Validation Engineer

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Job Description

We are seeking a dedicated Validation Process Engineer to join our team in a dynamic chemical manufacturing environment. You will play a critical role in validating manufacturing processes, particularly focusing on 190 proof Ethanol, and ensuring compliance with FDA regulations. This position offers a unique opportunity to work on diverse product lines and contribute significantly to our growth and innovation efforts.

Job Title : Validation Process Engineer

Job Description

We are seeking a dedicated Validation Process Engineer to join our team in a dynamic chemical manufacturing environment. You will play a critical role in validating manufacturing processes, particularly focusing on 190 proof Ethanol, and ensuring compliance with FDA regulations. This position offers a unique opportunity to work on diverse product lines and contribute significantly to our growth and innovation efforts.

Responsibilities

• Validate the manufacturing process for 190 proof Ethanol and the subsequent final drug product.
• Develop and execute validation protocols and ensure compliance with FDA regulations.
• Conduct validation testing and adjust equipment with precision to meet established standards.
• Collaborate cross-functionally with chemical compounders, operators, and the lab to ensure seamless implementation of validated processes.
• Prepare and oversee the production of three batches of the product as part of the validation process.
• Implement corrective and preventative actions based on audit findings.
• Draft validation documentation and ensure accurate record-keeping to pass customer audits.

Essential Skills

Additional Skills & Qualifications

Work Environment

The role is based in a chemical manufacturing environment, with time spent both on the production floor and in an office cubicle setting. The position involves hands-on work with various equipment and requires adherence to safety protocols.

Pay and Benefits

The pay range for this position is $55.00 - $65.00 / hr.

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

Workplace Type

This is a fully onsite position in Saint Louis,MO.

Application Deadline

This position is anticipated to close on Jul 16, 2025.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 due to a disability, please email actalentaccommodation@ for other accommodation options.

Seniority level

Seniority level

Mid-Senior level

Employment type

Employment type

Contract

Job function

Job function

Quality Assurance

Industries

Business Consulting and Services

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