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:

ultracurious – Apply your biggest ideas in courageous ways

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 the new state of the art Gene Therapy Manufacturing facility in Bedford, Massachusetts and the Analytical Equipment in QC labs located in Woburn, Massachusetts. 

You will work alongside senior team members and be focused on the planning for the Manufacturing Facility and/or Quality control Labs 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 Collaborate with different workstreams Execute testing on Manufacturing, QC and Utilities Equipment Documentation development Generate and maintain project trackers and spreadsheets Routinely execute simple and complex processes following established Demonstrate general knowledge of standard manufacturing practices and Strict adherence to current good manufacturing practices, standard operating procedures, and manufacturing Follow written procedures for clear and accurate documentation of equipment operation and process instructions. Monitor process operations to ensure compliance with Assist in the investigation of procedural Practice safe work habits and adhere to safety procedures and guidelines. Utilize knowledge to improve operational efficiency. Other duties as assigned Requirements: Pursuing a Bachelor’s degree in a relevant field of study (e.g., Engineering, Science), with minimum of 2 years completed Enrolled as a full-time student with plans to return to school in fall term This co-op is full-time (40 hours per week), from early July of 2025 until the end of December 2025. Knowledgeable of Microsoft Office Suite (Word, Excel, PowerPoint) Flexible; adapts work style to meet organization needs Meticulous attention to detail Strong ability to follow through with tasks Ability to exercise sound judgment, reasoning, and problem solving Capable of completing assigned responsibilities and keeping manager informed of work status GMP experience is a plus Ambitious and self-starting attitude to take on responsibilities and own process improvements Ability to collaborate fluidly with peers, supervisors and cross functional support groups required Exceptional written, oral communication, and organizational skills required independently and with strategic Physical Demands/Work Environment/Safety Considerations: Stand for extended periods of time wih periodic stooping / bending / kneeling. Ability to climb ladders and stairs of various heights. Able to lift, push, pull up to 50lbs. Work in a controlled environment requiring GxP gowning and wear protective clothing over the head, face, hands, feet, and body. This requires the ability to change clothes into appropriate gowning and personal protective equipment. Certain tasks may require use of a respirator; medical clearance will be required in advance. Must remove all make-up, jewelry, and contract lenses while in the manufacturing environment. Working in termperature-controled environments (cold rooms).   Full Time employees across the globe enjoy a range of benefits, including, but not limited to:   ·         Generous vacation time and public holidays observed by the company ·         Volunteer days ·         Long term incentive and Employee stock purchase plans or equivalent offerings ·         Employee wellbeing benefits ·         Fitness reimbursement ·         Tuition sponsoring ·         Professional development plans   * Benefits vary by region and country

Ultragenyx Pharmaceutical is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at talentacquisition@ultragenyx.com.

See our CCPA Employee and Applicant Privacy Notice. See our Privacy Policy.   Note to External Recruiters: All candidate activity and open positions are managed strictly through our Human Resources Department. Our Human Resources Department kindly requests that recruiters not contact employees/hiring managers directly in an attempt to solicit business and present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organization. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation.  Inquiries on developing a recruiting relationship with us, may be directed to: talentacquisition@ultragenyx.com.