Validation Engineer OSD Manufacturing

IT MINDS L.L.C.
  • New Albany, OH
  • Quick Apply
3 days ago

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.

Numbers & Facts

LocationNew Albany, OH

Skills

  • Capsulesunmatched
  • Corrective and Preventative Action (CAPA) Systemsunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Documentationunmatched
  • Drug Manufacturingunmatched
  • Engineeringunmatched
  • Equipment Validationunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Manufacturingunmatched
  • Manufacturing Equipmentunmatched
  • Manufacturing Operationsunmatched
  • Process Validationunmatched
  • Project/Program Managementunmatched
  • Quality Engineeringunmatched
  • Risk Analysisunmatched
  • Technical Supportunmatched
  • Validation Documentationunmatched
  • Validation Planunmatched

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