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7 Jobs Found 

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Manufacturing Engineer-2

Integer

New Ross
1 day ago
New Ross
1 day ago
At Integer, our vision and values are embedded in everything we do!
If you want to work for an organization that values customer focus, teamwork, respect, integrity, communication and innovation, apply now!
JOB SUMMARY:
Provide engineering support to production through improved methods, processes, jigs and fixtures, tooling and machine enhancements to improve standard times and employee efficiencies in order to manufacture quality medical guide-wires at the target costs. Validate and introduce new equipment and processes to production. Create and maintain Device Master Record (DMR) Documentation through the order entry and ECO process. Train employees to perform processes as documented by standard operating procedures.
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES:
Employees are expected to support the quality concepts inherent in the business philosophies of Lake Region Medical including a variety of job related tasks, which may not be specific to this position profile.
Accountabilities include:
+ Learn Lake Region manufacturing processes and equipment in order to understand them, so as to be competent in providing technical support to production.
+ Lead or participate in projects, working closely with Production, Maintenance and Quality departments to implement the required changes to stabilise and improve processes. Goals include reducing defects, increasing efficiencies and increasing process uptime.
+ Employ Lean Manufacturing and Six Sigma methodologies such as process mapping, control charting, as appropriate in project work.
+ Monitor manufacturing activities, measure significant process characteristics and analyse variation in order to detect and reduce waste / scrap. Support the manufacturing process by taking corrective and preventative action on production delays and deviations.
+ Project management using standard Lake Region methodology.
+ Transfer of automation and new process projects to production, both within and between sites.
+ Transfer of New Products to production, both within and between sites.
+ Assist in training employees in new or improved processes.
+ Process and product validation.
+ Process / layout design and implementation.
+ Develop and support related documentation: - ECO generation to introduce changes and maintain DMR documentation.
+ Order Entry processing.
+ Sourcing, specifying and purchasing production equipment.
+ Jigs and fixture specification and development.
+ Assist in the specification of spare part lists.
+ Be an active member of the Lake Region Medical Limited team and work with all employees to develop a world class lean manufacturing system.
+ Comply with the Lake Region Medical Limited behavioural standards.
SKILLS AND KNOWLEDGE:
+ Ability to communicate and work with people inside and outside the Department as necessary to execute these responsibilities.Ability to train and lead assigned employees.
+ Ability to understand and follow appropriate Departmental policies, procedures, practices and to understand inter-relationships of people and functions.
+ Knowledge of manufacturing operations, systems and project management, including procurement, inventory control, quality control, production planning and control, test and inspection, layout.Knowledge of engineering theories, methods and work measurement techniques.
+ Ability to apply engineering methods in the definition, design, research, development, utilisation, maintenance, and cost-control of processes and equipment to build Lake Region products and improve qualities and reduce costs of such processes and products. MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS: College graduate with degree in Engineering, or equivalent experience. PHYSICAL DEMANDS: Work effectively with close tolerance. MENTAL DEMANDS:
+ Ability to work in an organised fashion.
+ Attention to detail.
+ Self-starter. WORKING CONDITIONS:
+ Day-shift operation, but may be required to change working hours or work other shift patterns occasionally as project responsibility dictates.
Integer Holdings Corporation (NYSE:ITGR) is the largest medical device outsource (MDO) manufacturer in the world serving the cardiac, neuromodulation, orthopedics, vascular, advanced surgical and power solution markets. The company provides innovative, high quality medical technologies that enhance the lives of patients worldwide. In addition, it develops batteries for high-end niche applications in energy, military, and environmental markets. The company’s brands include Greatbatch Medical, Lake Region Medical and Electrochem. Additional information is available at https://integer.net .
Integer is committed to equal opportunity for all, without regard to race, color, religion, creed, national origin, ancestry, ethnicity, sex (including pregnancy and gender), age, physical or mental disability, citizenship, veteran or military status past, current, or prospective service in the uniformed services, genetic information, sexual orientation, gender identity, marital status, or any other characteristic protected under applicable legally recognized protected basis under federal, state or local law. Greatbatch Integer complies with the Americans with Disabilities Act (ADA), as amended by the ADA Amendments Act, and all applicable state or local law. Consistent with those legal requirements, Integer will make reasonable accommodations for qualified individuals with a known physical or mental limitations of otherwise qualified employees and applicants with a disability if such accommodation would allow the individual to perform the essential functions of the job, unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel believe you need a reasonable accommodation pursuant to the ADA, please contact us at
716-759-5739.
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Manufacturing Engineer

Sigmar

Waterford, Waterford
14 days ago
Waterford, Waterford
14 days ago

Are you a Manufacturing Engineer? Would you like to be part of an ever-growing team that understands the importance of on-time delivery and support to their customers while also providing high quality, reliable, and compliant products?

