Mr.Price Branded BargainsAnnacotty, 6 km from Limerick
and encourage team morale.
• Ensuring high store standards of cleanliness, merchandising and compliance with health & safety.
• Cash handling & till operation.
#AM
Job Type: Full-time
Benefits:
• Employee discount
• On-site parking
• Wellness program
Schedule...
Regeneron IrelandLimerick
GMP standards to ensure compliance with written procedures Tracking and supervising QC open compliance records ( CAPA's /Change Controls and Workflows) Reporting quality system metrics to the group and other QC functions Representing QC on interdepartmental teams and in meetings Participating in reg...
Regeneron IrelandLimerick
As a QC Electronic Data Management Specialist, a typical day might include, but is not limited to, the following: Work with cross-functional teams to define and prioritize electronic laboratory data systems projects and initiatives Ensure harmonization of electronic laboratory data systems use and m...
Regeneron IrelandLimerick
Lead-Related Activities include, but are not limited to, the following: Providing on-the-floor guidance and support to employees Ensuring employees' timesheets are completed on time Monitoring employee training to ensure that all requirements are met, including OJT Maintaining up to date training re...
Limerick
QA Specialist
This role participates in maintaining site compliance of operations inclusive of but not limited to Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities, Maintenance, Engineering, Materials Handling, and QA...
Regeneron Pharmaceuticals, IncLimerick
Within this role you will be responsible for working with cross-functional teams to drive activities that will ensure a state of continuous GMP compliance in Regeneron IOPS and to build inspection readiness capability across the organization...
Cook Medical IncorporatedLimerick
Overview
The primary function of this position is to manage a team of Engineers focused on design modifications of devices post release to market, for the purpose of maintaining device quality and compliance, securing regulatory approval, as well...
Cpl HealthcareLimerick
operations.The Associate Director QA is responsible for QA business processes including support of GMP and GLP compliance, regulatory inspection readiness, Quality Plan and continuous improvement projects and will provide leadership and direction to the QA team...
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Process Development Engineer
Limerick | Contract | www.cv-library.ie |
Process Development Engineer
Limerick - Hybrid Role
Company:
My client are a medical device company developing new and innovative invasive medical devices. As the Process Development Engineer, you will join an award winning Research and Development team focusing on the implementation of new projects and cutting edge devices.
Job Description:
Support the development and implementation of manufacturing and assembly processes associated with NPI, design feedback & input, as well as working with the suppliers key components. The PD Engineer will work closely with his/her counterparts responsible for device development and characterization, other development functions, and Quality.
The successful candidate will have be a self-starter, together with the required persistence and resourcefulness to succeed.
They will have hands-on knowledge and experience in both the development of Class III Medical Devices and the processes required to manufacture them.
Responsibilities:
• Develops manufacturing processes, materials, and methods as part of the product development team
• Designs, specifies, procures and qualifies process fixtures and equipment
• Develops Work Instructions and other supporting documentation (e.g. calibration and maintenance) for manufacturing processes
• Executes process characterisation and validation activities
• Becomes a technical expert in the assembly and manufacture of our products, and provides technical guidance to other team members
• Builds Quality into all aspects of work by maintaining compliance to all quality requirement
• Works with internal cross-functional teams and contract manufacturers or design firms to ensure system design, architecture, and verification/validation meets design input
• Supports cleanroom setup, fit-out & validation
• Evaluates relevant process & manufacturing technologies and strategically identifies opportunities to implement them
• Executes project plans, tasks and deliverables.
• Manages time to meet project deadlines.
• Uses structured problem-solving techniques and statistical methods for data driven analysis and decisions Skills,
Required Qualifications:
• Minimum of three years of medical device process development experience, and have either a primary or Master’s Degree in a relevant engineering discipline such as polymer, mechanical, manufacturing or biomedical engineering.
• Hands-on knowledge and experience in both the development of Class III Medical Devices
• Experience in fabrication and manufacture of Medical devices
• Product and process development, and new product introduction skills in medical devices are a must.
• In particular:
• Fixture and equipment design & specification
• Validation of processes and process equipment
• Development of Work Instructions and Calibration & Maintenance activities for manufacturing processes
For immediate consideration please forward your CV together with a covering note outlining your relevant experience and your availability notice
Limerick - Hybrid Role
Company:
My client are a medical device company developing new and innovative invasive medical devices. As the Process Development Engineer, you will join an award winning Research and Development team focusing on the implementation of new projects and cutting edge devices.
Job Description:
Support the development and implementation of manufacturing and assembly processes associated with NPI, design feedback & input, as well as working with the suppliers key components. The PD Engineer will work closely with his/her counterparts responsible for device development and characterization, other development functions, and Quality.
The successful candidate will have be a self-starter, together with the required persistence and resourcefulness to succeed.
They will have hands-on knowledge and experience in both the development of Class III Medical Devices and the processes required to manufacture them.
Responsibilities:
• Develops manufacturing processes, materials, and methods as part of the product development team
• Designs, specifies, procures and qualifies process fixtures and equipment
• Develops Work Instructions and other supporting documentation (e.g. calibration and maintenance) for manufacturing processes
• Executes process characterisation and validation activities
• Becomes a technical expert in the assembly and manufacture of our products, and provides technical guidance to other team members
• Builds Quality into all aspects of work by maintaining compliance to all quality requirement
• Works with internal cross-functional teams and contract manufacturers or design firms to ensure system design, architecture, and verification/validation meets design input
• Supports cleanroom setup, fit-out & validation
• Evaluates relevant process & manufacturing technologies and strategically identifies opportunities to implement them
• Executes project plans, tasks and deliverables.
• Manages time to meet project deadlines.
• Uses structured problem-solving techniques and statistical methods for data driven analysis and decisions Skills,
Required Qualifications:
• Minimum of three years of medical device process development experience, and have either a primary or Master’s Degree in a relevant engineering discipline such as polymer, mechanical, manufacturing or biomedical engineering.
• Hands-on knowledge and experience in both the development of Class III Medical Devices
• Experience in fabrication and manufacture of Medical devices
• Product and process development, and new product introduction skills in medical devices are a must.
• In particular:
• Fixture and equipment design & specification
• Validation of processes and process equipment
• Development of Work Instructions and Calibration & Maintenance activities for manufacturing processes
For immediate consideration please forward your CV together with a covering note outlining your relevant experience and your availability notice
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