Not rated - (view employer jobs)
Categories: QA - Quality Control, ManagementJob Description Schedule: Full-time Accenture's Life Sciences practice is dedicated to helping life sciences companies overcome industry challenges, achieve their business objectives and deliver improved health solutions to people around the globe. We serve all the top 10 global pharmaceutical companies, ...
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2. Regulatory Specialists   (Fulltime)15 hour(s) ago
Aerotek - United States, CA, Northridge - Not rated - (view employer jobs)
Categories: Admin - ClericalJob DescriptionLooking for Data Entry Candidates willing to perform the following job duties:-reviewing/verifying documents for the FDA response. - 1st shift (8-5 may vary by 30 minutes) or 2nd shift (3-11)- Reviewing documents- Documentation (must have good written and verbal skills)- No customer service - working with ...
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3. Regulatory Affairs Assistant   (Fulltime)20 hour(s) ago
Aerotek - United States, WA, Seattle - Not rated - (view employer jobs)
Categories: QA - Quality Control, ScienceJob DescriptionThe Regulatory Affairs & Safety Coordinator supports the Global Regulatory Manager on all projects for all markets throughout the products lifecycle. This position has a strong emphasis on safety and global compliance as is relates to raw materials and finished formulas.Current markets include: ...
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4. Regulatory CMC Scientist   (Temporary)23 hour(s) ago
System One - United States, VA, Elkton - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob is located in Elkton, VA.The Regulatory Document Coordinator will report to the Technical Operations Department. The Elkton plant is located in Virginia's Shenandoah Valley. The site employs a wide array of state of the art manufacturing technologies to support the production of pharmaceuticals including organic synthesis, biotechnology ...
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5. Sr. Regulatory Specialist, Biotech Center of Expertise~ San Diego, CA   (Fulltime)1 day ago
BASF - The Chemical Company - United States, CA, San Diego - Not rated - (view employer jobs)
Categories: BiotechJob DescriptionHow do you create chemistry? At BASF, is the world’s leading chemical company, we do it through the power of connected minds. Our portfolio ranges from chemicals, plastics, performance products and crop protection products to oil and gas. We combine economic success with environmental protection and social responsibility. ...
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6. Sr. Quality Regulatory Affairs Coordinator   (Temporary)1 day ago
Advanced Clinical - United States, PA, Malvern - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Number: 426098Sr. Quality Regulatory Affairs CoordinatorOVERVIEW Experience with TMFIdeally somebody that has submitted to different global Regulatory Authorities. Job Requirements
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7. Regulatory Compliance Specialist   (Temporary)1 day ago
OfficeTeam - United States, AZ, Tucson - Not rated - (view employer jobs)
Categories: Admin - Clerical, Customer Service, LegalJob DescriptionRef ID: 00220-9724749Classification: Office/Administrative Supervisor/MgrCompensation: $18.00 to $20.00 per hourOfficeTeam is currently looking for a Regulatory Compliance Specialist for a medical devices manufacturing company in Tucson. Responsibilities of the Regulatory Compliance Specialist include but are not limited to licensure, policy, research, ...
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8. Regulatory Compliance Specialist   (Fulltime)1 day ago
CareSouth - United States, GA, Augusta - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionJob Description Summary: The Regulatory Compliance Specialist serves as the initial point of contact on regulatory issues impacting patient care. This person maintains an extensive knowledge of Federal, State and Accreditation guidelines/regulations. Acts as a resource and advisor to the company and agency ...
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9. Regulatory Specialists   (Fulltime)1 day ago
Aerotek - United States, CA, Northridge - Not rated - (view employer jobs)
Categories: ManufacturingJob DescriptionLooking for Data Entry Candidates willing to perform the following job duties:-reviewing/verifying documents for the FDA response. - 1st shift (8-5 may vary by 30 minutes) or 2nd shift (3-11)- Reviewing documents- Documentation (must have good written and verbal skills)- No customer service - working with documents all ...
