Validation Analyst

Job Title: MES Validation & Support AnalystJob DescriptionThis role focuses on validating, testing, and supporting Manufacturing Execution Systems (MES) within a regulated manufacturing environment. You will work closely with technical and manufacturing teams to ensure systems function reliably, meet Good Manufacturing Practice (GMP) requirements, and accurately support electronic manufacturing documentation. This position emphasizes system validation and production support rather than system design or development, and offers a long-term opportunity to contribute to continuous improvement across the facility.Responsibilities

• Support the validation and testing of Manufacturing Execution Systems (MES) after system configuration and design activities are completed.
• Execute system testing according to established procedures and accurately document all test results.
• Create, complete, and maintain validation documentation and testing packages in compliance with GMP and regulatory expectations.
• Work closely with system designers, engineers, and technical teams throughout the validation lifecycle to ensure alignment and completeness.
• Provide day-to-day MES and related system support to manufacturing and production teams within the facility.
• Troubleshoot system and process-related issues, identify root causes, and assist in implementing appropriate resolutions.
• Learn and understand manufacturing processes and workflows to accurately interpret how they are represented and controlled within the MES.
• Support Electronic Batch Records (EBRs) and other electronic manufacturing documentation, ensuring accuracy and compliance.
• Collaborate with Manufacturing, Operations, Quality, and technical teams to ensure systems support operational and quality objectives.
• Assist with ongoing system support, regression testing, and continuous improvement initiatives related to MES and electronic documentation.
• Contribute to maintaining a compliant and efficient manufacturing environment by adhering to procedures and suggesting process enhancements where appropriate.

Essential Skills

• Experience working within a manufacturing or production environment.
• Good understanding of manufacturing processes and process flows.
• Strong computer and technical skills with the ability to quickly learn new systems.
• Experience with system validation, testing, technical support, or manufacturing systems.
• Ability to follow detailed procedures and accurately document testing results.
• Strong troubleshooting, communication, and problem-solving skills.
• GMP experience and familiarity with working in a regulated manufacturing environment.
• Experience within a pharmaceutical or similarly regulated manufacturing environment.
• MES validation experience, including execution and documentation of validation activities.
• Experience supporting Electronic Batch Records (EBRs).

Additional Skills & Qualifications

• Previous MES experience, particularly in a production or regulated environment, is preferred.
• Experience with FactoryTalk, PharmaSuite/PMX, or similar manufacturing systems is a plus.
• Electronic Batch Record (EBR) experience is highly desirable.
• Exp. in a pharmaceutical industry or other regulated environment is advantageous.
• Demonstrated ability to work effectively with cross-functional teams including Manufacturing, Operations, Quality, and technical groups.
• Interest in and aptitude for continuous improvement initiatives within manufacturing systems.

Work EnvironmentThis position supports manufacturing operations across a regulated, GMP-compliant facility and is offered as a long-term contract with a minimum 12month commitment and potential for extension. You will work in a production environment that relies on MES, Electronic Batch Records, and related systems such as FactoryTalk, PharmaSuite/PMX, or similar platforms. The role involves close collaboration with manufacturing, operations, quality, and technical teams, and requires adherence to established procedures, documentation standards, and regulatory requirements. The environment emphasizes accuracy, compliance, and continuous improvement, with a strong focus on reliable system performance to support safe and efficient manufacturing. Job Type & LocationThis is a Contract position based out of Columbus, OH. Pay and BenefitsThe pay range for this position is $33.65 - $38.46/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract position based out of Columbus, OH. Application DeadlineThis position is anticipated to close on Nov 13, 2026. Workplace TypeThis is a fully onsite position in Columbus,OH.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.