A global medical device company working on a new product introduction is seeking Junior and Senior Electrical Engineers to support on a 12-month contract basis. You&apos;ll work with a multi-disciplinary engineering team to support the design and development of bespoke electro-mechanical equipment. The role will cover electrical design, schematics, wiring harnesses, cabinet design, component selection, testing, and technical documentation. Essential Skills<ul><li>Electrical design experience</li><li>Product development / R&amp;D mindset</li><li>Electrical CAD experience</li><li>Technical documentation</li><li>Cross-functional engineering collaboration</li></ul>Desirable Skills<ul><li>Experience with automation, robotics, mechatronics, or machinery systems</li><li>Knowledge of safety, EMC, or relevant electrical standards</li></ul> This is a strong fit for engineers who want to stay close to hands-on design, early-stage development, and practical equipment build/testing. Desired Skills and Experience Electrical Design, Product Development, R&amp;D Engineering, New Product Introduction, NPI, Electro-Mechanical Systems, Electrical CAD, EPLAN, SolidWorks Electrical, Schematics, Wiring Harnesses, Cabinet Design, Technical Documentation, BOMs, Design Verification, Testing, Prototyping, Component Selection, Medical Devices, Regulated Manufacturing, Automation Equipment, Mechatronics, Robotics, Cross-Functional Engineering, Engineering Drawings, Control Cabinets, System Architecture, Requirements Definition, EMC, Electrical Safety, Risk Assessment, Machinery Directive, EN 60204-1, IEC 61010-1, Functional Safety, DFMEA, Design Review, Good Documentation Practice, GDP, Design Transfer, Manufacturing Equipment, Industrial Automation, Machine Design, Commissioning Systems, Control Systems, Instrumentation, Measurement Technology, Sensors, Actuators, PLC Exposure. Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement. To find out more about Real, please visit www.realstaffing.com Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales

R&D Electrical Engineer

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking an Associate QC Micro Analyst to join our Quality Control Microbiology team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When &amp; Where <ul><li>Shift Requirements: Shift pattern may be required based on business needs.</li><li>Location: Raheen, Limerick, Ireland.</li><li>This is a 12-month contract position. </li></ul>What You&#x2019;ll Do <ul><li>Perform microbiological testing and environmental monitoring activities to support product quality, patient safety, and cGMP compliance.</li><li>Collect and analyse samples from manufacturing areas, cleanrooms, and utilities using approved laboratory procedures.</li><li>Review laboratory data, complete documentation, and support investigations related to deviations, OOS, and OOT results.</li><li>Support microbiological validations, method transfers, and laboratory readiness activities.</li><li>Partner with Manufacturing, Quality, and other cross-functional teams to drive compliance and continuous improvement. </li></ul>The Environment And Physical Rhythms Of This Role <ul><li>Thrive in laboratory, manufacturing, and cleanroom environments.</li><li>Demonstrate strong attention to detail and a commitment to quality.</li><li>Work effectively both independently and within cross-functional teams.</li><li>Maintain accuracy and compliance while managing competing priorities.</li><li>Apply critical thinking and problem-solving skills to support investigations and process improvements. </li></ul>Let&#x2019;s Find Out If We&#x2019;re a Fit <ul><li>Requires a BS/BA in Life Sciences, Microbiology, Biotechnology, or a related field, or an equivalent combination of education and experience.</li><li>For Associate QC Micro Analyst: 0-2 years of relevant experience.</li><li>For QC Micro Analyst: 2+ years of relevant experience, preferably in the pharmaceutical or biotechnology industry.</li><li>Experience in a GMP-regulated laboratory environment is beneficial.</li><li>Strong communication, teamwork, and organizational skills with a focus on quality and compliance. </li></ul>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on&#x2011;site. Please speak with your recruiter and hiring manager for more information about on&#x2011;site expectations for your role and location. As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. For jobs in Canada: this posting is for an existing position.

