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Quality Technician REQ 1547

HID Global Corporation

Galway
22 days ago
Galway
22 days ago

Quality Technician REQ 1547

 

Securing your Future!

Build the future of digital identity! HID Global is a company that is ultimately involved in the dynamic and ever growing world of access control technology. Every day, we create the most innovative global authentication solutions for a variety of customer applications. We are a diverse, multidisciplined, growing multinational technical company that offers its employees a fun work environment, flexibility and career opportunity. We are the Evolution of Authentication.

 

What you will be part of:

HID Global powers the trusted identities of the worlds people, places and things. We make it possible for people to transact safely, work productively and travel freely. Our product and services are used by millions of people around the world to navigate their everyday lives.

 

Working at HID:

HID Global is an innovative fast paced organisation, with many possibilities to make a difference and add value. We empower our employees to achieve great things by taking ownership of their future career.

We value diversity and endorse an open-minded collaborative working environment. We are a company with integrity at our core. HID Global are committed to our employee engagement offering a range of employee benefits and  initiatives with events and activities happening all the time.

 

The Position:

You will be expected to inspect and test HID products, assemblies, subassemblies, components, parts and cards for conformance to specifications in accordance with written inspection instructions, procedures or verbal instructions.

This role will be working closely with the leadership team to identify and manage all supports required for value stream quality related tasks. You will collect and prepare data to ensure critical KPIs and data is available on a daily, weekly and monthly basis. As well as have the ability to communicate up and down the organisation to ensure KPIs and projects are being met as expected. 

This person will be responsible for raising SARs as appropriate for major supplier issues. You will manage and monitor for MRB reports and RMA transactions and analysis.

 

What we are looking for:

The ideal person will provide leadshership, guidance and support to technicians and inspectors. Ideally this person would have 5 years experience as a quality inspector in a simular role. They would be educated with a certificate or Diploma in quality or engineering discipline or equlivant. They would have experience of the following skills : metrology ,calibration, data collection and graphs, corrective action, DMAIC tools and supplier scorecards.

You will have excellent communication skills both verbally and writen in the English langage and will be able to demonstrate advance skills in data collection and analysis.

There are high customer expectations in this role and the ideal person would understand the customers requirements and also understands the consequences of inaccurate data. They will promote the importance of customer quality and report any issues that potentially will impact customers.

 

Why you should apply:

  • Excellent terms and conditions
  • Flexibility
  • On the job training and development
  • Work as part of a global team

Final Application Date: 17th February 2021

*No 3rd party agency engagement required for this role*

HID Global is an equal opportunities employer

HID Global powers the trusted identities of the world’s people, places and things. We make it possible for people to transact safely, work productively and travel freely. Our trusted identity solutions give people secure and convenient access to physical and digital places and connect things that can be accurately identified, verified and tracked digitally. Millions of people around the world use HID products and services to navigate their everyday lives, and over 2 billion things are connected through HID technology. We work with governments, educational institutions, hospitals, financial institutions, industrial businesses and some of the most innovative companies on the planet. Headquartered in Austin, Texas, HID Global has over 4,000 employees worldwide and operates international offices that support more than 100 countries. HID Global® is an ASSA ABLOY Group brand. For more information, visit www.hidglobal.com

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Manufacturing Engineer NPI/Projects

Sigmar

Galway, Galway
17 days ago
Galway, Galway
17 days ago

Manufacturing Engineer

Come join a company who is passionate about saving lives, developing the newest technologies for the treatment of some of healthcare’s toughest problems and the lives of their employees.

My client, a leading medical device company based in Galway, are seeking enthusiastic, technical and hard-working engineers to join their Manufacturing teams.

We have positions available in NPI, Projects and Line Support.

