A reputable engineering consultancy in North Leinster with a growing client base is looking to recruit a senior wastewater specialist engineer to work closely with clients on technical advice and troubleshooting. The role is mainly office based with regular travel to client wastewater treatment facilities for technical inspections and liaising with plant operators. Main responsibilities: Technical review of Wastewater treatment plant operations. [+]
A reputable engineering consultancy in North Leinster with a growing client base is looking to recruit a senior wastewater specialist engineer to work closely with clients on technical advice and troubleshooting. The role is mainly office based with regular travel to client wastewater treatment facilities for technical inspections and liaising with plant operators. Main responsibilities: Technical review of Wastewater treatment plant operations. Wastewater treatment plant operations manual review and compilation as necessary. Troubleshoot issues occuring in Wastewater treatment plants. Design wastewater treatment plant process to help improve plant operation. Support related environmental projects being carried out by clients, eg:Environmental Auditing, Due Diligence surveys, Monitoring and Sampling and other relevant areas. Required Qualifications and Experience: Degree level in a relevant Environmental or Engineering discipline, for example Degree in Civil and Environmental Engineering or Bachelor of Science in Environmental Management. 10+ years’ experience of wastewater treatment process with similar responsibilities. If you are interested in a role such as the above and hold a degree in a relevant environmental or engineering discipline, please send your application to Richard at Sigmar - see link below or to rwalsh@sigmar.ie. This job originally appeared on RecruitIreland.com. [-]
Instrument commissioning technician with safe pass required for Mullingar, Westmeath. Electrical background. References will be required. Please specify if you have your own transport.
Lead Equipment Engineer (pharmaceuticals. In this role, the successful candidate will provide technical expertise and leadership in ensuring that the equipment and facility requirements of the Process Development group are met and will represent the Process Development group at site and global equipment teams. Key Responsibilities. • Display a well-developed knowledge of engineering principles and cGMP requirements. [+]
Lead Equipment Engineer (pharmaceuticals. In this role, the successful candidate will provide technical expertise and leadership in ensuring that the equipment and facility requirements of the Process Development group are met and will represent the Process Development group at site and global equipment teams. Key Responsibilities. • Display a well-developed knowledge of engineering principles and cGMP requirements. • Become an SME in Process Development equipment and the site systems for equipment introduction. • Generate documentation to support facility/equipment specification, design and commissioning/qualification activities within a cGMP environment. • Apply a project management approach to develop, track and communicate plans for assigned projects, ensuring objectives are achieved on time and in budget. • Lead risk assessment activities involving cross-functional teams and make risk-based judgements on key project activities. • In conjunction with the Process Development process engineers and other key stakeholders, plan, design, specify and oversee the introduction of new facilities/equipment to support the delivery of key programmes and act as the PD representative on cross-functional project teams designated by the site engineering group to source major equipment. • Represent the Process Development department on cross-functional project teams to ensure delivery of key projects. • Analyse and provide resolution of technical issues. • Ensure that budgetary and CAPEX requirements are followed. • Encourage and support contributions from team members, promoting open discussion and collaboration, effectively managing conflict within the team. • Support FDA pre-approval and post-approval inspections by serving as technical expert for development operations. Present, where appropriate, technical data to internal / external audit groups (including HPRA & FDA) and commercial partners. • Present, where appropriate, technical data to internal / external audit groups (including HPRA & FDA) and commercial partners. • Ensure all company and departmental policies and procedures are adhered to. • Effectively communicate to stakeholders project activities and updates. Requirements for this role: • Third level qualification in Science, Engineering or related discipline. • Minimum of 5 years' engineering experience, preferably in the pharmaceutical industry , with detailed knowledge of process equipment and facilities (containment systems design and operation, dust extraction, solvent abatement etc.). • Strong technical and project management skills. • Demonstrated track record in generating technical options to resolve problems, prioritising solutions, selecting optimal solutions and implementing decisions. • Project Management skills an advantage. • Experience of formal risk-based assessment tools an advantage. • Adaptable to changing priorities. • Excellent verbal and written communication skills. This job originally appeared on RecruitIreland.com. [-]
Lead Process Engineer (pharma. This role is being offered as a 12 months' fixed-term contract. Working within the Process Development Group, the successful candidate will provide technical expertise and leadership for new and existing technology-based product development programmes. KEY RESPONSIBILITIES. • Manage experimental programmes for use in process development activities, involving investigational studies to provide indicative process/analytical data for identification of critical process parameter effects. [+]
Lead Process Engineer (pharma. This role is being offered as a 12 months' fixed-term contract. Working within the Process Development Group, the successful candidate will provide technical expertise and leadership for new and existing technology-based product development programmes. KEY RESPONSIBILITIES. • Manage experimental programmes for use in process development activities, involving investigational studies to provide indicative process/analytical data for identification of critical process parameter effects. Analyse the process and analytical data generated by these programs and report on same. • Design and lead process development activities focused on study of critical parameters to ensure that process conditions, at all scales, are consistent and not at “edge of failure”. Select appropriate parameters for prototype/finished dosage production to ensure product quality and reproducibility are achieved and a robust control strategy is developed. • Develop, execute and refine the methodology required for the generation of successful scale-up/optimisation process models. These models are required to accurately establish process operating windows at