Validation Analyst

MES Validation & Support Analyst

Job Description

We are seeking an MES Validation & Support Analyst to support manufacturing systems within a production environment. This position will primarily focus on system validation, testing, and production support, rather than system design or development. This individual will work closely with technical teams and manufacturing personnel to test system functionality, complete validation documentation, and provide ongoing system support. The ideal candidate will have strong technical aptitude, an understanding of manufacturing processes, and the ability to quickly learn specialized manufacturing systems.

Responsibilities

• Support the validation and testing of Manufacturing Execution Systems (MES) following system configuration and design.
• Execute system testing according to established procedures and accurately document results.
• Complete and maintain validation documentation and testing packages.
• Work closely with system designers and technical teams throughout the validation process.
• Provide day-to-day system support to manufacturing and production teams.
• Troubleshoot system and process-related issues and assist with identifying appropriate resolutions.
• Learn manufacturing processes and workflows to understand how they are represented within the MES.
• Support Electronic Batch Records (EBRs) and other electronic manufacturing documentation.
• Collaborate with Manufacturing, Operations, Quality, and technical teams.
• Assist with ongoing system support, testing, and continuous improvement activities.

Essential Skills

• Experience working within a manufacturing or production environment.
• Good understanding of manufacturing processes and process flow.
• 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.

Additional Skills & Qualifications

• Previous MES experience preferred.
• Experience with FactoryTalk, PharmaSuite/PMX, or similar manufacturing systems is a plus.
• Electronic Batch Record (EBR) experience is highly desirable.
• GMP experience.
• Experience within a regulated manufacturing environment.
• Previous pharmaceutical or similarly regulated manufacturing experience.
• MES validation experience.
• Experience supporting Electronic Batch Records (EBRs).

Work Environment

This long-term contract opportunity requires a minimum 12-month commitment with the potential for extension. The position will support manufacturing operations across the facility, working in a regulated environment typical of the pharmaceutical industry

Job Type & Location

This is a Contract position based out of Columbus, OH.

Pay and Benefits

The 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 & Location

This is a Contract position based out of Columbus, OH.

Application Deadline

This position is anticipated to close on Nov 9, 2026.

Workplace Type

This 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.