What they can offer you:

  • A Career with a Meaningful Purpose
  • A Collaborative Culture
  • A defined Career Development plan
  • The Opportunity to Develop and Innovate
  • Competitive Benefits
  • An excellent Work-Life Balance
  • Dedicated Corporate Social Responsibility

Your Responsibilities:

  • Troubleshoots new products / process working closely with product development.
  • Continually seeks to drive / improvements in process design, layout and operational performance.
  • Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements.
  • Actively promotes and participates in a cross -functional teamwork environment.
  • Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
  • Gives technical guidance to Associate Engineers and technicians.
  • Is an influential team member, fully motivated to achieve and demonstrate best practices in line with the department and Site objectives.
  • Demonstrate a primary commitment to patient safety and product quality.
  • Understands and comply with all the regulations governing the quality systems.

 

Your Background/Skills:

  • A Level 8 Degree (240 Credits) or equivalent in an Engineering or Science related discipline.
  • A minimum of 2-4 years’ experience working at Engineering level, ideally within the Medical Device industry or another highly regulated environment.
  • Project Management experience desirable but not essential.

For more information, please contact Emma on 091 455 307.

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.

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Extrusion Technician

Nordson

Galway
28 days ago
Galway
28 days ago

Collaboration drives Nordson’s success as a market leader in Industrial Precision Solutions and Advanced Technology. Our employees thrive in an environment where we help each other reach our personal best and enable our company to continuously improve and grow, and our customers to succeed. You will find Nordson employees sharing our success by giving back in the communities around the world where we live and work.

Nordson MEDICAL designs, engineers and manufactures complex devices and components with applications in wound healing, surgical and minimally invasive, fluid management, pulmonology and interventional and structural heart.Our pioneering Advanced Polymers team was the first to manufacture and supply medical balloons to the medical device industry. Nordson MEDICAL workswithdoctors, start-ups and large medical companies around the world at any point in the product lifecycle, from concept to launch and beyond. 

Purpose of position:

As an Extrusion Technician you will be involved with identifying, developing and introducing new extrusion technology. Liaising with sales, customers and suppliers and internal product design engineers to specify customer requirements with regards to dimensions, performance criteria and materials. Liaising with production to ensure extrusion equipment and processes are in place and capable. You also will be involved with the introduction of new equipment/technologies or new processes into the extrusion area or other assigned projects.

Principal Duties and responsibilities:

Manage, develop and validate new extrusion process including running extrusion trials for new product /product iterations and new technology to demonstrate capability and meet KPI’s.

Identify, specify, introduce, manage and validate new equipment and technologies in the extrusion area. Provide technical input and leadership on problem solving, resolve technical processing issues and implement process improvements in the extrusion dept.

Provide product line support for the engineering & production extrusion dept. creates documentation for extrusion equipment and process. Plan, write and execute validations for extrusion component process and technology. Control new product/process/technology introductions or changes and maintain records in accordance with the Nordson Medical quality systems to the requirements of ISO 13485 and FDC 21 CFR

Continually attain technical expertise in extrusion technologies and new materials and communicate and train extrusion personnel. Support the development of new business by working with internal design engineers, sales and customers on product and process development including costing review, feasibility studies, project timelines and technical capability assessments.

Drive the Nordson medical centre of extrusion excellence by relentlessly focusing on continuous improvement in processes, capability, equipment and business processes as well as identification of advancements in materials or equipment appropriate to be introduced to Nordson Medical.

Introduce improvement initiatives as assigned including investigations, trouble shooting, driving effective determination of root cause and championing a structured approach to problem solving using lean tools and 6 sigma principals.

Person Specification:

  • Primary degree or equivalent in Polymer, manufacturing or mechanical engineering;

  • 8 to 10 years Extrusion process experience;

  • 3 to 5 years Medical device or manufacturing experience is essential;

  • Hands on experience in extrusion and plastics material knowledge are essential;

  • Be a self-starter with good motivational and inter-personal skills;

  • A Practical level-headed individual with strong technical ability.

Travel: Less than 5% (other Nordson divisions and customers)

Collaboration drives Nordson’s success as a market leader in Industrial Precision Solutions and Advanced Technology. Our employees thrive in an environment where we help each other reach our personal best and enable our company to continuously improve and grow, and our customers to succeed. You will find Nordson employees sharing our success by giving back in the communities around the world where we live and work.

