Co-op, Validation

Job description

Why Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won’t go – challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life-changing treatments. We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in ways that are most meaningful for them. Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth – so employees can thrive in all areas of their lives, in and outside of work. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work. If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team . Position Summary: ultra dedicated – Your biggest challenges yield rare possibilities Ultragenyx has multiple Gene Therapy programs in development in the rare and ultrarare disease space, a robust pipeline. You will partner closely with the Engineering & Validation leadership team and will be responsible for upstream/downstream process & utility validation of GMP manufacturing systems at our state of the art Gene Therapy Manufacturing facility in Bedford, Massachusetts. You will work alongside senior team members and be focused on the planning for the Manufacturing Facility Validation This will give students a unique perspective on what it is like to support a gene therapy manufacturing site. This will not be a traditional on the floor hands on experience. The person who fills this role will be a part of a team that supports planning, execution, and decision- making for ongoing validation activities. Work Model: Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site and thus will be subject to certain on-site safety protocols during the pandemic. Responsibilities: • Attend Validation planning meetings <li data-leveltext="" data-font="Symbol" data-listid="40" data-list-defn-props="{"335552541":1,"335559685":360,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":&quo