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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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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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. • Standardization and Innovation: Design, develop, and improve global standards, Quality methods, practices, and tools. Drive the development of next-level capabilities, infrastructure, and innovations. • Process
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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
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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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May manage the study start up process in countries assigned (where SUPM not assigned) and/or oversee pCRO responsible for these activities as applicable Through the Site Care Partner/Country Trial
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& Insights. The individual will interact with multiple cross functional team members within the SPP Centers of Excellence (COE), Pfizer Business Technology, Pfizer Incentive Comp team, Pfizer Business