About the role Do you have Automation Engineer and Pharmaceutical Manufacturing experience, and are you seeking a new job? Cognizant is looking for a Senior Automation Engineer (DeltaV) in Dublin, and the role comes with an attractive salary and benefits package. You'll be working with a collaborative and inclusive company and will be involved in commissioning and on-site support activities. As a Senior Automation Engineer, you will join the projects Team in Dublin, where you will be involved in commissioning and on-site support activities. You will also generate functional specifications, design and test specifications for recipes, phase sequences, equipment modules, control modules, customized logic and HMI Graphics based on customer User Requirement Specifications (URS). In this role, you will: In your first few weeks in this Senior Automation Engineer role, you can expect to: Configuration and Testing of Recipes, Phases, equipment modules, Control Logic and Interlock Schemes based on design and test specifications Lead teams of Engineers and manage the project resources, scheduling task assignments, client interaction, coordination amongst different vendors and remote engineering office teams Batch Process upgrading on the DeltaV platform for pharmaceutical clients. What you must have to be considered Degree-qualified automation engineer with over six years of pharmaceutical manufacturing experience. You will also require the following: S88 / Batch Delta V expert Expert understanding of all project lifecycle phases and tasks Demonstrable project management skills Track record demonstrating ability to lead a complete project Ability to work independently. You'll receive an excellent salary and benefits package for your knowledge, expertise and flexibility. At Cognizant, taking care of employees is a priority: You can pursue innovative career tracks and opportunities here You can enhance your professional development through education and dedicated training We'll give you the skills you need to keep pace with the changing workplace while our compensation, benefits and wellness packages help you stay healthy and plan. Work model We strive to provide flexibility wherever possible. Based on this role's business requirements, this is a Hybrid position, based on our clients site 3 days per week. The working arrangements for this role are accurate as of the date of posting. This may change based on the project you're engaged in, as well as business and client requirements. Rest assured; we will always be clear about role expectations. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Senior Backend Engineer Role Details: Full-time for 40 contracted hours per week Salary: €80,000 Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV. - €92,000 Location: Ireland - Work from home or office based at ATU Sligo campus Who We Are Isla Health is a venture-backed healthtech startup, supporting our partners across the UK, EU and internationally. We have built a new category of healthcare technology which we refer to as the Digital Pathway Platform (DPP). Founded in 2019, we now support 25% of NHS Trusts and see 2 million submissions on the platform every year. As a company we are all laser focused on enabling a scalable model of care which empowers healthcare staff and improves patient outcomes. The DPP supports this by setting up digital pathways which are remote-first and asynchronous. As pathways harness sophisticated automation, clinical algorithms and intelligent cohorting, patients always take the optimised route through their pathway, thereby delivering a step change in clinical productivity. The Role We are looking for a Senior Node.js Engineer to work closely with our product & client facing teams, understand our customer challenges, and ship things quickly to test & learn. You will design, scope, build and deploy new features quickly for our users. Youll have high ownership over whole areas of the codebase and own features end-to-end, contributing to a platform that supports millions of patient interactions. You should be biased towards pace and experimentation and excited about solving the big challenges in healthcare. What Youll Do Build the platform that will allow our clients to look after their patients, integrating new data sources to drive our DPP, managing those complex clinical data flows to ensure that data is where it needs to be, and then writing updates back to 3rd party systems. Own services in production, including monitoring, debugging, and improving reliability over time. Collaborate with product and design to deliver user-focused solutions. Support and improve our cloud infrastructure. Outcomes Youll Be Responsible For Deliver high-quality, maintainable backend systems that scale with growing usage. Take ownership of features/services and ensure they are reliable in production. Support and mentor other engineers through collaboration and code review. Champion technical excellence and continuous improvement by driving best practices in software development, DevOps, and cloud infrastructure. The Team You will be joining a lean & high performing engineering organisation. We value pace, but also hold really high quality standards for each other. The structure: You will be a member of our Backend/Platform team. As a Senior Engineer, you will report directly to our Backend Lead. Cross-functional collaboration: Youll work in a tight loop with our Product, Design, and Frontend teams. Our tech & tools: We lean into modern, scalable infrastructure (Node.js, TypeScript, GCP). We prioritise tools that enable velocity - such as Terraform and automated CI/CD. We also lean heavily into AI, and youll be able (encouraged) to use whatever tools you need to scale your own and the teams workflows. Requirements As a Person You're a proactive Engineer who enjoys collaborating with all areas of the business and our customers directly. Youre passionate about solving complex problems in a team of