Westbourne Jobs in Ireland

The IM Lab Automation Analyst will manage and support IT activities related to a planned program of Laboratory Automation System deployments across Quality Control (QC) and Research & Development (R&D) laboratories. · Project manage the implementation of Laboratory Automation Sys ...

We are looking for a skilled Level 2 Deskside Support Engineer to provide advanced onsite technical support to end-users in our Cork office. · ...

The Validation Engineer will be responsible for the validation of Lab Systems in QCL Labs and Manufacturing Operations. · We are seeking an enthusiastic and experienced validation engineer to join our team on a long-term contract basis.The position will work within a collaborativ ...

We are looking for a skilled Level 2 Deskside Support Engineer to provide advanced onsite technical support to end-users in our Cork office. · ...

Job Summary · This Lab Automation Project Lead position involves managing IT activities for Laboratory Automation System deployments. · Responsibilities: · Develop validation documentation · ...

The IM Lab Automation Analyst will manage and support IT activities related to a planned program of Laboratory Automation System deployments across Quality Control (QC) and Research & Development (R&D) laboratories. · Project manage the implementation of Laboratory Automation Sys ...

We are currently looking to hire a · Lab method system script writer and Support Analyst to join our Lab IT services at the client site.Initially write SmartLab scripts for new and established analytical methods, training will be provided on SmartLab. · ...

+ LIMS technical support in GMP regulated environment. Manage and complete all Support tickets in timely manner. Work directly with level 3 administrators to resolve issues/requests. · Contribute to the support and maintenance of operating procedures pertaining to LIMS by reviewi ...

A leading company in the chemical and pharmaceutical sector is seeking to hire an Analytical Chemist. · ...

The QA Systems & Validation · Specialist is responsible for ensuring that all GMP-related changes, · systems, and validation activities comply with · regulatory requirements and site Quality standards.This role provides subject matter expertise across · change control, validatio ...