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Intern Jobs at Ultragenyx USA | Apply for Intern, Drug Substance Manufacturing Role

Intern, Drug Substance Manufacturing Role at Ultragenyx USA

Ultragenyx is now hiring an Intern for Drug Substance Manufacturing โ€“ Downstream and Central Services at its Bedford, MA facility. This is one of the most sought-after Intern jobs in biotech, offering hands-on exposure to downstream manufacturing, GMP operations, and real-world bioprocessing workflows. If you want to begin a career where science meets meaningful patient impact, this internship is the perfect gateway. Apply for Intern Jobs in the USA.

Job Details:

  • Position: Intern, Drug Substance Manufacturing โ€“ Downstream & Central Services
  • Shift: Mondayโ€“Friday, 2:00 PM โ€“ 10:30 PM
  • Location: Bedford, MA
  • Company: Ultragenyx
  • Work Model: Core Lab & Ops (majority on-site)
  • Duration: January 12, 2026 โ€“ December 23, 2026
  • Employment Type: Full-time Internship (40 hours/week)
  • Hourly Wage Range: $23.00โ€“$30.00/hour (based on experience and education)

About Ultragenyx:

Ultragenyx is a biopharmaceutical leader focused on transforming the future of rare disease medicine. Driven by innovation, scientific excellence, and patient-first values, Ultragenyx has built a collaborative ecosystem where new ideas thrive. The company challenges the status quo by creating therapies where unmet needs are highest. With a culture centered on learning, growth, and meaningful impact, Ultragenyx remains a top destination for students seeking Intern Jobs in cutting-edge biotech manufacturing and research.

Educational Requirements for Intern Role:

  • Candidates who are interested in the Intern Role should be:
  • Enrolled in a relevant degree program (Biotechnology, STEM major) OR recently completed a biotech training program
  • Familiar with basic lab techniques and documentation practices
  • Comfortable performing arithmetic calculations (fractions, decimals, percentages, algebra, geometry)
  • Proficient in Microsoft Excel, Word & Outlook
  • Able to read, write, and understand English
  • Experience in pharmaceutical or regulated industries preferred but not required
  • Viral vector experience preferred, not mandatory

Key Responsibilities for Intern Role:

  • Participate in daily Tier 1 manufacturing meetings to share operational updates
  • Support downstream drug substance manufacturing activities
  • Generate, review, and approve SOPs, batch records, and protocols
  • Assist with quality investigations, engineering activities, and continuous improvement
  • Maintain organization, safety, and upkeep of downstream areas
  • Follow cGMP procedures, manufacturing documentation, and aseptic techniques
  • Support filtration, tangential flow filtration (TFF), column chromatography, and related workflows
  • Practice safe work habits and follow all safety procedures

Skills Required for Intern Role:

  • Strong interest in drug substance manufacturing
  • Detail-oriented with strong troubleshooting abilities
  • Ability to work in fast-paced, regulated environments
  • Strong teamwork and communication skills
  • Ability to follow SOPs and document processes accurately
  • Self-motivated with strong problem-solving abilities
  • Comfortable with physical demands (lifting up to 50 lbs, gowning, working in cold rooms, climbing stairs/ladders)

How to Apply for the Intern Role?

Candidates can apply directly through the official Ultragenyx Careers page. You can also subscribe to website alerts to stay updated on Ultragenyx Intern Jobs and other future openings.

CLICK HERE TO APPLY

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