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conducting industry standard process safety testing to fully characterize materials, processes, and side streams prior to scale-up in laboratories and manufacturing facilities. You will collaborate with and
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manufacturing specialists for API synthesis in kilo-lab and pilot plant facilities, as well as provide support for technology transfer to Pfizer manufacturing sites and third party facilities. You will
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, team supply and investigational purposes Support transfer of processes to manufacturing sites Represent Conjugation on cross-functional teams Independently author technical reports and draft relevant
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pertinent industry-related experience and/or post-graduate specialty/residency are desirable Demonstrates effective relationship management and customer orientation Purpose Blueprint Contributions Analyzes
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the smallest particles of the universe to the building blocks of life. In this way, DESY contributes to solving the major questions and urgent challenges facing science, society and industry. With its
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achieve new milestones and help patients across the globe. How You Will Achieve It Develop purification processes to enable manufacturability assessment of biotherapeutic candidates. Deliver highly pure
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chemical or molecular-structural challenges. Support and contribute to the evolution of the ATCM Group's culture of teamwork and scientific excellence. Qualifications Must-Have 15+ years of industry
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Why Patients Need You Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate
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Nice-to-Have Experience working in the industry environment Background in cancer drug discovery related to ADC biology Experience in protein degradation and proteostasis is strongly preferred Additional
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and report progress into cross-functional project teams to meet customer expectations, project milestones and Good Manufacturing Practices {also cGMP} standards. Prepare and review technical documents