AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com . Follow @abbvie onLinkedIn, Facebook ,Instagram ,X andYouTube. Job Description Responsibilities : Perform cleanroom cleaning of the Biologics manufacturing areas which includes Core 1, Core 2, Core 3, Core 4, PFS and sterility suites. This includes performing post batch, routine and triple cleans in accordance with the relevant procedures. Ensuring the relevant areas are stocked with cleaning disinfectants/gloves/gowns/goggles and removal of waste from the area. Complete autoclave cycles and filter testing in compliance with procedures. Understand and follow gowning procedures and protocols assigned to assure consistent, reliable, and timely performance of contamination control responsibility within the team and to ensure minimal contamination of the clean room through inadequate gowning. Accurately complete documentation and logbooks on time, accurately and legibly. Report equipment issues to relevant departments Attend all the relevant training sessions and ensure training is completed in a timely manner. Complete eLMS training in a timely manner within due dates Ensure compliance with all EHS, Quality and housekeeping standards notifying management of any discrepancies. Participate in GEMBA’s and Process Confirmations to identify further improvement opportunities within the department Adhere to all policies and procedures in support of achieving site metrics. Qualifications Experience in Pharma/Medical Devices/Food Operations Strong communication and documentation skills High attention to detail and methodical in approach Ability to be a strong team player and work with cross-functional teams Outstanding organization, flexibility, and time management skills Ability to multitask and adapt in a fast-paced environment Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: #J-18808-Ljbffr
A global biopharmaceutical company in Westport, Ireland is seeking a dedicated professional for cleaning and maintaining Biologics manufacturing areas. Candidates should have experience in pharma or medical device environments, with strong attention to detail and ability to work collaboratively within a team. Responsibilities include performing cleaning tasks, ensuring compliance with health and safety standards, and maintaining thorough documentation. The role requires excellent communication skills and the capability to adapt to a fast-paced environment. #J-18808-Ljbffr
Job Description We are looking for a Warehouse Manager to join our supply chain team at our manufacturing site in North Dublin . In this role, you will report to the Supply Chain Director. This is a great opportunity to grow your career in supply chain / logistics. Lead materials planning, inventory control, and supply continuity across assigned operations. Ensure timely availability of materials to support production, service levels, and operational schedules. Partner with supply chain, operations, procurement, and quality teams to resolve shortages, delays, and planning issues. Monitor inventory accuracy, cycle count performance, and materials data integrity. Drive process improvement, standard work, and compliance with company policies and procedures. Strong competencies in leadership, problem‑solving, communication, cross‑functional collaboration, and analytical thinking. Manage site logistics security programs (AEO & Known Consigner). Qualifications Bachelor’s degree preferred in Supply Chain, Business, Operations, Logistics, or a related field. Relevant professional certification preferred, such as APICS/ASCM CPIM, CSCP, or equivalent. Prior experience with vendor management, production scheduling, or logistics coordination. Proven ability to lead teams and manage supervisors or frontline operations. Additional training in lean manufacturing, inventory management, or process improvement is beneficial. Experience in materials management, supply chain, inventory control, or manufacturing support. Strong working knowledge of ERP/MRP systems, planning tools, and Excel/reporting tools. Demonstrated ability to analyze data, identify risks, and make timely decisions. Experience in regulated environments, multi‑shift operations, or high‑volume pharmaceutical manufacturing environment. Continuous improvement experience such as Lean, Kaizen, or Six Sigma is desirable. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html #J-18808-Ljbffr
A leading pharmaceutical company in North Dublin is seeking a Warehouse Manager to join their supply chain team. The ideal candidate will lead materials planning, ensure timely availability of resources, and partner with various teams to resolve operational issues. Candidates should have a relevant degree, certifications in supply chain management, and substantial experience in logistics coordination. This role provides an excellent opportunity for career growth in a dynamic environment focused on innovation and integrity. #J-18808-Ljbffr
A global biopharmaceutical company in Sligo is seeking a Device Technician for evening shifts. You will be responsible for preparing and operating various production equipment, ensuring compliance with quality and safety standards. The ideal candidate will have at least one year of experience in a regulated manufacturing environment, capable of troubleshooting production issues and maintaining documentation as per GMP requirements. This role demands attention to detail and teamwork to meet production quality targets. #J-18808-Ljbffr
A leading pharmaceutical company in Westport is seeking a Packaging Operator for a 12-hour rotating shift role. The successful candidate will maintain a clean work area, execute packaging tasks, and troubleshoot equipment issues. Qualifications include a Leaving cert or equivalent, with mechanical experience being advantageous. Safety compliance and attention to detail are critical for this position. #J-18808-Ljbffr
Maintenance Excellence Planner – Westport Site As a Maintenance Excellence Planner at our Westport Site , you will play a key role in supporting the Maintenance Excellence Program (MEP) by planning engineering and maintenance activities using the company's computerised maintenance management system (CMMS). You will be a key facilitator and organiser within the AbbVie Westport team. Responsibilities Lead Maintenance Planning activity for a business unit and support 10 to 20 Technicians. Track, analyse and continuously improve Maintenance Excellence Program key performance indicators such as Schedule adherence, on time maintenance, reactive maintenance, backlog and efficiency. Run weekly meetings with Engineering, Planning and Production to agree schedule and maintain a 4 week lookahead. Set and optimise the maintenance schedule. Decide who will complete each work order and when it will be done. Demonstrate flexibility by adjusting the plan to suit business need. Communicate early and often with Operations, Engineering, Maintenance, Planning and MEP teams to maintain positive working relationships and drive high standards. Support shutdown planning. Train team on Maximo and Cognos as needed. Set up / update Assets and Preventive Maintenance routines on Maximo. Ensure adherence to company safety standards, policies and procedures. Qualifications A third level qualification in Engineering or a relevant discipline with 2+ years of experience or a trade qualification with 6+ years of experience. Proficient in the use of a Computerised Maintenance Management system such as Maximo is desirable. Strong interpersonal skills and a proven ability influence and unify stakeholders at multiple levels is an advantage. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. #J-18808-Ljbffr