Temp Assoc QC Micro Analyst

Permanent Contract This role will have responsibility to develop GQO Indirect category strategies, best practices processes, policies, procedures and project development to deliver sustainable margin results across a global network/sites. Identifies opportunities for value improvement and drives global leverage and efficiencies across network/site operations. Creates fact bases, strategic initiatives, business cases and recommendations. Will convert local strategies and initiatives into global strategies and constantly leads thinking on improving total GQ&amp;O efficiencies. Will execute deliverables in line with GQO strategies working closely with local, franchise, regional and global stakeholders. What you will do: <ul><li>Lead and execute category strategy across packaging, aligned with business and product roadmap priorities</li><li>Drive end-to-end sourcing strategy, including supplier segmentation, cost optimization, and long-term supply continuity planning</li><li>Negotiate and structure complex commercial agreements, including long-term contracts, volume commitments, and pricing frameworks with key strategic suppliers</li><li>Leverage market intelligence and industry trends to inform sourcing decisions, including advancements in plastics technology, materials innovation, and supplier capabilities</li><li>Partner cross-functionally with engineering, quality, and operations to align sourcing strategies with product development and manufacturing requirements</li><li>Identify and execute value creation opportunities, including cost savings, risk mitigation, and supplier consolidation initiatives</li><li>Ensure all sourcing activities, contracts, and supplier engagements align with company policies, governance standards, and compliance requirements</li><li>Any other duties as assigned. </li></ul>What you will need: <ul><li>Bachelor&apos;s degree in engineering, supply chain, operations or equivalent. </li><li>8-10 years of relevant experience, in medical devices or other highly regulated environments. </li><li>Category Management Level experience. Experience in Negotiation and Supplier Management</li><li>Strategic thinker, understands the details but can operate at a higher level. </li><li>Strong leadership &amp; interpersonal skills with the ability to engage &amp; influence senior stakeholders. </li><li>Experience with world-class strategic sourcing &amp; category management practices </li><li>Strong negotiation skills, negotiating and implementing commercial contracts to include supply and quality agreements (QAA). </li><li>Strong written &amp; verbal communication skills across all levels </li><li>Ability to multi-task and coordinate initiatives with a virtual, global/regional team. </li><li>Persuasive &#x2018;change agent&#x2019; capable of challenging conventional wisdom. </li><li>Track record of success in capturing value and driving spend to preferred suppliers. </li><li>Demonstrated ability to manage and improve vendor performance. </li><li>Hands-on mentality. </li><li>Ability to align with peers / stakeholders and build and maintain strong networks. </li></ul>#IJ Ireland Pay Ranges: <ul><li>Ireland: &#x20AC;88,000 - &#x20AC;146,000 EUR Annual </li></ul>At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker&#x2019;s comprehensive benefits package. If you&#x2019;d like to learn more about the salary or the benefits associated with this role, your recruiter will be happy to walk you through the details as you progress through the hiring process. Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Senior Sourcing Manager, Category Management

Job Ref 54502 Job Title Chef Location: Nenagh Salary On Application Closing Date For Applications 09-10-2026 Job Description Main purpose of the role: Ensure the food production area operates efficiently and effectively at all times and provide our customers with excellent products. The Ideal Candidate Will Have/be <ul><li>1 years&#x20AC;,, experience in a Supervisor/Manager role is desirable</li><li>2 years` experience in a role with an indept experience to fresh food</li><li>Experience in successfully achieving sales targets and KPIs</li><li>Fully trained in HACCP and food safety, and has experience in meeting the HACCP and food safety requirements</li><li>Experience in ordering for deli departments and managing waste within a fresh food department</li><li>Stocktaking experience</li><li>Ability to roster and adhere to budgets</li><li>Have a true passion for the food industry and, as such, be creative and innovative with the fresh offering</li><li>Customer focused and can build a quality and loyal customer base</li><li>The ability to inspire, lead and motivate employees through support and development. </li></ul>Main duties: <ul><li>Actively live Centra brand-values i.e. Proud, Energetic, Imaginative and Community-Based</li><li>Cook, prepare and display the food throughout the day</li><li>Oversee and ensure the smooth running of food production operations</li><li>Carry out stock takes and work out the cost price for product and portion control</li><li>Assess how the work is organised and delegate accordingly</li><li>Finish all orders to the highest standard</li><li>Attend regular management meetings as required and work to implement a programme of continuous improvement in line with these meeting actions</li><li>Assist in the induction, training and development of staff in the food production area</li><li>Attend any training or development programmes as directed by store management. </li></ul>Apply

