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    • Associate Director, Document Management T500-16913 - Hyderabad, India - Bristol Myers Squibb

    Bristol Myers Squibb
    Bristol Myers Squibb Hyderabad, India

    3 weeks ago

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    Description

    Job Description

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    The position of Associate Director, Document Management, is a strategic role that requires oversight and tactical support for Document Management activities. This includes authoring, review coordination, approval, issuance, implementation, periodic review, and retirement of documents. The goal is to ensure the performance of both routine operations and strategic initiatives related to global and local documents, as well as APQRs, continuously improves to meet compliance needs and business priorities.

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    This role involves managing stakeholder needs in balance to priorities and execution of document procedural adherence. It also requires ensuring up-to-date monitoring of review and approval ownership to prevent deviations from global document management and health authority requirements.

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    The Associate Director will develop forecasts, plans, and schedules to ensure timely document flow and completion reporting. They will act as a liaison with the business to ensure accurate document content and compliance with health authority regulations. Additionally, they will provide leadership and coaching on current industry trends and quality systems management.

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    Key responsibilities include providing strategy, oversight, and tactical support of Document Management run-the-business activities. The Associate Director will also ensure the performance of run-the-business and strategic initiatives associated with global and local documents, and APQRs, continuously improve to meet compliance needs and business priorities.

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    Requirements

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    A Bachelor of Science in Life Sciences (Chemistry, Biology) or Health Sciences is required. A post-graduate qualification is preferred. A minimum of 7 years of pharmaceutical industry GMP experience and demonstrated leadership in Quality and/or Compliance discipline with in-depth knowledge of global health authorities regulations and requirements is necessary.

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    Fluent English language skills, including reading, writing, and speaking, are essential. The ability to deliver clear and articulate presentations is also required. Commitment to Quality and a strong track record of delivering results in a fast-paced environment are highly valued.

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