About The Position

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. Internship program dates: June 8 - August 21, 2026 Education Required: Must be enrolled in an undergraduate, graduate, or PhD program preferably in chemical/mechanical/bio engineering, biochemistry, biotechnology, biology, and/or related discipline. General Description: The Process Engineering Intern will support the F&E Process Engineering team in the evaluation, documentation, and improvement of manufacturing process systems used to produce biological therapies. This role provides hands-on exposure to biotech process equipment, utilities, automation, and GMP-regulated environments while contributing to real engineering deliverables under supervision of senior engineers. By the end of the internship, the intern will: • Gain hands-on exposure to biotech manufacturing process systems and utilities. • Understand the role of process engineering within a GMP-regulated environment. • Develop practical engineering documentation and data analysis skills. • Learn how process improvements are evaluated and implemented in biologics manufacturing.

Requirements

  • Must be enrolled in an undergraduate, graduate, or PhD program preferably in chemical/mechanical/bio engineering, biochemistry, biotechnology, biology, and/or related discipline.
  • MS Office Suite or similar (required)

Nice To Haves

  • Familiarity with PFDs, P&IDs, CIP/SIP, and GMP principles.
  • Exposure to automation systems or process control concepts.
  • Experience with data visualization or basic statistical analysis.

Responsibilities

  • Process & Systems troubleshooting support
  • Assist in developing and updating PFDs and simplified P&IDs for manufacturing and utility systems across upstream and downstream operations
  • Collect and analyze historical manufacturing and utility data (e.g., batch cycle times, CIP/SIP)
  • Prepare trend charts, summaries, and visual reports
  • Support identification of efficiency and optimization opportunities
  • Draft or revise SOPs, work instructions, and process descriptions under supervision
  • Review vendor documentation and summarize equipment capabilities and limits
  • Assist in documenting automated recipes and mapping control steps to process intent
  • Support alarm and interlock documentation
  • Participate in recipe standardization/harmonization initiatives
  • Participate in team meetings, design reviews, and technical discussions

Benefits

  • Medical
  • Dental
  • Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness
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