brilliant people. You bring empathy and enthusiasm to help the wider team progress through mentoring. Youll bring strong experience in GCP and backend design, and support others through collaboration and knowledge sharing. Youll be super curious & love pushing the boundaries of agentic coding & scaling your own abilities. As a Developer Youll have professional experience as a Senior Developer, ideally in a startup, ideally ~5+ years as a developer. On that journey, youll have worked with lots of variety (exhaustive list below, not all required!): Writing code: Deep understanding of best practices when building Node.js applications with TypeScript & experience integrating with a variety of APIs, e.g. REST & SOAP. Cloud experience: Hands-on experience with cloud infrastructure. Ideally Google Cloud Platform, although not required. E.g: Datastore, Cloud Run, Cloud Functions, IAM, Docker. Networking: Solid understanding of VPCs, subnets, private VPNs. CI/CD: Automation, such as GitHub Actions. Infrastructure: Proven experience with unit testing frameworks such as Jest. Benefits Flexible working times - Work from home or our office based at ATU Sligo campus. Work abroad for up to 90 days per year. 25 days annual leave (on top of public holidays). Take your birthday off and another for a significant day of your choice. Generous well-being perks. An annual learning budget to support your growth. Delivering social impact through improved patient healthcare. Working at a well-funded and rapidly growing start-up, solving a global problem in a new way. Hiring Process Interviewing with us for the Senior Node.js & Cloud Engineer role will be split into 4 stages (all conducted virtually): A screening interview with someone from our People team - 15 minutes. A practical task you will complete independently. A technical interview with one of our Engineering Leads - 1 hour. A final interview with our co-founder CTO - 30 minutes. Diversity and Inclusion Isla is an equal opportunity employer and is committed to building an inclusive and diverse team. We encourage all qualified candidates to apply. Isla does not discriminate against anyone on the basis of their race, gender, disability, religion, national origin, age, or any other protected category. We choose to celebrate our teams differences and see them as one of our most valuable assets. Recruitment is not one-size-fits-all and we're happy to tailor our hiring process to better meet the needs of individual applicants. Using AI Tools for Your Application Most of our roles include several questions as part of the application process. AI tools such as ChatGPT might be useful in structuring or proof-reading your cover letter or your application answers. We encourage you to do your own research though to fully understand the company and the role you are applying to as you will be asked questions during any interview. Generic AI-generated answers are also really obvious. xsokbrc We'd like to get an idea of how you think early in the process; you should also make sure Isla is the right fit for you before you apply. Make AI tools work for you, not against you! Benefits: Work From Home

Quality Assurance Validation About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. Do not pass up this chance, apply quickly if your experience and skills match what is in the following description. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn . Are you driven to make a real difference in the lives of patients? We are seeking individuals who thrive in dynamic environments, embrace new ideas and are committed to making a meaningful impact. Location and Working Environment This position is 100% onsite in Tralee, Ireland. Purpose & Scope The role is part of the Quality Assurance function within the Astellas Ireland Co. Ltd. Tralee Plant Aseptic Manufacturing Facility. The QA Validation resource will be primarily responsible for the implementation, execution, and assessment of quality systems, procedures, and records to support compliant GMP operations. Responsibilities include ensuring adherence to agency regulations (GxP) and guidance, industry best practices, local regulations, and internal policies and procedures. This position works closely with Validation, Engineering, Manufacturing, Facilities, Document/Data Management, Quality Control (QC) and other GxP supporting functions to ensure compliance. This is accomplished by direct collaboration and oversight of Validation, Facilities/Engineering, Manufacturing Operations, QC activities and the review/audit of data and reports as specified by Standard Operating Procedures. Role and Responsibilities Build strong cross-functional relationships to ensure clear quality requirements and effective collaboration from project start. Provide hands-on QA oversight to staff and contractors, ensuring compliance with SOPs and GxP standards. Review and approve validation lifecycle documentation (plans, specifications, risk assessments, protocols, reports, deviations, and change controls). Partner with validation and stakeholders to define strategies, support project execution, and ensure timely, high-quality facility readiness in a cGMP environment. Author, review, and manage QA documentation and quality system records (SOPs, deviations, CAPA, change controls), including leading investigations and audits. Support leadership, external communications, and quality culture development while ensuring regulatory engagement and continuous improvement. Required Qualifications Science based degree with experience in a cGMP compliance environment, experience of QA function in an aseptic manufacturing plant essential. What awaits you at Astellas? Global collaboration and connection with like-minded life-science leaders. Real-world patient impact through transformative therapies. Relentless innovation at the forefront of scientific advancement. A culture of growth that supports your development and ambitions. Our Organizational Values and Behaviors