NordsonBoyle, 35 km from Sligo
machines, processes or products to bring concept to market, including essential product and process documentation.
• Uses a science-based approach to develop processes, process improvements and technology improvements.
• Understand current processes, taking...
Reperio Human CapitalIreland
Project ManagerI am currently recruiting for a retail bank in Dublin, and looking for an experienced Project Manager with full business change project lifecycle experience. ...
Wellington Professional RecruitmentIreland
As Project Manager, your duties will include but not be limited to: Support the advancement of wastewater treatment plant upgrades thoughout IrelandLeading project teams to deliver wastewater infrastructure projects within agreed scope, timeframes and budgets.
Ensuring project financial performance ...
Reperio Human CapitalIreland
They are looking to introduce a Data Engineer to join their growing team. Proven experience (4 years) in data engineering roles with a focus on the Microsoft stack. Familiarity with Azure cloud services, particularly Azure Data Factory and Azure DatabricksNice to have:Experience with.
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Specialist QA
Collins McNicholas | Sligo | www.collinsmcnicholas.ie |
This job offer is not available in your country.
Excellent opportunity for a QA Specialist with a leading Life Sciences company located in the North West of Ireland . The QA Specialist ensures product manufacturing complies with GMP and Regulatory standards.
Responsibilities include validating facility, equipment, and utilities, as well as reviewing and approving validation documentation .
This individual contributor role requires a self-starter with expertise in QA and validation , facilitating collaboration with departments like Quality Control, Manufacturing, Engineering, and Technical Services.
Overview of your responsibilities :
Provide technical expertise and guidance on QA and compliance topics , including validation strategy, new product introduction, and manufacturing issue resolution.
Manage assigned QMS areas , including Deviation, Change Control, CAPA, audits, complaints, vendor management, and approval of batch records and production materials.
Generate, review, and approve SOPs / documentation in designated areas.
Timely review and approval of site procedures to ensure GMP and regulatory compliance .
Review and approve validation protocols / reports to meet EU regulatory expectations.
Maintain GMP / validation document review to support technology transfers and NPI.
Apply Quality Risk Management principles as needed.
Lead QA activities in project work-streams involving cross-functional teams.
Knowledge, Skills and Experience Required for the Role :
Third-level qualification in relevant science or engineering discipline.
Minimum 5 years of experience in a GMP Quality environment.
Experience in Validation function with strong knowledge of Project Life Cycle and cGMP.
Excellent opportunity for a QA Specialist with a leading Life Sciences company located in the North West of Ireland . The QA Specialist ensures product manufacturing complies with GMP and Regulatory standards.
Responsibilities include validating facility, equipment, and utilities, as well as reviewing and approving validation documentation .
This individual contributor role requires a self-starter with expertise in QA and validation , facilitating collaboration with departments like Quality Control, Manufacturing, Engineering, and Technical Services.
Overview of your responsibilities :
Provide technical expertise and guidance on QA and compliance topics , including validation strategy, new product introduction, and manufacturing issue resolution.
Manage assigned QMS areas , including Deviation, Change Control, CAPA, audits, complaints, vendor management, and approval of batch records and production materials.
Generate, review, and approve SOPs / documentation in designated areas.
Timely review and approval of site procedures to ensure GMP and regulatory compliance .
Review and approve validation protocols / reports to meet EU regulatory expectations.
Maintain GMP / validation document review to support technology transfers and NPI.
Apply Quality Risk Management principles as needed.
Lead QA activities in project work-streams involving cross-functional teams.
Knowledge, Skills and Experience Required for the Role :
Third-level qualification in relevant science or engineering discipline.
Minimum 5 years of experience in a GMP Quality environment.
Experience in Validation function with strong knowledge of Project Life Cycle and cGMP.