Manager, Regulatory Affairs Job

Employer Name: PharmaceuticalCrossing	SpiderID: 2345339
Location: Milwaukee, Wisconsin	Date Posted: 7/5/2008
Wage:	Category: Medical/Health
Job Code:

Job Description:
Manage regulatory projects and provide regulatory and technical oversight to ensure timely submission and approval of CMC dossiers. 2. Effectively influence other functional areas to execute projects within area of responsibility. 3. Provide regulatory, compliance advice, consultation and support to Abbott's Pharmaceutical business units. 4. Manage change in compliance with applicable global regulations. 5. Identify regulatory CMC risks/opportunities for projects in area of responsibility and propose strategies to address risks. The individual is expected to work independently in these functions.6. Manage and provide oversight for regulatory relationships with Agency counterparts or Area groups within the scope of responsibility. The individual is expected to work mostly independent in this function. Skills/Experience Requirements Minimum three years of experience in a CMC technical position within R&D, Manufacturing Sciences, Quality Assurance and/or Regulatory Affairs. Education Requirements BS, MS, or PhD

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Job Criteria:
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Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
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Contact Information:

Contact Name: -	Company Type: Employer
Company: PharmaceuticalCrossing

City: Pasadena
State: California
Zip:

Web Site: http://www.pharmaceuticalcrossing.com