Job Responsibilities

  • Design manufacturing processes, procedures and production layouts.
  • Develop SOP’s and guide operations on training.
  • Ensure processes and procedures comply with relevant regulations.
  • Work with customers internally and externally as well as partners to deliver projects.
  • Utilize LEAN, Six Sigma and other best practices tools and principles daily.
  • Write and execute process and equipment validation (IQ/OQ/PQ).
  • Guide operations regarding design concepts and specification requirements.

Job Requirements

  • Level 8 in Mechanical, Biomedical or related Engineering/Science discipline.
  • Hands-on experience in Medical Device Assembly.
  • 4+ years of experience in a highly regulated environment.
  • Proven track record in the execution of protocols and validations.
  • Experience in managing validation activities and cost reduction projects.
  • Technical knowledge of Automated Systems (Pneumatic, Electro-pneumatic, Robotic)

For a confidential discussion on this or any other current job opportunity please contact Meggan on 021 235 9144 / mtully@sigmar.ie

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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Automation Engineer

BRIGHTWATER SELECTION (CORK) LIMITED

Waterford, Waterford
3 days ago
Waterford, Waterford
€55k - €65k Per Year
3 days ago
€55k - €65k Per Year

One of the South East's most attractive employers has a vacancy for an experienced Controls Engineer. Working in a dynamic and expanding site you will execute projects in a fast paced, multi-disciplined, cross-functional team environment. This role offers the opportunity to work on exciting new tech.

About the Job:

  • Manage production and the introduction of new technology through team leadership.
  • Provide technical and vision core competency support to Global Operations and Engineering on an as-needed basis, including possible off-hours, remote and onsite coverage rotation.
  • Provide Technical support and technical reference expertise to manufacturing and outside vendors in developing technical solutions for vision inspection technologies.
  • Project Management/ support of capital projects within the plant to drive increased volume and decreased cost across multiple manufacturing processes.
  • Provide Technical specification documents to external vendors for the purpose of trending and design/ build of new manufacturing equipment.
  • Support product, platform and cost improvement programs by delivering qualified vision systems. Interface with Engineering, SQA, QA and Operations to successfully validate software systems. Author and execute associated validation documents.
  • Provide technical and operations training on systems delivered.
  • Travel to vendor and other locations for on-site project support (domestic & international
  • Vendor management
  • Deliver projects on time and within budget
About You:
  • Electronics/ Electrical Engineering
  • Computer/Software development systems
  • PLC- Allen Bradley, Siemens
  • High Level language Programming e.g. C#, VB.net
  • Practical knowledge of machine vision systems including Cognex VPro and InSight desired
  • Methodical/Analytical approach to problem solving.
  • 3 - 5 years relevant experience
  • FDA regulated Medical Device
  • Project Management
  • PLC Software Development
  • Scada Software development
  • Manufacturing support
  • Development, documentation and approval of technical documentation

 

For more on the role call Nigel on 087 3618142 or send your CV for consideration.
T
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Material Characterisation Scientist, R&D

Teva Pharmaceuticals

Waterford
17 days ago
Waterford
17 days ago
Material Characterisation Scientist, R&D
Date: Feb 9, 2021
Location: Waterford, IE, X91
Company: Teva Pharmaceuticals
Who Are We?
We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us.
We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.
We are looking to fill positions in the Material Sciences group here at Teva Waterford. We are searching for talented and motivated individuals that would enjoy working in a team oriented, entrepreneurial environment.
A Day in the Life of...
+ You will evaluate and validate new characterisation techniques and equipment to assess the physiochemical properties of the API, the excipients.
+ You will evaluate techniques to aide and de-risk drug product development efforts (such as Raman & In vitro dissolution).
+ You will support the drug product bioequivalence assessments and identification of critical quality attributes of the drug product.
+ You will work within cross-functional teams to remediate technical issues in R&D and commercial.
Who we are looking for
Are you….
+ An excellent communicator in both written and oral formats?
+ Able to deliver high levels of customer service both to internal and external clients?
+ Skilled when it comes to planning and organising as well as able to adapt to changing priorities?
Do you have….
+ A Masters or Degree in a relevant subject or years of industry experience within the pharmaceutical industry?
+ Excellent project management skills and the ability to function effectively in a fast paced dynamic technical environment?
+ Knowledge of global regulatory and compliance requirements?
+ Experience in materials characterisation and validation of these techniques?
+ Experience of working to GMP and/or GLP and implementing policies and procedures in line with regulatory guidelines?
Function
Research & Development
Sub Function
Drug Development and Preclinical Studies
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Teva’s Equal Employment Opportunity Commitment
At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.
Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That’s why we’re constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice.
EOE including disability/veteran
I
I

