Manufacturing Associate II

Manufacturing Associate IILocation: Monksland, Athlone Competitive salary and benefitsContract: Permanent ContractShifts Initially: 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 - 14:45-23:00Moving to: 4 Cycle, 12.25 hr. Shift, 41.1 hr. Average Work Week (24x7 Operations) in Q2 2027Are 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 instrumentsComplete assigned tasks in a timely mannerConduct daily activities in an organised, efficient mannerPerform simple, routine, complex, and critical operationsTroubleshoot equipment issues, when necessaryEnsure process equipment is appropriately maintained for operationPerform and document operations in accordance with cGMP’sComplete equipment qualification protocols and validation protocolsRoutinely draft/develop and revise standard operating procedures, manufacturing batch records, and other documents as requiredRecognise, initiate process deviations and perform deviation investigations and closureSupport continuous improvement initiatives by identifying areas needing improvement, recommending strategies for improvement, and implementing those strategies once approvedEmbrace Alexion Core CompetenciesMaintain training compliance and train other staffCommunicate effectively, written and verbalEnsure a safe working environment for all staffPlan daily activities and schedule operationsInteract with other departmentsAseptic Filling with RABS in grade B backgroundCompounding/Formulation of productsSterile Filling of vials/syringes using IsolatorVisual Inspection of finished productCleaning and Sanitation of equipmentOperation of Parts washers and AutoclavesCIP/SIP of VesselsSupport regulatory auditsSupport all new product/process introductions on sitePerform data collection, compilation, and statistical analysisInteract with vendors and outside resourcesComplete assigned projectsBe the shift lead if required, providing instruction to the teamTroubleshoot and resolve operational problems during processingRepresent Manufacturing in cross-functional initiatives and meetingsMonitor and evaluate process trends and recommend and implement continuous improvement strategies as appropriateManage multiple projects independentlyPlan and implement complex changesPerform Environmental monitoring as requiredTechnical expert for entire area(s)Interact independently with regulatory agenciesDevelop and provide training on complex manufacturing processesPerform Manufacturing review and approval of critical documentsDevelop process validation protocolsMaintain good housekeeping and clean and sanitise classified areas as requiredAnalyse complex problems and determine and implement solutionsEssential Skills/Experience:Able to work within and adapt to complex electronic systems such as SAP and EQVAble to read, write, and converse in EnglishHave good solid understanding of MS Excel and WordAbility to work in an intense, fast-paced work environmentAbility to function, with guidance, in a rapidly changing environment while balancing multiple priorities simultaneouslyAbility to work independently and as part of a team2 years + experience in a cGMP biopharmaceutical manufacturing environmentDesirable Skills/Experience:BA/BSc in a scientific field or equivalent experienceWhen 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 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 Posted03-Sept-2026Closing Date16-Sept-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.