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Director Validation Jobs in Ohio (NOW HIRING)

CAI

Validation Engineer

Columbus, OH

$72K - $80K/yr

... work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or equivalent experience) - 2-4 years ...

CAI

Validation Engineer

Columbus, OH · On-site

$72K - $80K/yr

... work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or equivalent experience) - 2-4 years ...

CAI

Validation Engineer

Columbus, OH · On-site

$72K - $80K/yr

... work - Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or equivalent experience) - 2-4 years ...

RXinsider LTD.

Sr. Validation Engineer

Bedford, OH · On-site

$80 - $100/hr

Direct or indirect industry knowledge and the ability to learn new technical information and ... sciences or validations) having a minimum of 4+ years related experience or 3+ years related ...

CAI

Entry Level Validation Engineer

Columbus, OH · On-site

$60K - $70K/yr

... Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field preferred but not required - 0- 2 years work experience ...

CAI

Entry Level Validation Engineer

Columbus, OH · On-site

$60 - $80/hr

Direct small teams in document development and/or execution Qualifications and Experience * Bachelor's degree in a science or engineering field preferred but not required * 0- 2 years work experience ...

CAI

Entry Level Validation Engineer

Columbus, OH · On-site

$60K - $70K/yr

... Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field preferred but not required - 0- 2 years work experience ...

CAI

Entry Level Validation Engineer

Columbus, OH · On-site

$60K - $70K/yr

... Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field preferred but not required - 0- 2 years work experience ...

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Director Validation information

What does a director validation do?

A Director of Validation oversees the validation processes in industries like pharmaceuticals, biotechnology, or medical devices to ensure compliance with regulatory standards. They develop and implement validation strategies for equipment, processes, and systems, ensuring they meet quality and safety requirements. This role involves managing validation teams, coordinating with regulatory bodies, and maintaining documentation to support audits and inspections. The Director also ensures adherence to industry guidelines such as FDA, EMA, or ISO standards.

What are the typical daily responsibilities of a director validation in a regulated industry?

A Director Validation typically oversees the planning, execution, and review of validation projects to ensure compliance with regulatory requirements. Daily responsibilities include leading teams, reviewing validation protocols and reports, coordinating with quality, engineering, and regulatory departments, and addressing any deviations or issues that arise during validation activities. The role may also involve direct communication with regulatory agencies during audits and inspections. This ensures products or processes meet the highest standards of quality and regulatory compliance, ultimately supporting the company’s overall operational success.

What are the key skills and qualifications needed to thrive in the director validation position, and why are they important?

To thrive as a Director Validation, you need extensive experience in validation processes, regulatory compliance, quality assurance, and a relevant scientific or engineering degree. Familiarity with industry standards, validation lifecycle management software, and certifications such as Six Sigma or PMP are highly valued. Strong leadership, strategic thinking, and excellent communication skills help to drive complex projects and foster cross-functional collaboration. These skills are vital to ensuring validated processes meet regulatory standards and support organizational goals efficiently.

What are the most commonly searched types of Validation jobs in Ohio?

The most popular types of Validation jobs in Ohio are:

What are popular job titles related to Director Validation jobs in Ohio?

For Director Validation jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Director Validation jobs in Ohio look for?

The top searched job categories for Director Validation jobs in Ohio are:

What cities in Ohio are hiring for Director Validation jobs?

Cities in Ohio with the most Director Validation job openings:

Director Validation jobs near you
Infographic showing various Director Validation job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 10% Part Time, 1% Temporary, and 4% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Validation Engineer OSD Manufacturing

New Albany, OH • On-site

IT MINDS L.L.C.
See more jobs at IT MINDS L.L.C.external

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Validation Engineer OSD Manufacturing
Location: Ohio (OH)
Job Type: Contract
Duration: 1+ Year
Hours: 40 Hours/Week
Start Date: 09/21/2026 or 09/28/2026

Job Description

Our client is seeking a hands-on Validation Engineer with 5–10 years of pharmaceutical manufacturing experience, including strong Oral Solid Dosage (OSD) manufacturing experience.

The ideal candidate will be a self-directed validation generalist who can independently manage validation projects and work closely with operators on the manufacturing floor.

Responsibilities

  • Develop and execute validation protocols for registration batches and process validation.

  • Support IQ/OQ/PQ execution and equipment validation activities.

  • Develop batch records, sampling plans, risk assessments, and related validation documentation.

  • Write deviations and support CAPA investigations and implementation.

  • Coordinate sampling materials, containers, labels, and in-room execution with Operations.

  • Perform validation activities on OSD equipment, including:

    • Tablet presses

    • Encapsulators

    • Fluid-bed dryers

    • Coaters

  • Support technology transfer and process validation activities.

  • Perform hands-on validation activities on the manufacturing floor while completing required documentation and computer-based work.

  • Collaborate closely with Manufacturing, Operations, Quality, and Engineering teams.

Required Qualifications

  • 5–10 years of Validation Engineering experience in pharmaceutical manufacturing.

  • Strong Oral Solid Dosage (OSD) manufacturing experience is required.

  • Hands-on experience with tablet and capsule manufacturing equipment.

  • Experience developing and executing validation protocols.

  • Experience with IQ/OQ/PQ and equipment qualification.

  • Experience with batch records, sampling plans, and risk assessments.

  • Experience managing deviations and supporting CAPA investigations.

  • Strong understanding of GMP/cGMP requirements.

  • Self-directed with the ability to take ownership of projects with minimal supervision.

  • Comfortable working directly with operators on the manufacturing floor.

Preferred Qualifications

  • Cleaning Validation experience within OSD manufacturing.

  • Technology transfer experience.

  • Experience with process validation and registration batches.

  • Understanding of computerized systems from an equipment/validation perspective.