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5 Jobs Found 

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Manufacturing Engineer

Microchip

Ennis
30+ days ago
Ennis
30+ days ago

Company Description

Microchip Technology Inc. is a leading provider of embedded control applications. Our product portfolio comprises general purpose and specialized 8-bit, 16-bit, and 32-bit microcontrollers, 32-bit microprocessors, field-programmable gate array (FPGA) products, a broad spectrum of high-performance linear, mixed-signal, power management, thermal management, radio frequency (RF), timing, safety, security, wired connectivity and wireless connectivity devices, as well as serial Electrically Erasable Programmable Read Only Memory (EEPROM), Serial Flash memories, Parallel Flash memories, and serial Static Random Access Memory (SRAM). We also license Flash-IP solutions that are incorporated in a broad range of products.

Job Description

As a Manufacturing Engineer you will be a key member of the engineering team at Microchip, responsible for ensuring that our products meet customer needs and have the highest quality. Through part requirement analysis, definition, and selection, ensure product is correctly processed through screening and sampling operations as required by governing bodies and internal requirements. Create and maintain Process and Product definition with associated process controls and automation.

 Role Focus

  • Combining mechanical, electrical, and software principles and their application; identify, develop, and drive continuous improvement programs towards further automation within the facility.
  • Guide and drive on-site equipment appraisal initiatives for process standardization, quality improvement, and H&S developments where identified.
  • Understand HTRB and Burn-in screening principles, our products and processes to ensure compliance and maximum yield.
  • Understand DC and AC test principles, our products, related equipment and processes to ensure compliance and maximum yield.
  • Ensure compliance with DLA test methods. 

Key job responsibilities/duties include:

  • Review and disposition production lots based on electrical test screening.
  • Perform in-depth and controlled studies of specific/chronic problems and processes as required and specify corrective/preventative action as appropriate.
  • Responsible for analysis and performance improvement of key metrics for assigned processes and/or products.
  • Understanding of reliability theory and principles and application to Microchip products and processes.
  • Consult with international Microchip Divisions and test equipment suppliers to ensure best practices in the use of test and screening equipment.
  • Understand and implement Microchip Irelands’ Quality Manual and related in-house  procedures as they apply to assigned processes and new products.
  • Understand Government Specifications as they apply to assigned product and processes.
  • Implement Lean and support continuous improvement programmes.
  • Support in-house training programmes as required.
  • Ensure effective and professional communication with Microchip divisions, customers and vendors.
  • Take on other engineering duties as required and assigned.
  • Create and update internal product and process documents, in accordance with product requirements
  • Support Tactical Marketing, Planning and Engineering departments for new and existing product queries. Determine alternative product selection where required.
  • Understand and implement Microchip Quality Policies and related in-house procedures as they apply to assigned processes and new products.

Job Requirements

Qualifications and Experience

  • Level 8 Degree in Engineering (preferably Electronic Engineering) or Level 8 Degree in Physics.
  • Experience preferably in a component manufacturing, medical device or other highly regulated environment. 
  • User knowledge of LabVIEW and Minitab, JMP, Python, SolidWorks, CAD and AUTOCAD software packages.
  • Knowledge of DLA and/or ISO standards is an advantage.
  • Qualifications in, or previous exposure to Lean, Six Sigma, 5S, DOE, DMAICs or FMEAs is an advantage.
  • Experience in equipment appraisal towards CE compliance is an advantage.

 Competencies

  • Strong electronic and mechanical fundamentals aptitude, with good hands on approach.
  • Robust communications skills, fluent English is essential, with strong writing, editing, clarity and negotiation skills.
  • Must have a strong attention to detail, problem solving skills, and demonstration of logic.
  • Candidates will have the ability to work in collaboration with others on a project team and independently on tasks.
  • Good PC skills with proficiency in Microsoft Office packages.
  • The candidate should be self-motivated and eager to learn new skills, they need to be flexible, excellent team player and demonstrate the Microchip values.