relevant scale and identify appropriate in-process operating ranges to maintain both product quality and production efficiency. • Execute all aspects of team management as a leader of projects, from development through launch, associated with new formulation product or technology development programmes. • Interact with cross-functional and cross-site technical and CMC teams influencing and communicating on development projects. • Assess industry process advancements and introduce them to site as appropriate. • Act as site expert in resolution of technical issues by means of formulation, process or machine modifications, providing innovative solutions to issues at hand. • Manage and lead relative areas of responsibility through FDA pre-approval and post-approval inspections by serving as technical expert for development and processing operations. • Prepare Development Reports and CMC sections of DMFs or NDAs related to formulation development, process scale-up, process control and comparisons of development and commercial processes. • Ensure all company and departmental policies and procedures are adhered to and develop new or enhanced systems where appropriate. REQUIREMENTS FOR THIS ROLE: • Third level qualification in a Science or Engineering Discipline (to level 8 or higher) with minimum 5-8 years' relevant experience. • Experience of process development/engineering, formulation and related commercial scale-up/manufacturing, preferably in the pharmaceutical industry. • Strong technical and project management skills. • Demonstrated track record in generating technical options to resolve problems, prioritising solutions, selecting optimal solutions and implementing decisions in the pharmaceutical industry. • Strong experience in statistical analysis, sample sizing, Anova, DOE, regression analysis an advantage. • Excellent verbal and written communication skills. This job originally appeared on RecruitIreland.com. [-]
Lead Equipment Engineer (pharma. Youwill provide technical expertise and leadership in ensuring that the equipment and facility requirements of the Process Development group are met and will represent the Process Development group at site and global equipment teams. Key Responsibilities • Display a well-developed knowledge of engineering principles and cGMP requirements. • Become an SME in Process Development equipment and the site systems for equipment introduction. [+]
Lead Equipment Engineer (pharma. Youwill provide technical expertise and leadership in ensuring that the equipment and facility requirements of the Process Development group are met and will represent the Process Development group at site and global equipment teams. Key Responsibilities • Display a well-developed knowledge of engineering principles and cGMP requirements. • Become an SME in Process Development equipment and the site systems for equipment introduction. • Generate documentation to support facility/equipment specification, design and commissioning/qualification activities within a cGMP environment. • Apply a project management approach to develop, track and communicate plans for assigned projects, ensuring objectives are achieved on time and in budget. • Lead risk assessment activities involving cross-functional teams and make risk-based judgements on key project activities. • In conjunction with the Process Development process engineers and other key stakeholders, plan, design, specify and oversee the introduction of new facilities/equipment to support the delivery of key programmes and act as the PD representative on cross-functional project teams designated by the site engineering group to source major equipment. • Represent the Process Development department on cross-functional project teams to ensure delivery of key projects. • Analyse and provide resolution of technical issues. • Ensure that budgetary and CAPEX requirements are followed. • Encourage and support contributions from team members, promoting open discussion and collaboration, effectively managing conflict within the team. • Support FDA pre-approval and post-approval inspections by serving as technical expert for development operations. Present, where appropriate, technical data to internal / external audit groups (including HPRA & FDA) and commercial partners. • Present, where appropriate, technical data to internal / external audit groups (including HPRA & FDA) and commercial partners. • Ensure all company and departmental policies and procedures are adhered to. • Effectively communicate to stakeholders project activities and updates. Requirements for this role: • Third level qualification in Science, Engineering or related discipline. • Minimum of 5 years' engineering experience, preferably in the pharmaceutical industry , with detailed knowledge of process equipment and facilities (containment systems design and operation, dust extraction, solvent abatement etc.). • Strong technical and project management skills. • Demonstrated track record in generating technical options to resolve problems, prioritising solutions, selecting optimal solutions and implementing decisions. • Project Management skills an advantage. • Experience of formal risk-based assessment tools an advantage. • Adaptable to changing priorities. • Excellent verbal and written communication skills. This job originally appeared on RecruitIreland.com. [-]
What you need to know. Matrix Recruitment are looking to recruit a Process Technician for our Medical Device client based in Co. Galway. This is a permanent position and you will report to the Operations & Engineering Manager. Excellent salary and benefits package available in this expanding organisation. Your new job. Process and equipment setup and ready for production. Ensure the process area compliant and is audit ready at all times. [+]
What you need to know. Matrix Recruitment are looking to recruit a Process Technician for our Medical Device client based in Co. Galway. This is a permanent position and you will report to the Operations & Engineering Manager. Excellent salary and benefits package available in this expanding organisation. Your new job. Process and equipment setup and ready for production. Ensure the process area compliant and is audit ready at all times. Manage daily line performance and resolve technical issues. Develop manufacturing processes and ensure equipment is set-up. Support process validation activities. Establish and maintain manufacturing documentation including, equipment documentation, product routings, manufacturing procedures and logs and BOM’s. Provide ongoing support to production and drive continuous improvements in the area. Generate document updates in line with Quality Management Systems. Manager trouble shooting and resolving technical issues in a timely manner. What are we looking for? Diploma in Polymer Engineering or equivalent. 2-3 years’ experience within a medical devices environment and in a similar role. Strong technical understanding of set up and maintenance of manufacturing process with experience in validation and equipment design. Self-motivated with a good technical ability. Team player building effective relationships with Technicians and Engineers. Strong communication and problem-solving skills with great attention to detail. Apply for this job now or get in touch with Niall on 09064 90485. Matrix Recruitment Group is committed to providing a professional service where all CV's are kept confidential and will not be submitted to any clients without candidate’s knowledge or consent. This job originally appeared on RecruitIreland.com. [-]
