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 achieve this goal our vision is to lead the future of rare disease medicine. For us this means going where other biopharma companies wont 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 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 andpersonally 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 engineering support of GMP manufacturing systems at the new state of the art Gene Therapy Manufacturing facility in Bedford Massachusetts.
You will work alongside senior team members on engineering challenges and objectives and be expected to implement innovative and robust addition you would provide input on the development of engineering programs standards and processes for the new manufacturing site.
Work Model:
Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site.
Responsibilities:
- Attend MFG and Validation planning meetings and collaborate with different workstreams
- Execute simple and complex processes/testing.
- Demonstrate general knowledge of standard manufacturing practices and equipment.
- Strict adherence to current good manufacturing practices standard operating procedures and manufacturing documentation. Help to establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions and of process data.
- Monitor process operations to ensure compliance with specifications.
- Assist in the investigation of procedural deviations.
- Support the definition and execution of all activities in compliance with environmental health and safety (EHS) requirements and good manufacturing procedures (cGMPs)
- Assist in development of a single use database for the sites component library
- Supports quality investigations continuous improvement efforts and engineering activities as they directly impact the functionality of the manufacturing areas.
Requirements:
- Pursuing a Bachelors degree in a relevant field of study (e.g. chemical engineering bioengineering biochemistry) with minimum of 2 years completed and plans to return to school in the fall term.
- This is a 6 month co-op starting in January 2026 working until the end of June 2026.
- Available to work 40 hours/week during normal business hours
- 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 collaborators
Physical Demands/Work Environment/Safety Considerations:
- Stand for extended periods of time with periodic stooping / bending / kneeling
- Able to lift push pull up to 50lbs.
- Climb ladders and stairs of various heights.
- 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 the use of a respirator; medical clearance will be required in advance.
- Must remove all make-up jewelry and contact lenses while in the manufacturing environment.
- Working in temperature-controlled environments (cold rooms). #LI-Onsite
#LI-AJ1
U.S. Hourly Wage Range:
- $23.00-$30.00/hour
- The estimated hourly range reflectsan anticipatedrange for this position. The actual hourly wage offered will depend on the candidates school year/level.
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 .
See ourCCPA Employee and Applicant Privacy Notice.
See our.
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:.
Why Join UsBe a hero for our rare disease patientsAt 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 achieve this goal our vision is to lead the future of rare disease medicine. For us this means goi...
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 achieve this goal our vision is to lead the future of rare disease medicine. For us this means going where other biopharma companies wont 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 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 andpersonally 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 engineering support of GMP manufacturing systems at the new state of the art Gene Therapy Manufacturing facility in Bedford Massachusetts.
You will work alongside senior team members on engineering challenges and objectives and be expected to implement innovative and robust addition you would provide input on the development of engineering programs standards and processes for the new manufacturing site.
Work Model:
Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site.
Responsibilities:
- Attend MFG and Validation planning meetings and collaborate with different workstreams
- Execute simple and complex processes/testing.
- Demonstrate general knowledge of standard manufacturing practices and equipment.
- Strict adherence to current good manufacturing practices standard operating procedures and manufacturing documentation. Help to establish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions and of process data.
- Monitor process operations to ensure compliance with specifications.
- Assist in the investigation of procedural deviations.
- Support the definition and execution of all activities in compliance with environmental health and safety (EHS) requirements and good manufacturing procedures (cGMPs)
- Assist in development of a single use database for the sites component library
- Supports quality investigations continuous improvement efforts and engineering activities as they directly impact the functionality of the manufacturing areas.
Requirements:
- Pursuing a Bachelors degree in a relevant field of study (e.g. chemical engineering bioengineering biochemistry) with minimum of 2 years completed and plans to return to school in the fall term.
- This is a 6 month co-op starting in January 2026 working until the end of June 2026.
- Available to work 40 hours/week during normal business hours
- 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 collaborators
Physical Demands/Work Environment/Safety Considerations:
- Stand for extended periods of time with periodic stooping / bending / kneeling
- Able to lift push pull up to 50lbs.
- Climb ladders and stairs of various heights.
- 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 the use of a respirator; medical clearance will be required in advance.
- Must remove all make-up jewelry and contact lenses while in the manufacturing environment.
- Working in temperature-controlled environments (cold rooms). #LI-Onsite
#LI-AJ1
U.S. Hourly Wage Range:
- $23.00-$30.00/hour
- The estimated hourly range reflectsan anticipatedrange for this position. The actual hourly wage offered will depend on the candidates school year/level.
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 .
See ourCCPA Employee and Applicant Privacy Notice.
See our.
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:.
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Job Location:
Hourly Salary:
$ 23 - 30
Posted on:
30+ days ago
Vacancies:
1 Vacancy
