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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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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 an Associate Scientist, you will be
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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 Work under the guidance of a supervisor. With
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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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notifying instrument key operators of upcoming reagent/supply needs. Process samples for analysis or storage. Utilize PIMS/LIS computer system for the processing of samples. Collect biological samples from
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requires understanding of GCP and GMP to support the regulatory requirements and needs of different study types, quality management, inspection readiness, audit/inspection process, clinical trial processes
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pharmaceutical sciences, systems pharmacology, pharmacometrics, engineering, mathematics, physics or similar disciplines where modeling and simulation is emphasized. 2+ years of pharmaceutical industry or related
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Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related
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develop standard operating procedures and system support. Analyze operational process problems and recommend appropriate corrective and preventative actions. Manage change control authoring and execution
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disease pathogenesis . As a member of the discovery biology team, this individual will be playing a significant role in the drug discovery process including ideation and hypothesis testing, identification