Job Information
Motion Recruitment Partners MES Validation Engineer in Hillsboro, Oregon
MES Validation Engineer
Hillsboro, Oregon
Onsite
Contract
Up to $89.61/hr
Job Title: MES Validation Engineer
Duration: 4+ months (possible extension)
Location: Hillsboro Oregon 97124
Job Summary:
We are seeking an experienced MES Validation Engineer to support the multi-phase deployment and validation of Manufacturing Execution Systems (MES) within a regulated manufacturing environment. This role will focus on ensuring computerized systems are validated in compliance with applicable regulatory requirements and industry standards.
The ideal candidate will collaborate cross-functionally with IT, quality, automation, and business teams to develop and execute validation strategies that support efficient and compliant manufacturing operations. Key Responsibilities:
Develop, draft, review, and route validation documentation including test scripts, validation protocols, and final reports for computerized systems.
Ensure all validation activities comply with applicable regulatory requirements and industry standards (e.g., GxP).
Collaborate with IT/OT, system owners, quality assurance, and business process owners to align validation strategies with existing validated systems.
Provide input into overall project validation strategy and risk assessments.
Guide overall test strategy development and ensure integration with validated environments.
Execute formal validation activities in a GMP-regulated environment.
Identify, assess, and mitigate risks associated with computerized systems.
Support continuous improvement of validation processes and documentation practices.
Required Qualifications
Minimum 5 years of experience as a Validation Professional in a regulated environment.
Proven experience developing and executing validation protocols for computerized systems.
Strong knowledge of regulatory requirements such as FDA, EMA, GxP, and industry standards related to system validation.
Solid understanding of Computerized System Validation (CSV) principles.
Experience with Rockwell FactoryTalk PharmaSuite.
Experience managing testing plans and execution.
Experience with industry tools such as ERP systems, ValGenesis, LIMS, SCADA, and other regulated life sciences platforms.
Strong verbal and written communication skills.
Bachelor’s degree (or equivalent experience) in Biomedical Engineering, Regulatory Affairs, Chemistry, Biochemistry, Biology, Computer Science, Technology, or related life sciences discipline.
Preferred Qualifications
- Professional certifications in validation or related disciplines (e.g., Certified Quality Engineer (CQE), Certified Software Validation Specialist (CSVS)).
You will receive the following benefits:
Medical Insurance - Four medical plans to choose from for you and your family
Dental & Orthodontia Benefits
Vision Benefits
Health Savings Account (HSA)
Health and Dependent Care Flexible Spending Accounts
Voluntary Life Insurance, Long-Term & Short-Term Disability Insurance
Hospital Indemnity Insurance
401(k) including match with pre and post-tax options
Paid Sick Time Leave
Legal and Identity Protection Plans
Pre-tax Commuter Benefit
529 College Saver Plan
Motion Recruitment Partners (MRP) is an Equal Opportunity Employer. All applicants must be currently authorized to work on a full-time basis in the country for which they are applying, and no sponsorship is currently available. Employment is subject to the successful completion of a pre-employment screening. Accommodation will be provided in all parts of the hiring process as required under MRP’s Employment Accommodation policy. Applicants need to make their needs known in advance.
Specialization:
- Technical Engineering / Design / Support