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MES Validation Engineer (Biotech)
Job Location:
Job Location:
Hillsboro, IL - USA
Hourly Salary:
USD 65 - 70
Hourly Salary:
Posted:
15 October 2026 (6 days ago)
Posted:
Application Deadline:
12 January 2027
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Onsite in Hillsboro OR.
The Opportunity:
As part of the Process and Compliance Team in manufacturing you will perform a wide variety of tasks and operations that are required to design build test validate and maintain pharmaceutical production in a state-of-the-art highly-automated production and packaging facility. The MES Change Specialist works cross-functionally with manufacturing P&C ITOT Master data and many other departments to ensure the efficient construction and effective functionality of our electronic documentation for operations across HTO.
In addition to performing the responsibilities/tasks below the successful candidate will need to demonstrate the following traits and capabilities:
Who you are:
You hold a Bachelors degree in a relevant field plus 3-5 years of MES electronic batch record or computerized systems experience for regulated manufacturing OR Masters degree in a relevant field
You have prior experience with construction testing and validation of computerized systems
You have extensive prior experience working in electronic change management systems (trackwise Veeva etc.) to own changes and coordinate action items spanning multiple departments
Prior experience in IT OT or Software Technical Writing Quality Systems and Validation (CSV/CSA GAMP) preferably in a regulated industry.
You have a strong understanding of test requirements for electronic data systems for regulatory compliance
You have knowledge of the automation systems that include SAP Manufacturing Execution Systems (MES) Programmable Logic Controllers (PLC) and Human Machine Interfaces (HMI)
You have prior experience with sterile pharmaceutical manufacturing (solution prep equipment prep liquid/lyo vial filling PFS formulation inspection packaging etc)
Ownership of changes in a change management system (ex. Veeva) from initiation to closure
You have experience with troubleshooting Rockwell systems including remote or on-site support is strongly preferred
It is preferred you have prior experience on an EBR or MES deployment projects.
Nesco Resource offers a comprehensive benefits package for our associates which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical Vision Dental 401K and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race color religion age sex national origin disability status genetics protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal state or local laws.
The Opportunity:
As part of the Process and Compliance Team in manufacturing you will perform a wide variety of tasks and operations that are required to design build test validate and maintain pharmaceutical production in a state-of-the-art highly-automated production and packaging facility. The MES Change Specialist works cross-functionally with manufacturing P&C ITOT Master data and many other departments to ensure the efficient construction and effective functionality of our electronic documentation for operations across HTO.
In addition to performing the responsibilities/tasks below the successful candidate will need to demonstrate the following traits and capabilities:
- You will troubleshoot and identify resolutions for mechanical or automation related failures in production
- You will identify opportunities to improve leveraging data analytics of system performance to deliver reduced costs and increased efficiency.
- You will lead user requirement gathering for operational needs and perform initial requirement assessments for MES modifications
- You will own CSV functions including defining requirements writing and execution of test scripts
- Translate operational requirements into recipe and workflow requirements that will define CSV test protocols
- Development authoring and executing of protocols for configuration verification (CV) and functional verification (FV) testing of MES recipes and workflows according to approved procedures and CSV principles
- Investigate and assess exceptions and deviations from CV and FV protocol testing
- You will own plan execute and improve review of MES changes for a set of assigned manufacturing processes driven by the change management process including testing and implementation
- You will monitor project schedule and escalate concerns to leadership with appropriate time to mitigate
- You will assist with drafting test plans for MES changes including comprehensive test plans and/or reports for new recipes
- You will own MES-related deviations including high-complexity or multi-site deviations relating to MES defects. Ensure corrective actions resolve issues effectively
- You will support MES-components of other site initiatives including capitalized projects tech transfers Drug Substance/Drug Product (DS/DP) changes shutdown projects and new launches
- You will serve as an audit support for MES providing demonstrations presentations and answering questions as required. If topical support closure of any MES-related regulatory findings.
Who you are:
You hold a Bachelors degree in a relevant field plus 3-5 years of MES electronic batch record or computerized systems experience for regulated manufacturing OR Masters degree in a relevant field
You have prior experience with construction testing and validation of computerized systems
You have extensive prior experience working in electronic change management systems (trackwise Veeva etc.) to own changes and coordinate action items spanning multiple departments
Prior experience in IT OT or Software Technical Writing Quality Systems and Validation (CSV/CSA GAMP) preferably in a regulated industry.
You have a strong understanding of test requirements for electronic data systems for regulatory compliance
You have knowledge of the automation systems that include SAP Manufacturing Execution Systems (MES) Programmable Logic Controllers (PLC) and Human Machine Interfaces (HMI)
You have prior experience with sterile pharmaceutical manufacturing (solution prep equipment prep liquid/lyo vial filling PFS formulation inspection packaging etc)
Ownership of changes in a change management system (ex. Veeva) from initiation to closure
You have experience with troubleshooting Rockwell systems including remote or on-site support is strongly preferred
It is preferred you have prior experience on an EBR or MES deployment projects.
Nesco Resource offers a comprehensive benefits package for our associates which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical Vision Dental 401K and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race color religion age sex national origin disability status genetics protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal state or local laws.
Required Experience:
IC
About Company
Nesco Resource is a trusted staffing and employment agency delivering staffing services and recruitment solutions for employers and job seekers nationwide.