Impact Innovation Integrity One Astellas Accountability Courage Sense of Urgency Outcome Focus Benefits Learn more at: We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help. #LI-Tralee #LI-Onsite #LI-LG1 To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Area Sales Manager The full job description covers all associated skills, previous experience, and any qualifications that applicants are expected to have. - Ireland Pharma & Biotech | New Position | Excellent Package Candidates must have the right to work in Ireland. Unfortunately LOWENCO and Force are unable to offer visa sponsorship for this role. Force is delighted to be supporting LOWENCO in recruiting their first dedicated Area Sales Manager for Ireland, a landmark hire for a fast-growing international business making a decisive move into one of Europe's most significant life sciences markets. LOWENCO is an internationally operating business with an established presence on the US East Coast and in Germany, reporting into a Chief Sales Officer based in Denmark. Ireland represents their next major growth territory and with good reason. Ireland hosts the highest concentration of top-tier pharmaceutical and biotechnology operations in Europe, making this one of the most commercially exciting territories the company has entered. This is a true new business development role a hunter position for someone who thrives on building pipelines from the ground up, engaging senior stakeholders, and winning technical capital projects across the pharma and biotech sectors. The successful candidate will have the rare opportunity to shape LOWENCO's Irish market presence from day one, with the full backing of an experienced international team. Key Responsibilities Build and develop a strong sales pipeline across the pharmaceutical and biotechnology sectors Actively engage clients through in-person meetings with decision-makers, engineering departments, and site managers Prospect for and acquire new clients with a proactive, hunter-style approach Facilitate lunch & learn sessions and technical presentations for engineering firms Prepare and present accurate, compelling quotations and proposals Attend industry exhibitions and conferences in Ireland and selected European markets Collaborate with the internal sales team and Project Engineering Department Provide expert technical guidance and advice to clients Professional Background The ideal xsokbrc candidate will bring the following: Demonstrated success in technical project sales (CapEx) and direct sales roles Established network within engineering firms specialising in the pharmaceutical and biotechnology sectors Prior experience within the pharmaceutical and biotechnology industries Technical proficiency, possibly evidenced by an engineering background Proficiency in CRM systems is a mandatory requirement A minimum of 5 years' sales experience is expected To arrange a confidential discussion and to receive the full candidate pack, please call Shirley on or apply via the link. #Technical Sales Skills: Sales Engineering pharmaceutical biotech Business Development CRM Capex

About CAI: CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 700 people worldwide. Scroll down to find the complete details of the job offer, including experience required and associated duties and tasks. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries. Are you Ready? Our approach is simple; we put the client's interests first, we do not stop until it is right, and we will do whatever it takes to get there. As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally: We act with integrity, We serve each other, We serve society, We work for our future. With employee ownership, one person's success is everyone's success; we work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially. CAI agents will be exposed to cutting edge technologies in the advanced medicine space. You will have an opportunity to work with recognized subject matter experts allowing YOU to be a key player in bringing lifesaving therapies to market. As part of our company culture, we invest in YOUR future, and commit to hands on certifications as well as professional training. Our collaborative culture ensures that our customers benefit from exemplary work across our entire range of professional services. Requirements include: We are now seeking a CQV Engineer to join our growing operations in Ireland The role of a CQV Engineer in CAI is to: Conduct and lead Commissioning, Qualification, Validation team activities with a direct regard for Safety. Managing the C&Q documentation and execution lifecycle from SLIA generation through to OQ completion. Generating C&Q Procedures for projects. Approval of TOPs. Facilitate scoping / planning of commissioning spares and consumables. Deliver the C&Q activities as required to meet the schedule Track progress of C&Q activities as required. Preparation of Qualification Summary Reports (QSR), and management of Requirement Traceability Matrix (RTM) Execution of Design reviews, shakedown, commissioning, FAT's, IQ, OQ, PQ activities. Management of any aspect of C & Q, verification as requested i.e., Change Controls, Management of Contractors and Vendors, document control, punch list management. Coordinate with project contractors and equipment vendors to execute required tests. Allocate project resources for efficient execution of project deliverables. Coordinate support during C&Q execution - Position Requirements: BS or MS in a relevant science or engineering field, or equivalent 3+ years in CQV SME roles for life sciences - Clean Utilities/Filling experience preferable Excellent oral and written communication skills Excellent problem-solving skills Customer-service focused. Proficient in life science manufacturing processes in areas such as biotech, aseptic fill/finish, OSD, Gene Therapy or equivalent experience. Able to travel domestically and internationally if required. #LI-JD1$1 