Manufacturing Associate V - Nights

Alexion Pharmaceuticals, Inc.; Ireland; On-site; EUR 40,000 - 50,000; Full time

Job summary

A leading pharmaceutical company in Ireland is seeking a Manufacturing Associate V for permanent night shifts. The role involves implementing production schedules, completing batch records, and driving process improvements in a dynamic aseptic manufacturing environment. Essential skills include knowledge of automation systems like SAP and experience in cGMP Aseptic Filling processes. Applicants should exhibit strong communication skills and leadership qualities to mentor colleagues and maintain production schedules.

Benefits

Flexible working hours

Supportive environment for career growth

Qualifications

• Experience with SAP and Trackwise systems.
• Proven experience in a cGMP Aseptic Filling environment.
• Ability to work independently and in a team.

Responsibilities

• Perform core production tasks in various manufacturing areas.
• Engage in continuous improvement initiatives.
• Train colleagues in SOPs and process execution.

Skills

Understanding of process automation

Knowledge of Vial/Syringe Filling

Aseptic equipment familiarity

Communication skills

Independent work capability

Leadership experience

Education

BA/BSc in a scientific subject area

Job description

Manufacturing Associate V - Nights

Reports to: Manufacturing Supervisor

Location: Monksland, Athlone

Permanent Nights: 37.5 hours per week, 22:45-07:00 Sunday to Friday

Introduction to role:

At Alexion Athlone, we pride ourselves on our groundbreaking aseptic manufacturing facility dedicated to delivering rare and ultra-rare products to patients in need. We are expanding our team to foster a culture of manufacturing excellence, ensuring timely delivery and the highest quality standards. As a Manufacturing Associate V, you will be part of a high-performing team responsible for implementing production schedules using MCS automation, completing paper batch records, SAP materials consumption, routine maintenance checks, and driving continuous improvement in work processes and the environment.

Accountabilities:

• Complete Safety GENBA’s as per schedule, and raise safety events
• Independently perform all core production tasks in areas such as Formulation, Compounding, Pooling, Washing, Autoclaving, Sterilisation, Aseptic Filling, Visual Inspection, and equipment preparation.
• Develop individual specialisms as subject matter experts and display technical leadership by acting as a 'Champion' to drive improvements within the manufacturing operation.
• Embrace 5S and lean culture
• Support continuous improvemnet initiative
• Complete tasks according to SOPs and batch records in a cGMP environment with attention to detail and excellent documentation skills per ALCOA+ principles.
• Assist with operations deviations investigations through the QMS system and engage with relevant personnel.
• Train colleagues in SOPs, process execution, and equipment operation.
• Provide input into the creation and maintenance of area SOPs and batch records.
• Assist in Facility and Equipment start-up and Validation activities, providing input on equipment installation, operation, and troubleshooting.
• Serve as an 'Area lead,' providing leadership in the absence of the Manufacturing Supervisor.
• Demonstrate SME knowledge and experience in at least one area of operations.
• Lead process improvements within said area.
• Anticipate and troubleshoot operational issues and interface effectively with MCS.
• Engage with stakeholders including Technical Services, QA, and Automation colleagues to resolve issues.
• Organize work teams locally and maintain schedules.
• Mentor others and impart knowledge effectively.
• Set a positive example in EHS, GMP, and productivity.
• Act as designee for shift handovers and reporting out to DP LT/TS/Eng.
• Lead investigations/Change controls if required.
• Demonstrate a Lean mentality and lead by example.

Essential Skills/Experience:

• Ability to work within complex electronic systems such as process automation, SAP, and Trackwise investigation system.
• In-depth knowledge of Vial/Syringe Filling manufacturing processes and documentation such as batch records and SOPs.
• Familiarity with Aseptic equipment and systems like RABS, Isolators, glass washers, GIT’s, FIT’s, Capping, CIP&SIP of Vessels, VI machines, and WFI systems.
• Working knowledge of Grade A, B & C Manufacturing Environments.
• Knowledgeable of current Good Manufacturing Practices (cGMPs) and regulatory requirements.
• Strong verbal and written communication skills.
• Perform MBR Reviews and deviations.
• Ability to lead an area and motivate others to maintain schedules.
• Highlight production issues and contact relevant departments for support.
• Ability to work independently and as part of a team.
• Proven experience in a cGMP Aseptic Filling manufacturing environment.
• Provide in depth handover of task status
• Escalate issues as required

Desirable Skills/Experience:

• BA/BSc in a scientific subject area or equivalent experience preferred.

Please note: interviews will be held in January 2026

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 22:45-07:00 Sunday to Friday 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's Alexion division, we embrace an opportunity where work transcends the ordinary. Our closeness to patients brings us closer to our work and each other. With a pioneering spirit, we are unique in R&D and healthcare. Here, diversity is valued, inclusion is championed, and life-changing ideas can come from anywhere. We celebrate each other's successes while maintaining kindness as a core value. Join us to make a profound impact on patients' lives while growing your career in a supportive environment.

Ready to make a difference? Apply now to join our team!

Date Posted

17-Dec-2025

Closing Date

06-Jan-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.