![]() ![]() Sierra Space, based in Louisville, Colorado with operations in Madison, Wisconsin, Durham, North Carolina, and Kennedy Space Center, Florida, designs and manufactures advanced spacecraft, satellites, propulsion and environmental systems, spacecraft subsystems and components for the U.S. You'll apply, revise, and maintain our quality standards for receiving, in-process and final inspection. You'll inspect for structural flaws, internal defects, or missing welds, and accept, reject, or request rework of defective or malfunctioning units or systems. You'll be responsible for visually inspecting our materials, parts, and products at different stages of production, as well as recording observations and making recommendations for improving processes. Openness to quickly learn how to navigate in new IT systems and to communicate and collaborate with technical colleagues.Īll qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.If you are a seasoned quality inspection professional looking to make an impact in a rewarding industry, join our team! As a Quality Control Inspector III, you'll be using your skills and expertise to ensure that our incoming parts, in-process production, and shipped product fulfill all quality requirements.High proficiency in Excel and PowerPoint is required to support data analysis and creating presentations.Fast learner, open for feedback with able to work independently.Oncology experience/background strongly preferred.Must have strong communication (oral and written), multi-tasking, organizational, and project management skills.Background in operations supports digital marketing and digital data management.Background in project management, marketing, oncology and/or precision medicine.First preference is given to work in large pharma organization.Extremely professional executive administrative background required.STRONG project management/coordination skills.Associate's Degree with 5 years of job-related experience.There will generally be a lot of inputting data into systems, taking notes in meetings and following up on things etc.Providing up to date and accurate communications to external and internal, global & regional stakeholders, project management support, internal/external meeting management, liaising with vendor and cross functional teams to communicate status or needs, communicate status or needs and misc.In addition, responsibilities will include data analysis, compiling or synthesizing of data within projects. This resource will be providing administrative duties such as, preparing agenda/minutes, tracking timelines/deliverables, following up on action items, preparing data collection, managing schedules.This resource will be managing several projects, following up on teammates, project components and providing operational support and managing processes.It will also support the Precision Medicine team on a variety of projects related to the growth and scale of our fast-growing company.This role will have several aspects of general marketing support and business analysis.This job requires working on-site and client is mandating all on-site workers be vaccinated unless a medical/religious exemption is granted by the client. The manager would like this resource to be able to come into the office as needed. Location: Kenilworth NJ 07033 Note: This is an onsite/ Hybrid role.
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