Process Engineer I

SK Pharmteco

King of Prussia, PA

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JOB DETAILS

JOB TYPE

Full-time

SKILLS

Analysis Skills, Application Programming Interface (API), Automation Systems, Biology, Biotech and Pharmaceutical, CAD/CAM (Computer-Aided Design/Computer-Aided Manufacturing), Cell Cultures, Chemical Engineering, Cleanroom, Communication Skills, Contract Manufacturing, Cost Control, Cross-Functional, Current Good Manufacturing Practice (cGMP), Documentation, Fermentation, GMP (Good Manufacturing Practices), Manufacturing, Manufacturing/Industrial Processes, Materials Analysis, Physical Demands, Physical Science, Problem Solving Skills, Process Analysis, Process Engineering, Process Flow, Process Improvement, Project Engineering, Quality Management, Regulations, Scalable System Development, Small Molecules, Startup, Statistics, Team Player, Technical Support, Time Management, Writing Skills

LOCATION

King of Prussia, PA

POSTED

11 days ago

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.

About the Company

SK Pharmteco

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