Process Engineer I

SK PharmtecoKing of Prussia, PA
Onsite

About The Position

SKPT pharmteco (SKPT, the Corporation) is a U.S.-based global Contract Development and Manufacturing Organization (CDMO) that consolidates the operations of sites worldwide – Korea, France, Ireland, and the United States (CA and PA). Built on over 75 years of experience, SK pharmteco is a trusted partner specializing in the manufacture of small molecule APIs and intermediates, viral vectors for gene therapies, cell therapies, registered starting materials and analytical services for the pharmaceutical industry worldwide. We are seeking a motivated Process Engineer to join our growing team in a fast-paced environment. In this role, you will support the development and optimization of manufacturing processes, driving improvements in efficiency, quality, and cost. You’ll collaborate cross-functionally and contribute to building scalable, compliant manufacturing solutions.

Requirements

  • Bachelor's or Master's degree in Engineering or a Life/Physical Science (Chemical Engineering preferred)
  • 3–5+ years of experience developing, implementing, or improving manufacturing processes
  • Experience with bioprocess equipment, clean utilities, GMP facilities, and automation systems
  • Ability to independently own smaller processes or contribute to larger systems with guidance
  • Comfortable working hands-on in cleanroom environments
  • Strong understanding of cGMP regulations
  • Expertise in at least one biopharma area: cell culture, fermentation, or cell processing
  • Familiarity with CAD, Bluebeam, or similar tools
  • Knowledge of EHS and quality systems
  • Basic understanding of Lean principles
  • Strong problem-solving and analytical skills
  • Effective communication and teamwork abilities
  • Excellent time management and adaptability in a fast-paced environment
  • Understanding of process and industrial flow

Responsibilities

  • Develop and implement manufacturing solutions in a dynamic startup setting
  • Apply statistical methods to analyze products and processes for cost reduction and quality improvement
  • Identify and execute opportunities to improve manufacturing efficiency
  • Author engineering specifications, internal standards, and technical guidelines
  • Support engineering team readiness and documentation efforts
  • Contribute to special projects and other engineering initiatives as needed
  • Provide hands-on support in cleanroom manufacturing environments when required
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