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Co-op, Downstream Process Development

Ultragenyxpharmaceutical

Woburn, MA (United States) permanent

Posted: May 12, 2026

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Quick Summary

We're looking for a talented Co-op to join our team as a Co-op in Downstream Process Development. The ideal candidate will have experience in a similar field and be able to contribute to the development of life-changing treatments. The role involves working in a dynamic and fast-paced environment, and the ideal candidate will be able to work collaboratively with cross-functional teams to drive innovation and success.

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:

ultraimpact – Make a difference for those who need it most

We are seeking a motivated undergraduate or graduate student to join our AAV Downstream Process Development team. The successful candidate will support laboratory and data‑driven activities that directly contribute to commercial manufacturing, process development, and clinical compatibility studies. This position offers hands‑on experience in gene therapy downstream purification, exposure to GMP‑aligned development workflows, and the opportunity to learn industry‑relevant skills in chromatography, buffer preparation, and data analysis.

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:

1. Process Development

• Support development activities for AAV downstream processes, including buffer screening, filtration studies, and chromatography evaluations.

• Perform routine laboratory experiments under supervision, maintain detailed electronic lab notebook entries, and present results in team meetings.

2. Commercial Manufacturing Support

• Conduct laboratory studies to support commercial manufacturing needs, including column and resin lifetime extension studies required.

• Assist with investigations by providing experimental support, data review, or lab-based troubleshooting as needed.

3. ClinicalIn‑UseCompatibility Support

• Contribute to clinical in‑use compatibility studies, supporting material preparation, sample handling, and execution of defined protocols (as needed).

4. Laboratory Operations

• Prepare buffers and solutions according to established procedures to support ongoing experiments and team operations.

• Participate in core lab activities, including inventory management, equipment maintenance, and general lab organization.

5. Data Entry & Trending

• Assist with data entry and trending of manufacturing datasets.

• Support data management by compiling, organizing, and formatting process data

Requirements:

• Currently pursuing a bachelor’s or master’s degree in chemical engineering, Bioengineering, Biotechnology, Biology, Biochemistry, or a related scientific field.

• Strong interest in bioprocessing, AAV/gene therapy, or downstream purification.

• Ability to perform experimental studies on multiple AAV programs.

• Ability to follow protocols carefully and maintain attention to detail.

• Basic laboratory experience (academia or industry) preferred; chromatography or filtration exposure is a plus.

• Familiarity with Excel, data entry, or simple data analysis tools is advantageous.

• Strong communication skills, willingness to learn, and a team‑oriented mindset.

U.S. Hourly Wage Range:

• $23.00-$30.00/hour. The estimated hourly range reflects an anticipated range for this position. The actual hourly wage offered will depend on the candidate’s school year/level.

#LI-AJ1 #LI-Onsite

The typical annual salary range for this full-time position is listed below. This range reflects the characteristics of the job, such as required skills and qualifications and is based on the office location noted in this job posting. The range may also be adjusted based on applicant's geographic location.

This position is eligible for annual bonus and equity incentives. Actual individual pay is determined by demonstrated experience and internal equity alignment.

Pay Range
$1—$1 USD

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 [email protected].

See our CCPA Employee and Applicant Privacy Notice.

See our Privacy Policy.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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: [email protected].

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