Pharma Validation & Documentation Specialist
Listed on 2026-10-20
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Quality Assurance - QA/QC
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Pharmaceutical
Pharmaceutical Manufacturing, Pharma Engineer
Glatt Air Techniques Inc. in Ramsey, NJ is seeking a Technical Specialist / Validation to generate and oversee technical documents supporting pharmaceutical development, manufacturing, facilities, QA and QC.
You will develop SOPs, CAPAs, OOS and validation protocols for the Pharmaceutical Services Division with emphasis on fluid bed granulation, blending, milling, compression, encapsulation, coating and packaging.
This posting is for the Pharma Validation & Documentation Specialist role at Glatt Group, based in Ramsey, NJ, United States.
The following opportunity is for a Pharma Validation & Documentation Specialist with Glatt Group.
Our organisation is growing, and we are hiring a Pharma Validation & Documentation Specialist in Ramsey, NJ, United States.
This opportunity is for the Pharma Validation & Documentation Specialist role at Glatt Group.
We are seeking a motivated Pharma Validation & Documentation Specialist to join Glatt Group in Ramsey, NJ, United States.
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