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As a Senior Clinical Data Scientist at Pfizer, you will oversee clinical data processing, ensuring accuracy and consistency while leading data management projects. Your role involves guiding operational teams, managing timelines, and collaborating with various partners to enhance data quality and integrity in clinical studies.
The Sr. Associate will ensure optimal operations and services in fleet management in line with Pfizer's global policies. Responsibilities include vendor management, KPI reporting, data analysis, and supporting sourcing activities. The role involves collaboration with internal and external stakeholders to improve operational processes and compliance.
The Service Delivery Associate will support administrative HR tasks, monitor case management and HR systems, handle confidential information, maintain documentation, and propose process improvements while engaging with colleagues and contributing to business meetings.
The Antibody Drug Conjugate (ADC) Molecule Analytical Product Specialist will manage the transfer and validation of assays for antibody products, ensure compliance with ICH guidelines, and oversee analytical characterization for ADCs throughout development stages. The role involves collaboration with internal and external teams and supporting quality tasks necessary for drug efficacy and safety.
As a QC Planner, you will analyze chemical, biological, and microbiological products, ensuring compliance with quality standards. You will perform testing, maintain cGMP laboratories, develop training plans, and support audits, contributing to efficient operations in the pharmaceutical industry.
As a QC Scientist, you will support Pfizer's quality programs by analyzing chemical, biological, or microbiological products. Responsibilities include environmental testing, analytical testing, training junior colleagues, and participating in regulatory documentation. You will ensure compliance with quality standards and Good Manufacturing Practices while influencing team projects with your scientific expertise.
This position is likely focused on assisting with quality assurance and control tasks within Pfizer, contributing to maintaining product standards and compliance.
As a Validation/Qualification Officer at Pfizer, you'll evaluate and review clinical and commercial drug batches, ensuring compliance with established standards and quality practices. Your role entails approving audit reports, deviations, and manufacturing records while contributing to quality assurance and process improvement initiatives. You'll work collaboratively within teams to maintain inspection readiness and support corrective actions in manufacturing operations.
As a Legal Intern, you will handle administrative tasks, support digital campaigns, provide customer service, and engage in event planning. You will assist in optimizing digital platforms and maintaining compliance with regulations while developing your professional skills and knowledge in the legal field within the pharma industry.
As a Polymer Scientist, you will conduct R&D on new polymer materials, analyze their properties using advanced techniques, collaborate across teams, and develop innovative solutions for enhanced performance. You will also prepare reports and keep abreast of advancements in the field.
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