#LI-PT1

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Manufacturing Engineer

Edwards Lifesciences

Shannon
30+ days ago
Shannon
30+ days ago
The Company: Edwards Lifesciences is driven by a passion to help patients. The company collaborates with the world’s leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives.
The Role: We are looking to hire a Manufacturing Engineer who applies knowledge of technical principles and Edwards systems/procedures to optimize manufacturing processes.
Key Responsibilities:
+ Improve manufacturing processes using engineering methods (e.g., LEAN methods, basic statistics) for continuous process improvement
+ Develop basic experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
+ Analyze and resolve basic Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations)
+ Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
+ Establish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)
+ Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes
+ Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
+ Other incidental duties assigned by Leadership
Education and Experience:
+ Bachelor's Degree in in Engineering or scientific field
+ Minimum of 4 years’ experience of experience required
Additional Skills:
+ Good computer skills in usage of MS Office Suite including MS Project; CAD experience preferred (if applicable)
+ Basic documentation, communication (e.g., written and verbal) and interpersonal relationship skills
+ Basic understanding of statistical techniques
+ Previous experience working with lab/industrial equipment preferred (if applicable)
+ Good understanding and knowledge of principles, theories, and concepts relevant to Engineering
+ Good problem-solving, organizational, analytical and critical thinking skills
+ Good understanding of processes and equipment used in assigned work
+ Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to manage competing priorities in a fast paced environment
+ Must be able to work in a team environment, including immediate supervisor and other team members in the section or group; and may interact with vendors
+ Ability to build stable working relationships internally
+ Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide.
For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.
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Supplier Quality Engineer

Edwards Lifesciences

Shannon
21 days ago
Shannon
21 days ago
The Company: Edwards Lifesciences is driven by a passion to help patients. The company collaborates with the world’s leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives.
Apply knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution.
Key Responsibilities:
• Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.
• Develop moderately complex experiments and tests (including writing and executing protocols) to create, validate, and improve products (including evaluation of source materials and suppliers) and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports.
• Optimize moderately complex Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk.
• Develop, update, and maintain technical content of risk management files
• Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes.
• Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinate technician work.
• Other incidental duties assigned by Leadership
Education and Experience:
Bachelor's Degree in in Engineering or Scientific field , minimum of 2 years years experience Required or
Master's Degree or equivalent internship, senior projects, or thesis in Engineering or Scientific field including either industry or industry/education Required
Additional Skills:
• Good computer skills in usage of MS Office Suite
• Ability to read and interpret drawings
• Good documentation, communication and interpersonal relationship skills including negotiating and relationship management skills
• Basic understanding of statistical techniques
• Previous experience working with lab/industrial equipment required
• Solid understanding and knowledge of principles, theories, and concepts relevant to Engineering
• Solid problem-solving, organizational, analytical and critical thinking skills
• Solid understanding of processes and equipment used in assigned work
• Knowledge of and adherence to Quality systems
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast paced environment
• Must be able to work in a team environment, including the ability to manage vendors and project stakeholders
• Ability to build productive internal/external working relationships
• Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide.
For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.
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Process Development Engineer

Takeda Pharmaceutical

Ireland
2 days ago
Ireland
2 days ago

Job Description

  • Lead a cross-functional team during technical transfers (sending site) and new product introduction (NPI) (receiving site) projects in accordance with a pre-approved project plan, schedule and current project management best practice.  Ensure that critical manufacturing systems and support structures are in place for major technology transfer and NPI projects and provide technical advice on process engineering requirements as needed.  Liaise with technology transfer project counterparts in other Takeda sites;
  • Project manage the technical transfers to ensure a smooth transition;
  • Execute early stage feasibility, technical, process optimisation and process validation studies;
  • Liaise with the Engineering Process Support Team to identify process improvement opportunities for legacy products.  Propose and implement sustainable solutions to reduce processing times, improve yield, reduce defects and eliminate waste;
  • Identify cost-effective opportunities for the introduction of best-in-class manufacturing technologies. Design and introduce these technologies to manufacturing operations;
  • Review Change Records and Risk Assessments to assess potential process and validation impact;
  • Use statistical software packages for data analysis and in the identification and reporting of shifts, signals and trends in process parameters and product quality attributes;
  • Execute process improvement projects and deviation investigations using Six Sigma methodologies;
  • Liaise with other departments, vendors, external consultants & other Takeda sites as required;
  • Provide regular progress updates (written and verbal) on projects and activities within and beyond the Manufacturing Sciences Team as stated in project communication plans and/or as required by the relevant stakeholders;
  • Adhere to the compliance matrix of business processes and routine departmental tasks;
  • Comply with the relevant industry and Company quality standards and the cGMP pertaining to pharmaceutical production;
  • May be required to assume responsibilities of Process Support Engineer where applicable, from time to time and as directed by the Manager or Director.
  • Participate fully in any cross functional training initiatives;
  • Drive and promote the corporate values of Takeda-ism within the workplace;
  • Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business;
  • Ensure timely completion of all SOP reading, training and assessment;
  • Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
  • Degree qualified in a Science or Engineering discipline;
  • Masters in a related field is preferable.
  • Ideally 3 - 5 years’ experience as a Process Engineer with Pharmaceutical industry and New Product Introduction project experience;
  • Operations, process / technical support, projects or validation-based experience of oral solid dosage manufacturing processes an advantage;
  • Experience with technical transfers (sending site) for pharmaceutical products an advantage.
  • Excellent communication, report writing, presentation, interpersonal and time management skills.

