QA Validation Engineer

GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all...

GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all...

We Make Life More Rewarding and Dignified Location: Ballina Department: Quality Summary: The primary purpose of the Continence Care Validation Supervisor role is to lead the Continence Care QE Validation team and support any other QA activities on site as required. The primary Customers include Ballina Engineering, Manufacturing, Supply Chain Management,...

The role: PE Global is currently recruiting for a QA Validation Specialist on behalf of a leading pharmaceutical company based in Carlow. This is an initial 11-month contract role. Description: Carlow is offering an amazing opportunity for a Quality Assurance Specialist to join our quality team. In this role, you will play a vital role in supporting the...

QA Validation Specialist (New Product Introduction) 11 month contract On site Carlow AMC22404 I am on the lookout for a QA Specialist for Validation and NPI for a rapidly expanding biotechnology manufacturer in Carlow. You will be an essential member of the Technical transfer and Validation team responsible for managing development and manufacturer of...

Computer System Validation Engineer Ireland West Sligo Permanent Did you ever wish you joined a company at the start, when things where going from start up to ramp up? This is the prefect role for you to consider if you are looking to make a real impact and for you to be proud of being part of this great place to works company journey. I am looking to speak...

This is an 11-month initial contract. Purpose In this role, you will play a vital role in supporting the introduction of new products and Quality oversite of executed validation completed at our Carlow facility. As the QA Specialist for Validation and New Product Introduction (NPI), you will be an essential member of our esteemed Technical...

Team Horizon is seeking a Cleaning Validation Engineer for our Clients manufacturing facility in Sligo. In this role you will execute cleaning validation tests in accordance with approved protocols, procedures and guidelines.Why you should apply: * You will provide technical leadership in the area of cleaning validation and own the cleaning validation...

GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all...

Our client, a medical device engineering company in Sligo, is offering a range of development and manufacturing services from initial design assessment to the provision of sterile finished products for the European and US medical device market. They are seeking a Quality Assurance Engineer to join their team. Responsibilities include but are not limited...

Summary: Our client is a biopharmaceutical company based in Carlow looking for a Senior Validation Engineer to join its team for a significant expansion project transitioning the new facility from construction & project phase to a commercialisation of fully operational facility delivering life-saving products to patients. Responsibilities: Vial and Syringe...

Our client based in Sligo are looking to hire a QA Compliance Specialist on an initial 12 month contract. The Role: As the QA Compliance Specialist you will be responsible for documenting and establishing a quality system which ensures full compliance with all regulatory standards. You will be responsible for reporting on the effectiveness of the quality...

Senior Validation Engineer 12 month contract On site Carlow AMC22531 Start date ASAP I am looking for an experienced Equipment Validation Engineer to support the transition of a new biomanufacturing facility from project phase to a fully operational manufacturing facility. This role would be suitable for a CQV/lead Engineer with 6+ years experience in Vial...

Quality Assurance Specialist Validation and NPI An amazing opportunity has arisen for a Quality Assurance Specialistto join the quality team within a leading Biopharmaceutical Multinational. As a member of the Tech Transfer/Validation Team you will play a vital role in supporting the introduction of new products and Quality oversite of executed validation...

This is a 12-month contract with a view to extension. Purpose The role will require the leadership of an experienced, energetic, and committed Senior/ Lead Engineering (CQV/ Technical Engineer) with broad experience in Vial and Syringe Filling operations and the below key areas. Vial and Syringe Sterile operations Isolators, VHP, decontamination systems....

This newly created permanent position requires a specialised professional adept in cleaning validation, particularly within biologics manufacturing environments. This role will join a high performing and state of the art facility where you will have an opportunity to make a noticeable contribution. Key Responsibilities: - Validation Execution: Perform...

Computer System Validation Engineer Ireland West – Sligo Permanent Did you ever wish you joined a company at the start, when things where going from start up to ramp up? This is the prefect role for you to consider if you are looking to make a real impact and for you to be proud of being part of this great place to works company journey. I am looking...

Excellent opportunity for a CSV Engineer to join a global biologics company in the west of Ireland. Reporting to the Engineering Manager, this role will validate/qualify and maintain computer systems, including process automation systems, information Systems applications/infrastructure, and enterprise systems (e.g. ERP, Document Management Systems)....

The role involves working in a broad range of Quality Engineering disciplines, with particular focus on Validation and Compliance. The successful candidate will work closely with Engineering, Manufacturing and Continuous Improvement functions. Responsibilities: - Manage Change Control Requests as a quality resource - Planning, coordinating, executing,...

Our client based in Sligo are looking to hire a QA Compliance Specialist on an initial 12 month contract. The Role: As the QA Compliance Specialist, you will be responsible for documenting and establishing a quality system which ensures full compliance with all regulatory standards. You will be responsible for reporting on the effectiveness of the quality...