Sr. Tech, Operations

Overview
Job Description
A fantastic opportunity has arisen for a Senior Manufacturing Bioprocess Associate to provide operational support for manufacturing operations of our Late Stage and Launch Pipeline products at our new state of the art single use biotechnology facility in Dunboyne, Ireland.
Our facility in Dunboyne, Co.
Meath is a premier, state-of-the-art facility that enables and advances our best work.
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.
Our Dunboyne 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.
Our Dunboyne facility serves as a magnetic force that attracts, recognizes, and integrates people of diverse backgrounds and perspectives.
Employees will feel not only that they belong in the Dunboyne, but that the facility belongs to and is shaped by them.
Responsibilities
The Senior Manufacturing Bioprocess Associate will support end-to end production operations for both Fed Batch and Continuous Manufacturing.
Operate equipment according to electronic batch records, sampling plans and standard operating procedures.
Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
Ability to solve problems with a desire to continuously learn, improve and develop.
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.
Qualifications and Skills
Level 7 qualification in a science or engineering discipline desired.
A level 6 with a minimum of 3+ years' experience in a GMP Manufacturing requirement shall be deemed equivalent.
Competent in troubleshooting and show practical problem-solving capabilities.
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.
Proficiency in various SingleUse technologies in a manufacturing environment
Commissioning and Qualification experience
Understanding of Upstream and Solution Preparation Unit Operations
Understanding of both continuous and batch fed manufacturing processes.
We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.
As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.
Please do not hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.
We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.
Please feel free to speak to us about what flexibility means to you during your application.
Applying
So, if you are ready to invent solutions to meet unmet healthcare needs, please apply today.
Current Employees apply without links.
Current Contingent Workers apply without links.
Requisition ID: R355493
Job Posting End Date: 09/29/2025
Employee Status: Regular
Relocation: Not specified
VISA Sponsorship: Not specified
Travel Requirements: Not specified
Flexible Work Arrangements: Not Applicable
Shift: Not specified
Valid Driving License: Not specified
Hazardous Materials: Not specified
Required Skills: Adaptability, Biopharmaceutical Manufacturing, Contamination Control, Continuous Flow, Data Analysis, Equipment Maintenance, GMP Compliance, Good Manufacturing Practices (GMP), Manufacturing Operations, Master Batch Records, Material Selection, Organizational Compliance, Pharmaceutical Process Development, Production Planning, Production Support
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