The ideal candidate will be responsible for planning, coordinating, and implementing projects within the decided-upon budget, timeline, and scope. They will also effectively monitor and present project updates to relevant stakeholders, clients, or project team members. Responsibilities: Generation, Execution / Approval of Qualification Life Cycle documents from SLIA through to PQ and Fin...
Read moreValidation Engineer (Senior) – 12 month & 6 month contracts Onsite position (Western Ireland) – Potential to WFH on ad-hoc basis at discretion of manager. Joining team of approx. 6, reporting to Validation Team Leader. Overview: Coordinate the development & maintenance of validation programs in compliance with applicable regulatory and company requirements. Help direct, impl...
Read moreValidation Engineer (Senior) – 12 month & 6 month contracts Onsite position (Western Ireland) – Potential to WFH on ad-hoc basis at discretion of manager. Joining team of approx. 6, reporting to Validation Team Leader. Overview: Coordinate the development & maintenance of validation programs in compliance with applicable regulatory and company requirements. Help direct, impl...
Read moreThe role – As a QA CSQ/CQV Lead, you will play a pivotal role in ensuring the quality and compliance of validation and equipment qualification activities within a leading large molecule CDMO. This role involves overseeing computerised systems and lab equipment qualification, aligning with all relevant regulations, company policies, and contractual obligations. By reviewing and […]
Read moreTechnical Manager Central Ireland Overview A large global pharmaceutical organisation, providing a wide range of services for the development, manufacture and commercial launch of products for clients around the world. The Technical Manager is responsible for the management of R&D operations, chemists and labs at the site in central Ireland. Working closely with Team Leads, […]
Read moreQA Small Molecule Operations Scienta are teaming up with a leading Small Molecule Manufacturing site in the Scientific hub of Ireland. They now have an amazing opportunity for production QA Operations Specialist to join their young, expert, vibrant teams. Your roles objectives:* Manage quality-related matters specific to area of responsibility.* Responsible for approving appropriate quality-rel...
Read moreAssociate Director – QC Microbiology The Company: Scienta are teaming up with a Biotech Drug Substance Manufacturing Facility. This facility will be the most technically advanced manufacturing site and will include next-generation manufacturing technologies and advanced data collection and analysis platforms. Your role:* Provides leadership, direction, and governance for the QC microbiolo...
Read moreA global Pharmaceutical company are looking for an Affiliate Quality Lead to join the Irish Affiliate in Dublin. The Affiliate Quality Lead is responsible for the quality strategy and operations for their site in at their facility. You will be working closely with other department leads to ensure manufacturing and distribution meet standards and regulations. […]
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