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Procedural Document Manager

Company: Bristol-Myers Squibb Company
Location: New Brunswick
Posted on: August 15, 2019

Job Description:

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.Develop and/or revise procedural documents in R&D and GPS to support the business unit processes. Procedural management activities include, but are not limited to, working with subject-matter experts to ensure accurate document content and compliance with health authority regulations and expectations.Position Responsibilities

  • Develop procedural documents tosupport a GxP Quality Management System.
  • Reviewcurrent procedural documents with a compliance/regulatory mindset to identify key gaps and risks that SME teams need to remedy during the writing process.
  • Synthesize feedback from subject matter experts/ PD teams to identify and resolve issues in order to accurately document current and future PDs.
  • Proactively uses judgmentto manage risk and uncertainty, and to anticipate the need for and implement contingency plans.
  • Effectively manage projects, escalate issues as necessary and identify/meet key milestones.
  • Work with limited guidance to manage the development of PDs for key procedures, seeks input as needed.
  • Team leadership skills that contribute to meeting team goals and resolving complex issues.
  • Ability to think about solving problems through other mechanisms besides procedural documents.
  • Maintain a good understanding of FDA regulations and ICH Guidelines and other guidelines applicable to GxP. Regulations and guidelines include but are not limited to:
  • 21 CRF Parts 11, 58, 111, 210, 211, 610 and 820
  • ICH E6, Q7, Q8, Q9, and Q10
  • Exercise sound judgment, using a risk-based approach, to ensure compliance with PD regulations, practices, and policies.
  • Negotiate and influence solutions without direct authority.Experience Desired
    • Preferred: Bachelor's degree with 5-8 years' experience, Master's degree with 3-5 years' experience or PhD with 2-4 years' experience working in a pharmaceutical or highly regulated environment. or
    • Associate's degree or equivalent with at least 15 years' experience working in a pharmaceutical or highly regulated environment.Other Qualifications
      • Demonstrated ability to successfully manage competing deadlines and balance priorities while meeting or exceeding expectations
      • Ability to drive consensus, drive performance and to lead strategically.
      • Demonstrated knowledge of FDA regulations and ICH guidelines applicable to GXP. FDA regulations and ICH guidelines include, but are not limited to, the following:
        • 21 CRF Parts 11, 58, 111, 210, 211, 610 and 820
        • ICH E6, Q7, Q8, Q9, and Q10
        • High level of competency in PD writing including the appropriate use of grammar, syntax and organization of ideas
        • Knowledge of project management concepts and strategies
        • Knowledge of requirements for development, use and maintenance of controlled procedural documents
        • Demonstrated ability to resolve complex issues and differences in a creative, constructive and diplomatic manner
        • Demonstrated ability to work independently and mentor team members
        • Demonstrated ability to maintain a high level of productivity, accountability and energy
        • Proven team building skills and an ability to foster partnerships across projects and multidisciplinary teams
        • Demonstrated ability to follow up on open issues and drive results to completion
        • Demonstrated ability to effectively and decisively establish appropriate priorities for self and matrix teams
        • Proven track record for taking on challenges that are outside of normal book of work
        • Strong communication skillsBristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Keywords: Bristol-Myers Squibb Company, New Brunswick , Procedural Document Manager, Executive , New Brunswick, New Jersey

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