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To perform day to day laboratory testing, data review, routine duties and capable of enthusiastically taking responsibility for ad-hoc duties and projects. While working co- operatively as part of a team, will demonstrate drive, initiative and hunger for knowledge and quality of work
Role You will provide technical support to the QC Microbiology Lab & operations to ensure the continued manufacture and supply of quality pharmaceutical products in meeting the priorities of: Compliance, Supply, Strategy and Profit Plan. This role holds more senior responsibilities within the Microbiology Laboratory including (but not limited to) documentation development, report writing, execution […]
Support internal and external manufacturing operations remain operational, continuously improve, and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation
Primary responsibilities for the Validation Engineer include the following: Project validation support including conducting equipment performance qualifications (specifically cleaning and sterilization validation) Authoring project validation master plans; SOP and documentation updates; Authoring validation protocols and final reports, executing validation studies, analysis of validation data; Resolving technical issues encountered during study execution. This individual will be required to work
Project Design Manager is co ordinating the Design team for the project, broadly comprising of Engineering partner. Managing prioritisation and on-time delivery of design deliverables to mee the construction schedule Design pull by Construction). They will also help coordinate activities in the suite team to support the design activities, workshops etc. This includes design delivery and documentation, qualification efforts.
As QC Bioassay Analyst you will perform and review a range of techniques such as immunoassays, cell based potency bioassays and aseptic techniques as part of routine and non-routine testing and project work to ensure processes and end products comply with corporate and regulatory requirements to facilitate product release.
As part of the team, perform various Weigh and Dispense and material availability-related tasks to aid in the manufacture and reliable supply of products. Operate and/or monitor weigh and dispense activities and support equipment, using MES/DCS and PLC based systems, to ensure optimum equipment uptime and target outputs. Equipment will include, yet is not limited to, down flow booth and scales.
An amazing opportunity has arisen for a QC Analyst in Analytical Testing at a single use Multiproduct Biotech facility. In the site the role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and Analytical Methods. 11 month contract, onsite position with pay rate up to 30 euro per hour depending on experience.
Scientist role for pharmaceutical company based in Meath.11 month contract position with pay up to 33 euro per hour depending on experience. Hybrid working possible. Experience of pharmaceutical formulation development and/or clinical supplies manufacture is desirable. The Staff Scientist is required to possess a degree in Chemical Engineering, Pharmacy, Pharmaceutical Sciences or equivalent plus some industrial experience. Position will receive direction and support.
This is an amazing opportunity for a Quality Assurance Specialist to join our quality team. 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 Transfer/Validation Team. This team holds responsibility for managing the development and manufacture of vaccines and biologic