Pharmaceutical Operations Shift Supervisor

Join AbbVie as a dedicated and experienced Operations Shift Supervisor in our pharmaceutical manufacturing team. In this pivotal leadership role, you will ensure the safe and compliant production of drug product materials, upholding all regulatory, safety, and organizational standards.As a leader, you will guide a team of skilled pharmaceutical technicians, …

About the Role AbbVie is hiring Pharmaceutical Technicians for 6-month contracts in Sligo. These positions offer a chance to start a career in the pharmaceutical sector and gain hands-on experience on the production floor. What to Expect Pharmaceutical Technicians work as part of a team focused on producing high-quality medicines. The work supports patient health and contributes to ongoing improvements in healthcare. This is an entry-level opportunity with room to learn and develop new skills.

Purpose:The Technical Shift Leader for API is responsible for ensuring the production of API material aligns with organizational requirements and complies with all relevant regulations. This role involves leading the API Small Scale (SSC) manufacturing team in a pharmaceutical processing facility, ensuring adherence to safety, regulatory, and operational standards. Key Responsibilities:Oversee and implement pharmaceutical processing activities within the API SSC and associated locations to achieve operational goals.Provide leadership, motivation, and guidance to the manufacturing team, clearly communicating tasks and objectives to optimize performance.Ensure timely and accurate verification and updates of manufacturing control system transactions.Serve as the primary technical contact for the API SSC Business Unit, with shift technicians reporting directly to you.Communicate departmental objectives to ensure cost-effective product delivery within the AbbVie Class A supply chain framework.Collaborate with Supply Chain and Program Management to facilitate efficient planning, scheduling, and execution of commercial and NPI clinical manufacturing.Resolve operational and project-related issues by engaging with team members and project stakeholders.Drive operational excellence and meet key performance targets, including Overall Equipment Effectiveness (OEE) where applicable.Maintain compliance with all safety, environmental, and quality-related SOPs.Champion safety improvements and initiatives throughout the operations.Review, amend, and implement changes to SOPs while managing Corrective and Preventive Actions (CAPAs).Foster a culture of excellence and 'Right First Time' within the team.Coordinate with relevant departments and customers during the introduction and execution of NPI projects.Adhere to and promote all EHS & E standards, policies, and procedures.Work closely with other Technical Shift Leaders to ensure safe planning and execution of interdepartmental activities.Develop team members through appropriate training and performance evaluations.Assist HR in managing employee relations issues.Engage with internal and external customers regularly to address inquiries and clarify processes.

Join AbbVie as an Operations Leader in our OSD Manufacturing team, where you will play a pivotal role in driving operational excellence and efficiency. You will oversee production processes, ensuring adherence to regulatory requirements and quality standards. Your leadership will inspire a culture of continuous improvement, fostering collaboration and innovation within the team.

AbbVie Inc. is hiring a Drug Products Operations Specialist in Sligo. This full-time position focuses on supporting the production and quality assurance of pharmaceutical products. Role overview The Drug Products Operations Specialist helps keep manufacturing processes on track and ensures that finished products meet strict quality standards. Daily work involves collaborating with colleagues from different departments to uphold compliance and maintain efficient operations. What you will do Participate in the production of pharmaceutical products Support quality assurance activities to ensure products meet required standards Work with cross-functional teams to maintain compliance and resolve operational issues Requirements This role requires experience or interest in pharmaceutical manufacturing and quality assurance. Strong teamwork and attention to detail are important for success in this position.

Join AbbVie as an Aseptic Operations Engineer and play a pivotal role in ensuring the highest standards of aseptic processes in our state-of-the-art facilities. You will be responsible for overseeing aseptic manufacturing operations, implementing best practices, and ensuring compliance with industry regulations. This is an exciting opportunity to contribute to patient care through your expertise in aseptic techniques and operations.

