Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.
Title: Associate Regulatory Affairs II
Job ID: 22024
Location: Thousand Oaks, CA
Duration: 9 Month Contract
Pay Rate Range: Depends on Experience (W-2 all inclusive rate)
The Regulatory Professional under the direction of a Regional ...
The CFO supervises the Business Office and is the chief financial spokesperson for the organization. The CFO works for the Headmaster and with the Board of Trustees and directly assists on all strategic and tactical matters as they relate to budget management, cost benefit analysis and forecasting needs as well as supporting various Board of Trustees committees including Finance, Investment and Audit. The CFO is the Treasurer of the Roessler Chadwick Foundation. The CFO plans for and ...
The Surgical Regulatory Affairs Manager handles all regulatory development aspects for surgical devices as assigned. These include IOLs, Inserters and Solutions. The incumbent participates on the product development team to provide regulatory guidance for surgical devices assigned. They also manage relevant regulatory strategy components and interactions with Regulatory Authorities for their assigned surgical products and may perform due diligence efforts on new product opportunities.
The Principal Scientist will be the PKDM Development Project Team Representative on the Early and/or Global Development Teams in the area of Oncology. He/she will support small and large molecule drug development, registration, and post-marketing activities. He/she will be responsible for program-level strategic and resource planning, communication, scientific/technical deliverables, issue resolution, and functional representation for internal governance reviews, face-to-face interactions with global ...
Shall ensure regulatory and ISO 13485 comliance and obtain regulatory approval for medical devices, as well as, manage content, assembly, pre-final review, and filing of medical device applications including IDE's, 510k's and PMA's.
Would you like to join a company that has been voted top place to work several years in a row? Commensurate with experience top salary plus bonuses, 401(k), tuition, stock options, full medical, and 3 to 4 weeks paid flexible vacation time.
For complete details ...
Regulatory Affairs Specialist
Reporting to the General Counsel, the Regulatory Affairs Specialist ensures regulatory compliance on branding packaging, marketing materials and other corporate documents and affairs pertaining to labeling, legal items as well as compliance items regarding product development.
• Provide support in the dietary supplement categories by reviewing product descriptions, marketing material, labels and claims to determine compliance with the rules and regulations of federal ...
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