embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Project Engineer leadscross functionalprojects that support embecta' s injection products portfolio. This role plays a key part in delivering projects that ensure regulatory compliance, support product changes, and enable business continuity and growth. The position offers the opportunity to manage initiatives that are critical to thelong termsuccess of the business Responsibilities Leadcrossfunctional project teams delivering initiatives thatimpactcompliance, form/fit/function, cost reduction, line extensions, and other business opportunities. Actas a primary liaison between business leadership, functional management, and project team members. Collaboratewith functional managers to ensureappropriate resourceallocation and discretionary spending to meet project timelines. Planandfacilitateregular project meetings to ensure all stakeholders are informed, aligned, and completing assigned actions. Workclosely with Technical Subject Matter Experts (SMEs) to ensure all project tasks are clearly defined, planned, and executed. Assessthe impact of change requests, including risks, costs, and schedule implications. Manage, and in some cases execute, engineering change deliverables through all stages of the Change Control process. Provideregular project status updates to senior management, covering quality, schedule, cost, and overall progress. Promotestrong project planning, execution discipline, and rigor across all project activities to ensure successful outcomes. Experience & Education Bachelor'sdegree in an engineering ortechnology relateddiscipline. Experienceworking in a regulated Medical Devices and/orPharmaceuticalindustry environment. Experiencewith product lifecycle management inhigh volumemanufacturing environments. Solidunderstanding of structured product development processes, regulatory requirements, and quality systems. Experiencewith ISO standards, GMP guidelines, FDA regulations, medical device design controls, and manufacturing scaleup processes. Excellentinterpersonal and communication skills, with the ability toefficiently interact withdiverse audiencesand stakeholders Provenability to work effectively both independently and as part of across functionalteam. Strongattention to detail and commitment to quality and compliance. #LI-DF1 #LI-HYBRID embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The plant, based in Dun Laoghaire, runs 24/7 and is the Worldwide Centre of Excellence for Pen Needle Manufacturing within the embecta organisation, producing 4.6 billion medical devices annually. Here we employ approximately 450 people across operations, engineering, quality and R&D. We are now inviting application for our PQS Operator Talent Pool to (11-Month Fixed Term Contract) whose role is to meet operational needs across the site. This includes monitoring and maintaining production and quality performance to meet specified standards in accordance with GMP. This is a busy and varied role. Main responsibilities will include: The Operator will carry out the full range of responsibilities and duties required to meet current and future operational needs. This includes monitoring and maintaining production and quality performance to meet specified standards. Routine adjustments, repairs and maintenance of machines will be carried out by Operators. Operators will carry out all duties in line with Good Manufacturing Practices (GMP) and will record production and testing data in line with Standard Operating Procedures (SOPs). Operators will use existing technology and will embrace any requirements to acquire additional skills for new tools/equipment etc. Operators will participate in initiatives, projects & teams as required including Continuous Improvement, QIP (Quality Improvement Programme), Lean and 6 Sigma type teams. Must have excellent written and verbal communication skills as well as the ability to accurately document work performed. Ability to work primarily on your own initiative but experience working as part of a team will be required occasionally - You need to have a Strong planning and organizational ability. About you The successful candidate will have a minimum of 3 years' work experience in a manufacturing environment. You will have knowledge of using IT systems such as manufacturing. Regulated manufacturing/production environment and have a proven ability and willingness to learn. You will be technically qualified with a Leaving Certificate or substantial GMP manufacturing experience and a third level qualification in a technical discipline is desirable. You will need to have an excellent interpersonal and communication skills to execution systems, online self-service portals, training systems and barcode scanners required. Experience of working in a highly automated and high-speed environment and in a controlled clean room environment would be a distinct advantage. You will be hands on and have a sense of urgency. Ability to function as part of a team and work on own initiative. The ideal candidate will have some GMP/GDP experience and high level of safety awareness. This role will include Shift work, previous experience of Shift patterns is required. You must be willing to work on a 4-shift basis, the company will operate 24 hours/day, 7 days/week. embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Senior Process