Overview
A Senior Manufacturing Bioprocess Associate is sought to provide operational support for manufacturing operations of Late Stage and Launch Pipeline products at a state-of-the-art single-use biotechnology facility in Dunboyne, Ireland. The Dunboyne facility will provide Biologics Drug Substance manufacturing for Clinical Supply, Registration & Commercial Launch and is designed for multi-product operation with flexibility to adapt to pipeline changes. The facility aims to attract and include people from diverse backgrounds and perspectives, fostering a sense of belonging and ownership among staff.
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 key requirements.
* 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.
What Skills You Will Need
* 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 Single-Use 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 contact the Talent Acquisition Advisor assigned to this role if you need any support during the recruitment process.
We are committed to flexible working where possible and have introduced a hybrid working model for office-based colleagues. Please speak to us about what flexibility means to you during your application.
How to Apply
If you are ready to invent solutions to meet unmet healthcare needs, please apply today.
Current Employees apply here.
Current Contingent Workers apply here.
Search Firm Representatives: Merck & Co., Inc. does not accept unsolicited assistance from search firms for employment opportunities. No fee will be paid if a candidate is hired as a result of an agency referral where no pre-existing agreement is in place. Please, no phone calls or emails.
Employee Status: Regular
Relocation: Not Applicable
VISA Sponsorship: Not Applicable
Travel Requirements: Not Applicable
Flexible Work Arrangements: Not Applicable
Shift: Not Specified
Valid Driving License: Not Specified
Hazardous Material(s): Not Specified
Required Skills: Adaptability, Biopharmaceutical Manufacturing, Contamination Control, Continuous Flow, Data Analysis, Equipment Maintenance, GMP Compliance, Manufacturing Operations, Master Batch Records, Organizational Compliance, Pharmaceutical Process Development, Production Planning, Production Support
Preferred Skills: Not specified
Job Posting End Date: 09/29/2025
Requisition ID: R355493
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