CI Coach

Integer

New Ross
30+ days ago
New Ross
30+ days ago
At Integer, our vision and values are embedded in everything we do!
If you want to work for an organization that values customer focus, teamwork, respect, integrity, communication and innovation, apply now!
JOB SUMMARY:
The primary purpose of this position is to facilitate the creation and implementation of a continuous improvement culture of Operational Excellence for the New Ross Site. The successful candidate will lead and support significant projects, provide coaching and lean training across the site.
DUTIES AND RESPONSIBILITIES:
+ Develop best practice methods, workplace layout and workplace organization to gain improved Value streams, Process Flow Improvements & identify cost saving opportunities
+ To take part in and give guidance to cross-functional teams rolling out the Lean Operational Excellence initiatives throughout the Lake Region New Ross facility.
+ Coaching employees in Lean Techniques and Principles in order to develop an organization wide culture of change.
+ Deliver and teach Scientific Problem Solving Training (8 steps).
SKILLS AND KNOWLEDGE:
+ A thorough understanding of Lean Manufacturing Principles, Systems and Tools.
+ Strong written and oral communication skills; demonstrated ability to lead team activities; excellent problem solving skills; strong computer and presentation skills.
+ Knowledge of manufacturing operations, systems and project management.Knowledge of engineering theories, methods and work measurement techniques.Excellent problem solving skills with an innovative approach MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS:
+ Third level/ Master’s Degree or Diploma Lean/Industrial Engineering or Green belt in Lean or Six Sigma.
+ Experience in implementation of Lean Techniques/improvements is an advantage
Integer Holdings Corporation (NYSE:ITGR) is the largest medical device outsource (MDO) manufacturer in the world serving the cardiac, neuromodulation, orthopedics, vascular, advanced surgical and power solution markets. The company provides innovative, high quality medical technologies that enhance the lives of patients worldwide. In addition, it develops batteries for high-end niche applications in energy, military, and environmental markets. The company’s brands include Greatbatch Medical, Lake Region Medical and Electrochem. Additional information is available at https://integer.net .
Integer is committed to equal opportunity for all, without regard to race, color, religion, creed, national origin, ancestry, ethnicity, sex (including pregnancy and gender), age, physical or mental disability, citizenship, veteran or military status past, current, or prospective service in the uniformed services, genetic information, sexual orientation, gender identity, marital status, or any other characteristic protected under applicable legally recognized protected basis under federal, state or local law. Greatbatch Integer complies with the Americans with Disabilities Act (ADA), as amended by the ADA Amendments Act, and all applicable state or local law. Consistent with those legal requirements, Integer will make reasonable accommodations for qualified individuals with a known physical or mental limitations of otherwise qualified employees and applicants with a disability if such accommodation would allow the individual to perform the essential functions of the job, unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel believe you need a reasonable accommodation pursuant to the ADA, please contact us at
716-759-5739.
I
I

