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Manager is responsible for management of all engineering functions at the Henkel Cannon Falls facility. Manages the engineering staff to deliver a safe working environment and processes that result in
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, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines. What You
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changing needs of the regulatory environment Works with RQA colleagues on cross GxP audit plans as required Coaches colleagues - leads training for routine and non-routine site and process audits Advises
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environment with a cross-functional clinical team. BASIC QUALIFICATIONS PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD Strong written and verbal communication skills
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and regulatory operations and environment in countries under responsibility English is required. Prior Experience Demonstrated clinical research experience and/or study management/startup project
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, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines. What You
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transparent environment that encourages strong partnerships and mutual trust between teams, sub-teams, and therapeutics areas. Accountable to multiple project/core study teams and clinical sub-teams and manages
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within Fred Hutch. The successful candidate will enter a vibrant and dynamic research environment with an opportunity to lead basic, translational, clinical, and public health breast cancer researchers
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an educational, pharma, or biotech environment. Proficiency in compliance, regulatory affairs, strategy development, project management, developing budgets, fiscal monitoring, and financial projections using
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, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines. What You