Senior Manufacturing Bioprocess Associate
Dunboyne, Ireland | Posted on 10/28/2025
* Industry Pharma/Biotech/Clinical Research
* Work Experience 4-5 years
* City Dunboyne
* State/Province Meath
* Country Ireland
Job Description
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:
An amazing opportunity has arisen for a ManufacturingBioprocess Associate to provide operational support for manufacturingoperations of the Late Stage and Launch Pipeline products at our new state ofthe art single use biotechnology facility .
Requirements
Responsibilities:
The Senior Manufacturing Bioprocess Associate willsupport end-to end production operations for both Fed Batch and ContinuousManufacturing.
Primary activities/responsibilities:
* Operate equipment according to electronic batch records,sampling plans and standardoperating procedures.
* Work as part of a dedicated process team whereflexibility and teamwork are a key requirement.
* Ability to solve problems with a desire to continuouslylearn, improve and develop.
* Support weekend or out of hours work on select timeframes to support manufacturing activities.
* Conduct all work activities with a strict adherence tothe safety and compliance culture on site
* Support the Authoring of electronic batch records,sampling plans, work instructions and standard operating procedures.
Required Education, Experience and Skills:
* A level 6 with a minimum of 3+ years’ experience in a GMPManufacturing requirement shall be deemed equivalent
* Competent in troubleshooting and show practicalproblem-solving capabilities.
* Ability to work independently and within across-functional team.
* Familiarity with contamination control and batch releaserequirements
* Familiarity with Emerson DeltaV, Pas X, and the use ofAutomation in a manufacturing Process.
* Proficiency in various SingleUse technologies in amanufacturing environment
Preferred Experience and Skills:
* Commissioning and Qualification experience
* Understanding of Upstream and Downstream Unit Operationsfor mAb manufacturing
* Understanding of both continuous and batch fedmanufacturing processes
Reports to: Drug Substance Process Operations Manager
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