Chef

Build Our Future Together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Senior Instrumentation &amp; Controls (I&amp;C) Engineer to join our Site Engineering team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. Where <ul><li>Location: Raheen, Limerick. </li></ul>What You&#x2019;ll Do <ul><li>Acting as the primary I&amp;C representative within multidisciplinary project teams for projects from concept development through design, construction, commissioning, qualification and handover</li><li>Coordinating with Process, Mechanical, Electrical, Maintenance, Operations and Quality groups</li><li>Providing technical leadership for instrumentation and control systems across manufacturing, utility and facility infrastructure projects</li><li>Supporting troubleshooting and root cause investigations associated with instrumentation and control system performance issues</li><li>Specifying and evaluating field instrumentation including pressure, temperature, flow, level, load cells, pH, conductivity, TOC, UV and analytical instrumentation</li><li>Leading design reviews and approving instrumentation philosophies, P&amp;IDs, instrument indexes, I/O lists, control narratives, loop drawings and vendor packages</li><li>Participating in HAZOPs, risk assessments, constructability reviews and design verification activities</li><li>Reviewing and approving instrumentation wiring diagrams, panel designs and control architecture</li><li>Establishing, maintaining and continuously improving site instrumentation and controls engineering standards and specifications</li><li>Providing technical direction to engineering consultants, system integrators and construction contractors</li><li>Leading technical assessments for equipment obsolescence, instrument upgrades and functional equivalency evaluations</li><li>Supporting FAT, SAT, commissioning, qualification and startup activities for new systems and modifications </li></ul>The Environment And Physical Rhythms Of This Role <ul><li>You have excellent technical and analytical skills</li><li>Problem-solving and continuous improvement skills</li><li>You possess strong communication and collaboration skills</li><li>You are adaptable and can work in a fast-paced, regulated environment </li></ul>Let&#x2019;s Find Out If We&#x2019;re a Fit <ul><li>Bachelor&#x2019;s degree in Instrumentation Engineering, Electrical Engineering, Automation Engineering or related discipline.</li><li>Minimum 8 years of engineering experience with increasing responsibility in instrumentation, controls and automation systems.</li><li>Demonstrated experience leading I&amp;C engineering activities for projects within pharmaceutical, biotechnology or other highly regulated industries.</li><li>Strong knowledge of process instrumentation, industrial control systems and GMP regulated manufacturing environments. </li></ul>Thrive today. Grow tomorrow. #IRELIM #JOBSIEST #REGNIETO Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on&#x2011;site. Please speak with your recruiter and hiring manager for more information about on&#x2011;site expectations for your role and location. As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. For jobs in Canada: this posting is for an existing position. Salary Range (annually) &#x20AC;54,200.00 - &#x20AC;88,400.00