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10. Regulatory Affairs Associate/Consultant   (Fulltime)1 day ago
Lab Support, a division of On Assignment - United States, NJ, Rochelle Park - Not rated - (view employer jobs)
Categories: Manufacturing, QA - Quality Control, ConsultantJob DescriptionREGULATORY AFFAIRS CONSULTANT Seeking a RA Manager with prior experience in a medical device or regulated industry, preferably manufacturing environment. Prefer degree in Engineering or related Science. Advanced degrees accepted and prefered.Job RequirementsREQUIREMENTS Candidates must have experience and knowledge of the following: ...
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11. Quality Assurance & Clinical Documentation Specialist Position   (Fulltime)1 day ago
Aerotek - United States, MD, Rockville - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionJob Description: Quality Assurance & Clinical Document Specialist will assist in the coordination of activities and documents related to the conduct of clinical trials and participate in the development, editing and submission of clinical protocols, Investigator Brochures, INDs, and associated clinical materials as well as FDA submissions and ...
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12. Regulatory Affairs Specialist II   (Fulltime)2 days 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. The ideal candidate must be able to work in a team ...
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13. Sr. Regulatory Affairs Associate   (Fulltime)2 days ago
Thoratec Corporation - United States, CA, Pleasanton - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionPioneering Therapies, Transforming Lives. What does it mean to be part of the Thoratec Team? It means working in a fast-paced environment that inspires you. It means collaborating on projects that literally save patients' lives. We have an incredible opportunity for a Sr. Regulatory Affairs ...
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14. CTA/TMF Specialist   (Fulltime)2 days ago
Aerotek - United States, NJ, Cranbury - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionThis position will report to the Clinical PM who manages the TMF Project as part of inspection readiness.The CTA will independently work on the TMF to identify deficiencies and will work with the Project Manager to rectify any areas of deficiency noted during review; this reconciliation will be ...
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15. Regulatory Affairs Labeling Associate   (Fulltime)2 days ago
Aerotek - United States, NJ, Princeton Junction - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionSeeking (2) Regulatory Affairs Labeling Associates within pharmaceuticals.Responsibilities include:Prepare, review, approve and manage labeling for pharmaceutical products for FDA submission in accordance with FDA regulations.Responsible for the creation of pharmaceutical labeling drafts for submission to FDA based on Reference Listed Drug labeling, FDA requirements and client specific requirementsResponsible ...
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16. Sr./Principal Regulatory Affairs Associate   (Fulltime)2 days ago
MRIGlobalSearch - United States, MN, Minneapolis - Not rated - (view employer jobs)
Categories: ManagementJob DescriptionJob Classification: Full-Time RegularConnect confidentially with MRIGlobalMedDevice at: [Click Here to Email Your Resumé] Our client is a leading medical device manufacturer in the mid-west. They are continuing to grow and produce new products! They offer competitive salaries and comprehensive benefits! To be considered for this position, ...
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17. International Regulatory Affairs Coordinator   (Fulltime)2 days ago
Claddagh Resources - United States, GA, Atlanta - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionCoordinator of International Regulatory Affairs – Regulatory Affairs Specialist – Medical Technology Our client is a mid-sized (1200 employees), rapidly-growing medical affairs firm in Northeast Atlanta. The company is seeking a Regulatory Affairs individual with strong international background. Job Responsibilities As ...
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18. Regulatory Affairs Associate   (Fulltime)3 days 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, ...
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19. Senior Regulatory Affairs Specialist   (Fulltime)4 days ago
CR Bard - United States, MA, Woburn - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob Description Overview: Bard Davol Inc., a subsidiary of C. R. Bard, Inc., located in Rhode Island, 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, ...
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20. Senior Regulatory Affairs Specialist   (Fulltime)5 days ago
Method3 - United States, CT, Danbury - Not rated - (view employer jobs)
Categories: Health Care, OtherJob Description Overview A Senior Regulatory Affairs Specialist provides global Regulatory support to cross-functional teams working on a range of products in breast and skeletal health, including mammography, biopsy and densitometry devices. As part of a multi-disciplinary group, this position contributes to the design, development and launch ...
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