About Astellas Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women&apos;s health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com . Are you driven to make a real difference in the lives of patients? We&apos;re seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren&apos;t afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. Working Environment and Location <ul><li> This is a placement position for 3rd level 7 student </li><li> This position is based in Tralee, Ireland and requires you to be 100% on site / in the office. </li></ul>Purpose and Scope The student will support the Health and Safety Department under the guidance of experienced technical personnel, contributing to safe, compliant and efficient operations. They will gain practical experience in Health and Safety team operations in a manufacturing environment. Other activities will include assisting with activities that support Health and Safety schedule adherence, operational readiness and continuous improvement, developing an understanding of internal procedures and applicable regulatory, legislative and statutory requirements within a cGMP manufacturing environment and providing project and technical support to site initiatives while building cross-functional collaboration, problem-solving and communication skills. Role and Responsibilities Support EHS Compliance Activities <ul><li> Assist with monitoring compliance with site EHS procedures, GMP requirements, and applicable health and safety regulations. </li></ul>Participate in Risk Assessments <ul><li> Support the preparation and review of risk assessments, Job Safety Analyses (JSAs), and Safe Systems of Work under supervision. </li></ul>Conduct Workplace Inspections <ul><li> Participate in routine safety inspections and audits, documenting observations and tracking corrective actions to closure. </li></ul>Assist with Incident Management <ul><li> Support the reporting, investigation, and trending of safety incidents, near misses, and unsafe conditions to help identify preventive measures. </li></ul>Promote a Positive Safety Culture <ul><li> Actively participate in safety meetings, toolbox talks, and awareness campaigns while encouraging safe behaviours and adherence to site safety standards. </li></ul>Essential Qualifications <ul><li> Currently pursuing a relevant third-level qualification, preferably in a health and safety related course. </li></ul>Benefits Careers | Astellas Why Astellas <ul><li> Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients&apos; lives worldwide. </li><li> Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day. </li><li> Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you&apos;ll have the opportunity to shape the future of healthcare. </li><li> A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions. </li></ul>Our Organisational Values and Behaviours Integrity Innovation Impact One Astellas Accountability Courage Sense of Urgency Outcome Focus Skills And Capabilities Organizational Focus <li> </li>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&apos;s support team through LinkedIn Help.

Health & Safety Co-Operative Student

About SimoTech SimoTech provides manufacturing automation and IT systems engineering, project management and validation services. We partner with life sciences companies to design, build, operate and optimise critical process automation systems that deliver fast track project delivery, operational efficiency, improve manufacturing agility and achieve regulatory compliance. Why SimoTechWhat is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust and excellence, we play a critical partnering role to our clients&#x2019; life-changing supply of products to patients. In return, there is excellent salary, benefits, career progression, educational support and much more. MES Engineer SimoTech has a new opportunity for an experienced MES Engineer to join our team supporting a global pharmaceutical organisation onsite in their large Cork campus, which includes multiple high-technology manufacturing platforms. The ideal candidate for this role will have at least 5 years&#x2019; experience with Emerson Syncade systems through all aspects of the project lifecycle, within the life sciences industry. Key Responsibilities<ul><li>Process mapping of manufacturing processes and development, implementation, and support of MES recipes.</li><li>Take a leading role in recipe design sessions with Business Process SMEs.</li><li>Carry out testing and change control activities related to the MES recipes changes.</li><li>Develop, configure, and test MBRs from initial to final design.</li><li>Design, configure, and implement interfaces between Syncade MES and third-party systems.</li><li>Participate in MBR development design reviews including communicating cross-functionally with Automation, Lab Systems, ERP, and Quality groups.</li><li>Provide support and technical expertise for the ongoing development of the site MES system in development of MBRs and improving the MES business processes.</li><li>Take part in the training of all relevant EBR end-users and the ongoing development, review, and update of all relevant SOPs.</li><li>Carry out troubleshooting and fault-finding where required for MES and all relevant interfaces as required.</li></ul> Key Requirements <ul><li>5+ years&#x2019; experience as an MES Engineer within the life sciences industry</li><li>Bachelor&#x2019;s degree in engineering, computer science, life sciences, or similar.</li><li>A strong understanding of manufacturing processes and practices within a GMP environment across all aspects of the MES project lifecycle.</li><li>Broad technical experience in the delivery of MES systems/projects including design, configuration, and testing.</li><li>Experience with Emerson Syncade within a pharmaceutical API environment.</li><li>Proven analytical and problem-solving ability to identity the root-cause and solutions for technical issues related to MES systems, configurations, or integrations.</li><li>Strong communication and interpersonal skills with the ability to build solid working relationships that enable cross-functional cooperation and enhances stakeholder engagement.</li><li>Experience integrating MES systems to other systems such as DCS, SCADA or ERP is highly beneficial.</li></ul> What SimoTech Can Offer<ul><li>Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.</li><li>Develop new skills and enhance technical ability by working with innovative technologies in a multi-disciplined environment.</li><li>Opportunity to work with large corporate clients on exciting capital projects.</li></ul>