A Demand Planner on a 12-Month-Contract is required by CareerWise Recruitment for our Athlone, Westmeath based client. Two primary responsibilities include generating an accurate consensus forecast for the demand of rental and sales units as well as disposable products to support the one or more of the regional markets (i.e. APAC, MEA, etc…EMEA) and ensuring product in-stock rates at one, or more, regional distribution centers sufficient to meet customer requirements. [+]
A Demand Planner on a 12-Month-Contract is required by CareerWise Recruitment for our Athlone, Westmeath based client. Two primary responsibilities include generating an accurate consensus forecast for the demand of rental and sales units as well as disposable products to support the one or more of the regional markets (i.e. APAC, MEA, etc…EMEA) and ensuring product in-stock rates at one, or more, regional distribution centers sufficient to meet customer requirements. THE ROLE: * Lead the process of collaborative demand forecasting for sales and rental units in all assigned market regions. * Generate a baseline forecast through the statistical analysis of historical sales and rental data. * Gather qualitative inputs from the marketing, sales, and service teams to enhance the baseline statistical forecast and to improve accuracy and bias. This will include identifying future pricing strategies, sales promotions, and product line changes. * Facilitate demand review meetings with cross functional teams with the goal of finalizing a consensus forecast. * Provide analytical support the Sales and Operations Planning process. * Report and monitor forecast accuracy and bias. Identify root cause and corrective action when targets for accuracy and bias are not met. * Communicate stock level information to regional leadership. * Engage with Innovation Teams/New Product Teams to support supply chain planning associated with global new product releases. * Develop and co-ordinate stock-out mitigation plans across a cross functional group including: manufacturing, service and marketing. REQUIREMENTS: * Bachelors degree in Business, Statistics, Supply Chain, Engineering or a related field. * Minimum of 6 years of relevant work experience in supply chain planning, sales forecasting, or financial analysis. * Minimum of 2 years experience working with ERP, MRP II, MRP, SCP, or DRP systems. * Intermediate knowledge of meeting management including agenda design and group facilitation. * Intermediate to advanced knowledge of time series forecasting models such as moving averages. * Ability to establish and maintain effective interpersonal working relationships with internal customers, internal/external suppliers and fellow team members at all levels. * Intermediate proficiency with Microsoft Office Suite of applications (Excel, Access, Outlook, etc.) * Intermediate to advanced proficiency in visual data display and analysis including the appropriate use of tables, charts, and graphs. * Experience working effectively with cross functional teams with remotely located team members and stakeholders. * International travel required. * Oracle experience. * Demonstrated experience with Sales and Operations Planning. Please call Tom Devaney today for further information on 091-758771 or email: tdevaney@careerwise.ie. CareerWise Recruitment (In Search of Excellence. CareerWise Recruitment specialises in the multinational sector in Ireland which predominantly encompasses the Medical Device, Sciences/Pharma and ICT industries. We also work into the Indigenous Engineering and Food Processing/Agri sectors. Established in 1999, CareerWise Recruitment is recognised by many of the major indigenous and multinationals companies to be one of Irelands leading specialist Technical and Executive Recruitment firms. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway and Dublin. Supporting Business Demands & Growth since 1999. CareerWise Recruitment accepts that you do not wish your CV to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will be respected at all times. This job originally appeared on RecruitIreland.com. [-]
My client is a Start Pharma company looking for a Sterile Ops Technician to join their team.The Sterile Operations Maintenance Technician provides essential maintenance and technical support to manufacturing across the full range of sterile manufacturing equipment. The role involves developing preventative maintenance (PM) routines, completing PMs on time in addition to reacting to machine breakdown to support manufacturing performance. [+]
My client is a Start Pharma company looking for a Sterile Ops Technician to join their team.The Sterile Operations Maintenance Technician provides essential maintenance and technical support to manufacturing across the full range of sterile manufacturing equipment. The role involves developing preventative maintenance (PM) routines, completing PMs on time in addition to reacting to machine breakdown to support manufacturing performance. The role also plays a significant role in ensuring all equipment related documentation meets the cGMP standards expected. Key duties and Responsibilities: Works with manufacturing and quality colleagues as part of an Operations team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site. Prioritises safety and is diligent in the use of all appropriate safety tools and permits when maintaining equipment – champions safe working always. Provides maintenance support as required to include process systems, filling equipment, preparation equipment and clean utilities. Can provide basic automation and instrumentation support and liaises with automation/instrumentation specialists when required. Uses structured problem solving in the event of equipment failure and documents all equipment interventions as required by the maintenance system. Prepare preventative maintenance (PM) routines with other technical colleagues to minimise the risk of machine failure or equipment related deviations. Completes PM routines on time. Is trained and qualified to work in a grade B cleanroom and maintains this qualification. Is disciplined in ensuring personal hygiene at all time, and in following the garbing and hygiene expectations of working in a sterile manufacturing environment. Participates in bi-annual media fill studies to maintain qualification status. Is diligent in the completion and review of maintenance and related documentation required to meet GMP requirements of a sterile manufacturing site. Participates in and can lead continuous improvement teams. Proposes improvement ideas. Takes ownership of manufacturing equipment performance and builds relationships with key OEM support contacts. Key requirements. Familiar with pharmaceutical equipment and systems such as CIP/SIP, autoclaves, filling machines, isolators, clean utilities. Strong technical, troubleshooting and problem solving skills. Proficient in use of Microsoft Office and other computer applications i.e. CMMS. Strong team player with good proactive approach & manner. Knowledgeable of the regulatory and GMP requirements for maintenance activities. Degree/Diploma and/or technical certification / trade in a mechanical, electrical or related field. For more information or to apply please contact - Ruth.hayes@cpl.ie 019476289. This job originally appeared on RecruitIreland.com. [-]
