Within a manufacturing function you will be performing tasks supporting the manufacturing operations of both clinical and commercial manufacturing programs at Regeneron Ireland.
Working a shift pattern in a fully gowned, cleanroom environment, a typical shift might include, but is not limited to, the following :
Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors
Ensuring all associated documentation such as manufacturing batch records & logbooks are completed, accurate and verified in accordance with SOPs and cGMP Standards
Performing Equipment Cleaning, Preparation and Execution as well as completing associated documentation
Critical to the role is adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks
Performing various tests and in-process sampling
Maintaining housekeeping in designated area and adhering to the hygiene standards of the facility
Ensuring all required training is up to date and completed in a timely manner
This role might be for you if :
You enjoy working in a team that brings out the best in each other
You like tackling problems that need solving, using your verbal and written communication skills to ask questions and adapt quickly
You can adhere to the letter and spirit of policies and regulations
You can adapt to a changing environment and have the ability to adhere to a process-driven schedule
To be considered for this opportunity you must have a Leaving Certificate qualification to include maths and a science or engineering subject as a minimum or equivalent qualification.
Experience working shift in a GMP (Good Manufacturing Practice) environment / industry is preferred but not essential.
IREADV #JOBSIEST #LI-Onsite #REGNIEEC
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