Job Description We are now hiring a Device Technician to join our team in Abbvie Ballytivnan, Sligo . Here, you will work as a team member in production/operations areas in line with all safety, regulatory and organizational requirements, preparing equipment, work areas and materials and ensuring/verifying readiness of manufacturing operations. This is an evening shift position. A snapshot of your key responsibilities: Preparation and operation of moulding and ancillary equipment. · Preparation and operation of automated assembly and ancillary equipment. Preparation and operation of Pad Printing and ancillary equipment. Preparation and operation of manual assembly and ancillary equipment. Troubleshooting day to day manufacturing issues which may impact on efficiencies, safety or quality. Completion of quality checks and achieving production quality targets. Supplying materials to the operations and equipment in a timely and safe manner. Responsible for labelling and packing of components and finished products. Operating of Coordinate measuring equipment, and other advanced metrology equipment. Operate fully automated and complex computer-controlled systems, including robotic and vision system technology. Participate in divisional project team for New Product Introduction and Improvement Projects. Resetting equipment as necessary to ensure the manufacture of quality components. Team coordination to maximize the effectiveness of all the team members. Documentation of all activities in line with GMP requirements. Cross training within the team and training of new members. Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems. Execution of routine manufacturing documentation, commissioning and validation protocols on an ongoing basis. Ensuring compliance with the Quality, Regulatory, GMP requirements and adherence to all AbbVie policies and relevant legislation. Execute manual assembly and visual inspection as required. Qualifications What you will need: A minimum 1-year experience in a similar role in a regulated manufacturing environment AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. #J-18808-Ljbffr
A leading biopharmaceutical company in Westport, Ireland, is seeking candidates for a role focused on packaging tasks and maintaining safety and quality standards. You will be responsible for organizing the work area, following all SOPs and cGMP practices, troubleshooting equipment issues, and operating computerized production machinery. A Leaving Certificate or equivalent is required. Join a collaborative environment committed to innovation and community service. #J-18808-Ljbffr
About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description What you do, is what we need. Making a difference begins here. And takes all of us. Welcome to AbbVie! We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work. Purpose : The purpose of this role is to provide a Manufacturing Engineering service to the plant, in order to maximise the availability of our Manufacturing Equipment. You will also ensure the performance of day to day preventative, predictive and demand maintenance activity to maintain manufacturing and utilities equipment. This role is based on our Ballytivnan site. Flexibility to work shifts that include Days & Evenings is essential for this role. Responsibilities To liaise with Production to ensure equipment performance is maximized. Establish with the engineering team leader the department goals, schedules and timetables for activities. To maintain records and documentation on relevant Engineering Procedures and preventative & demand maintenance. To liaise with Internal/External Engineering personnel and contract maintenance providers in maintaining, troubleshooting and installing/commissioning equipment. To facilitate the implementation of equipment projects/ process improvements. Establish with the engineering team leader the department goals, schedules and timetables for activities. Contribute to successful external, Division and Corporate audits. Identification and implementation of manufacturing equipment related cost improvement plans and continuous improvement plans. Cross train within manufacturing engineering. Ensure safety standards are met and safe working practices adhered to. Support the Production Team in ensuring that manufacturing equipment is maintained to meet the output and yield requirements. Adhering to all relevant policies relating to Quality and regulatory. Supervision of external contractors carrying out work onsite. Required to undertake specific investigations, and equipment monitoring, with the view to improve manufacturing performance e.g. reducing plant, maximizing output and yield. Optimisation of elements of manufacturing machinery to adapt to process conditions in order to improve efficiency. Considerable and continual care and attention needed to avoid substantial damage to equipment. Adherence to the MEP (Maintenance Excellence Programme) is required to ensure increased reliability and decreased downtime for the plant. Business Skills. Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times. Requires proven problem-solving skills and the ability to adapt to new regulatory requirements. Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders. Strong communication skills both verbal and written are required for the execution of this role. Strong interpersonal skills are required. Demonstrates an ethos of Right First Time at all times. Each Engineering Technician is responsible for their own work and the execution of their tasks on a daily basis. Candidates must be flexible and support the business through working a 16/5 shift roster and on call rota as required. Qualifications 3rd level qualification in an Engineering discipline Trade qualified will also be considered 3-5 years experience in a regulated environment (GMP preferable) Strong IT knowledge is required. Strong troubleshooting and documentation skills Working knowledge of ATEX regulations and requirements Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html #J-18808-Ljbffr