Nordson MEDICAL designs, engineers and manufactures complex devices and components with applications in wound healing, surgical and minimally invasive, fluid management, pulmonology and interventional and structural heart.Our pioneering Advanced Polymers team was the first to manufacture and supply medical balloons to the medical device industry. Nordson MEDICAL workswithdoctors, start-ups and large medical companies around the world at any point in the product lifecycle, from concept to launch and beyond. 

Purpose of position:

As an Extrusion Technician you will be involved with identifying, developing and introducing new extrusion technology. Liaising with sales, customers and suppliers and internal product design engineers to specify customer requirements with regards to dimensions, performance criteria and materials. Liaising with production to ensure extrusion equipment and processes are in place and capable. You also will be involved with the introduction of new equipment/technologies or new processes into the extrusion area or other assigned projects.

Principal Duties and responsibilities:

Manage, develop and validate new extrusion process including running extrusion trials for new product /product iterations and new technology to demonstrate capability and meet KPI’s.

Identify, specify, introduce, manage and validate new equipment and technologies in the extrusion area. Provide technical input and leadership on problem solving, resolve technical processing issues and implement process improvements in the extrusion dept.

Provide product line support for the engineering & production extrusion dept. creates documentation for extrusion equipment and process. Plan, write and execute validations for extrusion component process and technology. Control new product/process/technology introductions or changes and maintain records in accordance with the Nordson Medical quality systems to the requirements of ISO 13485 and FDC 21 CFR

Continually attain technical expertise in extrusion technologies and new materials and communicate and train extrusion personnel. Support the development of new business by working with internal design engineers, sales and customers on product and process development including costing review, feasibility studies, project timelines and technical capability assessments.

Drive the Nordson medical centre of extrusion excellence by relentlessly focusing on continuous improvement in processes, capability, equipment and business processes as well as identification of advancements in materials or equipment appropriate to be introduced to Nordson Medical.

Introduce improvement initiatives as assigned including investigations, trouble shooting, driving effective determination of root cause and championing a structured approach to problem solving using lean tools and 6 sigma principals.

Person Specification:

  • Primary degree or equivalent in Polymer, manufacturing or mechanical engineering;

  • 8 to 10 years Extrusion process experience;

  • 3 to 5 years Medical device or manufacturing experience is essential;

  • Hands on experience in extrusion and plastics material knowledge are essential;

  • Be a self-starter with good motivational and inter-personal skills;

  • A Practical level-headed individual with strong technical ability.

Travel: Less than 5% (other Nordson divisions and customers)

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Manufacturing Engineer NPI/Projects

Sigmar

Galway, Galway
17 days ago
Galway, Galway
17 days ago

Manufacturing Engineer

Come join a company who is passionate about saving lives, developing the newest technologies for the treatment of some of healthcare’s toughest problems and the lives of their employees.

My client, a leading medical device company based in Galway, are seeking enthusiastic, technical and hard-working engineers to join their Manufacturing teams.

We have positions available in NPI, Projects and Line Support.

What they can offer you:

  • A Career with a Meaningful Purpose
  • A Collaborative Culture
  • A defined Career Development plan
  • The Opportunity to Develop and Innovate
  • Competitive Benefits
  • An excellent Work-Life Balance
  • Dedicated Corporate Social Responsibility

Your Responsibilities:

  • Troubleshoots new products / process working closely with product development.
  • Continually seeks to drive / improvements in process design, layout and operational performance.
  • Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements.
  • Actively promotes and participates in a cross -functional teamwork environment.
  • Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
  • Gives technical guidance to Associate Engineers and technicians.
  • Is an influential team member, fully motivated to achieve and demonstrate best practices in line with the department and Site objectives.
  • Demonstrate a primary commitment to patient safety and product quality.
  • Understands and comply with all the regulations governing the quality systems.

 

Your Background/Skills:

  • A Level 8 Degree (240 Credits) or equivalent in an Engineering or Science related discipline.
  • A minimum of 2-4 years’ experience working at Engineering level, ideally within the Medical Device industry or another highly regulated environment.
  • Project Management experience desirable but not essential.

