A leading recruitment agency is seeking a QC Micro Specialist for a pharmaceutical client in Dublin. The role is crucial for ensuring compliance, qualification, and effective operations in the Drug Substance facility. The ideal candidate will have 5 years of experience in a Microbiology Lab and a Bachelor's Degree in a relevant science field. Key responsibilities include supporting QC activities, maintaining cGMP standards, and managing deviations and CAPAs. #J-18808-Ljbffr
Our Westmeath based client is seeking a Quality Validation Engineer to join their team. Reporting to the Quality Manager you will be an integral figure in implementing and maintaining the Quality systems to the ISO 14001 and ISO 13485 standards. Please note that this is a Permanent on-site position on a Monday to Friday Daytime basis. Duties and responsibilities Maintenance of QMS systems to medical device standards to ISO 14001 and ISO 13485 standards Internal auditing to ISO 13485 Participation in new product development, collaborate with production on quality issues on products Validation duties such as generating and executing validation protocols, reports (IQ/OQ/PQ) Validating of equipment and new products Act as a point of contact to customers What we need from you Minimum bachelor’s degree in an Engineering/science field 3 years’ experience in a ISO 13485 environment Internal auditor qualified to ISO 13485 Exposure to equipment validation and statistical analysis Strong communication ability to liaise with different departments, and customers Apply for this job now by sending in a Word version of your CV or get in touch with Eugene at eugene@matrixrecruitment.ie or alternatively by phone at 0874075822. By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are kept confidential and will not be submitted to any clients without your knowledge and consent. We Value Your Trust. #J-18808-Ljbffr
Matrix Recruitment is seeking a Health & Safety Manager for our client in the Waste & Recycling industry, based in Co. Kildare You will lead Health & Safety across multiple sites, ensuring full compliance while driving a strong safety culture throughout the organisation. Your New Role Key Responsibilities: Lead H&S compliance across operations, ensuring all activities meet Irish legislation. Drive safety performance by improving KPIs, auditing sites, and managing accident reporting & investigations. Deliver H&S training including inductions, toolbox talks, and mandatory programmes. Maintain H&S systems & documentation — SOPs, risk assessments, and contractor compliance — while engaging teams in safety improvements. What You Need 3+ years’ managerial H&S experience , ideally in waste, recycling, services, or manufacturing industries. Level 8 Degree in Health & Safety (desirable). Strong communication & reporting skills with proficiency in MS Office. Flexible to travel nationwide and work across different business units. Full eligibility to work in Ireland and strong English language skills Please send your CV in Word format to Patricia. Full detailed job spec available on request. By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and retain it as outlined in our privacy policy. All CVs are confidential and will not be submitted to any clients without your permission. Please note that due to the high volume of applications, we can only reply to suitable candidates. We Value Your Trust. #J-18808-Ljbffr
A successful manufacturing company in Co. Cavan is seeking a Quality Manager to oversee internal process audits and drive quality performance. This permanent role requires strong leadership skills and a solid background in quality management, along with a Bachelor's degree in Quality Management or Engineering. You will manage quality engineers and technicians, develop process improvement strategies, and contribute significantly to customer satisfaction and reducing quality failures. #J-18808-Ljbffr
A Westmeath-based client is seeking a Quality Validation Engineer to join their team. In this permanent on-site role, you will implement and maintain Quality systems to ISO 14001 and ISO 13485 standards. Responsibilities include internal auditing, collaboration on quality issues, and validation duties. The ideal candidate has a bachelor's degree in engineering or science and a minimum of 3 years’ experience in an ISO 13485 environment. #J-18808-Ljbffr
A recruitment agency is seeking a Health & Safety Manager for a client in the Waste & Recycling industry located in Ireland. The role involves leading H&S compliance, driving safety performance, and delivering training. Candidates should have over 3 years of managerial H&S experience and a Level 8 Degree in Health & Safety is desirable. Strong communication skills and full eligibility to work in Ireland are essential. #J-18808-Ljbffr