Join AbbVie as a Technical Shift Lead, where you'll play a crucial role in ensuring the effective operation and management of our technical processes. In this dynamic position, you will lead a team of professionals, oversee daily technical activities, and ensure compliance with industry standards. You will be instrumental in driving innovation and continuous improvement, making a significant impact on our operational efficiency.

Purpose:The Aseptic Manufacturing Technical Lead will report directly to the Director of Aseptic Manufacturing. This pivotal role serves as a technical Subject Matter Expert (SME) for aseptic processes within the Global Network Aseptic Manufacturing team. The Technical Lead is tasked with providing essential troubleshooting support during significant aseptic events within the network, conducting hands-on assessments and investigations. The position is instrumental in driving standardization efforts by implementing and continuously updating best practices for aseptic procedures based on real-world events and technological advancements. Collaboration with various sites will be key to organizing and executing improvement initiatives aimed at proactively identifying, quantifying, prioritizing, and mitigating aseptic risks.The role involves close partnership with sites, the global aseptic team, and aseptic training programs to develop and deliver effective aseptic training and mentorship for operations leadership, ensuring adherence to good aseptic processing principles.Responsibilities:Provide on-site support for investigations related to significant aseptic events, including hands-on assessment and investigation aid.Proactively mentor and advise network team members, site peers, and senior management, sharing best practices.Contribute to the long-range strategy and planning for Aseptic Manufacturing, as well as the generation of capital plans.Organize and execute improvement events at manufacturing sites to proactively identify, quantify, prioritize, and mitigate aseptic risks.Drive standardization by implementing and continuously updating best practices based on operational events and technological advancements.Engage in aseptic audits, comparing procedures against actual practices on the floor, identifying risks, and facilitating solutions.Track and report site/network aseptic metrics to enhance aseptic performance to best-in-class standards.

Join Us in Making a Difference!Welcome to AbbVie!As a global, research-driven biopharmaceutical leader, we combine the innovation of cutting-edge biotech with the expertise of an established pharmaceutical giant. Our mission is to redefine possibilities in healthcare and enhance the lives of patients worldwide. We take pride in our commitment to fostering a great workplace culture.As a Quality Engineer at AbbVie Ballytivnan, you will play a vital role in documenting and establishing a quality system that ensures compliance with all regulatory and internal AbbVie standards. Your expertise will be key in assessing and reporting the quality system's performance to senior management. Collaborating closely with Quality Management teams and other stakeholders, you will drive advancements in quality, compliance, and operational efficiency.In this role, you will be responsible for achieving company objectives, fulfilling customer needs, and adhering to regulatory requirements set forth by the FDA, EU, and local health authorities.Key Responsibilities:Maintain strong relationships with the Quality Systems Manager and quality personnel across Business Units.Coordinate the quality system to ensure compliance with its requirements.Evaluate quality system performance and present findings at management reviews and quality performance meetings.Serve as the primary contact for various Quality System and Compliance activities, including training, documentation, metrics generation, and internal audit support.Support inspection readiness through preparation, logistics, and management of corrective actions.Uphold all Environmental, Health, and Safety (EHS) standards and policies.

The Process Engineer at AbbVie’s Sligo facility plays a key role in shaping and improving manufacturing processes. The position centers on developing and refining production methods to ensure they meet strict quality standards. Main responsibilities Develop and optimize manufacturing processes to support consistent product quality Maintain existing processes, identifying areas for improvement and troubleshooting as needed Contribute to AbbVie’s commitment to delivering advanced therapies to patients worldwide Location This role is based on site in Sligo. What this role supports Work in this position directly impacts AbbVie’s mission to provide high-quality therapies to patients around the globe.