For more information, please contact Emma on 091 455 307.

Following your application for this specific role, Sigmar may contact you regarding other positions that we feel you may be suitable for. If you do not wish to be contacted about other opportunities please let us know. For further information please refer to the Privacy Statement on our website.

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Quality Engineer (Projects) - Galway Job (Galway, G, IE)

Boston Scientific

Galway
18 days ago
Galway
18 days ago

There's never been a better time to be a part of Boston Scientific. This is an exciting moment: when our legacy of industry leadership intersects with the promise of a brilliant future. Today, we're 23,000 colleagues strong, with an impressive portfolio of 13,000 products. We’re at the forefront of the medical device industry – leading, evolving and transforming it into bolder and more amazing territories.

We are currently recruiting for an experienced Quality Engineer to join our Galway site on a fixed term basis with view to permanency.

 

Purpose

 

Demonstrates commitment to the Quality Policy (patient safety and product quality) through their daily execution of sound quality practices and the maintenance of an effective quality system.  Understands  and complies with all the regulations governing the quality systems. Ensures their direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work.

 

Responsibilities

  • Identifies and resolves complex exceptions to work assignments.
  • Summarizes, analyses, draws conclusions and makes appropriate decisions from test results or other process related findings.
  • Has the responsibility and independent authority to make decisions related to product quality, including the disposition of non-conforming product.
  • Participates in Customer Complaints investigation for areas under their control.
  • Continually seeks to drive improvements in product and process quality.
  • Knowledgeable on QSR and ISO/MDD standards, constantly promoting awareness of best industry practices, making appropriate decision on a daily basis utilizing the quality engineering manager/site QA Director as the final arbitrator on critical quality decisions.
  • Fully conversant with validation techniques and associated regulatory requirements including analysis of customer feedback and complaints.
  • Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
  • Knowledgeable on Risk Management , BSEN 14971 requirements.
  • Compiles and analyses operational, test and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.
  • May participate directly in a new product/technology transfer to ensure compliance to all internal and regulatory requirements.
  • Uses knowledge of Six Sigma, Statistical Analysis and Lean principles to investigate and solve problems and improve quality.
  • Gives technical guidance to Associate Quality Engineer, Technician and Inspection staff.
  • Is a good team member, fully motivated to achieve and demonstrate best practices in line with the department and Site objectives.
  • Deals with suppliers, other engineering disciplines within and outside of the Site and customers should the need arise.
  • Is familiar with the internal auditing process

Qualifications and Experience:

  • NFQ Level 8 (240 Credits) qualification in a STEM discipline
  • Minimum of 3-4 years experience in a Quality Engineering capacity.
  • Good technical capabilities, communication skills, teamwork abilities and initiative.
  • Proven ability to work well both as part of a team but also able to work on own with minimum supervision.
  • Proven ability to work well as part of a team & on own with minimum supervision.

     

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Manufacturing Engineer I / II Galway Job (Galway, G, IE)

Boston Scientific

Galway
9 days ago
Galway
9 days ago

 

For more than 30 years, Boston Scientific has advanced the practice of less-invasive medicine.  The Company's products help physicians and other medical professionals improve their patients' quality of life by providing alternatives to surgery.  Since 1994, employees in Galway have been at the forefront of some of these truly innovative medical device designs and manufacturing. 

Job Purpose

Provide scientific understanding and technical engineering skills to meet business goals and objectives. Ability to coach, lead and enhance the productivity of technical reports within the business. Provide a structured framework for training of technical reports. Build collaborative relationships through strong teamwork across the organization.

