At the new Alexion Bulk Drug Substance facility in College Park, Dublin we are constructing a newstate of the artbio-manufacturing facility. We are also building our team to create a manufacturing culture of excellence in everything we do. We will deliver on time for our patients with the highest quality product.
The Bio-Process Technician is a member of a high performing, empowered shift team, responsible for executing productionaccording to schedule using MCS automation, completing electronic batch records, SAP materials consumption, routine maintenance checks and continuous improvement of the work processes and environment.
Principal Responsibilities
Bioprocess technicians will be trained and competent to independently perform all core production tasks in the areas of cell culture, media preparation, purification, bufferpreparationand all ancillary tasks such as equipment preparation.
Bioprocess technicians will also develop anddemonstrateindividual specialisms as subject matter experts andare required todisplay technical leadership by acting as ‘Champion’ to drive improvements and excellence within specific aspects of the manufacturing operation within the shift team.
Responsible for execution of all tasks associated with the preparation for and production of Alexion products in cGMP environment ensuring full attention to detail and excellent documentation skills.
Assistinmaintaininga safe, cGMP compliant work environmentat all times
Responsible for completion of tasks according to SOPs and batch records (paper and electronic).
Perform initial troubleshooting of issuesidentifiedduring routine operations.
Assistwith the investigation of and operations deviations through the QTS system, engaging with all relevant personnel and functions asappropriate
Assistwhere necessary with the training of colleagues in SOPs, processexecutionand equipment operation.
Provide input into the creation and maintenance of area SOPs and batch records.
Seekand implement opportunities for Continuous Improvement.
Use Lean Tools as part of daily operations (Standard Work, 5S, Method 1, 2 etc.) tooptimizeefficiency and drive the culture of Continuous Improvement and Zero Defects
Where necessary assist in any in Facility and Equipment start up and Validation activities. Provide input on equipment installation, start-up, operation and troubleshooting to support introduction of new products into sustaining operations.
Shift working isrequired The shift pattern may be varied according to business requirements and will typically require weekend working and periodic rotation between day and night shifts.
Qualifications
Must beable to work within and adapt to complex electronic systems such process automation,SAPandTrackwiseinvestigation system.
Must have in-depth knowledge of biotech manufacturing processes and their translation into documentation such as batch records and SOPs
Must be familiar with biopharmaceutical equipment and systems such as bioreactors, centrifuges, autoclaves / glass washers, media/buffer systems, and purification systems.
Knowledgeable of current Good Manufacturing Practices (cGMPs) and regulatory requirements.
Mustpossessstrong verbal and written communication skills
Level 1 Entry level BSc. or diploma in a relevant vocational, science or engineering subject.
Level 2 Core Bioprocess Technician role. Requires 3+ years’ external experience in a cGMP biotech or closely allied pharmaceutical manufacturing environment, or 1.5 - 2 years at Level 1 and demonstration ofappropriate competencies
Competencies
Accountability: Holds self and others accountable for delivering results and puts patients first.
Decision Quality: Considers all relevant factors and uses appropriatedecision makingcriteria and communicates these appropriately.
Collaboration: Fosters open dialog and communication.
Cultivates Innovation: Can take a creative idea and put it into practice.
Perspective: Looks toward the broadest possible view of an issue/challenge
Planning: Accurately scopes out length and difficulty of tasks and projects
Problem solving: Uses rigorous logic and methods to solve difficult problems with effective solutions
Drive for results: Can be counted on to exceed goals successfully
Time Management: Can attend to a broad range of activities
Perseverance: Pursues everything with energy, drive, and a need to finish.
Date Posted
24-Jun-2026
Closing Date
07-Jul-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.
Alexion, AstraZeneca Rare Disease is focused on pioneering new possibilities for the rare disease community. We are driven by a mission to change what it means to live with a rare disease.
A leader in rare disease for more than three decades and today continues to build a diversified pipeline across disease areas with significant unmet need, using an array of innovative modalities.
As part of AstraZeneca, Alexion is continually expanding its global geographic footprint to serve more rare disease patients around the world. It is headquartered in Boston, US.
Alexion’s pioneering legacy in rare disease is rooted in being the first to translate the complex biology of the complement system into novel medicines. Alexion pushes boundaries to accelerate discovery of life-changing medicines. Headquartered in Boston, Massachusetts, Alexion has offices around the world and continues to expand its reach to benefit more people globally.
GL/NP/0116
GL/NP/0095
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