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 TrainingMaster of Science Pharmaceutical Systems Management,Expected inXXX3toNEW JERSEY INSTITUTE OF TECHNOLOGY-Newark,New JerseyGPA Pharmaceutical Systems ManagementBachelor of Science Biology,Expected in2008toRUTGERS 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 ExperienceSr. Software QA Engineer,05 XXX6toPresentAmazon 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.Product Quality Engineer,04 XXX6to04 XXX6Qorvo 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.Medical Technologist,04 XXX6to04 XXX6Interpath 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.Scientist I,07 XXX6to04 XXX6Thermo 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...  SEP  Our Client, an Innovative Company, has spent the past decade focused on the design and development of advanced technology for commercial applications. As they prepare for the next phase of their journey, they are in search of an accomplished and skilled Electrical Engineering Manager to join their team. In the role of Electrical Manager Director, you will play a pivotal part in overseeing comprehensive electrical systems architecture. Your responsibilities will encompass providing expert technical guidance for product design elements, fostering collaboration with various teams, and seamlessly integrating components into a unified system. Reporting directly to the Electrical Engineering Director, you will be instrumental in devising engineering strategies, initiating new projects, and ensuring the effective utilization of technology and resources to fulfill customer demands. This is an opportunity to work in a dynamic startup environment, where your contributions will make a tangible impact. Our Client values individuals who are eager to take on challenges, voice their ideas, and be accountable for their results. If you have experience working in Electrical Architecture with specific experience in DFMEA, Lean Engineering Principles, Power Electronics, High Voltage Systems, ISO26262 Compliance, and ASPICE framework, we would like to hear from you. Responsibilities Shape complete electrical systems architecture, ensuring a robust vehicle network strategy.Develop and refine engineering strategies and processes.Provide technical direction and guidance for comprehensive product design, particularly focusing on electrical architecture.Identify emerging opportunities and spearhead new projects.Contribute to the company s core activities through a solid understanding of principles and applications.Offer leadership and accountability to ensure successful execution. Requirements Bachelor s degree in Engineering required Master s degree preferred.A minimum of 10 years of experience in electrical system development and design, including electrical component development, validation, and launch.Strong analytical and decision-making skills.Experience in electrical engineering within an automotive context, with a minimum of 8 years of experience.Proven leadership abilities with excellent communication and interpersonal skills.Familiarity with problem-solving methodologies like DFMEA, six sigma design, and lean engineering.Experience with various automotive electrical systems.Understanding of ISO26262 and ASPICE processes.Awareness of cyber security risks and solutions.Capacity to develop innovative electrical architecture solutions.Occasional travel flexibility. Location Troy, Michigan (Onsite)Term Full-time, PermanentRate 130,000 - 150,000 - Negotiable on ExperienceBenefits 15 Target Bonus Program, excellent PTO and Holiday calendar, 401K Matching, Strong Healthcare More! If you meet the above qualifications and are excited about the prospect of joining our team, please submit your resume and cover letter for consideration. We look forward to hearing from you! At Human Capital Ventures, we are committed to promoting equality and diversity in all aspects of our business. We believe in creating supportive and inclusive environments where everyone can thrive, regardless of their race, ethnicity, gender, sexual orientation, religion, age, or ability. We strongly encourage applicants from diverse backgrounds to apply for our positions.

ATS compatibility: Potential Fit (score: 50.6)