 

Key Responsibilities

  • Providing technical leadership on product and process issues.
  • Leading technical improvement under the team’s VIP program.
  • Transferring and implementing processes either from development or from another manufacturing facility.
  • Liaison with quality and engineering both internal to the plant and externally within the corporation.
  • Participation, where appropriate, in the phase review process and the NPE meetings with respect to new products.
  • Ongoing manufacturing support in order to help the team meet its business objectives of quality, output and cost.
  • Maintain a valid capacity model in co-operation with the line Supervisor and conduct adequate advance planning for required capital.
  • Provide technical leadership/guidance for the Process Technician on the team (with specific responsibility to ensure that the preventative maintenance program is adequate and timely).
  • Development and implementation of appropriate supporting documentation, which complies with GMP in conjunction with the other team members.
  • Project planning, in detail, in support of major projects, product/process transfer etc.
  • Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
  • Responsible for other projects as assigned by the company.
  • Demonstrate a primary commitment to patient safety and product quality.
  • Understands and comply with all the regulations governing the quality systems
  • Ensures all direct reports are aware of their commitment to patient safety and product quality, are current with their training requirements and that they understand and comply with all other regulations governing their work.

Qualifications

  • NFQ Level 8 qualification (240 ECTS points) in engineering or a relevant field,
  • Minimum of 2 years' relevant experience to include line support engineering.
  • Medical Device or other highly regulated background highly desired.
  • Good technical capabilities, communication skills, teamwork abilities and initiative.
  • Project Management experience desirable.
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APU Test Engineer

Valeo

Tuam
Today
Tuam
Today
Job Description

Mission


Test Engineer is responsible for all the Test Equipment in the APU. This will include TRP (efficiencies), TLP (yield) and scrap. Continuous Improvement is an integral part of the job. Problem Solving, Root Cause Analysis and Corrective Action implementation are also a fundamental part of the job


Responsibilities

  • Define and implement TLR amp; TRP action plans to maintain and improve the companyrsquo;s KPI

  • Develop and take ownership of Test equipment inline with the APU resource plan

  • Generate Test System Process Qualification Plans in conjunction with the Quality Dept. i.e ; Capability Studies, Ramp;R Studies for presentation both internally and to Customers

  • Implement and maintain the process / product quality standards in line with the company / customer standards

  • Liaise with VVS Process Development Engineers (Hardware/Software amp; Mechanical), Manufacturing Engineers and Quality Engineers to ensure that solutions can be found to existing and future issues affecting camera output amp; yield.

  • Generation of Project Documentation ndash; Timing Plans, Build Reviews, Process Validation Reports, OEE Reports, Operator Instructions

  • Defining Training Requirements for Operations/Technicians following changes in Production ndash; product or process

  • Provide Test System development plans / cost to support the test improvement activities

  • Maintain amp; implement the 5S Principles

  • Presentation of the Test Systems to both internal amp; external Customers

  • Resolve Customer Quality Issues in conjunction with APU Process / Quality Eng. Or other resources as required

  • Support operations in resolving Technical Issues within sustaining Operations

  • Implement ECOrsquo;s and Production Permits and validate the changes

  • Ensure the process is maintained to V5000 amp; TS 16949 level or above at all times.

  • Ensure the Valeo Production Systems Requirements are respected and implemented as per agreed roadmaps.


Education

  • Degree in Electronics Engineer, Software Engineering or Equivalent Discipline

Professional Experience


  • Minimum 5 Years experience within Electronics Manufacturing Environment (ideally Automotive Electronics)
  • Experience with Pneumatics, GPIB, RS232C interfaces, sensors and PC/PXI I /O cards
  • Software Skills ndash; C, C++, Pyton programming or similar.
  • Experience in Camera Comms Stds ndash; LIN, CAN, Backchannel, Ethernet amp; I2C
  • Experience in Video Stds ndash; LVDS, NTSC, Ethernet amp; VPI
  • Experience with Automation equipment amp; handlers
  • Experience with NI Test Stand and/or Labview would be beneficial
  • Experience with vision based products/applications would be beneficial
  • Experience with dispense and UV based curing systems would be beneficial
  • Experience in document writing is required, ie. Procedures, specifications, reports, etc.
  • Knowledge of Shop Floor management systems amp; traceability required
  • Must have excellent debug amp; problem solving skills
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Engineering Manager