Join AbbVie Ballytivnan, a leading Centre of Excellence dedicated to Precision High Volume Moulding and Auto-Assembly, as we continue to innovate within our state-of-the-art Biologics aseptic fill finish facility. We are currently seeking a Technical Manager to spearhead technical support and program management for new product introductions (NPIs) across three departments: ADC conjugation, BT1, and ADCBT2. This position is based in Sligo and reports directly to the Technical Operations Manager. The ideal candidate will provide strong leadership to the NPI product team, process team, and ADC team, playing a pivotal role during an exciting phase of product innovation.Key ResponsibilitiesLead NPI activities for product, processes, and technology from initial development stages through to PPQ.Manage cross-functional teams with diverse skill sets to accomplish NPI objectives.Collaborate with teams across Process Development, Science & Technology (PDS&T), Quality, Manufacturing, Supply Chain, and ECM to ensure seamless product transitions from development to commercialization.Conduct site fit assessments for products in AbbVie’s pipeline and ECM opportunities.Provide technical oversight and coordinate NPI support across the biological manufacturing area.Coordinate with internal and external program management to keep NPI schedules aligned.Ensure resource availability for all NPI-related tasks.Foster a culture of innovation and continuous improvement within the team.Mentor operations personnel during NPI activities.Engage with external partners to ensure alignment and effective communication throughout NPI initiatives.Collaborate with partners to influence robust process control strategies and conduct process risk assessments.Prepare product transfer documentation to validate completion of deliverables prior to the product transfer stage gate review.Provide technical input and review/approve documentation for NPI activities.Ensure adherence to CGMP and EHS practices.Participate in NPI project gate reviews.Act as the subject matter expert for new products and technology transfers during audits by internal and external regulatory agencies.

Join our dynamic engineering team as an API Engineering Manager at our state-of-the-art facility located on Manorhamilton Road (MHR), Sligo. Reporting directly to the Operations Engineering Manager, you will lead a diverse team of engineers, technicians, and apprentices dedicated to our Active Pharmaceutical Ingredients (API) business unit. Your primary responsibilities will encompass team development, budget oversight, and collaboration with production to ensure alignment with policies governing Personnel, Quality, Engineering, Safety, and Finance.This multifaceted role requires you to foster cross-functional partnerships with contract maintenance providers, production teams, technical operations, quality assurance, and other stakeholders to optimize equipment performance. You will spearhead a variety of projects, ranging from continuous improvement initiatives to the introduction of new products, leveraging your extensive experience in an API manufacturing environment.Key ResponsibilitiesCollaborate with the Operations Engineering Manager to establish departmental goals, schedules, and activity timetables.Support and manage the development of manufacturing equipment.Ensure the API Engineering Team maintains manufacturing equipment to meet legal, divisional, and corporate standards.Develop and execute CAPA plans with defined timelines.Conduct specific investigations and monitor equipment to enhance manufacturing performance, with a focus on minimizing downtime and maximizing output and yield.Oversee equipment/process upgrades in a continuous improvement environment.Generate monthly engineering metrics and deliver timely management reports.Ensure budgets remain within targets and prepare capital expenditure requests as necessary.Facilitate successful external, divisional, and corporate audits.Maintain compliance with safety standards and promote safe working practices.Manage internal and external plant projects as required.Supervise and cultivate relationships with external contractors.Participate in relevant meetings and drive action items to completion.

Join AbbVie as a Quality Control Manager in our Sligo facility, where you will lead our quality assurance team to ensure compliance with industry standards. Your role will involve overseeing quality control processes, driving continuous improvement initiatives, and collaborating with cross-functional teams to achieve operational excellence.

Role Overview AbbVie Inc. is hiring a Senior New Product Introduction (NPI) Compliance Specialist in Sligo. This role focuses on ensuring new products meet all required compliance standards from early development through launch. What You Will Do Work closely with teams across departments to support the introduction of new therapies Guide compliance activities throughout each stage of the product lifecycle Help maintain high standards for regulatory and quality requirements as new products move toward market

Join AbbVie as a Senior Quality Control Analyst specializing in Microbiology. In this critical role, you will be responsible for overseeing the quality control processes within our microbiology lab. Your expertise will ensure that all microbiological testing meets stringent industry standards, thereby supporting our commitment to delivering top-tier pharmaceutical products.