Manufacturing Project Engineer Intern - cGMP/Capex

Cytiva

Logan (UT)

On-site

USD 18,000 - 28,000

Full time

14 days+

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Job summary

Cytiva in Logan, Utah invites a Summer Internship for engineering students to support equipment qualification and facility expansion efforts. You will engage with electro‑mechanical design, automation controls, and quality teams to learn professional skills and regulatory compliance.

The role offers exposure to IQ/OQ protocols, cGMP practices, and collaboration with multiple departments. Strong communication and initiative are essential for success in this hands‑on program.

Qualifications

  • Pursuing a Bachelor's degree in mechanical, industrial, manufacturing engineering or related field.
  • Excellent oral and written communication skills.
  • Availability Summer 2027 (Apr–Aug).

Responsibilities

  • Draft equipment qualification studies (system volume, mixer RPM setpoints, cleaning development).
  • Perform equipment qualification studies (gathering samples, recording data, compiling data).
  • Write engineering reports and test protocols.
  • Organize documentation for equipment (design files, P&ID, manuals, spare parts lists, PM schedules, protocols).
  • Support engineering priorities related to Capex efforts.
  • Evaluate safety, quality, production, and cost/efficiency of equipment.
  • Ensure activities comply with cGMP and company policies.
  • Design and develop production processes and qualification.
  • Create and execute IQ/OQ protocols.
  • Collaborate with third‑party engineering services and suppliers.

Skills

Communication
Cross-functional teamwork
Independent work
Initiative
Curiosity
Engineering mindset
Problem solving
Mechanical proficiency

Education

Bachelor's in Engineering

Job description

Cytiva in Logan, Utah invites a Summer Internship for engineering students to support equipment qualification and facility expansion efforts. You will engage with electro‑mechanical design, automation controls, and quality teams to learn professional skills and regulatory compliance.

The role offers exposure to IQ/OQ protocols, cGMP practices, and collaboration with multiple departments. Strong communication and initiative are essential for success in this hands‑on program.

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