Merit Medical

Galway, Galway
30+ days ago
Galway, Galway
30+ days ago
The Opportunity:
Vision, leadership and accountability, key attributes of the leader we are looking for to be a part the implementation of our systems and strategies to ensure development and growth in the Process Engineering Group. The Engineering manager will be tasked with ensuring a safe work environment, maximizing profitable growth, driving quality improvements, developing people, reducing operating costs, inventories and lead times through continuous improvement at every possible opportunity.
The Purpose:
Within the Engineering Team at Merit you will be a part of a dynamic and developing team who are working on projects and systems for multiple leading medical device products that have been acquired and developed out of our own R&D centre of excellence here in Galway. Our Engineers are directly involved in the development of innovative products for use in medical procedures. As the Engineering Manager you will lead a team of qualified, experienced, and energetic engineers and technicians of all levels to develop a world class Engineering Department.
Day to day:
* Create clarity and direction for roles and responsibilities for process engineering and technical support levels, ensuring structural alignment to the expectations and demands of the business
* Manage a team of manufacturing engineers and technicians in performing their respective responsibilities.
* Provide the leadership and drive to the successful roll out for all programs, incorporating good industrial engineering techniques for Target Deliverance of scrap and consumable cost reduction, increase in equipment availability and Problem Solving.
* Determine and drive improvement targets, meet and present the engineering metrics for all relevant performance goals.
* Establishes and supports a work environment of continuous improvement with close supervision of, and/or direct involvement in programs to develop & improve existing production / quality / performance.
* Determines appropriate staff levels for your team, participate in setting budgets, including wage increases and in job evaluation reviews.
* Engage with other stakeholders internally and establish service level agreements and set expectation and guidelines for the development of the group.
* Demonstrates and models through his / her management style and behaviour respect for our core values and a commitment to teamwork.
* Perform other related managerial tasks.
Your profile:
* Bachelor of Science or Engineering Degree in relevant technical discipline.
* Work related experience of at least six years of which at least f years' experience is in the medical device manufacturing industry in a similar role, coupled with a proven track record in a leadership role.
* Lean six sigma knowledge (preferably to Green Belt certification or higher). Experience of applying Lean tools / techniques to improve business processes & performance.
Merit Medical is an Equal Opportunities Employer
#LI-AD1 #
At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.
Key Benefits
* Fulltime Permanent contract
* Attractive Salary package
* Defined Contribution Pension Plan
* Health Insurance Cover
* Life assurance
Health & Wellbeing Events Calendar
Excellent career progression opportunities
Recognition scheme
Free Parking
Educational assistance
Internal training courses
Quality Subsidised Canteens & Barista Service
Active Sports and Social Club
We are Global
Merit Medical Galway commenced with 22 employees in 1993. Since then Merit has enjoyed year on year revenue growth and developed its workforce to over 900 employees. Headquartered in Salt Lake City, Utah, Merit maintains a diverse, multi-campus manufacturing footprint in Europe, North America, South America, Asia and Australia with a global distribution.
Medtech Company of the Year Winner
Merit Medical Galway are proud winners of the Medtech Company of the Year Award, a prestigious award recognizing those who are exceling in the MedTech industry
People Development
At Merit Medical Galway almost 60% of all roles are filled by internal employees! We focus on encouraging, believing in and providing a platform for you to progress your career!
Culture
A supportive and collaborative environment make Merit Medical a friendly, enjoyable place to work. We are proud of our energetic and dynamic culture. Diversity & Inclusion is evident here with an 50/50 ratio of male and female employees as well as 30 nationalities onsite! We value every employee as an individual.
To see more on our culture, go to www.merit.com/careers.
Follow Us:
Day in the Life:
Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled
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Service Technician

Salessense

Galway
30+ days ago
Galway
30+ days ago

The successful candidate will be required to repair and service Vehicles within the Service department. You will be required to deliver a high standard within the workshop in line with specifications set out by manufacturer and processes set out by the company/my client.