Quality Engineer III

Integer

New Ross
30+ days ago
New Ross
30+ days ago
At Integer, our vision and values are embedded in everything we do!
If you want to work for an organization that values customer focus, teamwork, respect, integrity, communication and innovation, apply now!
JOB SUMMARY
The Senior Quality Engineer will primarily be responsible for developing and maintaining all quality systems and monitoring production process for compliance to implemented process controls. Under minimal direction, manages Quality projects that may cover multiple sites. Duties will involve coordination, and scheduling of program or project activities. Assignments are broad in scope with the opportunity for the use of independent judgment. Essential Quality engineering skills are required.
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES
Employees are expected to support the quality concepts inherent in the business philosophies of Integer, including a variety of job-related tasks which may not be specific to this position profile.
POSITION REQUIREMENTS
Interfaces directly and regularly with customers (internal and external) staff. Often is included in critical business discussions with customers to bring deep insight to a problem or opportunity and establish a high level of credibility for Integer through demonstrated program management knowledge and expertise.
Proactively manage the risk associated with projects so that Integer’s and the customer’s business objectives are achieved. Minimize the uncertainties associated with projects relative to scope changes, customer expectations, business issues and other intangibles to enable successful completion of projects.
Involve and coordinate the input of all key functional groups and contributors to the proposed work plan.
Follows and develops Quality and Regulatory requirements including Integer’s policies, procedures, and appropriate regulatory requirements and have the standard Quality engineering skill set as outlined below.
Prepares or reviews documentation with a high degree of accuracy, completeness, and effectiveness using common Integer tools & templates were available.
As outlined above must have standard Quality engineering skills as outlined below:
1. Compliance with all Regulatory Standards, this includes:
Completion of internal audits to: ISO 13485 FDA QSR ISO 14000
b. Participation in Corporate auditing programs
c. Ensuring continued compliance with DMR
2. Develop and maintain a program ensuring only correctly validated equipment is used in production process. This will include:
Participation in validation protocol development Overseeing completion of validation or validation samples Supporting the engineering function to ensure compliance to related element of quality system
3. Liase with engineering departments on new product development projects to ensure;
All quality control requirements for non standard product are clearly understood All product samples for new product development qualification are inspected Relevant process controls are documented and transferred to production and suitably implemented with necessary training.
4. Monitor production process for compliance to implemented process controls to ensure quality product is shipped to customer and provide:
Trend analysis of data from the controls
Potential improvements for review with engineering based on the trends
Areas for Improvement to senior management
Review and propose changes to sampling plans based on trend analysis and changes to the system
5. Maintenance of customer concerns handling system in a timely manner including
Returned product analysis Organisation, filing and reporting of customer concerns
Ensure the requirements of the Electronic Documentation Management system
are understood and implemented at all levels of the organization.
Accountable to monitor manufacturing activities, measure significant process characteristics and analyse variation in order to detect and reduce waste
Ensure that in your absence, your area of responsibility is covered. Ensure that other departments are informed of your arrangements. Play a leadership role in encouraging the Company to achieve world class standards, above all by setting your own high professional standards as an example.
SKILLS AND KNOWLEDGE:
Ability to communicate and work with people inside and outside the department.
Excellent communicator: verbal, written and presentation skills.
Ability to train and lead assigned employees.
Ability to co-ordinate, plan and organise in a timely manner.
Knowledge of engineering theories and methods.
Rigorous attention to detail.
Ability to use Microsoft Office Suite (Excel, Project, Word, PowerPoint at a minimum) and ability to use / learn Oracle as the company ERP system (preferably Oracle)
MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS:
+ Demonstrate leadership in project management
+ Engineering, Science or Project Management Degree preferably with Quality Engineering included
+ Qualified systems lead auditor
+ Program Management certification or number of years experience
Integer Holdings Corporation (NYSE:ITGR) is the largest medical device outsource (MDO) manufacturer in the world serving the cardiac, neuromodulation, orthopedics, vascular, advanced surgical and power solution markets. The company provides innovative, high quality medical technologies that enhance the lives of patients worldwide. In addition, it develops batteries for high-end niche applications in energy, military, and environmental markets. The company’s brands include Greatbatch Medical, Lake Region Medical and Electrochem. Additional information is available at https://integer.net .
Integer is committed to equal opportunity for all, without regard to race, color, religion, creed, national origin, ancestry, ethnicity, sex (including pregnancy and gender), age, physical or mental disability, citizenship, veteran or military status past, current, or prospective service in the uniformed services, genetic information, sexual orientation, gender identity, marital status, or any other characteristic protected under applicable legally recognized protected basis under federal, state or local law. Greatbatch Integer complies with the Americans with Disabilities Act (ADA), as amended by the ADA Amendments Act, and all applicable state or local law. Consistent with those legal requirements, Integer will make reasonable accommodations for qualified individuals with a known physical or mental limitations of otherwise qualified employees and applicants with a disability if such accommodation would allow the individual to perform the essential functions of the job, unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel believe you need a reasonable accommodation pursuant to the ADA, please contact us at
716-759-5739.
No More Results

Posted

1 day ago

Description

At Integer, our vision and values are embedded in everything we do!


If you want to work for an organization that values customer focus, teamwork, respect, integrity, communication and innovation, apply now!


