Validating and analyzing production processes with minimum supervision
Building Static and Dynamic Simulation models with focus on throughput improvement, de-bottlenecking, buffer optimization, process improvement with minimum supervision
Building Static and Dynamic Simulation models with focus on under-the-roof material flow, fleet estimation, congestion analysis, layout optimization with minimum supervision
Building process charts to represent man-machine/process sequences (Cycle Time Charts - CTCs) with minimum supervision
Troubleshooting complex situations involving multiple variables and conditions with minimum supervision
Requirements
Bachelor’s Degree – Manufacturing Engineering or equivalent
Process Engineering professional to assist in the development of new manufacturing processes and equipment used in the production of medical devices.
Compensation
$73,900.00 – $116,000.00
Responsibilities
Assist in the design, development, verification, and validation of new manufacturing processes and equipment.
Support optimization of manufacturing processes through testing, data collection, formatting, and analysis of engineering studies and DOEs.
Participate in equipment start-up activities and execution of validation protocols.
Collaborate effectively with cross-functional development teams and contribute to technical design reviews.
Maintain quality system effectiveness and follow approved Design Control procedures in accordance with FDA guidelines.
Requirements
Associate’s degree in an Engineering or Technical discipline (Mechanical, Chemical, Electrical, or Physics preferred) or an equivalent combination of education and work experience.
Process Engineering professional to assist in the development of new manufacturing processes and equipment used in the production of medical devices.
Compensation
The base pay for this position is $73,900.00 – $116,000.00
Responsibilities
Assist in the design, development, verification, and validation of new manufacturing processes and equipment.
Support optimization of manufacturing processes through testing, data collection, formatting, and analysis of engineering studies and DOEs.
Participate in equipment start-up activities and execution of validation protocols.
Collaborate effectively with cross-functional development teams and contribute to technical design reviews.
Maintain quality system effectiveness and follow approved Design Control procedures in accordance with FDA guidelines.
Requirements
Associate’s degree in an Engineering or Technical discipline (Mechanical, Chemical, Electrical, or Physics preferred) or an equivalent combination of education and work experience.
As a Senior Analyst, Data Analytics, you'll play a key role in advancing investigative and detection capabilities within a highly visible team focused on protecting the organization and its clients. This role involves leveraging Python, SQL, data visualization and automation to transform large and complex datasets into actionable intelligence.
Compensation
$70,000 - $150,000
Responsibilities
Performs sophisticated data analytics to explore and identify known or previously unidentified criminal behaviours among customer and employee groups across BMO.
Supports investigations against people or property of BMO by providing key data or supporting the investigative process.
Applies knowledge of analytics algorithms and technologies to develop analytic solutions and support decision making.
Develops and implements the strategies for technology as related to business requirements.
Acts as a subject matter expert on BMO data and data modelling for criminal risk mitigation to guide management programs and investigation activities.
Senior Data Analyst in the Analytics team at Coupang Play, responsible for developing self‑serve data solutions, dashboards, and metrics to drive user engagement and monetization.
Responsibilities
Own the solution and drive cross‑functional effort to deliver analytics solutions
Quantify GTM engine and ensure data models and dashboards measure correct metrics
Define and reconcile metric definitions across stakeholders
Investigate and resolve data quality and system issues
Communicate findings to executives and operational teams
Requirements
Bachelor’s or Master’s degree in Computer Science, Information Systems, Data Science, or a related field
Support HCCI’s efforts to provide stakeholders with information to help them make informed decisions to improve the value of health care.
Compensation
This is a full-time, exempt, position with an annual salary range from $75,000 to $95,000, depending on experience.
Responsibilities
Apply working knowledge of health care claims structures to execute methodologically sound analyses.
Write and optimize complex SQL queries against large relational claims databases for analyses on health care spending, price, use, and quality.
Independently navigate database schemas to replicate documented existing analyses and develop code and documentation for new analyses, keep document specifications up to date.
Proactively benchmark findings to publicly available studies and internal research findings, enhancing reliability of analyses, initiating data quality and code audits as part of the results review process.
Partner with project leads to design and populate analyses with accurate, correctly structured data.
General supervisor in the Newborn Screening Laboratory responsible for planning, supervision, and quality assurance of laboratory testing for inherited disorders in newborns.
Compensation
Salary: $84,700
Responsibilities
Plan and direct daily activities and manage subordinate staff
Monitor test analyses and specimen examinations
Conduct laboratory testing analyses
Oversee training and orientation of laboratory personnel
Evaluate and document performance of testing personnel
Requirements
Bachelor's degree in laboratory science (Biology, Chemistry, Molecular Biology, Microbiology, Medical Laboratory Science) or related field
Master's degree in a related field may substitute for 1 year of experience
PhD degree in a related field may substitute for two years of experience
Manage semiconductor fabrication processes within the FAB, overseeing process qualification, production, and control methodologies.
Locations (2)
Borgaro Torinese, Piedmont, Italy
Torino, Emilia-Romagna, Italy
Responsibilities
Manage silicon wafer diode production processes across cost, quality and qualification, including photolithography, etching, dry and wet diffusion furnaces, PVD, PECVD, ion implantation, grinding and evaporation
Manage innovation technical projects (FAB process and methods, process automation, diode platforms)
Manage large datasets, statistical analyses and DOE modelling using JMP
Identify and evaluate new process opportunities, silicon suppliers and specifications, production and cost optimization initiatives, and root causes of yield and cost issues
Manage 8D problem‑solving activities and technical discussions with Quality and R&D departments
Conducts research activities on insect biology in arthropod systems in a contained laboratory environment, designing and performing genetic, proteomic, transcriptomic, imaging, biochemical and/or physiological experiments to elucidate factors critical for important insect traits.
Responsibilities
Conducts research activities on insect biology in arthropod systems in a contained laboratory environment
Designs and performs genetic, proteomic, transcriptomic, imaging, biochemical and/or physiological experiments to elucidate factors critical for important insect traits
Collects data and keeps detailed records of results, utilizing computer programs and databases to conduct analyses
Evaluates data, drafts figures, prepares research manuscripts and presents findings at conferences
Trains/supervises research support staff
Requirements
Ph.D. in Biology, Genetics, Biochemistry, Entomology or closely related field
Staff, Data Analyst (Analytics Team) - Coupang PlayCoupang · Singapore
Health Care Claims Data ProgrammerHealth Care Cost Institute · Washington, US
Public Health Scientist SupervisorArizona Department of Administration · Phoenix, US