Engineer is responsible for leading a team to deliver on Key Safety, Quality, Delivery and Cost Results in a high volume, fully automated manufacturing environment producing Pen Needle products. Responsibilities: Lead a team of engineers and/or technicians to provide direct support to the production and maintenance teams to resolve daily issues and assist with troubleshooting. Champion a data-driven approach to investigate and resolve process issues. Drive structured problem-solving with the technicians. Continuously strive to improve efficiency of the equipment by standardising and optimising equipment setup, upgrading equipment to improve process capability where necessary. Carry out frequent reviews of the preventative maintenance schedules to ensure that they are effective at mitigating equipment failure and improving uptime. Work closely with material suppliers to match machine and process capability, and ensure controls are robust throughout the value chain to maintain high levels of process stability and equipment uptime. Work closely with the development team on new equipment or processes to establish robust process windows and effective handover to production. Lead QN, Customer Complaint and CAPA investigations. Responsible for the change control process in the assigned area and ensuring that appropriate documentation and approvals are followed. Lead the training and development of technicians in the assigned process engineering area. Ensure that associates are working in a safe manner and that existing and new tasks are risk assessed. Ensure that all group activities are fully compliant with the Business Quality Policy Carry out performance reviews, set objectives, and follow the absence management process for direct reports. Any other reasonable duties which may be required by management from time to time. Educational Requirements and Relevant Experience: Bachelor's Degree in Engineering 10 years process engineering experience with people management Experience with high speed automation Experience with precision mechanical setup Knowledge, Skills and Abilities: Strong data analysis skills and experience applying Six Sigma or equivalent structured problem-solving approaches Knowledge of Lean techniques: Standard Work, TPM Familiarity with equipment validation and documentation within a regulated industry is advantageous #LI-DF1 #LI-ONSITE embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. As a maintenance technician you will provide support to operations through effective execution of the planned preventive maintenance program across the range of automated assembly equipment. You will collaborate cross-functionally with Operations Engineering, working closely with shift and day teams to deliver and continuously improve maintenance programs, while coordinating preventive maintenance for production equipment across the site. Responsibilities Execution of planned preventive maintenance activities across a range of high volume, fully automated assembly lines Working with reliability engineer on admin of maintenance plans, task lists and work orders in CMMS (SAP) Continual review of PM activities for effectiveness and improvement opportunities Deputize as needed for reliability engineer in scheduling, release, distribution and reconciliation of PM work orders Collaboration with wider engineering team to effectively and efficiently coordinate PM tasks Assist as required with validation and qualification of new and existing equipment including acceptance trials, and PM implementation. Deal/liaise with vendors, suppliers and local engineering shops; Involved in analysing customer complaints and internal quality issues and assist as needed in drawing up improvement programmes for equipment to eliminate these defects being produced. Assist with the training of other, new recruits and apprentices as required. Participate in companywide continuous improvement initiatives, working in teams as required and utilising appropriate quality tools as applicable. Maintain appropriate recording and reporting systems on all engineering related matters (e.g., breakdowns, maintenance etc.). Full utilisation of all current and new IT/processing systems e.g., SAP. Maintain highest standards of safety and housekeeping to ensure area, machines and equipment are maintained in a safe and clean condition. Correct and/or report unsafe conditions and other faults. Education & Experience Mechanical fitter trade preferred however alternative trades and/or other third level engineering qualifications will be considered. 