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Manufacturing Specialist Intern

Logo of KBI Biopharma

KBI Biopharma

1mo ago

🚀 Off-cycle Internship


AI generated summary

  • Enrolled in a Life Science or Engineering program, analytical, strong interpersonal skills, proficient in Microsoft Office, interest in biopharmaceuticals, able to work independently and in a team, physically capable of cleanroom work and handling hazardous materials.
  • The Manufacturing Specialist Intern at KBI Biopharma will be responsible for generating manufacturing and solution records, coordinating equipment preparation, troubleshooting and maintaining laboratory equipment, supporting change control and CAPA action plans, as well as assisting with compliance and quality activities to improve operations excellence.

Off-cycle Internship



  • Assist with drafting, and revision of manufacturing batch records, procedures, and supporting records.
  • Support new equipment enrollment qualification activities.
  • Assist SMEs with laboratory equipment supporting manufacturing operations troubleshooting, vendor calls, equipment repair coordination, operational changes, and system qualifications.
  • Support safety initiatives, compliance, and quality requirements on the GMP floor.


  • High school degree or equivalent; Currently enrolled in an undergraduate or graduate program in Life Science, Engineering, or a related field.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.
  • Proficient in Microsoft Office Suite (Excel, PowerPoint, Word, and Visio).
  • A demonstrated interest in the biopharmaceutical industry.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Able to stand on feet, bend, and move through cleanroom environment; able to lift equipment and samples. Must be comfortable working with hazardous materials and must comply to all health and safety regulations.

Education requirements

Currently Studying

Area of Responsibilities



  • Generation of batch records, solution records, equipment preparation records, processing assembly records, test sampling plans and process flow charts for specific manufacturing process units
  • Manufacturing laboratory equipment: work order initiation, follow up, assessments to support deviations, troubleshooting, and vendor coordination
  • Support change control deliverable implementations, and CAPA action plans as needed
  • Support compliance and quality activities with Operations Excellence Initiatives including: Standardization/5S and internal departmental auditing


Work type

Full time

Work mode