Production Operator
About Your New Employer
Days and evening shifts available with an expanding medical device company in Galway.
About Your New Job
Responsible for maintaining quality, monitoring and coordinating the necessary resources to ensure that production adheres to all Quality, Delivery, and Safety standards. This person will adhere to the build schedule to meet the product release plans. It is expected the person will be able to perform each of the work steps in the production of the units.
Key Responsibilities
* Assembles product in line with company needs and ensures the quality of the builds
* Investigates any process problems, abnormalities or defects, takes appropriate action and provides documentation
* Works with Operations Line Lead to ensure product release time goals are met.
* Performs incoming, in-process, final inspection, tests and audits per requirements on all supplier components
* Works with quality and engineering team to ensure the product meets requirements.
* Works with Operations Line Lead to coordinates resources and materials to ensure production is maintained.
* Assists with process/equipment validation and data analysis
* Aware of practices and processes utilizing current management tools
* Displays a high degree of teamwork, including completion of co-workers’ tasks where required.
* Assists in drafting all relevant SOP’s and ensures all SOP’s and standards are followed
* In compliance with established procedures, the position requires the completion of all tracking, inventory, processing, and safety documentation
* Oversees WIP and stock inventories
* Actively interacts with team members in support of day-to-day operating requirements.
What Skills You Need
* Leaving certificate minimum with ideally 1 year of medical device experience in production.
* Ability to read, understand, and apply the information contained in written procedures and Material Safety Data Sheets (MSDSs)
* Has knowledge of and is able to perform all jobs within area of oversight
* Must have good written and verbal communication skills and understanding of cGMP regulations. Good procedural writing skills.
* Computer literacy, numeracy and experience with all in-house applications. (e.g. Word, Excel)
* Must have demonstrated ability to work in a team environment
* Must be able to plan, organize, and implement multiple concurrent tasks; Possess a high level of self-motivation
What’s Next?
Click 'Apply Now' for more information or contact eward@sigmar.ie for more information.
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