Manufacturing Engineer
Contract
contract
14 Nov 2025
Cork City
Turrior AI analysis
Content + Source + Freshness • 16 Dec 2025 • 95% confidence
78 / 100
Offer value
This position offers a compelling salary and strong growth potential within the medical device sector, requiring relevant industry experience.
Pros
- Positions in the medical device industry are in high demand
- Challenging and rewarding work with the opportunity to impact patient care
- Strong focus on compliance and process improvement
Cons
- Requires specific industry experience
- Potentially stressful project timelines
- Can involve extensive documentation and compliance checks
Who it is for
Mid-level / Experienced • On-site
Good fit
- Candidates with a background in medical device manufacturing
- Professionals keen on improving manufacturing processes
- Individuals who thrive in regulated environments
Not recommended for
- Newcomers to the medical device field
- Candidates wanting flexible work arrangements
- Those uncomfortable with documentation-heavy roles
Motivation fit
Desire to contribute to healthcare advancementsInterest in process innovation and optimizationCommitment to quality assurance standards
Key skills
Manufacturing engineeringCompliance knowledgeDocumentation skillsAnalytical thinking
Score: 78/100 AI verified analysis
About the job
We're looking for a Manufacturing Engineer with expertise in the medical device industry on an hourly rate contracting basis. In this role, you'll be a key player in ensuring our manufacturing processes are robust, compliant, and efficient.
Responsibilities:
- Develop and approve validation protocols (IQ, OQ, PQ) and process characterization reports.
- Write, review, and approve Repeat Action Assessments (RAA) and Acceptance Equipment Lists (AELs).
- Update, review, and approve manufacturing instructions (SGOIs) and Manufacturing Execution System (MES) documents.
- Serve as the primary owner for DMR remediation NC/CAPAs as needed.
- Contribute to the completion of all DMR remediation activities, ensuring they are completed within required timelines.
What We're Looking For:
- A minimum of 2+ years of experience in a manufacturing, quality, or new product introduction (NPI) role within the medical device sector.
- Familiarity with medical device manufacturing documentation, including Standard Operating Procedures (SOPs), change control, and process risk assessments (PFMEA).
- Strong understanding of validation documentation (IQ, OQ, PQ) and their application.
- Experience with Design Master Record (DMR) remediation projects is a plus.
