Project Engineer - III (Senior
Listed on 2026-08-21
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering, Data Analyst
Location: West Point
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Source Inc.
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Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price.
Project Engineer - III (Senior)
Location:
Remote Role With 25% Travel Expected Duration: 12 Months Contract Pay Rate: $80.70/Hr on W2
Shift: Monday-Friday (8:00 AM to 5:00 PM) – 40.00 Hours/Week (Job Details)
Description:
Client is seeking a highly motivated individual for a technical operations contractor position. This role will primarily support the commercial manufacture of Drug Product (Form / Fill) at the client's External Partner network sites inclusive of the responsibilities below.
Education Minimum Requirement:
Bachelor's degree in Chemical / Biochemical Engineering, Pharmaceutical Science, or Chemistry/Biology, or other related science or engineering field.
Required
Experience and Skills:
- Minimum of 6 years post-bachelor's degree experience in a GMP functional area or support of a GMP functional area, such as Operations, Technical Operations, Technology, or Engineering
- Min 3 years of experience supporting sterile / aseptic drug product filling (vials, syringes, etc.)
- Statistics experience
- Strong communication and teamwork skills
- Demonstrated ability to independently manage projects/work to schedule/deadlines
- Travel may be required but not to exceed 25%
Preferred
Experience and Skills:
- Experience with isolator filling
Important Note:
REMOTE ROLE WITH 25% TRAVEL EXPECTED at the client's External Partner network sites.
Responsibilities include:
- Author, review, and maintain GMP technical documentation with clarity, accuracy, and compliance to applicable regulatory and quality requirements. Documents include:
- Change control ownership
- Protocols and technical reports
- Continued Process Verification (CPV) plans, data sets, trend analyses, and periodic reports
- Perform statistical data extraction and analysis to support proactive process analysis. Typical activities:
- Pull and validate production, quality, and process control data from relevant GMP sources or approved data trending systems
- Apply statistical process control (SPC), capability analysis, and other appropriate methods
- Create visualizations and summary metrics to support assessment outputs
- Contribute to continuous improvement initiatives, including data-driven process optimization and documentation standardization
- Floor support as needed for Person-In-Plant activities at External Partner
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Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.
Awards & Recognition
• America's Most Honored Businesses (Top 10%)
• Fastest-Growing Staffing Firm by Staffing Industry Analysts
• INC 5000 List for Eight Consecutive Years
• Top 100 by Dallas Business Journal
• Spirit of Alliance Award by Agile1 #LS01
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