3 + years experience in a high-volume manufacturing environment in medical device industry or other relevant industries such as Pharmaceuticals , Food Manufacturing Cross skilled technical experience on highly automated production equipment preferred with working knowledge of Mechanical, Electrical, Pneumatic and automated systems. A scientific approach to problem solving, blending analytical and experimental skills to maximise productivity and yield Excellent interpersonal and communication skills. #LI-DF1 #LI-ONSITE embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. JOB PURPOSE: The Shift Automation Technician will be a member of the Shift Maintenance team that provides engineering day to day and project support within the high volume, fully automated manufacturing environment, and will be responsible for and involved in troubleshooting, maintenance and continuous improvement of the production processes and equipment. RESPONSIBILITIES: Develop an in-depth knowledge of all control systems currently in use across the entire site including PLC's, motion systems, vision systems, electrical & safety systems and networks Operate as point of contact person for all automation related line down issues and projects Work closely with engineers and cross functional teams in monitoring equipment performance using proven troubleshooting and problem solving techniques / methods to solve to root cause Support the continuous improvement of all automated equipment using Lean / Six Sigma and Project Management techniques Ensure all new equipment and tasks are risk assessed, support investigation and near miss resolution, and proactively drive actions to reduce safety risks Support plant wide automation change control and manage software revision control systems in full compliance with business quality systems Carry out other relevant tasks as required by the Shift Engineer EDUCATIONAL REQUIREMENTS: Good knowledge of Electrical & Automation Systems associated with high volume manufacturing equipment and hold a Third Level Qualification in one of those disciplines or the National Craft Certificate together with additional specialized training and experience. PREVIOUS EXPERIENCE: At least 5 years' experience in a similar role with Equipment Automation, Software or related experience Proficient in Allen Bradley / Rockwell Automation PLC products with an ability to understand complex programming functions A proven track record in solving automation problems to root cause using structured problem solving Experience of High Speed Vision systems (Cognex Vision Pro/Insight) and Control Networks & Communication Systems (ControlNet, DeviceNet, Ethernet) Good understanding of Motion Control Systems (Allen Bradley, Emerson, Linmot) Experience of development, deployment & maintenance of SCADA / HMI systems (Allen Bradley, Schneider) Creative thinking team player with excellent communication skills, an ability to work on their own initiative combined with the ability to work seamlessly across various departments embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Process Engineer supports a high-volume, fully automated manufacturing environment, with responsibility for process development, troubleshooting, maintenance, and continuous improvement of production processes and equipment within the assigned area. Responsibilities: Develop, design, and evaluate equipment and/or processes. Requirement for novel and innovative approaches in relation to fixtures / jig design and scalability. Develop knowledge to become the subject matter expert for assigned processes. Drive process improvements through identification of problem areas/opportunities and collaborate with internal groups and external vendors using Lean / Six Sigma and project management techniques . Assist with Quality Non-conformances, Customer Complaints and CAPA investigations Liaise with external equipment manufacturers / suppliers in terms of equipment / fixture design and manufacture. Manage projects related to product & equipment development Adherence to current health, safety and environmental best practice, ensuring that all work is appropriately risk assessed. Liaise with R&D teams as required, providing design for manufacture input on component / assembly development projects. Provide support to operations, optimising existing processes as needed to ensure that engineering work orders / production related goals are met. Other work relevant to skills as requested by management Requirements Bachelors Degree in Engineering At least 3 years process engineering experience within a regulated manufacturing environment Process optimisation with strong background in design of experiments essential. Experience with Cognex or other Vision Systems, pick and place operations, and form fill seal would be desirable. High speed automation experience, test equipment fixture design and documentation is advantageous. embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. Job Purpose: Responsible for ensuring that products manufactured at the Dun Laoghaire site comply with all microbiological, ETO sterilization, GLP, and cleanroom requirements. This role provides technical microbiology and sterilization expertise, ensures adherence to regulatory and company standards, and maintains the site in a state of inspection readiness throughout the contract period. Responsibilities: Maintain up-to-date knowledge of all relevant international regulatory requirements related to microbiology, sterilization (including ISO 11135 and ISO 10993 ), and cleanroom controls applicable to Dun Laoghaire products. Maintain up to date knowledge of all relevant international regulatory requirements related to cleanroom operation (including ISO 14644 and ). Provide daily technical oversight and subject matter expertise for: ETO sterilization processes; product adoption, full/ reduce sterilization requalification ; GLP -compliant laboratory practices; and cleanroom behavior , controls, and environmental monitoring. Support Microbiology Technicians in the execution of microbiological testing, environmental monitoring, and sterilization activities. Set appropriate microbiological and