Locations

Bray, Ireland

Worker Type

Employee

Worker Sub-Type

Fixed Term (Fixed Term)

Time Type

Full time
T
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Process Development Engineer (Packaging)- 11 Month FTC

Takeda Pharmaceutical

Ireland
2 days ago
Ireland
2 days ago

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice, Privacy Policy and Terms of Use.

Job Description

  • Lead new packaging product introductions to P2 at TILGC.
  • Be a subject matter expert (SME) for packaging equipment and packaging systems.
  • Support primary and secondary packaging operations at P2 TILGC.
  • New Product Introductions
    • Lead Feasibility assessments for new packaging formats and new equipment
    • Technical Review of Artwork and Packaging
    • Lead optimisation and process validation studies
    • Parameter optimisation for vision systems, equipment and serialisation systems
    • Understand regulatory requirements and communicate them to the project team
    • Lead Capital Projects for equipment introductions as required
  • Packaging SME
    • Lead Root Cause Analysis for Packaging Processes
    • Troubleshooting and maintenance of Serialisation Systems
    • Troubleshooting and maintenance of Vision Systems
    • Troubleshooting and maintenance of Packaging Equipment
  • Operations Support
    • Liaise with QC, QA, CAPEX Team, Logistics, Supply Chain and Manufacturing to ensure adherence to schedule and efficient troubleshooting
    • Provide technical support and direction to manufacturing personnel in order to ensure that the manufacturing and ancillary facilities can be operated to optimum efficiency and that Plant Turnarounds are executed in an efficient manner. 
    • Actively participate in problem identification, problem solving and change initiatives in cooperation with other teams and services.  Continuous improvement with a cross functional focus is a core activity.
    • Investigate quality events as they arise and prepare deviation reports using site Trackwise system.
    • Complete required documentation relating to development and manufacturing activities in an accurate and timely manner. Such documentation would include (but not be limited to) BMRs and SOPs.
  • Support a culture of open communication, fairness and transparency.
  • Available to participate in ‘on call’ program and respond to ‘call out’ as required.
  • Participate in any required training and ensure team members are suitably trained.
  • Drive a continuous improvement mindset in line with AGILE programme at TILGC.
  • Uphold Company Code of Conduct.
  • Ensure that they themselves perform all operations in accordance with TILGC quality standards, GWPs, cGMPs and all other relevant policies, procedures, regulations and standards including Health & Safety and Environmental (HSE) Legislation.
  • Foster a safe work environment, ensuring all colleagues maintain safety as a priority.
  • Participate fully in any cross functional training initiatives.
  • Adopt  the corporate values of Vision 2025 and Takeda-ism within the workplace.
  • Foster, in cooperation with other TIL staff, an ethos of continuous improvement where CI is accepted as an integral part of the overall business.
  • Ensure timely completion of all SOP, reading, training and assessment.
  • Other duties as required and directed by the Manager, Finance or other Officer appointed by the Board of Directors.
  • 3rd Level Degree in Engineering or other relevant course.
  • Minimum 3 years experience in Pharma Manufacturing
  • Experience of Secondary Packaging systems
  • Experience of Primary Packaging Systems beneficial
  • Experience of Vision Systems
  • Experience of Serialisation Systems beneficial
  • Excellent written and verbal communication skills
  • Flexible, willing and positive attitude / mind-set
  • Excellent planning, scheduling and prioritisation ability
  • Excellent documentation skills and attention to detail.
  • Excellent knowledge of Microsoft products and systems skills.
  • Strong Quality orientation.
  • Ability to work under pressure & managing conflicting tasks at the same time.
  • Ability to work well with others to achieve organisational goals.
  • Safety focused.