MES Syncade Engineer

Overview Intern required for 6 months to support the R&amp;D Foods team. Role will involve supporting the following activities: Liquid and Powder ingredients concentrate and application issue resolution including bench top preparation and scale-ups and stability testing for our Sweet and Savoury portfolio of products. Analytical testing to support the foods forensics and brand stewardship team on issue resolution. Responsible for sweet and savoury finished products and application in project related lab analysis. Support global seasoning project through routine powder testing and new instrument method development Responsibilities <ul><li>Ensuring all instrumentation used in the testing is calibrated and are in a suitable for use.</li><li>Maintain good lab practice to a high standard /maintain accurate records</li><li>Prepare digital reports, interpret data and relay results in a timely manner</li><li>Contributing to safety assessments/risk assessments</li><li>Ensure compliance with EHS guidelines. </li></ul>Qualifications <ul><li>Undertaking BSc in Food Science/ Chemistry/ Nutrition (or related discipline)</li><li>Good verbal and written communication, skills.</li><li>Excellent people skills.</li><li>Team Player.</li><li>Self-starter, self-sufficient and eager to learn.</li><li>Interest in Food and the Food Industry.</li><li>Strong IT Skills in Word &amp; Excel. </li></ul>Additional Desired qualifications and/or experience: Understanding of powder and analytical instrumentation is desired, however training on specific equipment will be provided.

Flavor Science Intern (R&D) 2027

Company Overview: MACOM designs and manufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications. Headquartered in Lowell, Massachusetts, MACOM has design centers and sales offices throughout North America, Europe and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard. MACOM has more than 70 years of application expertise with multiple design centers, Si, GaAs and InP fabrication, manufacturing, assembly and test, and operational facilities throughout North America, Europe, and Asia. In addition, MACOM offers foundry services that represents a key core competency within our business. MACOM sells and distributes products globally via a sales channel comprised of a direct field sales force, authorized sales representatives and leading industry distributors. Our sales team is trained across all of our products to give our customers insights into our entire portfolio. MACOM is an Equal Opportunity Employer committed to a diverse workforce. MACOM will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, gender expression, national origin, ancestry, age, sexual orientation, marital or civil partnership status, pregnancy, disability, genetic information, veteran status, military obligations, or membership in any other category protected under applicable law. MACOM is looking for top talent to join our global organization of skilled Engineers based in our office in Eastgate, Little Island, Cork. Main Duties and Responsibilities: <ul><li> Simulate and design high-frequency integrated circuits using market-leading CAE tools </li><li> Characterise prototype designs in state-of-the-art laboratory </li><li> Work within a multi-disciplined project team </li></ul>Key Competencies Required: <ul><li> Good planning and organisational skills </li><li> Highly motivated </li><li> Deadline and detail oriented </li><li> Good interpersonal and communications skills </li><li> Ability to work well in a global team environment </li><li> Good understanding of RF concepts </li><li> Familiarity with high-frequency designs tools such as ADS and Cadence is preferred </li></ul>Minimum Qualifications: <ul><li> Degree in Electronic Engineering </li><li> Recent Graduate (or due to graduate in 2025)</li></ul>

