Senior Specialist, Quality Assurance Operations

<div class="content-intro"><div><strong>Why Join Us?</strong></div> <div> </div> <div><em>Be a hero for our rare disease patients</em></div> <div><em> </em></div> <div>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. </div> <div> </div> <div>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.</div> <div> </div> <div>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<em>. </em></div></div><h3 style="text-align: left;"><strong>Position Summary:</strong></h3> <p style="text-align: left;"><strong><em>ultra</em></strong><em>focused – Work together to fearlessly uncover new possibilities</em></p> <p style="text-align: left;">As Quality Assurance Drug Substance (DS) Specialist, you will be responsible for Quality Assurance activities at the new gene therapy manufacturing facility located in Bedford, MA. You will provide direct QA oversight and support for the core Drug Substance Manufacturing activities. Activities will include Production Batch Record review, deviation management, QA Manufacturing walkthroughs, logbook review and room/equipment tag-out for manufacturing use. The site is a multi-product facility which will be used for drug substance manufacturing, and aseptic filling of drug product. QA activities are primarily focused on the drug substance manufacturing areas but could also support Drug Product when required. Your role will partner with Manufacturing, Engineering, Validation, QC, Quality Systems, and MSAT functions to provide QA approval for various operating procedures, DS manufacturing processes, and batch records required for on-going manufacturing at the facility. You will report to the Associate Director, Quality Assurance at Ultragenyx Gene Therapy.</p> <h3 style="text-align: left;"><strong>Work Model: </strong></h3> <p style="text-align: left;">Core Lab Ops: This role typically requires that the majority of the work be conducted on-site.</p> <h3 style="text-align: left;"><strong>Responsibilities:</strong></h3> <p style="text-align: left;"> </p> <ul> <li style="line-height: 2;">Review/Approval of Master Batch Records and review/approval of executed DS Production Batch Records</li> <li style="line-height: 2;">Perform QA review/approval of DS area shutdowns/restarts after planned or unplanned maintenance/EM events etc.</li> <li style="line-height: 2;">Perform routine area walkthroughs, logbook reviews, inspection readiness assessments.</li> <li style="line-height: 2;">Responsible for writing, reviewing and/or approving documents such as SOPs, work instructions, policies, and standards to enable the execution of GMP manufacturing.</li> <li style="line-height: 2;">Work with various functions to resolve deviations and assess potential product and compliance impact. Escalate significant events to Quality Management and drive timely completion of effective investigations.</li> <li style="line-height: 2;">Drive or support continuo ... (truncated, view full listing at source)