Locations

Grange Castle, Ireland

Worker Type

Employee

Worker Sub-Type

Fixed Term (Fixed Term)

Time Type

Full time
No More Results

Posted

30+ days ago

Description

Company Description

Microchip Technology Inc. is a leading provider of embedded control applications. Our product portfolio comprises general purpose and specialized 8-bit, 16-bit, and 32-bit microcontrollers, 32-bit microprocessors, field-programmable gate array (FPGA) products, a broad spectrum of high-performance linear, mixed-signal, power management, thermal management, radio frequency (RF), timing, safety, security, wired connectivity and wireless connectivity devices, as well as serial Electrically Erasable Programmable Read Only Memory (EEPROM), Serial Flash memories, Parallel Flash memories, and serial Static Random Access Memory (SRAM). We also license Flash-IP solutions that are incorporated in a broad range of products.

Job Description

As a Manufacturing Engineer you will be a key member of the engineering team at Microchip, responsible for ensuring that our products meet customer needs and have the highest quality. Through part requirement analysis, definition, and selection, ensure product is correctly processed through screening and sampling operations as required by governing bodies and internal requirements. Create and maintain Process and Product definition with associated process controls and automation.

 Role Focus

  • Combining mechanical, electrical, and software principles and their application; identify, develop, and drive continuous improvement programs towards further automation within the facility.
  • Guide and drive on-site equipment appraisal initiatives for process standardization, quality improvement, and H&S developments where identified.
  • Understand HTRB and Burn-in screening principles, our products and processes to ensure compliance and maximum yield.
  • Understand DC and AC test principles, our products, related equipment and processes to ensure compliance and maximum yield.
  • Ensure compliance with DLA test methods. 

Key job responsibilities/duties include:

  • Review and disposition production lots based on electrical test screening.
  • Perform in-depth and controlled studies of specific/chronic problems and processes as required and specify corrective/preventative action as appropriate.
  • Responsible for analysis and performance improvement of key metrics for assigned processes and/or products.
  • Understanding of reliability theory and principles and application to Microchip products and processes.
  • Consult with international Microchip Divisions and test equipment suppliers to ensure best practices in the use of test and screening equipment.
  • Understand and implement Microchip Irelands’ Quality Manual and related in-house  procedures as they apply to assigned processes and new products.
  • Understand Government Specifications as they apply to assigned product and processes.
  • Implement Lean and support continuous improvement programmes.
  • Support in-house training programmes as required.
  • Ensure effective and professional communication with Microchip divisions, customers and vendors.
  • Take on other engineering duties as required and assigned.
  • Create and update internal product and process documents, in accordance with product requirements
  • Support Tactical Marketing, Planning and Engineering departments for new and existing product queries. Determine alternative product selection where required.
  • Understand and implement Microchip Quality Policies and related in-house procedures as they apply to assigned processes and new products.
     

Job Requirements

Qualifications and Experience

  • Level 8 Degree in Engineering (preferably Electronic Engineering) or Level 8 Degree in Physics.
  • Experience preferably in a component manufacturing, medical device or other highly regulated environment. 
  • User knowledge of LabVIEW and Minitab, JMP, Python, SolidWorks, CAD and AUTOCAD software packages.
  • Knowledge of DLA and/or ISO standards is an advantage.
  • Qualifications in, or previous exposure to Lean, Six Sigma, 5S, DOE, DMAICs or FMEAs is an advantage.
  • Experience in equipment appraisal towards CE compliance is an advantage.
     

 Competencies

  • Strong electronic and mechanical fundamentals aptitude, with good hands on approach.
  • Robust communications skills, fluent English is essential, with strong writing, editing, clarity and negotiation skills.
  • Must have a strong attention to detail, problem solving skills, and demonstration of logic.
  • Candidates will have the ability to work in collaboration with others on a project team and independently on tasks.
  • Good PC skills with proficiency in Microsoft Office packages.
  • The candidate should be self-motivated and eager to learn new skills, they need to be flexible, excellent team player and demonstrate the Microchip values.

#LI-PT1

Source: Microchip