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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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of new risks and evolving existing risks in relevant Quality Risk Management (QRM) tools. Provide feedback to QRM Business Process Owner (BPO) to continuously improve Integrated Quality Management Plan
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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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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve The Senior Associate Scientist is responsible
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve As a Senior Associate Scientist, you will be
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of new risks and evolving existing risks in relevant Quality Risk Management (QRM) tools. Provide feedback to QRM Business Process Owner (BPO) to continuously improve Integrated Quality Management Plan
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HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures. Field relevant inbound queries from HCPs via established triage process. In collaboration with Global
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colleagues. Ensures that all regulatory development process commitments are clearly communicated, monitored and met. Acts as the point of contact for all internal Pfizer communication regarding the status
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This posting covers two available positions (I&I and Rare Disease). Therapy area responsibility will be determined through the selection process. ROLE SUMMARY Specialty Care (SC) Medical Affairs
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This posting covers two available positions (I&I and Rare Disease). Therapy area responsibility will be determined through the selection process. ROLE SUMMARY Specialty Care (SC) Medical Affairs