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Validation Engineer OSD Manufacturing

IT MINDS L.L.C.

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.

Vacancy posted 2 days ago
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