For the given job description <<A Senior Software Engineer at O'Reilly Auto Parts develops and supports applications for internal and external systems including Inventory, Supply Chain, eCommerce, Retail Applications, Enterprise Search and more. Our teams are focused on the development, design and integration of various software systems, databases, and third-party packages utilizing tools and technologies including Java, JavaScript, Spring, Hibernate, and SQL. This particular position will be a full stack role working on Warehouse Management Applications; however, we will consider anyone with Supply Chain Application Development experience.
The base salary for this position is $116,000-$145,000 annually plus a 10% Annual Bonus. Exact compensation will be determined based on experience, however mid point around $126,000 - $131,000 would be more practical.
What You'll Do:Partner with key stakeholders to develop new features and enhance and support existing applications and programs.Work with business systems analysts and stakeholders to translate business to technical requirements and problem solve.Collaborate with project teams and cross functional teams to troubleshoot open issues and bug-fixes.Collaborate, coach and mentor team members on best practices, code reviews, internal tools, and process improvements.Write and maintain readable, sustainable, and efficient code in highly optimized and scalable architectures.Own applications from conception and design, to implementation and support.Debug and test code as needed.Create and update advanced technical documentation.
Skills and QualificationsRequired:High School diploma or equivalent.10+ years of software development experience.Strong knowledge of software engineering best practices of the full software development life cycle, including coding standards, code reviews, source control, testing, build and release engineering processes with focus on automation and end to end traceability.Experience in Java, Spring Boot, SQL Databases, and HibernateWorking understanding of databases including writing and amending queries in Oracle, SQL, PostgreSQL andor NoSQL.Experience working in DevOps including continuous integration and continuous deployment using open source technologies like GIT, Jenkins, JIRA and Confluence.Experience in effectively communicating with a broad base of end users and multiple management layers, including the ability to interact with vendors as needed.Ability to lead and mentor junior developer and effectively communicate with members of the team.Ability to work flexible schedule including nightsweekends.
Desired:Bachelor's degree in computer science or equivalent experience.Ability to articulate advanced technical concepts and teach others.Experience working with AgileScrum methodology.Experience in Microservice Architecture, Kubernetes, Containerization, MongoDB, SOLRExperience working in a remote, virtual or work-from-home environment.
Location: Remote, USA - This role can be remote, virtual or work-from-home anywhere in the United States.
 About UsO'Reilly Auto Parts IT department provides services to our corporate office, 6000+ stores, 28 distribution centers and 85,000 + team members.We have over 900 IT team members supporting 250+ small, medium and large web and software applications in addition to third party packages.We provide a collaborative environment and encourage knowledge sharingWe respect a healthy work-life balanceOur teams keep open communication through video conferencing, team messaging and daily stand-upsOur leadership values collaboration and encourages team members to bring creative problem-solving ideas from both a technical and functional perspectiveWe have several career paths, whether you want to be an individual contributor, manager, project manager, or stay technical - there's a documented growth plan to help you follow the path you chooseWe want to grow our people - we help to make you better by providing training for both technical and professional development>> the resume: <<Professional SummarySenior QA/Test Engineer with full system development lifecycle experience, including designing, developing, and implementing test plans, test cases, and test processes. Offer significant achievements driving cost savings, process efficiency, and fault-free audits. Skilled in Agile methodologies with strong leadership and strategic thinking skills. Proven ability to identify business needs and develop valuable solutions to improve accuracy and process efficiency. A strong team player with excellent communication and interpersonal skills.