My Client is a start up Pharma company looking for The Facilities Technician to provides maintenance and technical support to the site and to manufacturing across the full range of site facilities and utilities. The role involves developing preventative maintenance (PM) routines, completing PMs on time in addition to reacting to problems that may disrupt manufacturing activity. Key Duties and Responsibilities: Works with manufacturing and quality colleagues as part of an Operations team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site. [+]
My Client is a start up Pharma company looking for The Facilities Technician to provides maintenance and technical support to the site and to manufacturing across the full range of site facilities and utilities. The role involves developing preventative maintenance (PM) routines, completing PMs on time in addition to reacting to problems that may disrupt manufacturing activity. Key Duties and Responsibilities: Works with manufacturing and quality colleagues as part of an Operations team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site. Prioritises safety and is diligent in the use of all appropriate safety tools and permits when maintaining equipment – champions safe working always. Operates and maintains site black and clean utility systems including WFI, clean steam, HVAC, process air, boilers, compressors, etc. Uses structured problem solving in the event of equipment failure and documents all equipment interventions as required by the maintenance system. Prepare preventative maintenance (PM) routines with other technical colleagues to minimise the risk of machine failure or equipment related deviations. Completes PM routines on time. Supports Quality Control personnel in sampling of clean utilities and supports investigations into any out of trend results. Is diligent in the completion and review of maintenance and related documentation required to meet GMP requirements of sterile manufacturing site. Participates in and can lead continuous improvement teams. Proposes improvement ideas. Builds relationships with external equipment suppliers and service partners and coordinates service visits. Supports capital projects throughout equipment lifecycle and supports process development projects and associated validation activities. Reports accurately on all equipment downtimes to build history of equipment performance. Monitors site energy usage and reports on same. Coordinates instrument calibration partners to support calibration activity and instrumentation elements for process investigations. Is always prepared to escalate any safety, quality or performance risk observed. Key requirements. Familiar with pharmaceutical utility equipment such as WFI generation & distribution, clean steam generation & distribution, cleanroom HVAC, steam boilers, air compressors, etc. Strong technical, troubleshooting and problem solving skills. Proficient in use of Microsoft Office and other computer applications i.e. CMMS. Strong team player with good proactive approach & manner. Knowledgeable of the regulatory and GMP requirements for maintenance activities. Technical certification/trade in a business service, mechanical, electrical or related field. This job originally appeared on RecruitIreland.com. [-]
A key role within quality engineering QMS for Supplier Mgt & compliance related projects, ensuring technical correctness, & compliance with requirements of global regulations and part of an overall strategy for improved quality assurance for QMS, product quality. Reporting to the QA Manager you will : - Monitor current & assess potential new suppliers /service providers for technical, quality , & quality system capabilities. [+]
A key role within quality engineering QMS for Supplier Mgt & compliance related projects, ensuring technical correctness, & compliance with requirements of global regulations and part of an overall strategy for improved quality assurance for QMS, product quality. Reporting to the QA Manager you will : - Monitor current & assess potential new suppliers /service providers for technical, quality , & quality system capabilities. Implement continuous & innovative improvements with demonstrated & measurable results - Cost of Poor Quality etc. Drive supplier audit program by managing & conducting supplier audit s. Ensure proper root cause is found & implemented by supplier. Evaluate nonconforming supplied material & prepared Supplier Correction Action Requests to ensure resolution of root cause causing supplier quality issue. Ensure supplier files are compliant with regs & internal procedures. Partner with Site Purchasing & Divisional Supplier Quality team to ensure cross site competencies & drive improvements. Liaise with Operations, Supply Chain Mgt, Warehouse, Engineering & NPI to ensure uninterrupted supply of material s. Support NPIs by providing guidance on compliance with Company KPIs defined in material specifications, CTQ's, processes quality agreements etc. Ensure that requirements clear in the quality manual & SOPs are adhered too, & provide advice & guidance to all dept's regarding quality. Provide Operational QA Support for products & process. QUALIFICATIONS/EXPERIENCE. Degree in Quality , Engineering or a Science discipline with - 3-5 years' experience at quality engineering level within a regulated industry, ideally in Medical Device. Demonstrable knowledge of FDA 21CFR820 &/or ISO 13485 regulations. Audit experience in conducting supplier & or internal audit s. Certified Lead auditor qualification for ISO13485 is an advantage & statistical methods (FMEA etc. Familiarity with use of ISO 14971:2007 an advantage. Ability to communicate to mgt & peers, both orally & in reports. PERSONAL COMPETENCIES. Good project planning & organisational abilities. Strong interpersonal & communications skills, including oral & written reports. Pro-active with proven ability to work under own initiative, & strong team player. Solid technical ability & willingness to travel as part of duties. Please apply to the role and then we can discuss in detail. This job originally appeared on RecruitIreland.com. [-]
Our client is a IDA supported start up company, now hiring for a skilled Maintenance Technician from the Sterile or Pharma / GMP regulated manufacturing sector. The Sterile Maintenance Technician provides essential maintenance and technical support to manufacturing across the full range of sterile manufacturing equipment. The role involves developing preventative maintenance (PM) routines, completing PMs on time in addition to reacting to machine breakdown to support manufacturing performance. [+]
