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Validation Engineer

Net2Source

Devens, MA

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JOB DETAILS
SALARY
$48–$51.04 Per Hour
SKILLS
Agile Programming Methodologies, Asset Management, Biology, Change Control, Chemistry, Code of Federal Regulations, Communication Skills, Computer Systems, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Quality, Disaster Recovery, Document Control, Equipment Validation, GMP (Good Manufacturing Practices), Identify Issues, Industry/Trade Analysis, Leadership, Preventative Maintenance, Problem Solving Skills, Purchasing/Procurement, Quality Control, Quality Management, Regulations, Regulatory Requirements, Requirements Management, Risk Analysis, Root Cause Analysis, Scripting (Scripting Languages), Software Debugging, Software Testing, Standard Operating Procedures (SOP), System Validation, Team Player, Test Scripts, Validation Plan, Writing Skills
LOCATION
Devens, MA
POSTED
12 days ago
Join a Global Leader in Workforce Solutions – Net2Source Inc.
Who We Are
Net2Source 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.

Job Title: Validation Engineer
Location: Devens, MA 01434
Duration: 06+ Months (Extendable)
 
Pay Rate: $45.00 - 51.04/hr on W2
 
 
Must Haves:
• Bachelor's degree required
• Incumbents must have demonstrated experience in solving complex technical issues and have the skills and understanding to troubleshoot process defects
• Demonstrated success in cross functional influencing, strong communication, and collaboration skills
• Must have GMP experience
 
Responsibilities will include (but not limited to):
  • Manage the entire lifecycle of QC laboratory instruments from procurement to qualification to decommissioning, ensuring all activities are in compliance with applicable policies/regulations.
  • Design, execute, manage, and implement QC instrument/software qualification documents such as (but not limited to): User Requirement Specification (URS), Design Qualification (DQ), validation plans, equipment IOQ protocols, software test scripts, configuration specifications, risk assessments, qualification summary reports
  • Author/execute computer system validation scripts using an electronic validation database (ALM), or paper-based
  • Own change controls specific to the qualification of QC instruments and its associated software
  • Update the asset management database to reflect new assets, calibrations, preventative maintenances
  • Author instrument operational SOPs as needed
  • Coordinate/interface/host vendors on site
  • Champions qualification deviations/software defects, identifying root causes and Corrective Actions/Preventive Actions (CA/PAs)
  • Acts as the liaison between Digital Plant (IT) and lab departments
  • Execute periodic assessments/decommissioning, as needed
 
Qualifications and Experience Required:
  • Required Bachelor’s degree or Master’s degree in Engineering, Chemistry, Biology, or in a related, scientific/computer-based field.
  • Minimum of 2 – 4+ years’ experience in the biopharmaceutical industry or equivalent combination of education and validation/lab experience will be considered.
  • Quality management system experience including: document control/management, change controls, investigations, deviations, electronic validation databases, asset management database
  • Knowledge of cGMP regulatory requirements, computerized analytical systems, i.e., 21 CFR part 11, GAMP, electronic record/electronic signature, data integrity, disaster recovery
  • Incumbents must have demonstrated experience in solving complex technical issues and have the skills and understanding to troubleshoot process defects
  • Demonstrated success in cross functional influencing, strong communication, and collaboration skills
  • Must have GMP experience
  • Microsoft Office Applications, preferred.
  • Computer system validation experience, preferred
  • Equipment validation experience is a plus

Why Work With Us?
We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.
Our Commitment to Inclusion & Equity
Net2Source 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
Ready to Level Up Your Career?
Click Apply Now and let’s make it happen.

About the Company

N

Net2Source

Net2Source Inc. is a Global Workforce Management Solutions Company, headquartered in New Brunswick, NJ with its local offices in Texas, California, Florida, Illinois, Colorado and Michigan and its global operations in Canada, UK, Europe, UAE, Malaysia, Australia, China, Singapore and India. Net2Source offers a wide gamut of consulting solutions customized to specific client needs including but not limited to Application Development, Workforce Management and Project Consulting. Whether it’s a Fortune client, whether it’s a System Implementer or whether it is a Start -up, our recipe to success – Exceed expectations! Under promise, over deliver.
COMPANY SIZE
50 to 99 employees
INDUSTRY
Other/Not Classified
WEBSITE
http://www.net2source.com