Education and TrainingExpected inXXX3totoMaster of Science:Pharmaceutical Systems ManagementNEW JERSEY INSTITUTE OF TECHNOLOGY-Newark,New JerseyGPA:Pharmaceutical Systems ManagementExpected in2008totoBachelor of Science:BiologyRUTGERS UNIVERSITY & NEW JERSEY INSTITUTE OF TECHNOLOGY-Newark,New JerseyGPA:Biology
Skill HighlightsDesign engineeringAuditing proceduresQuality controlProcess improvementTest and Evaluation (T&E)Writing use casesExpert in data analysisMicrosoft OfficeShare PointAdvancedTeam Foundation ServerMicrosoft Test ManagerAnalytical problem solvingCross-functional teamwork
Professional Experience05/XXX6toPresentSr. Software QA EngineerAmazon Lab126–Cupertino,CA,Responsible for Software and System Verification and Validation activities intended for next generation Immunoassay Chemistry In Vitro Diagnostics Analyzer.Designed, developed and implemented effective tests protocols to verify that the system complied with requirements.Used Orthogonal Arrays Test Strategy to lead testing in the pursuit of high quality test designs.Performed continues integration testing across multiple platforms, resulting in fast defect discovery.Testing the application structures and functionality's for grey box and black box testing.Drove test execution within fast-paced, agile development environment.Developed, maintained and approved quality related processes to continually improve performance.Managed and drive test schedule and related activities.Demonstrated debugging skills in a complex automated instrumentation environment, including hardware, software, and mechanical components.Collaborated with software and hardware development team for verification and validation activities.Evaluated and analyzed qualification data collected during projects, while verifying acceptability of the data and compliance with the approved protocols.Used monitoring tools such as Dev Track ,Team Foundation Server, MTM and RdExpert.04/XXX6to04/XXX6Product Quality EngineerQorvo–Apopka,FL,Responsible for leading Methods Integrations V &V test activities in bridging the functions and validating of instrument system development and assay development for ADVIA Centaur XP/XPR Immunoassay in vitro diagnostic (IVD) instruments and accompanying laboratory automation.Supervised, assigned tasks and provided technical guidance to the V&V team during the test protocol development and test execution phases.Monitored testing progress, tracked and reported quality goals for the project.Design experiments and provide rapid and accurate diagnostic testing for clinical laboratories working with infectious diseases, oncology, cardiac markers, fertility testing, thyroid function, and other clinical applications.Created systems validation plans that outlined the systems validation approach.Selected the proper testing techniques and methodologies to use in the design studies development.Developed business-focused regression test scenarios and test scripts for existing systems to ensure that previous errors are fixed, no new errors are introduced and the system functions as intended.Developed design studies based on the software, system, system user interface, system use cases and hardware requirements.Implemented design changes by creating, executing, analyzing and reporting on verification and validation activities for immunoassay systems.Researched field complaints and performed root cause investigations to identify solutions.Assessed field safety issues by performing cross-functional risk assessments and generating product safety reports detailing safety risks, severities, probabilities, and mitigations.Investigated and resolved Corrective and Preventive Action Plans (CAPAs).Reviewed and analyzed test results and documented deviation found using Defect Tracking Systems and Application Lifecycle Management tools.Generated validation summary reports that concluded the test results and the overall quality level for the project.Participated in formal systems design reviews, requirements analysis and change control board meetings.Notable projects: Reagent Check Volume Errors, Reagent Carryover Mitigations, Sample Integrity.04/XXX6to04/XXX6Medical TechnologistInterpath Laboratory–Kirkland,WA,Concurrent with graduate education in Pharmaceutical System Management, prepare specimens and conduct laboratory assays in Special Coagulation in support of disease diagnosis, treatment, and prevention.Develop novel test methods, protocols, and reference ranges for in-house Special Coagulation tests, perform validation and statistical analysis of performance of all reagents and instrumentation, and prepare, edit, and cross-check reports of lab results.Employ standard laboratory test and measurement controls to regularly assess quality control levels in