Job Description

What if the work you did every day could impact the lives of people you know? Or all of humanity?At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.Position Summary:This position requires an individual who must work with minimal supervision to manage the system development life cycle for the Illuminas Laboratory Information Management System (LIMS). This person will join a dynamic, fast paced organization supporting new product development teams, as well as sustaining operations. This person is responsible for compiling relevant information related to product and process definition, analyzing business and compliance requirements, assessing risks for impact, and procuring accurate information for use in global systems. In addition to product configuration, development, and change activities, tasks include support and iteration of LabVantage LIMS, management of Engineering Change Requests and Change Orders (ECRs/ECOs), workflow process development, and identification and participation in product and process improvements initiatives.Responsibilities:Own, Support, and iterate system development life cycle for LIMS to develop and optimize manufacturing process flowsDrive improved utilization of LabVantage for laboratory areas with respect to both configuration and core functionality, and act as voice of the customer for manufacturingOversee development of drivers for Scientific Data Management System (SDMS) for instrument connectivity and seamless data integrationUnderstanding of master data and the roles played by PLM, ERP, MES, LIMS, etc. in support of manufacturing and product releaseReview and monitor implementation activities to ensure the change has been completed properlyResponsible for the accuracy of system data through process evaluation and validationDevelop and maintain product and process configurations and collaborate on the implementation of solutions in LIMS, PLM and ERP. Candidate must have a solid understanding of LIMS/PLM/ERP and changes to downstream cross functional areas and systemsAble to work independently and requires minimal guidance to perform required tasksWork with peers and/or subordinates to ensure timely completion of projects and tasksTake initiative to develop and implement new processes to strengthen data accuracy or enhance efficiencyDemonstrate effective communication style working with all levels of organizational structure, through multiple departments, and across global sitesAll listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.Requirements:Experience with software programming languages, Java, Groovy preferred (5+ Years)Hands-on experience with 3rd Party interfaces that are commonly interfaced with LIMS applications like ERP, PLM, MES, SDMS, Instruments, etc.Technical background in manufacturing, preferably in a life sciences, diagnostic, and/or medical device environmentDirect hands-on experience managing configuration change management in LIMS, LabVantage LIMS preferred.Proven ability to convert process flows into automated workflow modelsExperience in configuration management, operations, and/or quality within a regulated industrySolid understanding of computer system and system validationsExperience with Software Development Life Cycle of quality systemsExperience with process and material change and configuration activities within an Enterprise Resource Planning (ERP) system, SAP preferredProduct Lifecycle Management (PLM) experienceWorking knowledge of ISO 13485 and cGMP requirements desiredHigh degree of initiative and ownership, as well as a proven history of delivering results while working with several different departments in a fast-paced environmentBe able to work in AMR time zones on a consistent basisAll listed requirements are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.

Illumina