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Jobs (16 Matches)
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1. Regulatory Affairs Coordinator   (Fulltime)20 days ago
Medix - United States, IL, Lombard - Not rated - (view employer jobs)
Categories: Science, PharmaceuticalJob DescriptionJob Duties: Administers and maintains the Company’s Annual Product Review including generating the reports. Supports administering and maintaining the Company’s Documentation Change Control System for compliance documentation. Uses Food and Drug Administration (FDA) monographs and other regulations ...
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2. Cleaning Validation Specialist   (Fulltime)20 days ago
ADDITIONAL STAFFING GROUP - United States, NC, Wilson - Not rated - (view employer jobs)
Categories: Pharmaceutical, QA - Quality Control, ManufacturingJob Description Cleaning Validation Specialst ~ Pharmaceutical Manufacturing We are now hiring an experienced Cleaning Validation Specialists for a long-contract position within the biotech/pharma industry. Call today for more details (919-844-6601)! Qualified candidates will have experience coordinating cleaning validation activities. Executing protocols and reports for ...
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3. Regulatory CMC Specialist   (Fulltime)21 days ago
Sancilio & Company, Inc. - United States, FL, West Palm Beach - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionCompany Overview Sancilio and Company, Inc. (SCI) is a biopharmaceutical company focused on Advanced Lipid Technology™ (ALT) and complimentary products. Unlike most research stage companies, SCI has developed a portfolio of commercialized products that are developed, manufactured and distributed by our own dedicated people in our own cGMP manufacturing ...
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4. Regulatory Affairs Specialist   (Temporary)21 days ago
Pinpoint Pharma - United States, IL, Vernon Hills - Not rated - (view employer jobs)
Categories: Research, QA - Quality Control, MarketingJob DescriptionThe Regulatory Affairs Associate is responsible for supporting compliance to FDA and International regulations, listings and licenses. This position will assist in compiling and submitting Regulatory documents according to requirements. Additionally, it provides support for all Regulatory compliance activities including labeling ...
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5. Sr. Regulatory Affairs Specialist   (Fulltime)21 days ago
iRhythm Technologies - United States, CA, San Francisco - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionReports to: Director QA/RA  Description: iRhythm Technologies, Inc. is a San Francisco-based medical device company combining novel diagnostic device with advanced data analysis concepts to create new approaches to cardiac rhythm monitoring. iRhythm’s Quality Assurance & Regulatory Affairs team is looking for a strong candidate to fill ...
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6. Regulatory Affairs Specialist   (Fulltime)21 days ago
Atrium Staffing - United States, NJ, Wayne - Not rated - (view employer jobs)
Categories: ScienceJob DescriptionOur client is a global specialty bio-pharmaceutical company, with a huge line of products and brands. Salary/Hourly Rate: $40-45/hr Position Overview: The successful candidate will have an understanding of current US, EU, Japan and International GMP / GDP regulatory requirements and be able to ...
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7. Regulatory Affairs Clinical Associate   (Fulltime)21 days ago
Amneal Pharmaceuticals LLC - United States, NY, Hauppauge - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionThe Associate I assists, with minimal guidance, the Director Regulatory Affairs Clinical-NDA with all IND/NDA related activities: Day to day regulatory activities for all IND/NDA projects including submission of all required filings Track recurring regulatory activities and manage submission timelines Study Material release coordination Submission/tracking of all types of clinical regulatory ...
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8. Clinical Compliance Specialist   (Fulltime)21 days ago
Ultimate - United States, CA, East Irvine - Not rated - (view employer jobs)
Categories: Pharmaceutical, QA - Quality Control, ResearchJob DescriptionA global medical device company in Irvine is seeking a linical Compliance Specialist for a long term engagement with our client. Please see below for further details:The Clinical Compliance Specialist will be responsible for conducting internal, site and vendor audits for ...
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9. Quality Assurance Nurse   (Fulltime)21 days ago
Kelly Scientific Resources - United States, FL, Jacksonville - Not rated - (view employer jobs)
Categories: Biotech, Research, ScienceJob DescriptionKelly Clinical Research has an exciting opportunity for a Quality Assurance Nurse and a Quality Assurance Nurse Supervisor.  These are long-term project opportunities in Jacksonville, FL that come with benefits!The Quality Assurance Nurse is a Healthcare Educator who represents the company to investigate, evaluate ...
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10. Global Product Surveillance and Safety Specialist   (Fulltime)25 days ago
Valeant Pharmaceuticals - United States, NY, East Rochester - Not rated - (view employer jobs)
Categories: PharmaceuticalJob DescriptionValeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by ...
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11. Lead Regulatory Document Specialist   (Fulltime)27 days ago
Thermo Fisher Scientific - United States, NV, Sparks - Not rated - (view employer jobs)
Categories: WarehouseJob DescriptionWhen you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.Responsibilities: The ...
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12. Regulatory Associate   (Temporary)27 days ago
Corporate Brokers - United States, MI, Spring Lake - Not rated - (view employer jobs)
Categories: Information Technology, Legal Admin, PharmaceuticalJob DescriptionThe Regulatory Assistant provides support for global regulatory submissions and general administrative support of the global regulatory organization. This role may also provide support to the CMC group in the form of computer system support and maintaining key electronic documentation to current ...
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13. Regulatory Affairs and Communications Specialist   (Temporary)27 days ago
Paladin - United States, IL, Deerfield - Not rated - (view employer jobs)
Categories: General BusinessJob DescriptionJob Classification: ContractOur client, a well-known pharmaceutical company located in Deerfield, is seeking a Regulatory Affairs and Communications Specialist to join their team for 3 to 6 months. As the Regulatory Affairs and Communications Specialist, you will provide daily monitoring of health authority and trade association websites ...
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14. Regulatory Affairs Associate   (Temporary)27 days ago
Lab Support, a division of On Assignment - United States, CA, South San Francisco - Not rated - (view employer jobs)
Categories: QA - Quality ControlJob DescriptionLab Support is seeking a Regulatory Affairs Associate for a growing biopharmaceutical company in South San Francisco. This is a contract position through the end of the year. The Regulatory Affairs Associate will be responsible for assisting with compiling information necessary for the NDA submission. A successful ...
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15. Regulatory Affairs Coordinator   (Fulltime)27 days ago
Aerotek - United States, CO, Broomfield - Not rated - (view employer jobs)
Categories: Admin - Clerical, Biotech, QA - Quality ControlJob DescriptionA fast-growing medical device company in Broomfield, CO, is seeking two Regulatory Affairs Coordinators to join their team. The positions are 6+ month contracts and pay $20-24/hr. Please review the job description below and apply if interested!Job Duties:Coordinates support ...
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16. Entry Level Regulatory Affairs Clerk   (Fulltime)27 days ago
Aerotek - United States, CO, Broomfield - Not rated - (view employer jobs)
Categories: Biotech, QA - Quality Control, ScienceJob DescriptionRegulatory Affairs ClerkMedical Device CompanyBroomfield, CO Pay: $20-24/hour DOECurrently looking for entry level regulatory affairs clerks to join a medical device company in Broomfield, Colorado. This position will entail assisting the regulatory affiars team as well as researching regulatory files and ...
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