Electronic Design Engineer

Summary: We currently have an opportunity for an Electrical Engineer to join our team. The successful candidate will support a variety of projects in the pharmaceutical, biopharmaceutical and medical device industries. Responsibilities:<ul><li>Delivery of projects including detailed design, scope issue, field construction and commissioning through handover.</li><li>Will be involved in the preparation of cost estimates for clients including timelines and justifications.</li><li>Carry out site surveys.</li><li>Carry out the design of areas such as lighting, small power, fire alarms, LV distribution and cable sizing etc.</li><li>Assist with the preparation of projects schedules and monitor progress, ensuring critical path is maintained and implementing mitigation plans as necessary.</li><li>Help develop a strong safety culture within the company, proactively drive towards continuous improvement and achieving best in class standards.</li><li>Generate User Requirements Specifications with stakeholders.</li><li>Review design packages from consultants.</li><li>Involvement in the issuing of tender enquiries for consultants, contractors and vendors.</li><li>Interface with project management and project engineers during the design, execution and start-up phase of projects.</li><li>Support field installation and commissioning of larger projects.</li></ul> Qualifications &amp; Experience:<ul><li>Degree in Electrical Engineering or similar.</li><li>Working knowledge of CAD a distinct advantage.</li><li>Minimum 3 years&#x2019; post graduate experience in project delivery in a medical device or pharmaceutical manufacturing environment.</li><li>Technical knowledge of MV and LV power infrastructure, Building Management Systems (BMS), data and IT infrastructure.</li><li>Project planning, design, cost control.</li><li>Ability to coordinate of multiple stakeholders, contractors and vendors.</li></ul>

Electrical Design Engineer

Research Associate - Ireland, Cork - Initial 12-Month Contract - Life Sciences Are you interested in joining a world leading biopharmaceutical company, focused on developing advanced and innovative treatments for those suffering with rare diseases? This is a fantastic opportunity to work in a state-of-the-art facility in Cork. You will be joining a leading Biopharmaceutical company who focus on a range of products which are life-changing for individuals. Our client is currently seeking a Research Associate. What You&apos;ll Deliver <ul><li>Execute and complete projects independently.</li><li>Generate and review data, makes data analysis.</li><li>Maintain up-to-date documentation of laboratory work carried out including documentation storage and archiving in accordance with GLP.</li><li>Support updates of lab instructions, BPDs, SOPs, templates.</li><li>Support maintenance and calibration of lab equip </li></ul>What you&apos;ll need: <ul><li>Experience in daily operations with microbial cell culture, including cell thawing and cell banking, seed train expansion etc.</li><li>Experience in fermentation process, including fermenter inoculation, daily monitoring, sampling and in-process analysis utilising standard bioprocess analytical equipment.</li><li>Basic understanding of mammalian cell expansion and it&#x2019;s difference in comparison to microbial operations.</li><li>Experience in processing of inclusion bodies is desirable. </li></ul>If this role is of interest, please apply now!