sterilization quality standards for products and ensure consistent application across the site. Ensure full compliance with internal sterilization procedures, cleanroom requirements, GLP expectations, and global Quality System regulations. Review sterilization cycles, microbiological data, and processed product lots; approve lots for release in accordance with quality standards. Lead or support root cause investigations involving microbiological or sterilization-related non-conformances. Act as microbiological and sterilization technical specialist for the Dun Laoghaire site and collaborate with relevant technical specialist groups. Support the site in always maintaining audit and inspection readiness (internal, external, Notified Body, and regulatory). Maintain laboratory safety, equipment readiness, and compliance with data integrity expectations. Perform any other duties as reasonably required by management during the contract period. Educational Requirements and Relevant Experience: Degree in Science or a related Quality discipline, specializing in Microbiology. Minimum 5 years' experience in medical devices, pharmaceutical, or biotech sectors. Demonstrated expertise in: GLP principles and laboratory governance; cleanroom operations and environmental monitoring. Experience with process validation and cleanroom compliance. Terminal Sterilization / Ethylene Oxide Sterilization and ISO 11135 advantageous. Knowledge, Skills and Abilities: Excellent interpersonal, communication, and team-building skills. Proven ability to work within cross-functional teams in a regulated environment. Strong understanding of ISO 13485, FDA QSR/QMSR, and sterilization standards. Strong analytical and problem-solving skills with experience in investigations and CAPA. High level of computer literacy, including Microsoft Office applications. Ability to manage complex technical activities independently with minimal supervision. embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. Job Purpose: Responsible for ensuring that products manufactured at the Dun Laoghaire site comply with all microbiological, ETO sterilization, GLP, and cleanroom requirements. This role provides technical microbiology and sterilization expertise, ensures adherence to regulatory and company standards, and maintains the site in a state of inspection readiness throughout the contract period. Responsibilities: Maintain up-to-date knowledge of all relevant international regulatory requirements related to microbiology, sterilization (including ISO 11135 and ISO 10993 ), and cleanroom controls applicable to Dun Laoghaire products. Maintain up to date knowledge of all relevant international regulatory requirements related to cleanroom operation (including ISO 14644 and ). Provide daily technical oversight and subject matter expertise for: ETO sterilization processes; product adoption, full/ reduce sterilization requalification ; GLP -compliant laboratory practices; and cleanroom behavior , controls, and environmental monitoring. Support Microbiology Technicians in the execution of microbiological testing, environmental monitoring, and sterilization activities. Set appropriate microbiological and sterilization quality standards for products and ensure consistent application across the site. Ensure full compliance with internal sterilization procedures, cleanroom requirements, GLP expectations, and global Quality System regulations. Review sterilization cycles, microbiological data, and processed product lots; approve lots for release in accordance with quality standards. Lead or support root cause investigations involving microbiological or sterilization-related non-conformances. Act as microbiological and sterilization technical specialist for the Dun Laoghaire site and collaborate with relevant technical specialist groups. Support the site in always maintaining audit and inspection readiness (internal, external, Notified Body, and regulatory). Maintain laboratory safety, equipment readiness, and compliance with data integrity expectations. Perform any other duties as reasonably required by management during the contract period. Educational Requirements and Relevant Experience: Degree in Science or a related Quality discipline, specializing in Microbiology. Minimum 5 years' experience in medical devices, pharmaceutical, or biotech sectors. Demonstrated expertise in: GLP principles and laboratory governance; cleanroom operations and environmental monitoring. Experience with process validation and cleanroom compliance. Terminal Sterilization / Ethylene Oxide Sterilization and ISO 11135 advantageous. Knowledge, Skills and Abilities: Excellent interpersonal, communication, and team-building skills. Proven ability to work within cross-functional teams in a regulated environment. Strong understanding of ISO 13485, FDA QSR/QMSR, and sterilization standards. Strong analytical and problem-solving skills with experience in investigations and CAPA. High level of computer literacy, including Microsoft Office applications. Ability to manage complex technical activities independently with minimal supervision. embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Engineering Maintenance Technician is responsible for the hands-on maintenance, troubleshooting, and technical performance of high-speed, automated manufacturing equipment within the OBI manufacturing