Job ID: JOB-12226
Location: Spiddal, Galway
We are looking to speak with experienced Manufacturing Technicians about this great new job opportunity in Galway with one of our leading clients. This company stands out for their culture, exceptional career development pathways and unrivalled rewards and recognition packages.
This exciting new job opportunity in Manufacturing is located in Galway. Galway, voted “Europe most Friendliest City 2020”!
Apply to us to find out more about this great job opportunity in Manufacturing in Galway and we can talk through if it’s the right job for you.
About the Role:
The position requires a proven candidate with a background in providing high-value manufacturing engineering support within a GMP-regulated medical devices industry. Candidates must have a minimum of 3 years of experience in providing process, continuous-improvement and compliance support within an ISO-8 (or higher) clean environment. Due to exciting growth on a number of new product/ technology introductions in 2020, the successful candidate will liaise heavily with cross-functional NPI (new product introduction) teams which can encompass R&D, manufacturing-engineering, maintenance, EH&S, quality-engineering and supply-chain functions. He/ She will work as part of a team to maintain high quality/performance/safety standards on all assigned implant-products. Reporting to the Engineering Manager, the position will be challenging, involve exposure to the latest Tier1- company implant product-designs and will require an ability to work autonomously.
Duties and Responsibilities:
- Provide high-value support to manufacturing operations through daily collaboration with production staff and Manufacturing Engineer supervisors, working with cross-functional colleagues to resolve production floor issues.
- Identify and implement manufacturing projects which improve product quality, reduce lead times and reduce costs.
- Deploy the principles of lean and six sigma in identifying and implementing the optimum areas for improvement in manufacturing operations.
- Assist New Product Introduction (NPI) teams with key input into design for-manufacturing and product flow/layout development. Take ownership for the execution of process qualification related builds.
- Key member of PFMEA-generation workshops.
- Ownership of IQ, OQ, PQ protocol-generation, execution and reporting.
- Maintain, update and review manufacturing, quality and engineering related documentation as required – driving and reviewing all Engineering Change Notice (ECN) proposals.
- Assist with training of product builder staff on key operational tasks.
- Enjoy a multi-departmental approach to problem-solving where everyone has a voice and is respected for their input in driving root-cause-analysis reviews.
- Always strive to meet or exceed the expectations of our customers.
- Perform facility-based EH&S, layout or energy-savings projects as required.
- Overseeing the maintenance and calibration of critical equipment systems.
- There will be a strong linkage with the Quality Assurance department in supporting the Regulatory and Compliance requirements of an ISO13485 organisation. This will encompass NCR and CAPA ownership and resolution.
- Make appropriate decisions daily, using the Manufacturing Manager and Senior Quality Assurance representatives as needed as the final arbitrators on critical quality-related decisions.
- Performs other related duties, as assigned.
Skills and Experience:
- Successful candidate must have a strong track record of execution within in a medical device environment. This role will involve production-support of Tier1-multinational-customer products – and as such, experience is essential.
- A Bachelor’s degree in manufacturing engineering, biomedical engineering, quality engineering, or related field and 3 years’ minimum experience is required.
- Experience in the areas of medical textile technologies (such as polymer/wire-braiding, weaving, knitting etc) and polymer coating/grafting technologies is desirable.
- Strong familiarity with FDA GMP/QSR; ISO 13485 and medical standards is required.
- Experience of transferring products from design into commercialmanufacturing, is highly desirable
- Solid knowledge of PFMEA development, IQ/OQ/PQ validation is required.
- Candidate must be highly motivated and passionate about meeting production targets with excellent time-management, presentation, communication skills, technical writing skills and organizational skills with the ability to work independently or as part of a team.
- Possess strong analytical skills, with a hands-on approach.
- Project management experience is desirable.
For further information on this role please contact Dominic Courtney on 086 8395533 / firstname.lastname@example.org
Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/
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Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.
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