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Manufacturing Bioprocess Associate-Drug Substance, Drumree
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Client:
Location:
Drumree, Ireland
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
304cbc1fbbd7
Job Views:
6
Posted:
01.06.2025
Expiry Date:
16.07.2025
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Job Description:
Job Description
About PSC Biotech
Who are we?
PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.
‘Take your Career to a new Level’
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.
Overview:
By integrating leading-edge technology with a dynamic, activity-based workspace, the facility will support seamless connection and collaboration within and across teams and functions. Facility will provide Biologics Drug Substance manufacturing for Clinical Supply, Registration & Commercial Launch.
The facility is designed to be operated in a multi-product mode which requires flexibility to adjust as the pipeline of clinical and commercial biologics-based medicines demands change.
An amazing opportunity has arisen for a Manufacturing Bioprocess Associate to provide operational support for manufacturing operations of the Late Stage and Launch Pipeline products at our new state of the art single use biotechnology facility in Ireland.
This role will involve supporting manufacturing operations on a Shift Rotation basis.
Facility serves as a magnetic force that attracts, recognizes, and integrates people of diverse backgrounds and perspectives.
Reports to: Drug Substance Process Operations Manager
Requirements
Role Functions:
* The Manufacturing Bioprocess Associate will support end-to end production operations for both Fed Batch and Continuous Manufacturing.
* Shift role 24/7 (Onsite)
* Support on floor manufacturing of pipeline products on a shift rotation
* Operate equipment according to electronic batch records,sampling plans and standard operating procedures.
* Work as part of a multi-disciplined, diverse and dedicated process team where flexibility and teamwork are an essential requirement
* Support weekend or out of hours work on select time frames to support manufacturing activities.
* Conduct all work activities with a strict adherence to the safety and compliance culture on site
* Support the Authoring of electronic batch records, sampling plans, work instructions and standard operating procedures.
Skills and Education required:
* Level 6 qualification in a science or engineering discipline desired.
* 2+ years experience in a GMP Manufacturing requirement shall be deemed equivalent
* Ability to work independently and within a cross-functional team.
* Familiarity with contamination control and batch release requirements
* Familiarity with Emerson DeltaV, Pas X,and the use of Automation in a manufacturing Process.
* Experience with various SingleUse technologies in a manufacturing environment
Preferred Experience and Skills:
* Understanding of Upstream and Downstream Unit Operations for mAb manufacturing
#LI-AP1
Requirements
Level 6 qualification in a science or engineering discipline desired. 2+ years experience in a GMP Manufacturing requirement shall be deemed equivalent Familiarity with Emerson DeltaV, Pas X Understanding of Upstream and Downstream Unit Operations for mAb manufacturing The Manufacturing Bioprocess Associate will support end-to end production operations for both Fed Batch and Continuous Manufacturing. Shift role 24/7 (Onsite) #J-18808-Ljbffr