quality technician jobs

Near galway, galway
13Jobs Found

13 jobs found for quality technician jobs Near galway, galway

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Senior Manufacturing Engineer

Sigmar

Galway, Galway
5 days ago
Galway, Galway
5 days ago

Senior Manufacturing Engineer

Here in Galway, I'm recruiting for an experienced Senior Manufacturing Engineer to join a small but expanding medical device company. This is a permanent job and you will join a team of 4 experienced Engineers within the Manufacturing Group. You will focus on manufacturing and process development activities while working closely with R&D.

Your Responsibilities:

  • As as a Senior Engineer, you will frequently interact with product stakeholders (e.g. external vendors, production, quality, etc.) to identify opportunities and develop appropriate strategies
  • Work with and lead internal cross-functional teams and contract manufacturers or design firms to ensure system design, architecture, and verification/validation meets design input.
  • Evaluate external technologies and strategically identify opportunities to implement them.
  • You will serve as a key communicator from the customer to the design team.
  • As the Technical Expert (subject matter expert), you will be responsible for contributing and solving complex projects/issues as they arise.
  • Project Management: Create, drive, communicate & execute project plans, tasks and deliverables.
  • Develops processes, materials and solutions through in house and out of house development paths.
  • Use structured problem-solving techniques and statistical methods for data driven analysis and decisions
  • Build Quality into all aspects of work by maintaining compliance to all quality requirements
  • Provide technical guidance to other engineers & technicians.

Your Background:

  • Level 8 Engineering or Science Degree.
  • Experienced Engineer with 5 years in a medical device environment.
  • Experience with medical products such as large calibre delivery systems is an advantage
  • Product and process development skills in medical devices a must
  • Strong knowledge of materials and process capabilities for catheter based medical device implants
  • Strong working knowledge and ability to use statistical techniques, six sigma and DFSS methodology
  • Proficient in solid works, ACAD and FE
  • Ability to work within a team; fully motivated to achieve and demonstrate best practices in line with company objectives.
  • Excellent verbal communication skills to enhance collaboration and written skills to prepare/execute/communicate plans and reports
  • Strategic Planner with successful scheduling & execution results

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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Manufacturing Engineer NPI/Projects

Sigmar

Galway, Galway
5 days ago
Galway, Galway
5 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 Technician I/ II (Defined-Term) - Multiple Shifts Job (Galway, G, IE)

Boston Scientific

Galway
4 days ago
Galway
4 days ago

We're 23,000 colleagues in 40 countries across six continents. But together, we're one global team. Everything we do combines purpose and passion. It's our passion that fuels our desire to make a difference. And it's our extraordinary sense of purpose that drives us to innovate, create and collaborate. We never plan on stopping. Working at Boston Scientific, you're given the space and freedom to wonder ‘what if?' We know that a single idea can make a big difference in the lives of patients.

 

We are currently looking for an experienced Quality Technician I/II to join our team. This is initially 12 months contract with a view to permanency. Multiple shifts available.

Role: Quality Technician (Manufacturing Support) - 12 months Defined Term contracts

Shift: Multiple

 

Purpose

 

  • Controlling closed Exception Reports/Non Conformances Reports, Line Audits & Non Conforming Report Board Reports that are generated. Compiling Non Conformance Board Reports each month & compiling various documents for Management on an ad hoc basis. Carrying out Plant-wide Internal Audits & Internal Audits as per relevant schedules. Compiling Yield & Scrap Reports.

 

Responsibilities

 

  • Ensure compliance to all applicable regulatory standards and current GMP procedures and practices.
  • Perform product defect analysis.
  • Routine final functional testing, product release criteria testing/inspection and recording of test results.
  • Review and update of QA Documentation.
  • Control of non-conforming product.
  • Problem solving and continuous improvement investigations.
  • Perform internal and plant wide audits as required.
  • Review and update of QA Documentation.
  • Review and update of QA Documentation.
  • To provide assistance and support to the Quality Engineering and Operations function.
  • Provision of excellent service to all internal customers for the production group or functional area in which they work.
  • Decision making ability coupled with the ability to work on one s own initiative and with minimum supervision is required.
  • Good interpersonal skills and organisational skills.
  • Excellent attention to detail.
  • Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.

 

 

Qualifications/ Experience

 

  • NFQ level 6 or above in Science or Engineering Discipline. Minimum of 2-3 years in a similar role.
  • Medical Device background would be highly desired.
  • Decision making ability coupled with the ability to work on one’s own initiative and with minimum supervision is required.
  • Good interpersonal skills and organisational skills.
  • Excellent attention to detail.
  • Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.
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Quality Technician REQ 1547

HID Global Corporation

Galway
30 days ago
Galway
30 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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Quality Engineer (Projects) - Galway Job (Galway, G, IE)

Boston Scientific

Galway
26 days ago
Galway
26 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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Controls Engineer

Crest Solutions

Galway
17 days ago
Galway
17 days ago


Crest Solutions have an open position for an Equipment Engineer to join our team. This is a 12-month contract.


Responsibilities:

·        Work on Mechanical/Electronic troubleshooting, hardware/software interfacing.

