Validation Engineer

Responsibilities

• Support validation execution and gap assessments tied to equipment qualification, tank qualification, mixing studies, smoke studies, aseptic technique, and instrument/equipment qualification.
• Auditor-driven project focused on equipment validation, particularly tanks used for drug substance mixing and drug product filling.
• Assess existing IOQ/OQ documentation for robustness, identify gaps between OQ and PQ, and determine if current qualifications support performance qualification expectations.
• Evaluate product-specific mixing study needs, including understanding tank qualification, viscosity considerations, matrix/bracketing approaches, risk assessment, and validation gap identification and mitigation.
• Support smoke study execution in an aseptic processing environment, including understanding aseptic technique, equipment operation, and driving execution as a validation representative.
• Lead and guide internal resources, manage execution, and keep the validation effort moving forward.

Requirements

• Bachelor's degree in Engineering, Science, Life Sciences, or related technical discipline preferred.
• Equivalent hands-on validation experience can be considered.
• Must have validation execution experience in a pharmaceutical, biotech, or aseptic manufacturing environment.
• Equipment qualification experience.
• Strong understanding of IOQ/OQ/PQ expectations.
• Ability to perform gap assessments.
• Tank qualification experience.
• Mixing study experience or strong understanding of equipment-based mixing qualification.
• Aseptic processing experience.
• Smoke study experience or strong understanding of smoke study execution.
• Ability to support protocol execution and documentation.
• Ability to assess whether qualification packages are robust enough.
• Ability to identify validation gaps and recommend mitigation strategies.
• Ability to handle a strong personality and drive work forward without being timid.