Our client is a IDA supported start up company, now hiring for a skilled Maintenance Technician from the Sterile or Pharma / GMP regulated manufacturing sector. The Sterile Maintenance Technician provides essential maintenance and technical support to manufacturing across the full range of sterile manufacturing equipment. The role involves developing preventative maintenance (PM) routines, completing PMs on time in addition to reacting to machine breakdown to support manufacturing performance. The role also plays a significant role in ensuring all equipment related documentation meets the cGMP standards expected. Main Duties: Works with manufacturing and quality colleagues as part of an Operations team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site. Prioritises safety and is diligent in the use of all appropriate safety tools and permits when maintaining equipment – champions safe working always. Provides maintenance support as required to include process systems, filling equipment, preparation equipment and clean utilities. Can provide basic automation and instrumentation support and liaises with automation/instrumentation specialists when required. Uses structured problem solving in the event of equipment failure and documents all equipment interventions as required by the maintenance system. Prepare preventative maintenance (PM) routines with other technical colleagues to minimise the risk of machine failure or equipment related deviations. Completes PM routines on time. Is trained and qualified to work in a grade B cleanroom and maintains this qualification. Is disciplined in ensuring personal hygiene at all time, and in following the garbing and hygiene expectations of working in a sterile manufacturing environment. Participates in bi-annual media fill studies to maintain qualification status. Is diligent in the completion and review of maintenance and related documentation required to meet GMP requirements of a sterile manufacturing site. Participates in and can lead continuous improvement teams. Proposes improvement ideas. Takes ownership of manufacturing equipment performance and builds relationships with key OEM support contacts. Supports capital projects throughout equipment lifecycle and supports process development projects and associated validation activities. Reports accurately on all equipment downtimes to build history of equipment performance. Is always prepared to escalate any safety, quality or performance risk observed. Education/Experience: Familiar with pharmaceutical equipment and systems such as CIP/SIP, autoclaves, filling machines, isolators, clean utilities. Strong technical, troubleshooting and problem solving skills. Senior trade in a mechanical, electrical or related field or Degree/Diploma and/or technical certification. Proficient in use of Microsoft Office and other computer applications i.e. CMMS. Strong team player with good proactive approach & manner. For more information or to apply, call 01 254 2278 send your CV in confidence to peter.godwin@ cpl.ie. This job originally appeared on RecruitIreland.com. [-]
Matrix Recruitment are currently recruiting a number of R&D Engineer’s for a global medical devices company in Galway. What you need to know. You will work as an R&D Engineer for our medical device client in Galway. These are contract positions initially with excellent opportunities for career progression in a global medical device organisation. You will work in the Cardiac and Vascular space and you will develop innovative products for use in medical procedures. [+]
Matrix Recruitment are currently recruiting a number of R&D Engineer’s for a global medical devices company in Galway. What you need to know. You will work as an R&D Engineer for our medical device client in Galway. These are contract positions initially with excellent opportunities for career progression in a global medical device organisation. You will work in the Cardiac and Vascular space and you will develop innovative products for use in medical procedures. Your new job. Key duties & responsibilities: Work as part of the R&D team on the development of new medical device products. Ensure the products are designed efficiently to ensure success. Maintain manufacturing documentation. Provide technical support to product and process development and in clinical programs and compliant investigations. Lead multidiscipline teams in planning and implementing the introduction of new products. Support introduction/implementation of product/process/materials changes to operations. Understand sourcing, testing and approving materials. Monitor and evaluate safety practices and ensure compliance with legislation. Document design/development and test activities as required. What are we looking for? Desirable: BEng or Masters qualification in Mechanical, Biomedical or a related engineering discipline. 3-4 years’ experience ideally in a medical device environment. Medical device technology experience ideally in interventional vascular devices. Experience in biomedical materials and processing knowledge and medical device design procedures. Proven experience in innovative design and development/manufacturing implementation programs. High level of enthusiasm and motivation. Dynamic team player who can work effectively with cross functional teams. Strong interpersonal skills and displays the highest level of integrity. Apply for this job now or get in touch with Niall on 09064-90485. Matrix Recruitment Group is committed to providing a professional service where all CV's are kept confidential and will not be submitted to any clients without candidate’s knowledge or consent. This job originally appeared on RecruitIreland.com. [-]
Webrecruit Ireland- Co Westmeath, Co Dublin, Meath
Project Engineer – Plastic Moulding Products. Westmeath, Co Westmeath. €Excellent DOE Plus Pension, Healthcare Insurance Cover for Family, 26 Days’ Holiday. If you’re an analytical project engineer seeking a fresh, new challenge, this is a superb opportunity to develop your career with an international business. Our client utilises the world’s latest technologies to provide innovative technical plastic moulding solutions to the automotive, industrial and healthcare sectors. [+]
