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A pioneering biotechnology company in Oxford seeks a Process Development Scientist to support downstream process development. The successful candidate will design experiments, manage schedules, and ensure compliance with GMP requirements while contributing to breakthrough therapies. Ideal applicants will have a background in molecular biology or biochemistry and experience in laboratory settings.
Job Description
Process Development Scientist, Downstream - Oxford
Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company dedicated to developing and commercializing transformative medicines to address unmet patient needs in oncology, infectious diseases, and autoimmune diseases. Our R&D leaders are recognized globally as some of the most successful drug developers in the biotech industry. We foster an environment that encourages collaboration, innovation, and the pursuit of big questions.
We focus on delivering first-in-class biological therapies, including our highly innovative soluble TCR platform. Our ImmTAX molecules represent a new class of precision-engineered drugs that harness the immune system to treat diseases with high unmet medical needs.
At Immunocore, we value the contributions of each individual and embrace our core values: Science, Trust, Respect, Integrity, and Entrepreneurship (STRIDE). These values drive our mission and create a thriving, inclusive workplace where ideas flourish.
We are committed to developing breakthrough therapies that improve patients' lives and support our team in these efforts. Immunocore is an equal opportunity employer, dedicated to fostering an inclusive environment where everyone feels valued and respected. We encourage applications from individuals of all backgrounds, regardless of race, gender, sexual orientation, gender identity, age, disability, or any other protected characteristic.
Role Overview:
This role involves designing and conducting experimental investigations to support downstream process development of emerging drug candidates, including the establishment of manufacturing and clinical production processes. Key responsibilities include protein purification, implementing chromatography and separation techniques, and analytical assessments of purity (e.g., SDS-PAGE, HPLC). The candidate must work independently and collaboratively under tight deadlines, maintaining accurate records and communicating effectively with external partners for GMP manufacturing and regulatory compliance.
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