To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Graduate Onsite Support Engineer (2 year FTC) About Astellas At Astellas we are making treatments that matter to people. Do you have the right skills and experience for this role Read on to find out, and make your application. We are tackling the toughest health challenges, placing the patient at the heart of everything we do. Through our global vision for Patient Centricity, we integrate the patient experience into our everyday working practices. We have developed ground breaking medicines in immunology, oncology and urology, improving and saving the lives of patients worldwide. Learn . Are you driven to make a real difference in the lives of patients? We are seeking individuals who thrive in dynamic environments, embrace new ideas and are committed to making a meaningful impact. Location and Working Environment This position is 100% onsite in Kerry, Ireland This is a 2 year FTC September 2026 Start This position will require on-site work and may require occasional evening or weekend work. Purpose and Scope: The On-Site Support Engineer is responsible for providing comprehensive onsite technology support and services to ensure optimal performance of all IT infrastructure and systems at assigned sites. This role involves installation, maintenance, troubleshooting, and repair of hardware and software, as well as providing excellent customer service to resolve technical issues efficiently. Role and Responsibilities Onsite Support: Learn and work with IT technical support for hardware, software, and networking issues. Understand routine maintenance and upgrades on IT systems and equipment. Diagnose and provide technical information with computers, servers, networks, and other technological components Follow onsite team guidance and perform hardware repairs, replacements, and system updates as needed. Customer Service: Involve in customer interactions to clients for addressing their technological concerns promptly and professionally. Communicate effectively with clients to understand their requirements. Train and support end-users on technology usage and best practices. Documentation and Reporting: Follow IT team guidance, Document and maintain accurate records of all onsite activities, including service requests, incident reports, and maintenance logs. Document configurations, procedures, and troubleshooting steps for future reference. Provide regular status updates and reports to management. Compliance and Security: Ensure compliance with company policies, industry standards, and regulatory requirements. Follow company standard and security protocols to protect client data and IT infrastructure. Role and Responsibilities continued Work as one team Work together with counterparts within and between the sites to share knowledge and improve processes Work together with other support teams which are on-site. (e.g Lab support , AV support) Work together with remote teams to provide the best possible service. (e.g Infrastructure , Security) Be the hands and eyes for remote teams when needed. (e.g. Network , Server , Security team) Required Qualifications Minimum degree level qualification with I.T or Equivalent Must be a recent graduate or finished degree before September 2026 Preferred Qualifications & Skills Good knowledge of computer hardware, software, networking, and operating systems. Good Knowledge and willingness in troubleshooting and repair of IT equipment and systems. Good customer service and communication skills to interact with users Ability to work independently and manage multiple tasks effectively. Fluent in written and verbal business English Valid driver's license and willingness to travel to other local sites as required. What awaits you at Astellas? Global collaboration: Work within a connected global community dedicated to improving patient lives. Real-world patient impact: Contribute to life-changing therapies that make a difference worldwide. Relentless innovation: Join a company pushing scientific boundaries. A Culture of Growth: Thrive in a supportive environment that fosters development and progression. Our Organisational Values and Behaviours Impact Innovation Integrity One Astellas Accountability Courage Sense of Urgency Outcome Focus Benefits Careers | Astellas We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. #LI-Kerry #LI-Onsite #LI-MO1 To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

We are now looking for a catering/kitchen assistant to join the existing catering team in Waterford Nursing Home. Increase your chances of reaching the interview stage by reading the complete job description and applying promptly. This is a permanent full time role. Applicants must be available to work full time, weekdays and weekends included. What does this role entail? To assist in the preparation and service of food and in the cleaning of the kitchen and dining area. Main Activities Assist in the preparation and service of all meals and beverages for residents, visitors and staff to the required company standards of hygiene and economy. Preparation of resident trays and dining areas ensuring that the necessary equipment, utensils, and food is available in the required quantities and at the required time. Clear and clean kitchen, dining areas and catering utensils using appropriate cleaning techniques and equipment as directed by the Catering Manager/Cook. Advise residents on menu choice in a way as to give maximum choice. Adhere to good practice with regard to hygiene, health and safety, HACCP and COSHH Regulation at all times meeting all legislative requirements. Assists with record keeping as directed by Catering Manager/Cook. Carry out other duties as directed by line Manager. What are the skills/experience needed? Experience working in kitchen/catering HACCP trained Excellent communication skills Must be reliable & keep to schedule Can work as part of a team Good conversational English All posts are subject to satisfactory references, medical and Garda vetting. Note This job description is intended to give the post holder an appreciation of the role envisaged for the catering/kitchen assistant. Given the nature of the work it must be stressed that maximum flexibility is required to work in the home. Specific tasks and objectives will be agreed with the post holder and the Manager. To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