Research Associate

Responsibilities We are recruiting for a Graduate Welding Engineer within the Quality Department, DQ, and will report directly to the Manager, Quality, or his/her delegate. This role provides an excellent opportunity for a graduate to develop a career in welding engineering within a supportive and technically focused environment. The successful candidate will receive structured training, mentoring and practical on-the-job experience to develop the knowledge, skills and competencies required to progress as a professional Welding Engineer. The employee will be expected to attain and maintain an appropriate standard of independent certification to ensure competency required for the role of Welding Engineer. The Company is committed to supporting the employee&#x2019;s professional development and where the employee does not already hold an appropriate qualification as an EWE/IWE (European/International Welding Engineer), training and support will be provided. Further certification may be required if the requirements of the appropriate international standards for the welding engineering knowledge base dictate it or as may be required by the company when these are identified. Responsibilities shall include, but are not limited to the following: <ul><li> Complete agreed graduate objectives and development activities.</li><li> Attend and complete relevant training courses, including training associated with new or existing equipment, processes, systems, standards and procedures.</li><li> Develop knowledge and experience in tasks and responsibilities identified in ISO14731 Annex B in support of the company management systems and standards.</li><li> Coordinate welding management and related activities.</li><li> Prepare relevant reports in a timely and professional manner using appropriate company equipment e.g. computers, digital cameras, NDT equipment etc.</li><li> Make use of computer-based systems including CAD, BAAN, LIKV, LIDA systems available within LCC and other software packages e.g. E-mail, Word, Excel, etc.</li><li> Liaise and communicate with personnel and departments within LCC and any external companies as may be necessary from time to time.</li><li> Investigate quality / production /welding issues in a professional and diligent manner.</li><li> Strive to drive continuous improvement in LCC.</li><li> Support and develop quality management systems and support the certifications held by LCC (ISO9001, ISO 3834-2, EN1090 etc.).</li><li> Support, cooperate and assist other engineers and inspectors in the course of their duties as necessary.</li><li> Keep records of work and control inspections carried out, including new records which may be introduced as necessary to demonstrate product quality, quality control and completion of inspections.</li><li> Cooperate in the management of welding activities throughout the company.</li><li> Carry out or assist in welder certification and testing.</li><li> Monitor the quality of welding on a continuous basis and report findings to both production and management personnel as necessary with relevant KPI&#x2019;s.</li><li> Carry out weld testing using whatever means are necessary or required e.g. visual examination, hardness testing, weld macro examination etc. and other duties may be necessary from time to time as directed by MQ and management.</li><li> Produce, coordinate, and document Welding Procedure Qualification Reports / Testing, Welding Procedure Specification and other documentation as may be required to control monitor and demonstrate good practices in welding management.</li><li> Assist other control inspectors or carry out other quality department functions. </li></ul>Qualifications Requirements And Experience <ul><li> A degree in Mechanical Engineering.</li><li> Relevant knowledge in all aspects of steel fabrication.</li><li> Good knowledge of Engineering Materials and Physical Metallurgy will be an advantage.</li><li> Good computer skills, with experience in CAD being a distinct advantage.</li><li> Good organizational and time management skills.</li><li> Willingness to travel. </li></ul>Benefits What We Offer: <ul><li> Competitive Salary</li><li> Paid overtime</li><li> End of Year Bonus</li><li> Pension Scheme</li><li> Service Pay</li><li> Early finish on a Friday</li><li> 21 days annual leave + Length of service days</li><li> Company Fixed Days</li><li> Subsidised canteen</li><li> Sports and Social Club</li><li> Retailer Discounts</li><li> Life Assurance</li><li> Refer a friend Scheme</li><li> Maternity Pay</li><li> Educational assistance</li><li> Career Progression Opportunities</li><li>Please note, CV&apos;s will not be accepted directly by email.</li><li>We do not require the assistance of recruitment agencies for this role. </li></ul>#LCC Have we awoken your interest? Then we look forward to receiving your online application. If you have any questions, please contact Emily O Connor. One Passion. Many Opportunities. The Company Liebherr Container Cranes Ltd. is one of the world&apos;s leading manufacturers of ship to shore cranes, rail mounted gantry cranes and rubber tyre gantry cranes. From its base in Killarney, Ireland, the company designs, builds and exports container cranes worldwide. Founded in 1958 as the first Liebherr factory outside of Germany, today, container cranes manufactured by Liebherr in Ireland are renowned for their quality, longevity and productivity. Location Liebherr Container Cranes Ltd. Killarney Ireland (IE) Contact Emily O Connor Emily.OConnor@liebherr.com