Senior Instrumentation & Controls Engineer

The Lead Research and Development Engineer will be a technical leader and/or growing subject matter expert, applying engineering principles to solve complex technical challenges and ensuring products meet clinical needs, safety requirements, and quality standards.Leading a team in the development of drug-device combination products with a focus on the drug side. They should have working knowledge of designing and executing stability establishing studies in accordance with ICH guidelines and working knowledge of the analytical test methods required for characterisation of APIs. In this role, they may have the following responsibilities:<ul><li>Lead medium to large projects/programs while also supporting other project teams, as needed.</li><li>Collaborate across functional department(s), grow and advance their area of technical expertise, and provide guidance and technical leadership across multiple projects within their area.</li><li>Work with senior leadership to identify focus area(s) for research and best practices.</li></ul> It would be an advantage if the candidate also has working knowledge of the following areas: <ul><li>Polymer characterisation techniques</li><li>Pre-filled syringe combination product design requirements</li><li>Sustained release or hydrogel based formulation design</li><li>Embolization product design</li><li>Development of the formulation for a drug product</li><li>Completion of CMC (chemistry manufacturing controls) development of that product.</li><li>Execution of stability testing of the drug product.</li><li>Successful market approval for the drug product through interactions with relevant regulatory agencies (e.g. FDA).</li><li>Continue to perform the functions, duties, and expectations of the Senior Research and Development Engineer at a high level, as applicable.</li></ul> Education and/or Work Experience<ul><li>Bachelor&#x2019;s degree in Engineering and 7 years&#x2019; relevant experience. Relevant advanced degrees (Master&#x2019;s or PhD) may reduce the experience requirement by 2-4 years.</li><li>Experience in a technical role within Medical Device or regulated industry/adjacent experience.</li><li>Project/technical leadership experience.</li><li>Experience working closely with senior leadership.</li><li>Experience in successfully mentoring, guiding, and training employees within an area of expertise is preferred.</li></ul> Knowledge and Skills and/or Abilities<ul><li>Strong analytical and critical thinking skills.</li><li>Strong technical writing.</li><li>Proven ability to work with cross functional teams to solve complex problems.</li><li>Proven ability to develop and lead elements of new products and processes in achieving functional objectives.</li><li>Knowledge of relevant ISO, EU, FDA medical devices standards regulations.</li><li>Strong influencing skills required to secure support/buy-in across the function, driving acceptance and understanding of new concepts and/or approaches.</li><li>Project management methodology and skills is preferred.</li><li>This role requires fluency in Artificial Intelligence (AI) and data concepts, including the ability to critically evaluate AI outputs, improve workflows using approved tools, identify and mitigate bias or inaccuracies, and communicate AI-driven insights clearly and responsibly to peers and managers.</li><li>Demonstrated fluency in both written and spoken English, and in other local language(s), as applicable.</li></ul>

Research and Development Lead

Responsibilities <ul><li>Provide first-class cost-effective design solutions for automated equipment for next generation Med Tech manufacturing equipment.</li><li>Deep working knowledge &amp; demonstrated capability to design automation equipment &amp; processes.</li><li>Generate Design concepts in 2D and 3D CAD of proposals to help drive project solutions and recommendations.</li><li>Have an understanding of FEA techniques to verify design, preferably able to use FEA software to verify design.</li><li>Formulate and recommend engineering policies and technical work in accordance with project objectives. Ensure that sound technical engineering concepts are applied.</li><li>Maintain a network and open lines of communication with other technology teams across J&amp;J, ensuring awareness and alignment with key stakeholder needs and new technology developments.</li><li>Lead and develop new value propositions that employ the latest technologies to bring increased efficiencies to the manufacturing supply chain</li><li>Develop Proof of Principle (POP) activities to de-risk proposed solutions and drive these POP activities to completion, iterating the design where needed.</li></ul> Expectations<ul><li>Provide a clear/concise Communications with both key stakeholders and Engineering Teams</li><li>Ensure customer requirements are met and that customer feedback/recommendations are sought to allow closure of successful use cases.</li><li>Manage key equipment partners and integrators for the development of automated manufacturing systems.</li><li>Establish effective working relationships and develop new partnerships to optimize product development with partners across the organization.</li><li>Establish Strong Relationships with new and potentially Key Vendors.</li><li>Support and lead where appropriate in developing the following Project Management requirements:</li><li>Project Charters.</li><li>Project scopes / Planning &amp; Defining scope / Costing Estimates.</li><li>Schedules / Activity Planning &amp; Sequencing / Time Estimates.</li><li>Report generation and project progress reporting.</li><li>Key delivery metrics as per the stage gate process.</li><li>Risk Analysis / Managing Risks and Issues.</li></ul>

