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:
Quality Technician
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
As a Quality Technician, 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 providing quality system support to the Solventum Morden manufacturing site
Tasks / Systems within scope (as assigned):
- Release finished product for sale by DHR review, perform quality audits on finished product
- Assemble and maintain device history records for all medical products.
- Support NCN investigations.
- Perform incoming components inspection and release for all raw materials.
- Perform product testing.
- Maintain 5S environment in lab and in office areas.
- Support the Morden CAPA (Corrective action, Preventive action) system.
- Support the Morden CAPA (Corrective action, Preventive action) system – act as database coordinator
- Administer the Document Control System under the Morden Quality Management System as follows: maintain documentation database, create and revise standards as required, administer routing for signatures/approvals, distribute final standards. Maintain status of documentation as current and in compliance by annual review of all documentation for accuracy.
- Support Internal auditing system by provide maintaining certification and performing as a qualified auditor.
Your Skills and Expertise
To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:
- High School Diploma/GED or higher from an accredited institution
- Experience working in a Medical Device manufacturing environment.
In addition to the above requirements, the following are also required:
- Experience in one or more of the following environments: Quality, technical, lab, manufacturing and/or plant (course work and internships considered)
Additional qualifications that could help you succeed even further in this role include:
- Familiarity with manufacturing processes
- Demonstrated experience conducting quality systems audits
- Strong customer focus and consultative skills, with a proven ability to develop solutions to difficult problems.
- Excellent written, verbal, presentation, and interpersonal communication skills
- Strong analytical, decision-making, and problem-solving skills
- Statistical knowledge and practice with Gage Repeatability and Reproducibility (R&R) studies, Statistical Process Control (SPC) and Process Capability, Sampling Plans, Design of Experiments (DOE), Analysis of Variance (ANOVA) and Regression, Process and Product Understanding (PPU), and Lean Manufacturing
Work location:
Travel: May include up to 10% domestic/international travel
Relocation Assistance: Is not authorized.
Must be legally authorized to work in the country of employment without sponsorship for employment visa status (e.g., 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.
Solventum Canada welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.
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
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