Quality Engineer

Sentior, Ltd.; Limerick; Hybrid; EUR 52,000 - 74,000; Full time

Benefits offered by this job

Competitive hourly rate

Job summary

Johnson & Johnson Vision in Limerick is seeking a Senior Quality Engineer to lead quality system design, audits, and compliance assessments across manufacturing processes. You will drive improvements using GMP, ISO standards and SPC-based analytics, and coordinate with cross-functional teams on new product introductions and process transfers.

The role requires a degree in science or engineering with 3–5 years in medical devices/pharma, CAPA/RCI experience, and strong data analysis skills.

Qualifications

• Degree qualified in science or engineering field.
• 3–5 years of relevant experience in Medical Devices/Pharmaceutical industry for senior level.
• Experience with GMP, ISO, and process excellence tools desirable.

Responsibilities

• Lead quality system design and audits, and support steady-state manufacturing.
• Drive data-driven quality improvements and monitor quality systems.
• Oversee CAPA, NCR, audits, and management reviews; report metrics to leadership.

Skills

Statistical analysis

Quality tools

Cross-functional collaboration

Education

Degree in science or engineering

Tools

Minitab

Excel

pFMEA

SE

SPC

Job description

ICTZZP toegestaan# Quality EngineerJohnson & Johnson Limerick 3 maandenGepubliceerd 1 uur geleden · Opportunity ID: 1061434Tarief indicatie —Uren 40 u/wStart 30 Nov 2026Duur 3 maandenInteresse in deze opdracht?## De opdrachtSenior Quality EngineerLocation: LimerickDuration: 12 MonthsHours: 39Provides leadership and support to root cause investigation activities, and ensures good QualityEngineering practices are used in investigations. Drives continuous improvement through data driven approaches and monitoring of quality systems.Roles and Responsibilities- Provides complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes- Utilizes multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), equipment engineering system (EES), and international organization for standardization (ISO).- Addresses and corrects product and process complaints.- Reports on contract manufacturer performance metrics and ensures management reviews.- Oversees audits of all quality system categories to assess compliance to process excellence standards.- Ensures comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, presenting reports to management - Handles complex technical issues for manufacturing processes that are to be transferred to satellite facilities.- Responsible for supporting the activities of Operations/Engineering/information management in building quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness- Leads and executes upgrades to Quality System- Support QA programs in assuring compliance to the pertinent regulation - Identify and lead cost and technical improvements under the departments’ continuous improvement program.- Provide key inputs and leadership into transformational process developments.- Project Management - provide timely and accurate reporting on project activities.- New Product Introductions & Product Transfers- Lead or actively participate in cross-functional teams to ensure New Product Introduction/Research and Development projects are completed in a timely and efficient manner.- Actively interfacing with cross-functional team members, always practicing good team work in support of day to day operating requirements.- Demonstrate strong leadership and a clear identifiable work ethos within the team.- Develop and maintain a Credo & Behavioural Standards based culture within the group.- Ensure effective closure on Quality System documents (Audit Actions, NCR’s, CAPA’s, Maps, etc).- Ensure all process developments, NPI etc are managed in accordance with the Quality management system.- Implementation of safety/environmental requirements on purchase of all new equipment.- Work with team leader to develop and implement strategic engineering Goals & Objectives.- Support the implementation of all engineering and plant strategic initiatives.- All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform- Maintains and develops risk management lifecycle.- Ensuring continuous improvement and understanding of measurement systems used on-site , driving down variance in test methodology.- Develops site knowledge on manufacturing process knowledge, and monitors inputs and outputs to the processes , and implements and drives corrective actions. - Sustains and advocates Credo based standards in all aspects of work.- Supervise others if requiredHow to SucceedEssential Requirement for Quality Engineer- Degree Qualified with science or Engineering DegreeEssential Requirements for Senior Quality Engineer- Degree Qualified with science or Engineering Degree with 3-5 years relevant experience in Medical Devices/ Pharmaceuical IndustryDesirable- Excellent working knowledge of process excellence / QE tools such as pFMEA , SE , statistical analysis , SPC- Excellent IT skill eg , experience in minitab , excel reports- CAPA and RCI experience- Risk management experience- Automated process controls experience - Good presentation skills- Supervision of othersBenefitsThis role offers a very competitive hourly rate. This contract will run for 12 months.about Johnson & Johnson VisionJohnson & Johnson Vision brings together cutting-edge insights, science, technology and people. We partner with eye care professionals and help more people around the world preserve and restore sight. Our portfolio includes the best selling contact lens brand in the world, ACUVUE, plus consumer eye health solutions, dry eye treatments, refractive (Lasik) and cataract products. Contribute to the next healthcare breakthrough, create a world connected by SIGHTTM with your next project at Johnson & Johnson Vision. https://jnjvisionpro.co.uk/Application ProcessWe are looking to process the first round of applications within the next 2 working days.We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, LTD & Umbrella options are available. Diversity, Equity & InclusionFor more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.