Associate Director, Supplier Quality

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Knowledge:
Demonstrates excellent verbal, written, and interpersonal skills.
Demonstrates a thorough knowledge of compliance requirements and an understanding of current global and regional trends in compliance.
Is capable of taking a leadership role in updating and preparing the company for changes in regulations.
Is capable of leading a small team in development of systems and procedures and implementation.
Is well recognized as a knowledgeable resource for QA compliance advice in other departments.
Specific Education & Experience Requirements:
10+ years of relevant experience in the pharmaceutical industry and a BS or BA.
8+ years of relevant experience and a MS.
Specific Job Responsibilities:
Supports Compliance management in maintaining the company’s Compliance program.
May manage the day-to-day activities of one or more individual contributors, including task assignment and prioritization, monitoring task performance, and conducting performance reviews.
Ensures awareness of compliance requirements and responsibilities within the function.
Establishes excellent working relationships with compliance/quality groups.
Responsible for maintaining current knowledge of applicable compliance requirements through attendance at industry and regulatory agency sponsored meetings and seminars.
Responsible for providing guidance on interpretation and application of existing and new requirements. Provide guidance to assigned departments and management when specific compliance issues arise.
Assists in evaluation and implementation of standard operating procedures and systems needed to comply with requirements.
Leads various types of audits or projects or supervises contractors. Audits may include internal systems audits, external vendor audits, or document reviews.
Assists in regulatory agency inspections. Assists in coordination of responses to any regulatory agency findings.

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For Current Gilead Employees and Contractors:

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