Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

• Perform Incoming Inspection
• Perform DHR Review
• Perform Product Release
• Perform Internal/GMP Audits
• Perform complaint documentation reviews.
• Coordinate & perform routine environmental sampling, monitoring & trending
• Coordinate the collection of samples for QDA testing
• Control of Non-conforming material
• Assist in the development, analysis and improvement of site Quality Metrics
• Assist in the issuance, review and processing of NCMRs
• Assist in the analysis and resolution of problems
• Assist in the review and update of Work Instructions
• Assist in the execution of process validations
• Assist in the development and update of process FMEAs
• Provide Quality support to Manufacturing
• Ensure continuous compliance for Product Manufacturing, Packaging and Labelling.
• Will abide to Environmental, Health and Safety (EHS) Policies and any relevant other EHS documentation.
• Will comply with all relevant training required and adhere to relevant associated documentation.
• Follow strict adherence to the requirements of CGMP.
• Actively contribute to the enhancement of compliance initiatives for areas of responsibility.

• Qualification in Quality, Science or Engineering, and/or relevant experience.

• Three (3) years’ experience working in a regulated environments, specifically medical device, FDA or ISO 13485 registered work environments is preferrable.

• Strong computer skills (MS Excel, Power Point, Word etc.)
• Familiarity with statistical tools such as Pareto charts and trend charts.
• Familiarity with root cause analysis tools.
• Ability to effectively communicate, both verbally and in writing, to both non-technical and technical associates.

• Onsite – Athlone, Ireland

• The role will be on a 2 cycle shift.
• Mon- Wed 7pm-7am and Mon – Thursday 7-am -7pm.

• Flexible and available to support business need, as required