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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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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
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to accelerating research advances from bench to bedside through brilliant science and distinctive approaches to collaboration among scientific investigators and academic and industry partners. The NCI-designated
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medicinal chemistry experience in the biopharmaceutical industry Contemporary knowledge of the key Medicinal Chemistry concepts and design tools required for pharmaceutical drug discovery PREFERRED
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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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responsibilities in compliance with current Good Manufacturing Practices/ Good Laboratory Practice (cGMP/GLP) and all other regulatory agency requirements. Assist in updating and writing documents associated with
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productively in a fast-paced, highly collaborative, and diverse team environment. Preferred Work experience in an industry setting highly desired NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
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industry/CRO. Clinical Research experience in the phase 3/pivotal space in Oncology, ideally on the side of the sponsor and with a track record of successful regulatory submission, inspection, and regulatory