Matrix Recruitment are currently recruiting for a QC Micro Specialist on behalf of our client based in Dublin. Your New Role: A great opportunity has arisen for a QC Microbiology Specialist. The QC Microbiology Specialist role is a critically important role to ensure efficient and effective compliance, qualification, and operation of the company Drug Substance facility. Key Duties and Responsibilities: Perform and support QC analytical activities including in-process, release and stability related testing. Provide day to day direction and scheduling to the QC analyst team. Responsible for the qualification, maintenance, and/or integration of the QC methods, in compliance with up-to-date data integrity, regulatory, and industry standards. Responsible for driving a culture of Continuous Improvement. Ensure that cGMP standards are maintained at all times. Accountable for change control process and mechanisms required to maintain a state of continued compliance for the methods. Manage deviations, CAPAs and change controls. Author/review technical documents, standard operating procedures and actions for the performance of laboratory methods. Participate in risk assessments and implement and follow-up on corrective / preventative measures. Serve as an SME for regulatory and internal inspections and audits. Work cross-functionally to build and operate testing capability within the lab. Escalate potential cGMP or compliance issues effectively in a timely manner for proper resolution to ensure product quality. The desire to continuously learn, improve and develop. Follow up-to-date analytical practices with reference to pharmacopoeias, specifications, regulations, and industry standards. Writing and updating SOPs. Ensure training is current for all job functions performed. Maintain data integrity and ensure compliance with company SOPs, specifications, and cGMP regulations. What you need: 5 years industry experience with significant knowledge and experience working in a Microbiology Laboratory in a pharmaceutical company. Bachelor's Degree Qualification (Science, Microbiology preferred). Experienced in testing as per the pharmacopeia’s. Working knowledge of QC Digital Systems (eLogs, Electronic Lab Notebook, LIMS etc.). #J-18808-Ljbffr
What you need to know: You will work as a Quality Manager for our client, a highly successful and well-established manufacturing company in Co. Cavan . As a Quality Manager you will oversee internal process audits and analyses and drive quality performance data through communication, standard setting and problem solving. This role is a Permanent opportunity where the working hours operate 8:15 AM to 4:45 PM Monday to Friday. Occasional travel required to customer locations. Key Duties and Responsibilities: Manage and develop the Quality Process Engineers and Technicians. Develop C implement strategies to improve production processes working closely with Design, Production and Industrial Engineering teams. Maximise customer experience and company profitability through Right First Time Design and monitor new and existing quality gates for early detection of failures. Educate staff and provide high quality instructions for manufacturing processes. Eliminate quality failures through root cause analysis and corrective actions. What you Need? Bachelor’s Degree in Quality Management or Engineering. Lean or Six Sigma an advantage. 5-7 years of experience in a senior quality role in a manufacturing environment. Preferably 2-3 years in a people management role. In depth working knowledge of root cause analysis and problem solving tools. Proven record of delivering results through collaborative process improvements. Expertise in quality management systems, methodologies, and standards (e.g. Six Sigma, Lean ). Meticulous and thorough in inspecting products and reviewing processes and data. Ability to analyse data, identify root causes, and implement effective solutions. Accounting for and driving down the cost of poor quality. Apply for this job now or get in touch with Brenda on 087-4343544. #J-18808-Ljbffr
A global financial services company in Limerick is seeking a Senior Financial Reporting Accounting Consultant for a 6-month contract role. This position offers a hybrid working model and requires strong experience in investment management or audit industries. The ideal candidate will ensure compliance with accounting standards and mentor junior staff. Interested applicants should email their CV or Rena at the provided email. #J-18808-Ljbffr
What you need to know New job alert!!! My client in the manufacturing industry based in Co. Longford is looking to expand their team and hire a Maintenance Facilities Technician As the Maintenance / Facility Technician, you will play a key role in ensuring the smooth and efficient operation of equipment, machinery, and facility systems across the facility. THIS IS A 4 SHIFT-CYCLE PERMANENT JOB WITH COMPANY BENEFITS THE ROLE IS 12 HOUR SHIFTS DAYS/NIGHTS4 SHIFT CYCLE ROSTER Key duties & responsibilities: Carry out rebuilds on the machines and infrastructure. Involved in projects focusing on areas such as machinery efficiency and breakdown reduction. Troubleshoot/repair equipment and machinery on the facility of the company. Follow Preventative Maintenance schedule. Keep maintenance reports and make records for all the repair work conducted on the machinery. Carefully maintain inventory for the tools and place orders for new ones when they are required. What are we looking for? Bachelor's degree in mechanical engineering or a Leve6/trade qualification Experience carrying out maintenance in a manufacturing environment Knowledge of Maximo Asset Management system or equivalent would be an advantage. Apply for this job now - By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are kept confidential and will not be submitted to any clients without your knowledge and consent. Please note that due to the expected high volume of applications we can only reply to applicants suitable for the position. In the interest of protecting your data and informing you of your rights we will notify you should we retain your information by issuing an acknowledgement email and a request for consent where not already expressly given. We Value Your Trust. Skills: Maximo systems experience or related manufacturing maintenance experience Manufacturing, Maintenance, Technician. Benefits: pension contributions up to 4% Shared Value Plan after two years