Senior Project Design Engineer

Build Our Future Together At Regeneron, we use science and innovation to develop life-changing At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a QC Analyst (Drug Product) to join our QC Chemistry, Drug Product Testing team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. As part of the Drug Product Testing team, you will support the testing and release of biopharmaceutical products for commercial and clinical drug product programs. When &amp; Where <ul><li>Shift Requirements: 12/7 or Days</li><li>Location: Raheen, Limerick </li></ul>What You&apos;ll Do <ul><li>Perform testing in accordance with approved procedures to support product release and stability programs.</li><li>Review laboratory testing documentation and data to ensure compliance with GMP requirements and quality standards.</li><li>Support the validation, qualification, and transfer of analytical test methods and procedures.</li><li>Investigate laboratory events and collaborate with cross-functional teams to support fact-finding and resolution activities.</li><li>Write, revise, and maintain controlled test procedures and standard operating procedures (SOPs).</li><li>Participate in required training activities and maintain training compliance.</li><li>Manage laboratory supplies and materials required for routine operations.</li><li>Support continuous improvement initiatives and projects that enhance laboratory performance and efficiency. </li></ul>The Environment And Physical Rhythms Of This Role <ul><li>Thrive in a fast-paced, quality-focused laboratory environment.</li><li>Quickly learn new techniques, procedures, and technologies while working independently.</li><li>You possess strong trouble-shooting and problem solving skills.</li><li>You have strong attention to detail &amp; excellent written and oral skills. </li></ul>Let&apos;s Find Out If We&apos;re a Fit <ul><li>Requires a BS/BA in Life Sciences or a related field.</li><li>QC Analyst: Minimum of 2 years of relevant industry experience.</li><li>Previous experience reviewing analytical testing performed within a GMP-regulated laboratory environment is preferred.</li><li>Strong organizational, communication, and teamwork skills with a commitment to quality and compliance. </li></ul>Thrive today. Grow tomorrow. #IRELIM #JOBSIEST #REGNIRLQC Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on&#x2011;site. Please speak with your recruiter and hiring manager for more information about on&#x2011;site expectations for your role and location. As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. For jobs in Canada: this posting is for an existing position. Salary Range (hourly) &#x20AC;18.34 - &#x20AC;28.70

QC Analyst (Drug Product)

Build Our Future Together As a Facilities Engineer, you will provide engineering support, troubleshooting, &amp; subject matter expertise to the Facilities Operations, Utilities &amp; HVAC teams. Where <ul><li>Location: Raheen, Limerick </li></ul>What You&#x2019;ll Do <ul><li>Building and specifies cGMP clean/grey utilities, &amp; HVAC equipment, piping, ducting and/or controls</li><li>Managing small-to-mid sized projects related to utilities &amp; HVAC equipment &amp; services</li><li>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</li><li>Assisting in the design review, site acceptance and installation of equipment</li><li>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</li><li>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</li><li>Implementing corrective/preventative actions for existing equipment and maintenance processes</li><li>Preparing engineering evaluations and test plans for and executes modification change control documentation</li><li>Interpreting P&amp;IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs </li><li>Maintains a clean and safe working environment by enforcing procedures, policies, and regulations </li></ul>The Environment And Physical Rhythms Of This Role <ul><li>You have strong analytical and interpersonal skills</li><li>You are able to prioritise and re-prioritise as needed and adapt to change</li><li>You are comfortable working in a fast-paced setting </li></ul>Let&#x2019;s Find Out If We&#x2019;re a Fit <ul><li>Sr Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 5 years&#x2019; experience </li><li>Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 2 years&#x2019; experience </li></ul>Thrive today. Grow tomorrow. #IRELIM #JOBSIEST Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on&#x2011;site. Please speak with your recruiter and hiring manager for more information about on&#x2011;site expectations for your role and location. As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. For jobs in Canada: this posting is for an existing position. Salary Range (annually) &#x20AC;46,200.00 - &#x20AC;88,400.00

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