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.

Job Description:

3M Health Care is now Solventum

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long Legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.

We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.

The Impact You'll Make in this Role
Providing Quality support to processes, materials, and products; Assuring Quality standards are maintained; Assist with the implementation of and compliance to the Quality Management program and for supporting company goals, objectives, policies, procedures, quality systems and compliance with regulatory requirements.

As a Quality Lead, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

• 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.

Your Skills and Expertise

To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:

Education:

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

Experience:

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

Skills:

• Strong computer skills (MS Excel, PowerPoint, 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.

Work location:

• Onsite - Athlone, Ireland

Work Type - Shift:

• The role will be on a 2 cycle shift.

• Mon- Web 7pm-7am and Mon - Thursday 7-am -7pm.

Travel:

• Flexible and available to support business need, as required

Must be legally authorized to work in country of employment without sponsorship for employment visa status (eg, H1B status).

Supporting Your Well-being

Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.

Diversity & Inclusion

(*) We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, gender, sexual orientation, age, civil status, disability, family status, or membership of the travelling community.

Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.

Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain of @solventum.com. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.

Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.

Solventum Global Terms of Use and Privacy Statement

Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.

Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with the
terms.