area. This is a technical maintenance role, with clear ownership for planned, preventative, and reactive maintenance, fault diagnosis, and equipment reliability. The Engineering Technician works closely with Engineering, Operations, and external vendors to ensure equipment operates safely, reliably, and at optimal performance. Key Responsibilities Carry out planned, preventative, and reactive maintenance on a wide range of automated production equipment. Perform mechanical, electrical, pneumatic, and controls-based fault finding to diagnose equipment issues and restore production safely and efficiently. Support equipment overhauls, modifications, installations, and recommissioning activities as required. Act as a technical specialist for assigned equipment or production areas. Analyse equipment performance data, downtime trends, and OEE metrics to identify recurring issues and reliability improvement opportunities. Drive continuous improvement initiatives focused on downtime reduction, waste elimination, and equipment robustness. Apply structured problem-solving methodologies (RCA, 5-Why, Fishbone, etc.) to prevent recurrence of technical failures. Provide technical input into validation documentation and activities, including equipment changes, upgrades, and process improvements. Support engineering assessment of drawing and specification changes and assist with their controlled introduction. Liaise with equipment vendors, suppliers, and local engineering shops to support maintenance, repairs, and upgrades. Maintain equipment, tools, and work areas to the highest standards of safety, housekeeping, and compliance. Ensure all maintenance activities are carried out in line with site safety procedures and regulatory requirements. Education & Experience National Craft Certificate (Electrical / Mechanical / Mechatronic) or a third-level qualification in Engineering. Proven hands-on experience in a high-volume manufacturing environment (medical device, pharma, semiconductor, food, or similar regulated industry). Demonstrated experience in equipment troubleshooting, fault diagnosis, and maintenance ownership. Desirable Experience with PLC-controlled systems, vision systems (e.g. Cognex), and pick & place automation. Experience analysing equipment data to drive OEE and reliability improvements. Familiarity with validation, change control, and working within regulated manufacturing environments. Key Skills & Competencies Strong hands-on troubleshooting and diagnostic capability Logical, analytical, and methodical approach to technical problem-solving Ability to work independently while collaborating effectively with Engineering and Operations Clear technical communication skills Good PC and systems skills for maintenance reporting and documentation #LI-ONSITE #LI-DF1 embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Senior Process Engineer - Packaging is responsible for leading a team to deliver on key Safety, Quality, Delivery and Cost Results in the packaging cell. The role will act as the SME for fully automated, high-volume, high speed packaging machines, and is responsible for day-to-day production support and driving improvements in the area. Lead a team of technicians to provide direct support to the production and maintenance teams to resolve daily issues and assist with troubleshooting. Champion a data-driven approach to investigate and resolve process issues. Drive structured problem-solving with the technicians. Carry out frequent reviews of the preventative maintenance schedules to ensure that they are effective at mitigating equipment failure and improving uptime. Work closely with material suppliers to match machine and process capability, and ensure controls are robust throughout the value chain to maintain high levels of process stability and equipment uptime. Work closely with the development team on new equipment or processes to establish robust process windows and effective handover to production. Lead QN, Customer Complaint and CAPA investigations. Responsible for the change control process in the assigned area and ensuring that appropriate documentation and approvals are followed. Lead the training and development of technicians in the assigned process engineering area. Ensure that associates are working in a safe manner and that existing and new tasks are risk assessed. Ensure that all group activities are fully compliant with the Business Quality Policy Carry out performance reviews, set objectives, and follow the absence management process for direct reports. Any other reasonable duties commensurate with the level and scope of the role as required by management from time to time. Experience and Education Bachelor's Degree in engineering At least 10 years process engineering experience with people management. Strong practical knowledge of packaging equipment and packaging processes is desirable Experience in improving maintenance programmes and driving overall equipment effectiveness Strong data analysis skills and experience applying Six Sigma or equivalent structured problem-solving approaches Knowledge of Lean techniques: Standard Work, TPM Familiarity with equipment validation and documentation within a regulated industry is advantageous. Familiarity with Good Manufacturing Principles #LI-ONSITE #LI-DF1 embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. TPBN1_IJ