·      Group SME on the debugging and troubleshooting of PLC (Allen Bradley) / PC hardware and software issues on manufacturing equipment.

·        Acts as an escalation point for group technicians for Controls / Software issues on their shift.

·        A strong electrical troubleshooting competancy is essential.

·        Interface with a variety of site personnel and with outside vendors when necessary while performing the above.

·        Take responsibility for preventative maintenance procedures with an assigned process or area.

·        Responsible for machine performance and up time.

·        Assists in implementing technical improvements under the teams C.I.P. program.

·        Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.

·        Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.


In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

For those individuals that supervise others, the following statements are applicable:

·Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the sites Quality Policy.

·Establishes and promotes a work environment that supports the Quality Policy and Quality System.

·Not applicable.


Requirements:


A developing professional. Working knowledge and application of business and technical concepts, procedures and practices. General knowledge of industry practices, techniques, and standards. General understanding of business unit/group function. Exercises judgment when interpreting company policies and procedures to resolve a variety of issues.


·        Strong Controls / Automation background. Excellent PC (Allen Bradley) / PLC hardware / software troubeshooting skills required. Strong understanding of Controls systems (motion control, vision systems, robotics, plc, pc, pneumatics) required.

·        A strong electrical troubleshooting competancy would be an advantage.

·        Degree Qualified


Why Join Crest Solutions?


 Crest Solutions we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Crest Solutions benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. An example of what is offered to our team members is as follows:

ü Competitive salary

ü Full healthcare cover, leave benefits, life assurance, flexi-time and pension scheme

ü A varied and exciting career with Crest Solutions with opportunities to work in a cutting-edge, innovative technological environment

ü A structured approach to professional development opportunities with an educational assistance program


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Controls Engineer

Crest Solutions

Galway
17 days ago
Galway
17 days ago


Crest Solutions have an open position for an Equipment Engineer to join our team. This is a 12-month contract.


Responsibilities:

        Work on Mechanical/Electronic troubleshooting, hardware/software interfacing.

      Group SME on the debugging and troubleshooting of PLC (Allen Bradley) / PC hardware and software issues on manufacturing equipment.

        Acts as an escalation point for group technicians for Controls / Software issues on their shift.

        A strong electrical troubleshooting competancy is essential.

        Interface with a variety of site personnel and with outside vendors when necessary while performing the above.

        Take responsibility for preventative maintenance procedures with an assigned process or area.

        Responsible for machine performance and up time.

        Assists in implementing technical improvements under the teams C.I.P. program.

        Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.

        Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.


In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

For those individuals that supervise others, the following statements are applicable:

Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the sites Quality Policy.

Establishes and promotes a work environment that supports the Quality Policy and Quality System.

Not applicable.


Requirements:


A developing professional. Working knowledge and application of business and technical concepts, procedures and practices. General knowledge of industry practices, techniques, and standards. General understanding of business unit/group function. Exercises judgment when interpreting company policies and procedures to resolve a variety of issues.


        Strong Controls / Automation background. Excellent PC (Allen Bradley) / PLC hardware / software troubeshooting skills required. Strong understanding of Controls systems (motion control, vision systems, robotics, plc, pc, pneumatics) required.

        A strong electrical troubleshooting competancy would be an advantage.

        Degree Qualified


Why Join Crest Solutions?


 Crest Solutions we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Crest Solutions benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. An example of what is offered to our team members is as follows:

 Competitive salary

 Full healthcare cover, leave benefits, life assurance, flexi-time and pension scheme

 A varied and exciting career with Crest Solutions with opportunities to work in a cutting-edge, innovative technological environment

 A structured approach to professional development opportunities with an educational assistance program


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

Boston Scientific

Galway
17 days ago
Galway
17 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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Customer Quality Engineer

Valeo

Tuam
7 days ago
Tuam
7 days ago
Job Description



  • Highlight the main responsibilities

  1. MISSION

    1. Enhance awareness of customer expectations by:

      1. Maintaining a permanent dialogue with quality staff at the customer site

      2. Participating in periodic quality briefing meetings.

      3. Constantly communicating customer expectations to site

      4. Periodically distributing briefing notes to the Group.

    2. Eliminate line failures, Coordinate cooperation between the site and Customer involved

      1. Key point for the customer: ensure normal flow very quickly.

      2. Key points for the site: characterize the problem in the QR PDCAcompleting 5W2H, doing first level analysis and send it to concerned APU

      3. Speed-up the return of bad parts and if possible good part(s) to be compared with.

      4. Managing sorting operations (at Customer and on advanced platforms): put in place the needed resources, systematically prepare a detailed instruction sheet, follow the progress of the activity, reporting the time spent for each operation and sorting results.PDCA/FTA-LLC: Challenge the logical thinking of the PDCA analysis.. If no progress done on PDCA improvement required, inform levels N+x, escalate to Plant QRQC,if necessary, the Product Groups or Business Groups Functional Department concerned (follow escalation process)..

      5. Response time: should the plants fail to respond on time required by the Customer / Valeo, inform levels N+x and, if necessary, the Product Groups or Business Groups Functional Department concerned (follow escalation process).