JOB SUMMARY:


Provide engineering support to production through improved methods, processes, jigs and fixtures, tooling and machine enhancements to improve standard times and employee efficiencies in order to manufacture quality medical guide-wires at the target costs. Validate and introduce new equipment and processes to production. Create and maintain Device Master Record (DMR) Documentation through the order entry and ECO process. Train employees to perform processes as documented by standard operating procedures.


ESSENTIAL JOB DUTIES AND RESPONSIBILITIES:


Employees are expected to support the quality concepts inherent in the business philosophies of Lake Region Medical including a variety of job related tasks, which may not be specific to this position profile.


Accountabilities include:


+ Learn Lake Region manufacturing processes and equipment in order to understand them, so as to be competent in providing technical support to production.

+ Lead or participate in projects, working closely with Production, Maintenance and Quality departments to implement the required changes to stabilise and improve processes. Goals include reducing defects, increasing efficiencies and increasing process uptime.

+ Employ Lean Manufacturing and Six Sigma methodologies such as process mapping, control charting, as appropriate in project work.

+ Monitor manufacturing activities, measure significant process characteristics and analyse variation in order to detect and reduce waste / scrap. Support the manufacturing process by taking corrective and preventative action on production delays and deviations.

+ Project management using standard Lake Region methodology.

+ Transfer of automation and new process projects to production, both within and between sites.

+ Transfer of New Products to production, both within and between sites.

+ Assist in training employees in new or improved processes.

+ Process and product validation.

+ Process / layout design and implementation.

+ Develop and support related documentation: - ECO generation to introduce changes and maintain DMR documentation.

+ Order Entry processing.

+ Sourcing, specifying and purchasing production equipment.

+ Jigs and fixture specification and development.

+ Assist in the specification of spare part lists.

+ Be an active member of the Lake Region Medical Limited team and work with all employees to develop a world class lean manufacturing system.

+ Comply with the Lake Region Medical Limited behavioural standards.


SKILLS AND KNOWLEDGE:


+ Ability to communicate and work with people inside and outside the Department as necessary to execute these responsibilities.Ability to train and lead assigned employees.

+ Ability to understand and follow appropriate Departmental policies, procedures, practices and to understand inter-relationships of people and functions.

+ Knowledge of manufacturing operations, systems and project management, including procurement, inventory control, quality control, production planning and control, test and inspection, layout.Knowledge of engineering theories, methods and work measurement techniques.

+ Ability to apply engineering methods in the definition, design, research, development, utilisation, maintenance, and cost-control of processes and equipment to build Lake Region products and improve qualities and reduce costs of such processes and products. MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS: College graduate with degree in Engineering, or equivalent experience. PHYSICAL DEMANDS: Work effectively with close tolerance. MENTAL DEMANDS:


+ Ability to work in an organised fashion.

+ Attention to detail.

+ Self-starter. WORKING CONDITIONS:


+ Day-shift operation, but may be required to change working hours or work other shift patterns occasionally as project responsibility dictates.


Integer Holdings Corporation (NYSE:ITGR) is the largest medical device outsource (MDO) manufacturer in the world serving the cardiac, neuromodulation, orthopedics, vascular, advanced surgical and power solution markets. The company provides innovative, high quality medical technologies that enhance the lives of patients worldwide. In addition, it develops batteries for high-end niche applications in energy, military, and environmental markets. The company’s brands include Greatbatch Medical, Lake Region Medical and Electrochem. Additional information is available at https://integer.net .


Integer is committed to equal opportunity for all, without regard to race, color, religion, creed, national origin, ancestry, ethnicity, sex (including pregnancy and gender), age, physical or mental disability, citizenship, veteran or military status past, current, or prospective service in the uniformed services, genetic information, sexual orientation, gender identity, marital status, or any other characteristic protected under applicable legally recognized protected basis under federal, state or local law. Greatbatch Integer complies with the Americans with Disabilities Act (ADA), as amended by the ADA Amendments Act, and all applicable state or local law. Consistent with those legal requirements, Integer will make reasonable accommodations for qualified individuals with a known physical or mental limitations of otherwise qualified employees and applicants with a disability if such accommodation would allow the individual to perform the essential functions of the job, unless the accommodation would impose an undue hardship on the operation of our business. If you are interested in applying for an employment opportunity and feel believe you need a reasonable accommodation pursuant to the ADA, please contact us at


716-759-5739.
Source: Integer