Biotech Associate

PSC Biotech Corporation; Dunboyne; On-site; EUR 42,000 - 60,000; Full time

Job summary

Dunboyne, Ireland – PSC Biotech Corporation is hiring for a manufacturing technician role within our self-directed work team (SDWT) in a state-of-the-art single-use biotech facility. The BTA will execute automated biologic drug substance production under GMP and EHS standards, supporting inoculation, cell culture, filtration, and purification processes.

You will work on a dedicated process team, drive lean improvements, and help ensure right-first-time delivery while maintaining safety and

Responsibilities

• Execute commercial manufacturing processes according to established work instructions and SOPs.
• Complete COMMIT cards to highlight ways of working within SDWTs and Hubs.
• Maintain manufacturing documentation to support GMP compliance.
• Provide safety feedback and support continuous improvement of behaviours.
• Take part in shift handovers and tier 1 meetings, escalating issues as needed.
• Liaise with other groups to plan tasks and ensure site schedule alignment.
• Act as an ERT during emergency situations if trained.

Job description

Dunboyne, Ireland | Posted on 10/07/2026

• Industry Pharma/Biotech/Clinical Research
• Work Experience 1-3 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:

• This role will be part of Manufacturing Self Directedwork team/ Hub in our new state of the art single use multi-product biotechfacility. The organizational structure at the site will be based onself-directed work teams (SDWT) where decisions will be made at the level wherethe data exists.
  
• The BTA is responsible for all procedures and processesassociated with the manufacture of Drug Substance at Our Company’s manufacturingfacility, at the highest standards of Safety, Quality and Compliance.
  
• The BTA will be responsible for undertaking manufacturingoperations involved in the production of biologic drug substances on theirdesignated shift. Key responsibilities include the execution of an automatedrecipe using paperless technology in order to progress the drug substancethrough inoculation and cell culturing activities, leading to filtration andpurification of the product in a state-of-the-art single use technology basedfacility. The incumbent will be involved in setting up the single use equipmentbetween runs, carrying out the production process according to world class GMPand EHS principles. The BTA will also be involved in driving to optimize andimprove the processing activities through use of standard work and leanprocessing techniques while supporting operations team to consistently deliveron specific Key Performance Indicators (KPIs). At all times this role isfocused on delivery to the patient through living the culture including acommitment to safety, focusing on right first time in everything we do and aconcentration on the engagement and development of self and peers.
  
• Complete COMMIT cards to highlight ways of working withinour SDWT’s and Hubs and across our site that support our COMMIT culture.
  
• Provide immediate feedback to others at any time toreinforce good safety and improvement of behaviors and acts.
  
• Execute commercial manufacturing processes according toestablished work instructions and Standard Operating Procedures (SOPs).
  
• Ensure that all assigned task related to manufacturingdocumentation support is in accordance with good manufacturing practices.
  
• Routinely talk about any safety issues you are concernedabout.
  
• Work as part of a dedicated process team whereflexibility and teamwork are a key requirement.
  
• Generate SOPs/ Work Instructions (WIs) to ensurecompliance with regulatory standards.
  
• Adhere to Right First-Time principles.
  
• Provide assistance and/or support for maintenance,engineering, quality or other colleagues as requested.
  
• Escalate issues as appropriate to manager/designee.
  
• Maintain a high level of personal expertise and workingknowledge of all aspects of the manufacturing process and process equipmentthrough continuous training and development.
  
• Liaise with other groups and individuals to ensureplanning of tasks is effective and linked into the manufacturing process planand site schedule.
  
• Challenge and identify improvements to the safety andenvironmental programmes on site.
  
• Celebrate with use of proactive recognition tools thatinspire teams and individuals you collaborate with.
  
• Take part in shift handovers and tier 1 meetings, raisingconcerns or issues promptly and providing options for resolutions.
  
• Act as an ERT during emergency situation if trained.