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PSC Biotech Corporation in Dunboyne, Ireland, is seeking a New Material Introduction & Material Qualification Specialist. The role focuses on evaluating and qualifying materials, ensuring regulatory compliance, and managing supplier collaborations to support product integrity and patient safety.
The successful candidate will lead NMI activities, drive material qualification, and partner with multiple stakeholders across QA, regulatory, procurement, R&D, and operations in a hybrid work
Dunboyne, Ireland | Posted on 10/22/2026
About PSC Biotech
Who are we?
PSC Biotech is a leading Biotech Consultancy firm foundedin 1996, headquartered in Pomona, California, USA, with Global operations inIreland, India, Singapore, Australia and the US, serving 350 clients in morethan 23 countries worldwide. We provide cloud-based software solutions forQuality Management and Regulatory Inspections, pharmaceuticals contractmanufacturing professionals, and metrology services to our clients.
‘Take your Career to a new Level’
PSC Biotech disrupts the conventional consultancy modelby aligning our EVP as one of the unique selling point which includes theopportunity to work with the most talented cohort of like-minded professionalsoperating in the Pharma/ Biotech Industry. We offer a permanent contract ofemployment giving exposure of working in Top Pharmaceutical client sites in adiverse-cultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech, we provideunparalleled empowering career development though Learning & Developmentin-house training mentorship through constant guidance to facilitate careerprogression. We believe in creating high performing teams that can exceed ourclient’s expectations with regards to quality of all scalable and business unitdeliverables, staying under budget and ensuring timelines for our deliverablesare being met.
Overview:
The New Material Introduction & MaterialQualification Specialist will be responsible for the evaluation, qualificationand lifecycle management of materials used in site. You will ensure new andexisting materials meet regulatory, quality and safety requirements throughrigorous testing, supplier qualification and cross functional collaboration,enabling reliable, compliant and cost effective supply to support productintegrity and patient safety.
Key Accountabilities
Preferred experience:
Other Job Requirements