Sobre este puesto de Co-op, Process Engineer en Ultragenyx Pharmaceutical
Position Summary:
ultradedicated – Your biggest challenges yield rare possibilities
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 solutions. In 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 site’s component library
- Supports quality investigations, continuous improvement efforts and engineering activities as they directly impact the functionality of the manufacturing areas.
Requirements:
- Pursuing a Bachelor’s degree in a relevant field of study (e.g., Chemical Engineering, Chemistry), 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 January 11 until the end of June 2027.
- Knowledgeable of Microsoft Office Suite (Word, Excel, PowerPoint)
- Strong organizational skills
- Flexible; adapts work style to meet organization needs
- Meticulous attention to detail
- Strong ability to follow through with tasks
- Good verbal communication skills; Ability to write clearly and effectively
- 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
General Manufacturing: Drug Substance/Central Svcs:
- 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).
*The pay range for this position is $23 - $28/hour.
#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.
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.