Project Engineer – Plastic Moulding Products. Westmeath, Co Westmeath. €Excellent DOE Plus Pension, Healthcare Insurance Cover for Family, 26 Days’ Holiday. If you’re an analytical project engineer seeking a fresh, new challenge, this is a superb opportunity to develop your career with an international business. Our client utilises the world’s latest technologies to provide innovative technical plastic moulding solutions to the automotive, industrial and healthcare sectors. They are now looking for a Project Engineer to join their team in Westmeath. Fostering a fast-paced environment that nurtures excellence, our client provides all of their employees with opportunities to enhance their abilities and progress their careers. As a Project Engineer, you will oversee a range of product development projects, from design phase through to mass production. Initially focusing on automotive projects, you will: - Liaise with customers regarding product design and development. - Select key tooling suppliers and manage their performance. - Lead project review meetings. - Co-ordinate and perform pre-production trials, both at supplier sites and in-house. - Perform process capability studies to ensure that new projects meet quality, cost and delivery standards. - Manage changes to existing products. - Lead and participate in continuous improvement activities. To be considered, you will need: - Experience as a project engineer. - Strong project management skills. - Excellent knowledge of design and visualisation software, such as AutoCAD. - Advanced MS Office skills, including MS Project and Excel. - A BS degree in engineering or a related field. Decisive and organised, as a Project Engineer, you must have superb prioritisation and time-management skills. You must also be a confident communicator with a team player mentality. To apply for the role of Project Engineer (Plastic Moulding Products), please apply via the button shown. This vacancy is being advertised by Webrecruit Ireland Ltd. The services advertised by Webrecruit Ireland Ltd are those of an Employment Agency. Additional Keywords: Project Engineer, Plastic Moulding Products, Product Design Engineer, New Product Design Engineer, NPD Engineer, Engineer, Engineering, Technical Project Engineer, Engineering Project Manager, Engineering Project Co-ordinator. Working hours: Monday – Friday, 8:00 – 16:00. Notice period: 2 months. This job originally appeared on RecruitIreland.com. [-]
Contact: Caroline Kingston. Email: caroline@hero.ie. Telephone: 0868395531. Senior Projects Engineer. Our client, a medical device company in Westmeath are currently looking to recruit a Senior Projects Engineer for their site. Our Purpose. At our Projects Engineering Department in the company we focus on providing stable, flexible and cost effective solutions to enhance our processes and systems that produce the highest quality products through innovative engineering projects, programs and solutions. [+]
Contact: Caroline Kingston. Email: caroline@hero.ie. Telephone: 0868395531. Senior Projects Engineer. Our client, a medical device company in Westmeath are currently looking to recruit a Senior Projects Engineer for their site. Our Purpose. At our Projects Engineering Department in the company we focus on providing stable, flexible and cost effective solutions to enhance our processes and systems that produce the highest quality products through innovative engineering projects, programs and solutions. Project Engineers are directly involved in planning and executing strategic project programs designed to continuously improve our manufacturing processes, systems, quality and regulatory compliance to the highest standards. Our Offer. You will lead strategic projects for the facility. You will be responsible for the planning, management, execution and oversight of the projects assigned, working closely with cross-functional project teams and departments. You will ensure meticulous planning, execution and leadership utilizing standardized systems, processes and templates for project execution and governance and regular reporting on project performance to senior management. You will set and track scope, schedules, budgets, deadlines, deliverables, resources and performance data throughout the project life cycle. You shall work closely with cross functional groups such as R&D, Engineering, Quality, Opex and Manufacturing team members to ensure projects are delivered to plan. You will advise senior management of project performance on a consistent basis and on solution responses to potential delays or deviations from original plans. Qualifications. Your Profile. We are looking for a qualified person with a minimum Bachelor`s Degree in a Science/Technology/Engineering related discipline (Mechanical, Manufacturing, Automation or equivalent. Ideally, you should possess a formal Project Management Certification (PMP, IPMA Level C or equivalent. You have a minimum of 5+ year`s successful demonstrated experience in project engineering ideally within Operations functions, preferably within the highly regulated Medtech sector. You are a dynamic team player and can work effectively and proactively on cross-functional teams. You can demonstrate your experience in the successful delivery of multiple projects from conception through to completion, meeting schedules and budgets. You are methodical and are experienced in the use of systems for project engineering and project managing. You can demonstrate your experience in project planning and execution and the delivery of projects to meet original scope, schedule and budget targets. You possess leadership and people management skills in project and/or functional management. You have technical knowledge of automated manufacturing systems and processes. You have a high level of proficiency and experience with MS Project, MS Office (Excel), Data analysis and Lean/Six Sigma. You are energetic, self-driven with a tenacious drive for results. You are highly focused and inner-directed to ensure on-time, high-quality delivery of projects in accordance with plant KPIs. You can take both logical and creative approaches to problem solving. You have a strong business and financial acumen, analytical, data and systems driven. You are well organised and resourceful and will do what it takes to get the job done on time. You have proven leadership ability, approachable and collaborate with others with ease. You are curious and questioning and establish risks and pitfalls to ensure surprises are minimized. You are an effective communicator with all levels of the organisation and comfortable with presenting to senior leadership. You are energised by tough challenges and persevere to achieve the final result, yet are objective and escalate issues early. You can manage and resolve conflict quickly. You must be capable of demonstrating the following leadership expectations: Thinks Critically and Makes Sound Decisions, Sets High Standards, Initiates and Leads Change, Instils Operational Excellence, Drives Accountability and Models Ethical Behaviour. Leadership Expectations provide the framework for what we expect from all employees at the company - outlining the actions and behaviours we must develop and demonstrate in pursuit of our Mission and global growth goals. For further information on this Senior Projects Engineer role in Westmeath Galway please contact Caroline Kingston on 0868395531 / caroline@hero.ie. Check out all our open jobs on our HERO Recruitment website - www.hero.ie. Please Note: HERO Recruitment will not forward your details to any company without your prior approval. This job originally appeared on RecruitIreland.com. [-]
Ref: 96979. Service Technician. County Westmeath. €29000 - €32000. Our Client is currently expanding its service & maintenance business and is seeking to recruit a Service Technician to join their expanding team. Servicing systems throughout Ireland, UK and Europe the role will involve extensive travel. Duties will include: Maintenance and inspection of pump units and sprinkler systems. [+]
