Overview PE Global Healthcare are delighted to assist their client, a leading Alzheimer healthcare service to recruit for a Day Centre Manager. The service works across the country in the heart of local communities to provide dementia specific services and advocating for the rights of people affected by dementia through quality supports and services. Responsibilities Assess and provide appropriate client care in the centre: Supervise, co-ordinate and support the work of all staff assigned to him/her: Carry out the administration required to provide an efficient and effective Day Care Centre: Ensure there is an awareness of the issues relating to dementia at a local level and promote the services provided locally by the Society: Keep the chairperson/committee informed on issues for their Support the committee in fundraising activities from time to time e.g. Tea Day, Christmas sales etc Attend training courses, conferences and meetings with the regional manager as required Carry out any other duties that may be assigned from time to Candidate Requirements Degree or foreign equivalent (validated by NQAI) ideally in Nursing, Social Care, Applied Social Studies in Social Care, Applied Social Studies, Social Studies At least 5 years’ post qualification experience in the heath/social care or voluntary sector At least 3 years’ of management experience in a similar role Experience of working with people with complex needs in a variety of different situations Demonstrated knowledge of the voluntary sector, older people issues and dementia Full clean driving license Please call Claire PE Global Healthcare 083 208 5507 or email Claire.osullivan@peglobal.net Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland PE Global Healthcare specialises in providing contract and permanent Healthcare professionals to the private and public sector. PE Global Healthcare finds jobs for Healthcare Staff in all specialties in Ireland. Register today to keep your finger on the Job Opportunity Pulse #J-18808-Ljbffr
A biopharmaceutical company is seeking a Principal Scientist in Dublin for a 12-month contract. The successful candidate will support upstream and downstream manufacturing processes in drug substance production, requiring strong knowledge of cGMP and data analytics. Responsibilities include providing technical support, implementing process improvements, and troubleshooting. Candidates should have a minimum BSc and at least 6 years’ experience in the biopharmaceutical industry. Interested individuals can apply by sending their CV to the provided email. #J-18808-Ljbffr
A leading healthcare service provider in Ireland is seeking a Day Centre Manager to oversee client care and support staff in a dementia-focused environment. The ideal candidate will have a degree in Nursing or Social Care, with at least 5 years of post-qualification experience and 3 years in management. Responsibilities include supervising staff, managing client care, and engaging with local communities. The role requires a full clean driving license and a commitment to advocacy for individuals affected by dementia. #J-18808-Ljbffr
PE Global is currently recruiting for a Principal Scientist on behalf of our client based in North Dublin: 12 month initial contract Our clients Multi Product Cell Culture (MPCC) Facility is seeking to recruit a contract upstream and/or downstream Manufacturing Support Scientist. The Manufacturing Support group (in MS&T) are responsible for continued process technical support to the cell culture, primary recovery and downstream unit operations for the commercial manufacture of multiple mammalian cell culture processes in the Multi Product Cell Culture facility. The successful candidate will be key contributor to this dynamic and highly technical team. This position will build collaborations with Manufacturing, Manufacturing Science & Technology (MS&T), Upstream and Downstream teams, Engineering, Quality Assurance, Quality Control and Global Regulatory Sciences groups to name a few. Key Responsibilities Have a thorough knowledge of the science behind each molecule and associated drug substance manufacturing processes with fundamental knowledge of one or more of the following relevant principles: Upstream (Cell Culture Focus) including media preparation, large scale cell culture bulk drug substance manufacturing processing (vial thaw, scale up, single use systems, seed and production bioreactors and harvest centrifugation/clarification); Downstream (Purification Focus): to include buffer preparation, purification and viral reduction steps, including chromatography, ultrafiltration, viral reduction filtration and viral inactivation technologies and DS formulation and bulk fill. To identify and implement process improvements, e.g. yield, cycle time reduction through evaluation of process performance using data analytics tools. Provides process subject matter expertise for regulatory inspections and other interactions with regulatory agencies (e.g. health authority query support – timely responses / data gathering etc.), representing the site. To provide on the floor support for troubleshooting processing issues and to lead manufacturing investigations into process deviations and resolution. Identify or support process improvements (through change control or CAPA) and participate in implementation of Lean initiatives at site. Authoring of technical documents, including protocols, reports and SOPs supporting the validation of the manufacturing process. To generate documentation protocols and lead the execution of plant supporting studies and technical studies on the manufacturing floor at commercial scale. Document and appropriately communicate aspects of work and learnings at internal and external fora (may include participation at scientific meetings). Qualifications & Experience Minimum BSc or equivalent with at least 6 years’ experience in drug substance manufacturing technical support in the biopharmaceutical industry. You have demonstrated awareness of cGMP compliance and regulatory agency requirements as well as strong oral communication and technical writing skills. Good interpersonal skills coupled with demonstrated ability to effectively work in a cross-functional global environment matrix organization, and in local group settings. Ability to develop, build, present and defend technical and scientific approaches in both written and verbal form. Can effectively partner with and influence stakeholders without direct solid line authority. Drives technical decisions balancing product quality and operational requirements. Please note that this role may infrequently require periods of extended hours or a modified work schedule and may require on-call availability. On-site Protocol Physical presence at the worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well‑being and engagement, and it enhances the Company culture. Interested candidates should submit an updated CV. Please click the link below to apply, call Audrey on 0214297900 or alternatively send an up-to-date CV to audrey.mccarthy@peglobal.net. #J-18808-Ljbffr
