Gene Therapy Manufacturing Intern (GMP)

Ultragenyx Pharmaceutical; Bedford; On-site; GBP 24,000 - 29,000; Full time

Benefits offered by this job

Generous vacation time and publicholid

Volunteer days

Long term incentive and ESPP

Employee wellbeing benefits

Tuition sponsoring

Job summary

Ultragenyx Pharmaceutical in Bedford offers a Manufacturing Associate role focused on downstream and central services in a GMP setting. The position involves supporting batch records, SOPs, quality investigations and continuous improvement while maintaining a clean, compliant facility.

Strong collaboration and attention to detail are essential for success in this fast-paced environment. The role requires a high school diploma to BS, biotech certification, and 1–2 years in a regulated industry.

Qualifications

• High school to BS in any field; enrollment in Biotech Certificate Program preferred.
• Preferably 1–2 years in a regulated industry; experience in downstream/solution prep is a plus.
• Ability to perform arithmetic, read and follow procedures, and use Microsoft Office.
• Willingness to work in a fast-paced environment with strong collaboration.

Responsibilities

• Attend daily manufacturing tier 1 meetings and communicate operation status.
• Generate, review and approve SOPs, batch records, and protocols for Downstream/Central Services.
• Support quality investigations and continuous improvement activities affecting manufacturing.
• Maintain facility and processes within Downstream/Central Services manufacturing.
• Collaborate effectively with diverse teams and ensure EHS and cGMP compliance.

Skills

Attention to detail

Teamwork

Communication skills

Microsoft Office

Education

Biotech Certificate Program

High School Diploma or equivalent

BS in any field

Tools

Microsoft Office

Job description

Ultragenyx Pharmaceutical in Bedford offers a Manufacturing Associate role focused on downstream and central services in a GMP setting. The position involves supporting batch records, SOPs, quality investigations and continuous improvement while maintaining a clean, compliant facility.

Strong collaboration and attention to detail are essential for success in this fast-paced environment. The role requires a high school diploma to BS, biotech certification, and 1–2 years in a regulated industry.