Validation Lead About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. Increase your chances of an interview by reading the following overview of this role before making an application. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn . Are you driven to make a real difference in the lives of patients? We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. Location and Working Environment This position is 100% onsite in Tralee, Ireland. Purpose & Scope Lead the daily operations of the Validation function, managing Validation Engineers (staff and outsourced providers), coordinating activities, and improving operational efficiency. Ensure facilities, utilities, equipment, computerized systems, manufacturing processes, cleaning procedures, analytical methods, and aseptic operations perform as intended and reliably produce safe, effective, and compliant biopharmaceutical products. Provide strategic leadership across the validation lifecycle-planning, execution, review, approval, and maintenance-aligned with GMP, data integrity principles, and risk-based methodologies. Own the Site Validation Master Plan (VMP), champion cross-functional governance, and drive continuous improvement to maintain a validated state. Role and Responsibilities Lead and develop the Validation team; foster an engaged, psychologically safe, high-performance culture aligned with Astellas values. Ensure stable supply and delivery of departmental objectives; resolve issues, prioritise effectively, and drive continuous improvement via ambitious KPIs. Maintain compliance with GMP, GDP, environmental, safety, and governance requirements; ensure audit readiness and robust data integrity. Contribute to site and global strategy; deliver strategic projects on time and within budget while anticipating future trends and skill needs. Lead implementation of new products, technologies, systems, and procedures; ensure compliant change management and effective knowledge transfer. Build strong cross-functional and global partnerships; support business continuity, mitigate risks, and deputise for site leaders as required. Required Qualifications Bachelor's degree (or equivalent) in an Engineering or Scientific discipline, or proven relevant in-depth experience. Preferred Qualifications Extensive experience in a similar role with strong technical competence and validation leadership capability (cGMP start-up experience advantageous). Proven ability to progress complex technical projects, support commissioning/maintenance of cGMP manufacturing, and manage multiple priorities. Excellent organisational, interpersonal, verbal, and written communication skills; able to work independently and collaboratively; open to new ideas. What awaits you at Astellas? Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives. Real-world patient impact: Contribute to transformative therapies that reach patients around the world. Relentless innovation: Join a company at the forefront of scientific breakthroughs. A culture of growth: Thrive in a supportive environment that champions your development. Our Organizational Values and Behaviors Impact Innovation Integrity One Astellas Accountability Courage Sense of Urgency Outcome Focus Benefits Learn more: We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help. #LI-Tralee #LI-Onsite To be considered for this role you will be redirected to and must complete the application process on our careers page. xsokbrc To start the process, click the Apply button below to Login/Register.

We are seeking a Contracts Manager to join our team at Elliott Group. Overview: The successful candidate will oversee the design, construction, and delivery of projects, ensuring completion on time and within budget while meeting client expectations. This key senior role involves leading site management teams, fostering client relationships, maintaining high standards in safety, quality, and programme compliance, and contributing to the strategic direction of the company as part of the Senior Management Team. Key Responsibilities: Manage site teams, subcontractors, and client relationships. Drive excellence in construction standards, safety, and quality. Ensure programme and budget compliance. Implement effective communication strategies and company systems. Conduct regular project reviews and progress reporting. Training: The role requires relevant certifications (e.g., Safe Pass, Manual Handling) and proficiency in Microsoft Office and project management software. A full job description is available upon request. To be considered for this position, please click APPLY below to send us your up-to-date CV.

We are currently recruiting for a SHO in Psychiatry for a Hospital in Ireland. · Recent experience in Psychiatry · Junior Doctors will be considered · Well-developed interpersonal skills · Ability to work as part of a diverse team · Strong commitment to high-quality patient care We are happy to talk to you further if you require any more information. We also offer referrals to anyone who helps with successful placements of medical staff. Please call 064 667 0001 and ask for Mike or send your most updated CV to michael@redchairmedical.ie Apply for this job You can apply for this job via the application form below. Name * Phone number * Email address * Upload your CV * Max. file size: 5 MB. Any comments? Privacy Consent * I consent to you collecting my details above. * This form collects your details above so we can contact you back in relation to your application. Please see our privacy policy for more information. #J-18808-Ljbffr