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for the site engineering group and its deliverables. YOUR SKILLS B.S. in Chemical or Mechanical Engineering. Strong working knowledge in both disciplines. 10 years process engineering experience preferred
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wide range (non-routine) complex audits (minimal to no oversight - as needed). Execute audit strategy and lead process audits. Act as a reviewer of audit reports from outsourced or routine audits. Assess
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. Utilize critical thinking skills and demonstrates fact-based decision-making capabilities to address areas of deficiency. Recognize, identify, and engage in opportunities for continuous process improvement
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development and execution of control plans Utilize operational performance data to characterize state of control, improvement opportunities and drive process and system optimization Deliver effective business
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Procedures (SOPs) to ensure compliance with good clinical practice (GCP), regulatory agencies, Institutional Review Boards (IRBs), and Pfizer processes. Apply knowledge gained within the Early Clinical
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regulations Independently conducts wide range of routine/(non-routine) complex investigator site audits (minimal to no oversight - as needed) Executes audit strategy, leads/supports process audits, and may
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experience in Automation Engineering Experience with process controls equipment; design and debugging skills Broad understanding of systems architecture and operations, and related components Excellent project
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throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external
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conveying messages in a clear and concise manner. Analyzes, interprets , and distills data and other information to create documents . Applies comprehensive knowledge of relevant regulatory requirements and
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and internal quality procedures. Investigate opportunities for regulatory innovation / promote the use of novel approaches within project teams to resolve issues and problems. Develop effective