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
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.
ResponsibilitiesDevelop 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.
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.
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.
| Location | New Albany, OH |
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