compliance with CAP, safety, and risk-management guidelines and all other governing regulations and protocols; maintain cleanliness of lab equipment, instruments, and work area.Provide technical supervision and mentoring to new associates in laboratory processes and procedures.Conducted well-received research study, "Can ETP Be Used as a Clinical Assay in a Clinical Laboratory Setting?" for XXX1 annual meeting of The American Society of Hematology (ASH).Commended by supervisors for timeliness and precision in completing routine and special laboratory assays of patient blood and plasma specimens.Performed Special Coagulation assays to include bleeding and clotting time, lupus inhibitor, mixing studies, general thrombophilia, and pregnancy tests.Conducted ELISA assays including Protein Z, FX Antigen, Free Protein S Antigen, Protein C, Protein S, Immunoglobin G & M, and Collagen Binding assays.Facilitated Special Coagulation Molecular Biology assays such as FV Leiden, Prothrombin, MTHFR C677, and MTHFR 1298 gene mutation tests.Successfully collaborated with cross-functional team to clearly communicate test results to physicians, pathologists, and lab supervisor in support of provision of exemplary patient care.Substantially increased departmental productivity and reduced turnaround by always completing and reporting patient test results within established timeframes.Designed and formatted technical specification documentation, including architecture diagrams and process flows, to describe necessary system changes during test development and QA phases.07/XXX6to04/XXX6Scientist IThermo Fisher Scientific Inc.–Jacksonville,FL,Structured and conducted analytical and physical tests on raw materials, diligently following United States Pharmacopeia (USP) Monograph and Food and Drug Administration (FDA) guidelines for active and inactive drug substances to optimize pharmaceutical quality control / management operations.Performed physical tests to include particle size analysis, bulk density, tap density, sieve analysis, loss on drying, heavy metals, residue on ignition, assay by titration, pH, identification tests on infrared (IR), ultra violet (UV) testing, thin layer chromatography, microscope testing, and diverse identifications tests; calibrated and utilized balances, Karl Fischer titrator, ATM sonic sifter, bulk tap density tester, gauge meter, Fourier transform infrared spectroscopy (FT-IR), UV-vis spectrophotometer, atomic absorption spectrometer, and Accumet pH meter.Provided comprehensive project support to High Pressure Liquid Chromatography (HPLC) Lab and Analytical and Formulation Research and Development (R&D) Department.Performed IR and UV tests on raw materials of R&D samples, stability samples, finished products, and in-process samples.Ensured seamless compliance with corporate standard operating procedures (SOPs) and Current Good Manufacturing Practices (cGMPs) through exact generation of logbooks, data printouts, databases, and notebooks outlining daily assay, process validation, and cleaning validation activities.Provided on-going environmental monitoring of hazardous liquid chemical environment, immediately reporting incidents to supervisor in support of OOS and OOT deviation reporting.Honed solid command of USP pharmacopoeia, ICH guidelines, and FDA rules and regulations.Knowledge of quality regulations and standards.
SkillsProtein Z, FX Antigen, Free Protein S Antigen, Protein C, Protein S, Immunoglobin G & M, and Collagen Binding Molecular Biology assays: FV Leiden, Prothrombin, MTHFR C677, and MTHFR 1298 gene mutation tests Immunoassays: Allergy, Anemia, Bone, Cardiovascular, Diabetic, Hepatitis and HIV, Immunosuppressant, Liver Fibrosis, Metabolic, Reproductive Endocrinology, Sepsis, TDM, Thyroid Function, ToRCH and Special ID, Tumor Markers/ Oncology Physical tests: Particle size analysis, bulk density, tap density, sieve analysis, loss on drying, heavy metals, residue on ignition, assay by titration, pH, identification tests on infrared (IR), ultra violet (UV) testing, thin layer chromatography Equipment:	Siemens ADVIA Centaur XP/XPR Immunoassay (IVD) instruments, Siemens BCSXP for special coagulation assays, Stago CAT, Stago STAR evolution XPS for clotting assays, Invader GenMark eSensor for molecular assays, Chronolog Aggregometer, Hologic TECAN, balances, Karl Fischer titrator, ATM sonic sifter, bulk tap density tester, gauge meter, Fourier transform infrared spectroscopy (FT-IR), UV-vis spectrophotometer, atomic absorption spectrometer, Accumet pH meter, medical devices Software:	Dev Track ,Team Foundation Server, MTM, RdExpert, Lotus Notes, Microsoft Office Suite, Visio, MS Project Continued... Continued... Continued...>>. The result is, Good Fit

Fit assessment: Good Fit