Manufacturing Process Engineer
Job in
West Columbia, Lexington County, South Carolina, 29172, USA
Listed on 2026-03-04
Listing for:
Insight Global
Full Time
position Listed on 2026-03-04
Job specializations:
-
Engineering
Validation Engineer, Quality Engineering, Process Engineer, Pharma Engineer -
Pharmaceutical
Validation Engineer, Quality Engineering, Pharma Engineer
Job Description & How to Apply Below
WILL PROVIDE RELOCATION TO CHARLESTON, SC!!
Position: Pharmaceutical Process Engineer II
Location: Charleston, SC
Length: FULL TIME HIRE
Rate: $100,000 - $110,000
Exact compensation may vary based on several factors, including skills, experience, and education
Required Skills
- Bachelor’s degree in Engineering
- 3+ years of experience supporting sterile pharmaceutical manufacturing
- Experience with process validation, investigations, and technology transfer
- Strong working knowledge of cGM
NICE TO HAVE SKILLS AND EXPERIENCE
- Liquid fill dosage forms
- Lyophilization and sterilization processes
- Process scales up and optimization
- Pharmaceutical technology transfer
Insight Global is seeking a Process Engineer (Sterile) II to support a pharmaceutical manufacturing client of ours in Charleston, SC. This individual will provide hands‑on technical support in a fast‑paced manufacturing environment, supporting process validation, technology transfer, investigations, and continuous improvement initiatives.
Key Responsibilities- Provide technical support for sterile manufacturing processes, including process transfer and validation activities
- Analyze existing manufacturing processes and implement improvements to increase efficiency, reduce costs, and improve product quality
- Develop or modify processes, equipment, and layouts to meet production goals
- Author and execute process validation, cleaning validation, and process optimization protocols
- Define critical process parameters, sampling plans, and testing requirements
- Write validation reports and technical improvement documentation
- Monitor manufacturing processes during production runs and troubleshoot issues
- Support aseptic operations, including sterilization, depyrogenation, lyophilization, and sanitization
- Participate in deviations, investigations, and CAPAs
- Utilize FMEA to troubleshoot and mitigate processing risks
- Support capital projects, including scope development and design review
- Ensure compliance with cGMPs and all required training
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