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
As a(n) Snr Quality Systems Engineer, 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:
* Representing Quality function in Site Management meetings as required.
* Acting as a delegate for the Quality Lead.
* Act as Quality Systems Software Validation Lead for site.
* Leading and implementing significant process improvements, projects and cost saving initiatives using data & quality tools to drive quality decisions. Initiating project plans, identifying resource allocations, performing and guiding technical activities such as risk documentation, procedural updates, test methods, process/software validation that have major importance to the business.
* Leading investigations and providing technical guidance to peers in relation to Software Validation, CAPAs and NC and to address compliance issues and providing guidance to engineering. Leading the implementation of robust solutions. Independently assess and provide guidance to Quality and Engineering disciplines.
* Performing and leading Internal and Supplier Audits.
* Facilitating and participating in external regulatory body audits, e.g. ISO and FDA.
Your Skills and Expertise
To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:
* Bachelor’s Degree or higher in Engineering or Science related field (minimum level 8).
* Five (5) years’ experience working in a regulated environment, specifically medical device, FDA or ISO 13485 registered work environments is preferable.
Additional qualifications that could help you succeed even further in this role include:
* Lead Auditor or Internal Auditor certification an advantage.
* Experience with the use of JIRA, Qtest and VERA for documenting software lifecycle is advantageous but not essential.
* Knowledge and experience of Oracle, FactoryTalk applications, PEMAC and Bartender is advantageous.
Work Type: Hybrid Eligible (Job Duties allow for some remote work but required to work onsite 2-3 days per week, in Athlone).
Work Location: Athlone, Co. Westmeath
Travel: May include up to 5% domestic/international
Relocation Assistance: Not authorized
Must be legally authorized to work in 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.
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.
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