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regulatory affairs in Los Angeles

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  1. Director of Regulatory Affairs

    A Director of Regulatory Affairs job opportunity needs to be filled immediately by Adecco Medical & Science. This is a direct hire opportunity in Valencia, CA. You will be responsible for developing global regulatory strategies and submissions to ensure compliance and approval from the FDA. Additionally, you will advise on regulatory requirements, prepare submissions, negotiate their approval, and assure compliance. Moreover, you must be able to function in a start-up like environment and be hands-on ...

  2. Sr. Regulatory Affairs Specialist

    A Sr. Regulatory Affairs Specialist job opportunity needs to be filled immediately by Adecco Medical & Science. This is a direct hire opportunity in Valencia, CA. You will be responsible for the content, assembly, pre-final review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) submitted to the FDA and foreign regulatory agencies. Additionally, you will be identifying and resolving quality issues as they present themselves. Moreover, you will apply regulatory expertise to ...

  3. Regulatory Affairs Specialist

      ~~ Requisition # :  44307  Assignment Information    Date Submitted :  7/17/2014 9:50:56 AM  Positions : 1  Start Date :  7/31/2014  End Date :  10/31/2014  Order Status :  Open  Order Type :  Requisition for Contract Labor  Required Travel :  No Travel Required     Work Environment :  Professional   Anticipated Schedule :  Typical 8 Hour/Day    Required Dress Code :  Business Casual     Contractor Work Location:  Northridge, CA USA   Job Description    Labor Category :  Quality Regulatory ...

  4. Regulatory Affairs Specialist-307

    3 Month Contract in Northridge CA Job Title:  Regulatory Affairs Specialist-307   Job Duties:  Ensure compliance to the FDA Quality System Regulations, European Requirements, and other regulatory requirements. Prepare required documentation (510(k)s, technical files, dossiers) for domestic and foreign submissions and registrations. Attend design review meetings regarding design controls. Interacts with other departments to assist in determining the Regulatory pathways required for products ...

  5. Business Operations Manager

    Location Los Angeles, CA 90016 Department Operations Supervisor Chief Executive Officer Employment Salaried / Full-time Benefits Among others; Medical / Dental / Vision / Paid Holidays & Time Off   Position Overview EcoSmart Inc is seeking a smart, talented and motivated Business Operations Manager to execute efficient, streamlined, and profitable management and growth of our Operations department. In this dynamic and challenging role, you’ll provide leadership to a team that manages warehouse ...

  6. Sr. Regulatory Compliance Specialist - (ID:450)

    Job Title: Sr. Regulatory Compliance Specialist Location: Los Angeles / Anaheim area Salary: Dependent on Experience Reports To: VP of Technology The Company: The Company is a well-established, family-owned blender and packager of cleaning products and sanitizers for the household, industrial, and institutional markets.   Job Overview: The Senior Regulatory Specialist must be detail-oriented, flexible, and eager to make a positive impact at client sites, specifically with a small, but fast ...

  7. Vice President of Global Regulatory Affairs

    NW Recruiters is seeking a Vice President of Global Regulatory Affairs. This role will be responsible for assisting in analyzing public policy developments, drafting responses to public policy, legislative and regulatory initiatives.​ Analyze regulatory frameworks in jurisdictions where the firm is or is considering carrying on business, preparing presentations relating to public policy, developing and operationalizing the firm’s South American strategy.​   Responsibilities Deepen the firm’s ...

  8. Regulatory Affairs Director

    Overview The Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies to secure market access for Class II/III medical devices in coordination with key internal and external stakeholders.  This individual will be the Regulatory subject matter expert for all applicable medical devices. S/he will need to identify, assess and communicate regulatory development and submission strategies, regulatory risks, interface with relevant regulatory ...

  9. VP/GM (California, Hawaii and Nevada)

    Empowering healthcare starts with you. At McKesson, whether you work in HR or marketing, finance or public affairs, you're making a difference. You'll spark a chain reaction that results in millions of people getting more from their healthcare. As the nation's leading healthcare services company, we touch virtually every aspect of healthcare. We empower our customers by delivering vital supplies and solutions. And we empower our employees through a supportive environment where opportunity and ...

  10. Regulatory Affairs Associate (4159)

    Summary: Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical and scientific data and reports required for submission in support of products. Responsibility: Track of status and progress of regulatory documentation • Review, edit and proofread regulatory documentation • Assist in preparation and review of labeling, SOP’s, and other departmental documents • Compile under supervision regulatory ...

  11. Chief Compliance Officer

    The Chief Compliance Officer (CCO) is primarily responsible for overseeing and managing compliance with the organization, ensuring that the company and its employees are complying with all regulatory requirements and with internal policies and procedures.  This position supports the Mission of the Hospital through the provision of distinctive and compassionate care to our patients. Essential Functions: This position is the architect & steward of enterprise compliance. Maintaining current ...

  12. Clinical Supply Chain

    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: Clinical Supply Chain Job ID: 23654 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 24 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: Under minimal supervision, manage demand and supply of Pre-Clinical and ...

  13. Quality Control Publisher I (Expert in  Adobe Acrobat 7.0)

    Title: Quality Control Publisher I Job ID: 23830 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 18 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   This position will provide Publishing Quality support for Global Regulatory Affairs and Safety. Perform quality control checks of PDF components for electronic regulatory submissions by adhering to company’s guidelines and use of QC check list. These checks focus on the formatting of and ...