Ref: 96979. Service Technician. County Westmeath. €29000 - €32000. Our Client is currently expanding its service & maintenance business and is seeking to recruit a Service Technician to join their expanding team. Servicing systems throughout Ireland, UK and Europe the role will involve extensive travel. Duties will include: Maintenance and inspection of pump units and sprinkler systems. Fault finding and installation of pumps, engines and motors. Stripping of pumps and alarms. Fault finding and installation of control panels. Managing own reporting on IPAD and detailing work orders/repairs. Experience Required: At least 5 years previous experience in a similar role. Background experience in diesel engines, mechanical or electrical is essential. Full clean driving licence is essential. Extensive travel throughout Ireland, UK and Europe. Good IT skills. Proven experience completing reports. Strong attention to detail. Excellent communication skills. A fantastic opportunity to join a well established organisation, immediate interviews, do not delay, contact Gary Browne on 045-448800 or email your CV in confidence to gary@hrconsultants.ie. This job originally appeared on RecruitIreland.com. [-]
Overall Purpose: The Process Engineer provides technical support and expertise in the build-out, equipment procurement, commissioning, validation, and tech-transfer activities associated with the start-up of the new Aerie Ireland manufacturing facility. For the on-going commercial operation of the facility, the Process Engineer will provide key technical support in the areas of process control, manufacturing process troubleshooting, process optimization, process development, and product transfer. [+]
Overall Purpose: The Process Engineer provides technical support and expertise in the build-out, equipment procurement, commissioning, validation, and tech-transfer activities associated with the start-up of the new Aerie Ireland manufacturing facility. For the on-going commercial operation of the facility, the Process Engineer will provide key technical support in the areas of process control, manufacturing process troubleshooting, process optimization, process development, and product transfer. The Process Engineer will report to the Technical Services Manager. Essential Duties, Functions and Responsibilities: Works with manufacturing and quality colleagues as part of an Operations team whose shared goal is to realise the safety, quality, delivery and cost objectives of the site. Prioritises safety and is diligent in the use of all appropriate safety tools and permits when maintaining equipment – champions safe working always. Will program manage and technically lead receiving site activities necessary for the successful transfer of new products onto the Athlone site via a structured and compliant NPI (new product introduction) process. Will prepare site process descriptions by developing a PCS (process control strategy) for the processes and in identifying and agreed with Quality the process CPPs (Critical Process Attributes) and CQA (Critical Quality Attributes) for products. Provides technical support for product PPRs (Periodic Product Review. Is the process SME for the compounding and filling process and supports manufacturing and maintenance in the operation and maintenance of these systems. Supports manufacturing by leading/supporting deviation investigations, and is familiar with structured problem solving and root cause analysis. Supports validation activity in process manufacturing areas. Leads continuous improvement projects and initiatives and is owner of yield performance and cycle time improvement. Provides training and mentoring to build technical capabilities among teams. Supports capital projects throughout equipment lifecycle. Skills/Knowledge Required: Strong technical knowledge of aseptic manufacturing techniques, procedures and theory. Knowledge of best practices in pharmaceutical product development, scale-up and technology transfer. Specific knowledge of sterile pharmaceutical manufacturing processes and technologies. Strong analytical skills, documentation skills and research skills. Very strong problem-solving skills, ideally using formal tools e.g. FMEA. Strong understanding of pharmaceutical industry regulatory requirements. Clear understanding of the needs of cGMP and validation (DQ-PQ. DoE knowledge desirable. Knowledge of sterilization principles and practices. Strong communication and interpersonal skills. Highly motivated with ability to work effectively with multidisciplinary teams or independently. Strong team player. Good proactive approach & manner. Education Required : Bachelors Degree in Mechanical Engineering, Pharmaceutical Sciences, or related Science discipline. Further qualification (Masters) in related discipline ideal. Experience Required: At least 8 years relevant experience in a pharmaceutical manufacturing environment, with at least 5 years experience in a comparable process engineering/technical services role. Must have experience working in a sterile manufacturing environment. Ophthalmic manufacturing experience a plus. Experience with many of the following processes: Product introduction and transfer. Cycle time and yield improvement initiatives. Continuous improvement projects. Equipment engineering runs, cycle development, PQ, Eng Runs, Media Fills and PV. Regulatory audit preparation and follow-up. Equipment and component specification. Component preparation – autoclaves, etc. Vial or bottle filling of sterile solutions. Cleaning (CIP/SIP) and sterilisation technologies. Isolator technology incl. VHP. Compounding – dispensing, formulation, sterile filtration, etc. Primary container closure components. For more infromation or to apply please contact peter.godwin@cpl.ie or call 01 947 6227. This job originally appeared on RecruitIreland.com. [-]
Matrix Recruitment is currently recruiting a Senior Facilities Engineer for our pharmaceutical client based in Co. Offaly. What you need to know. You will work as an Senior Facilities Engineer and will work for our pharmaceutical client based in Co. Offaly . This is a permanent opportunity with excellent opportunities for career progression. You will work in the Engineering Department and have responsibility for all maintenance and calibration systems. [+]
