- ResponsibilitiesPerform routine and non-routine microbiological testing with accurate documentation.Manage lab operations: scheduling, equipment, stock control, and maintenance.Ensure a safe, compliant lab environment aligned with SOPs and quality standards.Maintain quality systems (cGLP), including SOPs, validations, investigations, and trend reviews.Collaborate cross-functionally to support projects and continuous improvement.Lead contamination control eResponsibilitiesPerform routine and non-routine microbiological testing with accurate documentation.Manage lab operations: scheduling, equipment, stock control, and maintenance.Ensure a safe, compliant lab environment aligned with SOPs and quality standards.Maintain quality systems (cGLP), including SOPs, validations, investigations, and trend reviews.Collaborate cross-functionally to support projects and continuous improvement.Lead contamination control e
- ResponsibilitiesDeveloping dashboards, examining data, and compiling reports for business discussions.Stay up to date with market trends to identify new lead opportunities.Support the team with increasing effectiveness of business development initiatives.Identify process improvement opportunities to promote team productivity and operational goals.Building partnerships with new and existing clients.RequirementsKnowledge of the pharmaceutical industry or relResponsibilitiesDeveloping dashboards, examining data, and compiling reports for business discussions.Stay up to date with market trends to identify new lead opportunities.Support the team with increasing effectiveness of business development initiatives.Identify process improvement opportunities to promote team productivity and operational goals.Building partnerships with new and existing clients.RequirementsKnowledge of the pharmaceutical industry or rel
- ResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.ActResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.Act
- We are currently recruiting for a packaging operator with a client of ours within the pharmaceutical industry based in Tallaght The role is offered on an initial 6 month contract with a possibility of extension. Expected hours are 7:30am - 3:30pm Monday - Friday (39 hours per week) Duties & Responsibilities Responsible for in process weight, volume and quality checks are carried out as per SOPs. Perform line setups, clearances and reconciliations as per SWe are currently recruiting for a packaging operator with a client of ours within the pharmaceutical industry based in Tallaght The role is offered on an initial 6 month contract with a possibility of extension. Expected hours are 7:30am - 3:30pm Monday - Friday (39 hours per week) Duties & Responsibilities Responsible for in process weight, volume and quality checks are carried out as per SOPs. Perform line setups, clearances and reconciliations as per S
