Process Engineer; NPI
Listed on 2025-11-02
-
Engineering
Process Engineer, Quality Engineering
- Industry Pharma/Biotech/Clinical Research
- Work Experience 4-5 years
- City Carlow
- State/Province Carlow
- Country Ireland
About PSC Biotech
Who are we?
PSC Biotech is a leading Biotech Consultancy firm foundedin 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in morethan 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 Careerto a new Level’
PSC Biotech disrupts the conventional consultancy modelby 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 adiverse-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 ourclient’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:
New exciting opportunity now exists on our Carlow Sitefor a Process Engineer to join the Process Engineering Group on site and reportto the Technical Engineering Manager
Our new team member will serve as technical support fornew product introduction (NPI) and commercial manufacturing and will participate and/or lead cross functional or single function teams including liaising with vendors or above site groups. You will typically have prior related work experience; ideally in manufacturing, preferably GMP Setting butwe will consider applicants from other working environments as long as theyhave technology transfer experience
Knowledge of process monitoring systems, automation systems(Delta
V), operational intelligence & data systems (Pi System) within a GMPmanufacturing environment would be beneficial and desirable but not a necessity for this role
Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical,Automation, Capital Projects, Maintenance, Safety, Process Development,Technical Services, Utilities and Validation.
RequirementsResponsibilities:
- Design/Author/Review/Approve/Execute qualification/validation documentation and process development studies in linewith the standard approval process
- Design/Author/Review/Approve/Execute Execution/development of change controls
- Contribution to Kaizen events as appropriate
- Technical input into quality notification by authoring/reviewing/approving investigations
- Execution of equipment/qualification validation programs;including re-qualification and re-validation
- Support continuous improvement through Lean Six Sigma methodologies
- Perform root cause analysis of system failures,substandard performance, using standard tools and methods, to resolve machine and system issues
- Serve as technical engineering representative for internal technical group discussions and represent technical Operations Carlowat global technical forums
- Drive compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, ensuring consideration of the impact on GMP and compliance and decisions made. Accountable for compliance via documentation completion, risk assessments, closing out corrective action, participate in audits and inspections and proactively highlighting any issues around compliance
- Work collaboratively to drive a safe and compliant culture in Carlow
- May be required to perform…
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