Manufacturing Associate II

Location: Monksland, Athlone

Competitive salary and benefits

Opening date: 27/02/2026

Closing date: midnight 15/03/2026

Day/Evening 16/5 Shifts (8 hr shift x2 shifts per day x5 days Rotation)

37.5 hours per week - Monday to Friday 07:00-15:15 - 14:45-23:00

Are you ready to make a difference in the world of biopharmaceuticals? As a Drug Product Manufacturing Associate II at the Alexion Athlone Manufacturing Facility, you'll play a pivotal role in ensuring operational readiness and excellence. You'll be an expert in various unit operations throughout the Fill Finish manufacturing process, performing batch operations with precision and under limited supervision. Dive into a dynamic environment where your skills will contribute to life-changing medicines.

Accountabilities:

Operate manufacturing equipment and instruments
Complete assigned tasks in a timely manner
Conduct daily activities in an organised, efficient manner
Perform simple, routine, complex, and critical operations
Troubleshoot equipment issues, when necessary
Ensure process equipment is appropriately maintained for operation
Perform and document operations in accordance with cGMP’s
Complete equipment qualification protocols and validation protocols
Routinely draft/develop and revise standard operating procedures, manufacturing batch records, and other documents as required
Recognise, initiate process deviations and perform deviation investigations and closure
Support continuous improvement initiatives by identifying areas needing improvement, recommending strategies for improvement, and implementing those strategies once approved
Embrace Alexion Core Competencies
Maintain training compliance and train other staff
Communicate effectively, written and verbal
Ensure a safe working environment for all staff
Plan daily activities and schedule operations
Interact with other departments
Aseptic Filling with RABS in grade B background
Compounding/Formulation of products
Sterile Filling of vials/syringes using Isolator
Visual Inspection of finished product
Cleaning and Sanitation of equipment
Operation of Parts washers and Autoclaves
CIP/SIP of Vessels
Support regulatory audits
Support all new product/process introductions on site
Perform data collection, compilation, and statistical analysis
Interact with vendors and outside resources
Complete assigned projects
Be the shift lead if required, providing instruction to the team
Troubleshoot and resolve operational problems during processing
Represent Manufacturing in cross-functional initiatives and meetings
Monitor and evaluate process trends and recommend and implement continuous improvement strategies as appropriate
Manage multiple projects independently
Plan and implement complex changes
Perform Environmental monitoring as required
Technical expert for entire area(s)
Interact independently with regulatory agencies
Develop and provide training on complex manufacturing processes
Perform Manufacturing review and approval of critical documents
Develop process validation protocols
Maintain good housekeeping and clean and sanitise classified areas as required
Analyse complex problems and determine and implement solutions

Essential Skills/Experience:

Able to work within and adapt to complex electronic systems such as SAP and EQV
Able to read, write, and converse in English
Have good solid understanding of MS Excel and Word
Ability to work in an intense, fast-paced work environment
Ability to function, with guidance, in a rapidly changing environment while balancing multiple priorities simultaneously
Ability to work independently and as part of a team
2 years + experience in a cGMP biopharmaceutical manufacturing environment

Desirable Skills/Experience:

BA/BSc in a scientific field or equivalent experience

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why this essential worker role works Monday to Friday 07:00-15:15 - 14:45-23:00 (Rotation early/late), onsite. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

At AstraZeneca, you'll find an environment where innovation thrives. Our patient-driven culture encourages exploration of new ideas that have a profound impact on lives. Diversity is valued here, fostering an inclusive atmosphere where life-changing ideas can emerge from anywhere. We celebrate achievements together, ensuring kindness is integral to our ambition to succeed for those in need. Our commitment extends beyond our work, as we take pride in giving back to the communities we serve.

Ready to embark on this exciting journey? Apply now to join our team!

Date Posted

27-Feb-2026

Closing Date

15-Mar-2026

Our 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.

Manufacturing Associate II

Job Description