Matrix Recruitment is currently recruiting a Senior Facilities Engineer for our pharmaceutical client based in Co. Offaly. What you need to know. You will work as an Senior Facilities Engineer and will work for our pharmaceutical client based in Co. Offaly . This is a permanent opportunity with excellent opportunities for career progression. You will work in the Engineering Department and have responsibility for all maintenance and calibration systems. You will ensure the proper maintenance and calibration of all process equipment and utilities. Salary and package is negotiable for the right candidate and dependent on experience. Your new job. Key duties & responsibilities: Management of the PEMAC Maintenance and Calibration system to ensure all manufacturing equipment and utilities are fully maintained. Ensure all equipment on site is captured, and proper maintenance and calibration procedures are in place. Ensure all records are kept accurately and accessible for audits. Work with engineering technicians for the day to day operations and maintenance of all utilities and systems to support manufacturing. Management of temperature mapping and validation of various plant items including fridges, autoclaves and incubators. Communicate with QA and validations to ensure scheduled validation and calibration work on equipment and utilities is carried out correctly. Management of environment systems on site and ensure all environmental requirements are achieved. General maintenance duties as required. Take part in Quality and Safety regulatory audits as needed. What are we looking for? Desirable: Degree/Diploma/Apprenticeship in relevant engineering discipline or equivalent. 3-5 years’ experience in high volume pharmaceutical/healthcare industry. Experience in calibration and validation of utilities and equipment including freezers, incubators and autoclaves. Excellent project management skills. Ability to plan and manage tasks and ensure deadlines are achieved. Ensure clear records are maintained. Excellent communication and organizational skills. Apply for this job now or get in touch with Niall on 09064-90485. Matrix Recruitment Group is committed to providing a professional service where all CV`s are kept confidential and will not be submitted to any clients without candidate’s knowledge or consent. This job originally appeared on RecruitIreland.com. [-]
Lead Process Engineer - Process Development - Westmeath. Our pharmaceutical client is looking for the ideal candidate to provide technical expertise and leadership for new and existing technology based product development programmes. This will be a maternity cover role (12 months. Responsibilities: Manage experimental programmes for use in process development activities, involving investigational studies to provide indicative process/analytical data for identification of critical process parameter effects. [+]
Lead Process Engineer - Process Development - Westmeath. Our pharmaceutical client is looking for the ideal candidate to provide technical expertise and leadership for new and existing technology based product development programmes. This will be a maternity cover role (12 months. Responsibilities: Manage experimental programmes for use in process development activities, involving investigational studies to provide indicative process/analytical data for identification of critical process parameter effects. Analyse the process and analytical data generated by these programs and report on same. Design and lead process development activities focused on study of critical parameters to ensure that process conditions, at all scales, are consistent and not at “edge of failure”. Select appropriate parameters for prototype/finished dosage production to ensure product quality and reproducibility are achieved and a robust control strategy is developed. Develop, execute and refine the methodology required for the generation of successful scale-up/optimisation process models. These models are required to accurately establish process operating windows at relevant scale and identify appropriate in-process operating ranges to maintain both product quality and production efficiency. Execute all aspects of team management as a leader of projects, from development through launch, associated with new formulation product or technology development programmes. Interact with cross functional and cross site technical and CMC teams influencing and communicating on development projects. Assess industry process advancements and introduce them to site as appropriate. Act as site expert in resolution of technical issues by means of formulation, process or machine modifications. Manage and lead relative areas of responsibility through FDA pre-approval and post-approval inspections by serving as technical expert for development and processing operations. Prepare Development Reports and CMC sections of DMFs or NDAs related to formulation development, process scale-up, process control and comparisons of development and commercial processes. Requirements: Third Level Degree in a Science or Engineering Discipline. 5-8 years relevant experience, preferably within the pharma' industry. Strong technical and project management skills . Demonstrated track record in generating technical options to resolve problems , prioritising solutions, selecting optimal solutions and implementing decisions in the pharmaceutical industry. Strong experience in statistical analysis , sample sizing, Anova, DOE, regression analysis. This job originally appeared on RecruitIreland.com. [-]
What you need to know. Matrix Recruitment is working with a world leader in developing and marketing high quality surgical equipment, in the recruitment of an Inventory Controller/Planner . This is a 3 -4 monthcontract job and based in Co. Offaly . Inventory Controller/Planner will be responsible for analysing/monitoring inventory, across many of the company’s divisions. This role will work alongside the Supply Chain team and report into Inventory Manager. [+]
What you need to know. Matrix Recruitment is working with a world leader in developing and marketing high quality surgical equipment, in the recruitment of an Inventory Controller/Planner . This is a 3 -4 monthcontract job and based in Co. Offaly . Inventory Controller/Planner will be responsible for analysing/monitoring inventory, across many of the company’s divisions. This role will work alongside the Supply Chain team and report into Inventory Manager. Salary: €30k -€33k. Your new job. Key duties & responsibilities. Responsible for monitoring inventory for sales. Ensuring administration of Company policies and procedures for field inventory management. Responsible for analysing inventory utilization, publishing field inventory metrics, assisting with inventory field audits, and performing reconciliations. Initiate cycle counts and research, resolve/report any inventory discrepancies. Continuous improvement projects. Carry out cross functional transactions on ERP system. Work with Materials team on materials procurement. Making sure documentation is correct on incoming and out going products. What are we looking for? Desirable: APICS qualified would be a distinct advantage. 2+ years’ experience working in inventory management or supply chain functions within a Materials Department. Excellent Microsoft office skills with ERP systems experience a must. Good time management, communication and organizational skills. Apply for this job now or get in touch with Breda on 09064-90485. Matrix Recruitment Group is committed to providing a professional service where all CV`s are kept confidential and will not be submitted to any clients without candidate’s knowledge or consent. This job originally appeared on RecruitIreland.com. [-]
