Senior Technical Analytical Specialist

Role Overview AbbVie Inc. is hiring a Senior Technical Analytical Specialist in Sligo. This position focuses on supporting key projects and strengthening analytical processes across the site. The role combines technical expertise with analytical problem-solving to help maintain high quality standards. What You Will Do Support critical projects by applying ad…

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 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.

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.

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.

AbbVie is seeking a Quality Assurance Compliance Specialist to support compliance activities within the Quality Assurance department at the Sligo site. This entry-level position focuses on maintaining high standards in product quality and upholding regulatory requirements. Role overview The Quality Assurance Compliance Specialist works alongside experienced team members to help ensure products meet internal and external quality standards. This position plays a part in supporting compliance initiatives and contributes to the company's commitment to healthcare quality. What you will do Assist with compliance processes and documentation within the Quality Assurance team Support efforts to maintain product quality and regulatory adherence Contribute to ongoing quality improvement initiatives Requirements Entry-level role; suitable for candidates starting a career in quality assurance or compliance Interest in product quality and regulatory standards Strong attention to detail and willingness to learn

Join AbbVie as a Senior Product Quality Assurance Manager, where you will lead a dedicated team to ensure the highest quality standards for our innovative products. In this critical role, you will oversee quality assurance processes, implement best practices, and collaborate with cross-functional teams to drive product 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 our dynamic Product Development Science and Technology (PDS&T) team at AbbVie as a Senior Engineer in Sligo. Reporting to the Associate Director, PDS&T – Combination Products, Aesthetics & Devices (CAD), you will play a pivotal role in supporting a variety of medical devices including catheters, autoinjectors, syringes, and pumps. This role calls for a leader with exceptional technical expertise and communication skills to drive innovative solutions across multiple sites. Your engineering acumen will be crucial in successfully completing complex projects aligned with the strategic objectives of Product Development Science and Technology.Key Responsibilities:Design and implement engineering solutions for product processes; facilitate the transition of products from late-stage development to manufacturing, assist with regulatory submissions, and lead significant line improvements.Oversee the PDS&T elements of projects with local significance, ensuring thorough planning and coordination.Serve as the technical lead for Design Verification activities within PDS&T for projects of global relevance, for both new and existing products.Investigate product functional issues, developing effective technical solutions.Enhance and transfer testing methods for combination devices and related components.Provide expert guidance to AbbVie and third-party manufacturing sites to resolve product functional issues, ensuring compliance with AbbVie’s standards.Independently design and conduct essential experiments that align with project objectives.Implement innovative experimental protocols and techniques.Maintain a deep understanding of project goals and demonstrate high proficiency across all initiatives.Develop and execute strategic plans to accommodate product modifications and updates.Adhere to corporate standards concerning conduct, safety protocols, material handling, GxP compliance, and animal care where applicable.Work effectively in a self-managed environment with minimal oversight.Perform other duties as assigned.Travel may be required up to 10% of the time.

Are you driven by a commitment to delivering exceptional service and technical expertise? Do you aspire to ensure that consumers enjoy a consistently high-quality product experience? If yes, this opportunity might be the perfect fit for you.Your main responsibility will be to maintain and service dispensing equipment for a prominent drinks client.At CPM, every member of our team plays a vital role in our business growth. Our people form the heart of CPM’s value proposition, and as an essential team member, you will be expected to make a significant impact on client delivery. This position demands initiative, a strong customer-centric approach, and a dedication to best practices and continuous improvement. A proactive, can-do attitude is essential.

Join AbbVie, a global biopharmaceutical company committed to discovering and delivering innovative medicines. We are currently seeking a dedicated Quality Assurance Specialist in Manufacturing Compliance to join our team in Sligo. In this role, you will ensure compliance with regulatory standards and support our commitment to quality and patient safety.

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.