Manufacturing Associate III (24-month Fixed Term Contract)

Reports to: Operations Supervisor, Drug Product Operations

Location: Monksland, Athlone

FTC: 4 Cycle, 12.25 hr. Shift, 41.1 hr. Average Work Week (24x7 Operations)

Introduction to role:

Are you ready to make a difference in the world of biopharmaceuticals? As a Drug Product Manufacturing Associate III at Alexion Athlone Manufacturing Facility, you'll play a pivotal role in ensuring operational readiness and delivering batch operations with precision. This position offers the opportunity to become a subject matter expert in various unit operations throughout the Fill Finish manufacturing process. Working on a 24/7 operations shift, you'll be part of a dynamic team dedicated to producing life-changing medicines.

Accountabilities:

• Sterile Filling of vials / syringes using Isolator
• Aseptic Filling with Isolator Technology in Grade C background
• Complete Safety GENBA’s as per schedule, and raise safety events
• Maintain process equipment for operation through Cleaning and Sanitation
• Perform and document operations in accordance with cGMP’s
• Embrace 5S and lean culture
• Support continuous improvement initiatives
• Maintain training compliance and train other staff
• Aseptic Filling with RABS in grade B background
• Compounding / Formulation of products
• Visual Inspection of finished product.
• Troubleshoot and resolve operational problems during processing
• Perform Environmental monitoring as required.
• Maintain good housekeeping and clean and sanitise classified areas as required.

Essential Skills/Experience:

• Able to work within and adapt to complex electronic systems such as SAP and Trackwise
• Able to read, write and converse in English
• Possess a proven 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
• Proven experience in a cGMP biopharmaceutical manufacturing environment
• Provide in depth handover of task status

Desirable Skills/Experience:

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

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 full time 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

Closing Date