Graduate Welding Engineer

Analytical / QC Technology Transfer Specialist | 12-Month Contract | Tralee, Co. Kerry Summary:A 12-month contract opportunity in Tralee, Co. Kerry for an experienced QC/Analytical professional supporting a sterile pharmaceutical Technology Transfer programme. You&#x2019;ll take ownership of the analytical workstream for product transfers, with a particular focus on analytical method transfer and verification. Key Responsibilities:<ul><li>Own analytical method transfer/verification protocols and reports, working closely with QC.</li><li>Liaise with sending-site analytical teams to secure method packages, reference standards and comparator data.</li><li>Plan and track analytical method transfer activities alongside the wider product transfer schedule.</li><li>Support analytical investigations and provide analytical input into FMEA/risk assessments.</li></ul> Requirements:<ul><li>Typically 4+ years&#x2019; QC/Analytical experience within a GMP pharmaceutical environment.</li><li>Experience in analytical method transfer or verification, with knowledge of analytical method validation/transfer principles such as ICH Q2.</li><li>Degree in Chemistry, Biochemistry, Pharmaceutical Science or a related discipline; sterile fill-finish analytical experience is advantageous.</li></ul>

Analytical / QC Technology Transfer Specialist

At Cadence, we hire and develop leaders and innovators who want to make an impact on the world of technology. Cadence is a pivotal leader in electronic design, building upon more than 30 years of computational software expertise. The company applies its underlying Intelligent System Design strategy to deliver software, hardware and IP that turn design concepts into reality. Cadence customers are the world&#x2019;s most innovative companies, delivering extraordinary electronic products from chips to boards to systems for the most dynamic market applications including consumer, hyperscale computing, 5G communications, automotive, aerospace industrial and health. At Cadence, we hire and develop leaders and innovators who want to make an impact on the world of technology. Job Title: Principal Analog Design Engineer (SERDES) Location: Cork Reports to: Design Engineering Group Director Job Overview The Principal Analog Design Engineer will take a Technical Leadership role on the PMA design team as part of a SERDES Product Team located at Cork, Ireland. Job Responsibilities <ul><li>Design of High Speed SERDES products at data rates up to and exceeding 112 Gbps on leading edge technology nodes (e.g. 5nm FinFET CMOS)</li><li>Design and development of analog/mixed signal IC circuit blocks from initial concept/specification through final verification of conformance to customer specifications</li><li>Work closely with Physical Design Engineers to design IC circuit blocks and PMA sections</li><li>Participate in technical leadership of the team in the areas of circuit design and SERDES architectures</li><li>Work with global teams (US, west coast and east coast), which work in different time-zones </li></ul>Job Qualifications <ul><li>Candidate&#x2019;s background should include a minimum of 7 years of experience in CMOS SERDES or high-speed I/O IC design and development</li><li>BEng, MEng or PhD Qualified</li><li>Working knowledge of a set of common SERDES standards and their electrical requirements</li><li>Must have a thorough understanding of jitter and signal equalization techniques</li><li>Proficient design experience in many of the following SERDES circuit blocks: Driver, Receiver, Serializer, Deserializer, Phase Interpolator, Low jitter PLL, High Speed Clock Distribution, Bias and Bandgap, Voltage Regulators</li><li>Excellent problem-solving skills, analog aptitude, good communication skills and ability to work cooperatively in a team environment </li></ul>Skills Additional Skills/Preferences: Cadence tool experience and design experience at &gt;10Gbps and in <li>Lab test experience as part of silicon evaluation is advantageous</li><li>Interest in publishing academic papers and presenting at conferences e.g. ISSCC, JSSC </li>Additional Information Cadence is committed to equal employment opportunity and employment equity throughout all levels of the organization. We strive to attract a qualified and diverse candidate pool and encourage diversity and inclusion in the workplace. Travel: &gt;5% We&#x2019;re doing work that matters. Help us solve what others can&#x2019;t.

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