Our client is seeking a highly technical and experienced leader for their Director, OSD Validation opening at their Ohio facility. The Director, Validation will be responsible for all clinical and commercial manufacturing support through facilities, equipment, filter, cleaning, and manufacturing process validation, support commissioning and qualifications of capital projects, computer systems qualification, and oversite of the entire validation program.

Be one of the first applicants, read the complete overview of the role below, then send your application for consideration.

For further details and responsibilities, apply here or reach out directly to Hannah Ferguson at hferguson@germerintl.com

Strong OSD Cleaning, Equipment, Process, and Product Validation and Tech Transfer experience is required.

Qualifications Bachelor’s Degree in relatable field required. Oral Solid Dosage validation required. 12+ years’ experience in cGMP pharmaceutical manufacturing environment. Supervisory Experience: minimum of 6 years. Detailed working knowledge of GMPs, FDA Aseptic Processing Guideline, EU “Orange Book”, GAMP, and ICH guidelines.