    3. Communicate with the Customer:

      1. React quickly when customersrsquo; contacts become dissatisfied and send information to Valeo sites, escalate if necessary, to the Product Groups or Business Groups Functional Department concerned (follow escalation process).

      2. Protect the customer by managing sorting operations, implementing surveys, preventive inspections,

      3. When review of PDCA analysis is requested by the Customer, present the PDCA/FTA-LLC with representatives (ie: APU manager, plant manager) or on behalf of the Product Groups or Business Groups

      4. Serve as the point of access for customer contacts seeking information or a contact at Valeo (in case of no GRE present at customer location)

      5. Provide the Product Groups or Business Groups with detailed information about the customer#39;s organization and operating methods.

      6. Define and communicate to Customer and internally back-up Valeo contacts when not available (ie.: holidays, business trip)

      7. Support Product Groups or Business Groups, communicating to Customer the issues under Customer responsibility detected on Valeo lines (ie.: damaged packaging, transportation issues)

      8. Support Product Groups or Business Groups in case of language issue with the Customer

.

  • Highlight the main responsibilities

  1. Help make products easier to assemble and ensure that they are used properly by:

    1. Informing the customer of the correct conditions of use and of Valeo#39;s recommendations.

    2. Informing the plants of the actual conditions of use and their evolution.

    3. Detecting any Non-Conformance in the use of Valeo products at the customer site and immediately informing the customer.

  2. Participate in measuring Quality by:

    1. Being informed of customer Quality indicators that apply to Valeo products:

      1. PPM Line Returns.

      2. Specific customer indicators.

    2. Knowing how indicators are measured at the customer site and by keeping Valeo informed of possible changes.

    3. Knowing customer contacts who process and consolidate Quality data in IT systems, so as to help Valeo sites ensure that their own Quality data are correct.

    4. Formalizing the numerous quot;in the fieldquot; quality data which is not covered by indicators.

    5. Ensure Line QRQC

    6. Participate in Stop Scrap Projects amp; Systems

    7. Enforcing Work Instruction Compliance

  1. CONTACTS

    1. In Customer plant: Technicians, Quality Analysts and Quality Department managers, Manufacturing Quality staff and Operators, Procurement agents and Logistics managers, Advanced platform managers, Sorting company managers, Group Resident Engineers, Independent Resident Engineers, Contractors

    2. With Valeo : APU Managers, Plant Managers, Logistics Managers, Projects Managers, Ramp;D engineers amp; Managers, APU Quality engineers, Quality Managers (site,, Product Group, Business Group, Group)

  2. RESOURCES

    1. To carry out his/her assigned tasks effectively, the Customer Quality Engineer must develop and maintain a knowledge of Valeo#39;s products, methods and network by:

      1. Regularly visiting Customer sites (personnel, product and process knowledge).

      2. Getting training in PDCA/FTA, QRQC, LLC

    2. The Customer Quality Engineer should have working equipment such as PC, Phone, Digital Camera, connections to network with high speed access in order to be able to communicate quickly with Valeo sites, when at customer sites.​​​​​​​



Education level are necessary for the position

Diploma/ Degree in an Engineering discipline

5 minimum years in Automotive or Aerospace Business

Experience in Operations or development

Job Type

Full Time

Posted

5 days ago

Description

Senior Manufacturing Engineer

Here in Galway, I'm recruiting for an experienced Senior Manufacturing Engineer to join a small but expanding medical device company. This is a permanent job and you will join a team of 4 experienced Engineers within the Manufacturing Group. You will focus on manufacturing and process development activities while working closely with R&D.

Your Responsibilities:

  • As as a Senior Engineer, you will frequently interact with product stakeholders (e.g. external vendors, production, quality, etc.) to identify opportunities and develop appropriate strategies
  • Work with and lead internal cross-functional teams and contract manufacturers or design firms to ensure system design, architecture, and verification/validation meets design input.
  • Evaluate external technologies and strategically identify opportunities to implement them.
  • You will serve as a key communicator from the customer to the design team.
  • As the Technical Expert (subject matter expert), you will be responsible for contributing and solving complex projects/issues as they arise.
  • Project Management: Create, drive, communicate & execute project plans, tasks and deliverables.
  • Develops processes, materials and solutions through in house and out of house development paths.
  • Use structured problem-solving techniques and statistical methods for data driven analysis and decisions
  • Build Quality into all aspects of work by maintaining compliance to all quality requirements
  • Provide technical guidance to other engineers & technicians.

Your Background:

  • Level 8 Engineering or Science Degree.
  • Experienced Engineer with 5 years in a medical device environment.
  • Experience with medical products such as large calibre delivery systems is an advantage
  • Product and process development skills in medical devices a must
  • Strong knowledge of materials and process capabilities for catheter based medical device implants
  • Strong working knowledge and ability to use statistical techniques, six sigma and DFSS methodology
  • Proficient in solid works, ACAD and FE
  • Ability to work within a team; fully motivated to achieve and demonstrate best practices in line with company objectives.
  • Excellent verbal communication skills to enhance collaboration and written skills to prepare/execute/communicate plans and reports
  • Strategic Planner with successful scheduling & execution results

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.