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Process Engineer I

SK Pharmteco
Posted 7 days ago, valid for 19 days
Location

King Of Prussia, Montgomery 19406, PA

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • SKPT pharmteco is a global Contract Development and Manufacturing Organization (CDMO) specializing in pharmaceutical manufacturing with over 75 years of experience.
  • They are looking for a Process Engineer with 3 to 5+ years of experience in developing and improving manufacturing processes, preferably in Chemical Engineering.
  • The role involves developing manufacturing solutions, analyzing processes for quality improvement, and providing hands-on support in cleanroom environments.
  • Candidates should have a strong understanding of cGMP regulations, expertise in biopharma areas, and effective communication skills.
  • The position offers a competitive salary, which is not specified in the job description.
Company Overview:
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.

Position Summary:
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.

What You’ll Do
  • 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
Qualifications
  • 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
Key Skills & Competencies
  • 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
Physical Requirements
  • Ability to sit for extended periods and work on a computer
  • Ability to lift up to 15 pounds as needed
Note: This job description is intended to convey information essential to understanding the scope of the job role. It is not intended to be an exhaustive list of qualifications, responsibilities, and skills required. Additional duties may be assigned as necessary.

SK pharmteco Inc., is an equal opportunity employer who prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants.

 



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