  • FETAC or City & Guilds Qualification
  • Experience in vehicle services and repairs
  • Ability to work in a team
  • Ability to work on own initiative
  • Display a keen interest in Motor Vehicles
  • Interested in working in a fast-paced environment
  • Attention to detail is fundamental to ensure quality is consistently delivered
  • Continuous improvement mindset
  • A full and valid driving license is essential for the role
  • Build strong interdepartmental relationships and pay close attention to other departments requirements
  • Work independently in a busy, active environment, managing own time and workflow effectively
  • Present a consistently professional image to both internal and external customers, through attitude, behaviour and personal appearance
  • Strong problem-solving ability to identify and resolve queries

  • Diagnosis, repairs and servicing of Mercedes-Benz vehicles to the highest standards and to the appropriate manufacturer specification
  • Through the use of diagnostic equipment and a systematic approach, ensure vehicle faults are diagnosed and rectified
  • Ensure full understanding of latest technology introduced on the vehicle range and how to diagnose and repair faults on them
  • Complete relevant service documentation (Job sheets, PDI’s, service reports) in line with ISO, warranty and Dealership requirements
No More Results

Posted

22 days ago

Description

Quality Technician REQ 1547

 

Securing your Future!

Build the future of digital identity! HID Global is a company that is ultimately involved in the dynamic and ever growing world of access control technology. Every day, we create the most innovative global authentication solutions for a variety of customer applications. We are a diverse, multidisciplined, growing multinational technical company that offers its employees a fun work environment, flexibility and career opportunity. We are the Evolution of Authentication.

 

What you will be part of:

HID Global powers the trusted identities of the worlds people, places and things. We make it possible for people to transact safely, work productively and travel freely. Our product and services are used by millions of people around the world to navigate their everyday lives.

 

Working at HID:

HID Global is an innovative fast paced organisation, with many possibilities to make a difference and add value. We empower our employees to achieve great things by taking ownership of their future career.

We value diversity and endorse an open-minded collaborative working environment. We are a company with integrity at our core. HID Global are committed to our employee engagement offering a range of employee benefits and  initiatives with events and activities happening all the time.

 

The Position:

You will be expected to inspect and test HID products, assemblies, subassemblies, components, parts and cards for conformance to specifications in accordance with written inspection instructions, procedures or verbal instructions.

This role will be working closely with the leadership team to identify and manage all supports required for value stream quality related tasks. You will collect and prepare data to ensure critical KPIs and data is available on a daily, weekly and monthly basis. As well as have the ability to communicate up and down the organisation to ensure KPIs and projects are being met as expected. 

This person will be responsible for raising SARs as appropriate for major supplier issues. You will manage and monitor for MRB reports and RMA transactions and analysis.

 

What we are looking for:

The ideal person will provide leadshership, guidance and support to technicians and inspectors. Ideally this person would have 5 years experience as a quality inspector in a simular role. They would be educated with a certificate or Diploma in quality or engineering discipline or equlivant. They would have experience of the following skills : metrology ,calibration, data collection and graphs, corrective action, DMAIC tools and supplier scorecards.

You will have excellent communication skills both verbally and writen in the English langage and will be able to demonstrate advance skills in data collection and analysis.

There are high customer expectations in this role and the ideal person would understand the customers requirements and also understands the consequences of inaccurate data. They will promote the importance of customer quality and report any issues that potentially will impact customers.

 

Why you should apply:

  • Excellent terms and conditions
  • Flexibility
  • On the job training and development
  • Work as part of a global team

Final Application Date: 17th February 2021

*No 3rd party agency engagement required for this role*

HID Global is an equal opportunities employer

HID Global powers the trusted identities of the world’s people, places and things. We make it possible for people to transact safely, work productively and travel freely. Our trusted identity solutions give people secure and convenient access to physical and digital places and connect things that can be accurately identified, verified and tracked digitally. Millions of people around the world use HID products and services to navigate their everyday lives, and over 2 billion things are connected through HID technology. We work with governments, educational institutions, hospitals, financial institutions, industrial businesses and some of the most innovative companies on the planet. Headquartered in Austin, Texas, HID Global has over 4,000 employees worldwide and operates international offices that support more than 100 countries. HID Global® is an ASSA ABLOY Group brand. For more information, visit www.hidglobal.com

Source: HID Global Corporation