Technical Expert eLIMS CoE QC Operations

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.comAs guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: QualityJob Sub Function: Quality SystemsJob Category:ProfessionalAll Job Posting Locations:Horsham, Pennsylvania, United States of America, Malvern, Pennsylvania, United States of America, Raritan, New Jersey, United States of AmericaJob Description:Johnson & Johnson Innovative Medicine is recruiting for an Analyst – Technical Expert within the eLIMS Center of Excellence. This position can be based at any of our Innovative Medicine operating companies in Europe and North America.Principle responsibilities:In this role, you will play a key part in driving and shaping digital laboratory processes across global QC Operations. As a technical expert in eLIMS, you will ensure high-quality data eLIMS configurations that enable efficient, compliant, and paperless laboratory workflows, including product release and Certificate of Analysis generation. You will work independently to design, maintain, and continuously improve data setups while ensuring alignment with current business processes and regulatory requirements.You will act as a bridge between business and IT, translating laboratory needs into robust system solutions. Your responsibilities will include integrating laboratory instruments and applications into the eLIMS system, reviewing and testing system updates, and creating and maintaining system documentation and standards. You will proactively find opportunities for process improvements and contribute to global harmonization and standardization efforts.A strong sense of ownership is essential in this role, as you will be responsible for delivering incoming requests in a timely and high-quality manner. You will develop a deep understanding of site-specific laboratory processes and master data requirements to ensure accurate and complete system configurations. In addition, you will lead or contribute to projects within QC Operations, such as continuous improvement initiatives related to the iLAB’s Base Business process.Beyond your technical responsibilities, you will support the growth of the team by mentoring, coaching, and training colleagues, sharing your expertise and fostering collaboration across regions. You will maintain close relationships with local laboratories and interested parties while ensuring clear and effective communication with the eLIMS CoE leadership.Qualifications:You hold a bachelor’s degree or equivalent education and bring 4 to 6 years of experience in a regulated industry such as pharmaceuticals, medical devices, or diagnostics. You have strong experience with LIMS/eLIMS systems and quality environments, and any exposure to analytical testing, quality control, or IT is an advantage. You demonstrate a solid understanding of cGMP principles, FDA regulations, ICH guidelines (Q8, Q9, Q10), and risk management.You are organized, able to manage multiple priorities, and comfortable working in a dynamic environment where flexibility is required. Strong communication skills in English (minimum level B2) and the ability to effectively train and engage partners are essential. You demonstrate a strong customer focus, build trustful relationships across global teams, and are committed to delivering high-quality results.You demonstrate an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices. You are comfortable using AI tools to enhance efficiency and productivity, including the ability to craft effective prompts to support day-to-day work.This is a highly visible role within a global Center of Excellence, offering the opportunity to contribute to the future of digital QC laboratories, drive innovation, and make a meaningful impact across Johnson & Johnson’s global network. Travel requirements are minimal, up to 5%.Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):Switzerland - Requisition Number: R-075742Ireland and Netherlands - Requisition Number: R-076441US - Requisition Number: R-076443 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.Required Skills:Preferred Skills:Analytical Reasoning, Business Alignment, Business Behavior, Coaching, Collaborating, Communication, Compliance Management, Data Compilation, Data Quality, Data Savvy, Document Management, Problem Solving, Quality Auditing, Quality Control (QC), Quality Management Systems (QMS), Quality Services, Quality Standards, Systems Analysis, Training PeopleThe anticipated base pay range for this position is :79 000,00Additional Description for Pay Transparency:127 650,00SummaryLocation: Raritan, New Jersey, United States of America; Horsham, Pennsylvania, United States of America; Malvern, Pennsylvania, United States of AmericaType: Full time