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The Global Mark-Up Exchange Inventory Manager is responsible for managing the Global Inventory Cube and conducting data submissions, ensuring compliance and data quality. The role involves collaboration across departments to deliver effective inventory reporting and analysis, support financial accounting processes, and implement continuous improvement initiatives. This position requires strong leadership skills and the ability to engage with various stakeholders to facilitate timely inventory data submissions.

The R&D Finance Associate collaborates with finance and clinical teams to prepare budgets, forecasts, and financial analyses for studies. Responsibilities include managing relationships with partners, maintaining forecast data, and ensuring compliance with finance policies. The role requires solid analytical skills and proactive problem-solving abilities.

The McPherson Rotational Associate role at Pfizer is an entry-level position within the Global Supply Rotational Development Program. It involves rotating through multiple disciplines and gaining hands-on experience in Engineering, Manufacturing, Quality, and more, aimed at delivering key company goals and fostering personal growth.

The Antibody Drug Conjugate (ADC) Molecule Analytical Product Specialist manages the transfer and validation of release assays for ADC products, ensuring compliance with ICH guidelines. Responsibilities include collaborating with teams across various departments, managing the analytical characterization and stability studies, and leading regulatory submissions for ADC products.

The Quality Analytical Development Scientist is responsible for designing, developing, and implementing analytical test methods, troubleshooting methods, supporting QC investigations, and leading method optimization projects. This role requires strong technical expertise and substantial laboratory experience to improve analytical processes and ensure compliance.

As a Scientist, you will conduct microbiological testing on various products, ensuring compliance with quality and regulatory standards. You'll be responsible for documenting results, maintaining laboratory operations, assisting with investigations, and supporting method validation while striving for continuous improvement in laboratory practices.

The role involves leading quality assurance for packaging and labelling in a pharmaceutical context, ensuring compliance with regulations and quality standards. Responsibilities include overseeing quality programs, managing packaging lifecycle documentation, and leading investigations. The manager will also provide guidance on packaging regulations, participate in audits, and collaborate with various teams to foster quality improvements.