QC Engineer Salary at Ccice BETA

WHO WE ARE LARQ was started with a simple vision where innovative technology can be combined with inspirational design to help people access pristine drinking water easily and sustainably. Our products look as good as they make you feel. We are confident these are the most beautiful hydration products in the world. We make it easy to choose a healthier and sustainable choice, anytime and anywhere. And we are just getting started. You are what you drink. So drink brilliantly. WHAT WE’RE LOOKING FOR LARQ is looking for an organized, analytical, and ambitious Manufacturing Engineer to join our growing team. This is an exciting time to join LARQ as we prepare to introduce several new products this year and expand our manufacturing footprint into new regions including the US, Mexico, and the EU. The ideal candidate will have a strong background in manufacturing engineering, experience working with external partners, and a passion for driving efficiency, quality, and innovation. This role wi

Job Title: Sr. Manufacturing Engineer Location: San Jose, CA Zip Code: 95134 Start Date: Right Away Job Type: Contract - 6 months Pay Rate: $70.00 - $80.00 /hr DoE Shift: 8am-4:30pm M-F with some weekend work Keywords: #SrEngineeringJobs #ManufacturingEngineeringJobs #SanJoseJobs A Sr. Manufacturing Engineer job is available with our client in San Jose, CA. As a Manufacturing Engineer, you will learn and Apply knowledge of electrical components, interiors, systems integration or structural assembly and installation to collaborate and influence our multidisciplinary Product Design Engineering, Quality, Manufacturing and Facilities teams in the development of a new aircraft. To be considered for this role, you will have a Bachelor's Degree and 5+ years of relevant work experience in the aerospace industry. US Citizenship is required. JOB RESPONSIBILITIES: Assist on and off aircraft builds for electrical components, interior closeouts, metallic and composite assemblies, wiring harnesses,

Job Title: Composite Manufacturing Engineer Location: San Jose, CA Zip Code: 95134 Start Date: Right Away Job Type: Contract - 6 months Pay Rate: $55.00 - $70.00 /hr DoE Shift: 2nd - 3pm-11:30pm W-Sun OR Tues-Sat A 2nd Shift Composite Manufacturing Engineer job is available with our client in San Jose, CA. As a Manufacturing Engineer, you will learn and Assist aircraft build up and modifications to electrical components, mechanical composite assemblies, and wiring harnesses and to collaborate and influence our multidisciplinary Product Design Engineering, Quality, Manufacturing and Facilities teams in the development of a new aircraft. To be considered for this role, you will have a Bachelor's Degree and 5+ years of relevant work experience in the aerospace industry. US Citizenship is required. JOB RESPONSIBILITIES: Assist aircraft build up and modifications to electrical components, mechanical composite assemblies, and wiring harnesses. Utilizes various forms of engineering and techni

SUMMARY Senior Manufacturing Engineer represents the Operations department on projects to support transfer of designs from R&D into Manufacturing. The individual will be a key member of cross-functional teams, performing activities associated with process development and design transfer. The individual will be responsible for presenting technical updates to the team, supporting the development team in areas such as Design for Manufacturability, process control/characterization, manufacturing documentation, and providing production support during engineering builds. Additionally, the individual will support manufacturing activities both internally and with contract manufacturers. PRINCIPAL DUTIES AND RESPONSIBILITIES Design experiments, develop protocols, perform process validations and data analysis, draw conclusions, and communicate results. Troubleshoot/improve manufacturing processes. Design/select equipment & fixtures and qualify them for manufacturing. Establish process flow and p

Job Overview: Responsibilities: Full-Project Involvement: Engage in every stage of the project, from design and prototyping to mass production and sustaining Design Feedback: Review designs and provide feedback on manufacturability to ensure smooth production transitions Contract Manufacturer (CM) Collaboration: Work closely with CMs to establish build readiness, including designing, reviewing, and implementing production fixtures Managing BOMs and PLM systems Serve as the primary technical point of contact for CMs to drive project progress Investigate and root-cause problems, driving fixes back to engineering teams or CMs Process Improvement: Learn from past projects and proactively refine manufacturing processes to enhance efficiency and quality across all projects Requirements: 5+ years of experience in Manufacturing Product, Process, or NPI Engineering within networking equipment manufacturing environments Strong expertise in DFx principles (DFM, DFA, DFT, DFQ, DFR), production fix

Manufacturing Engineer II (Catheter) Department: NC2 - Engineering Location: Santa Clara, CA START YOUR APPLICATION (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req_id=3012353&source=3012353-CJB-0) This position is located on-site in Santa Clara, California ABOUT THE COMPANY More than just another design shop or contract manufacturer, Cirtec offers a uniquely comprehensive range of vertically integrated capabilities. Cirtec specializes in complex, difficult to produce components and devices in today-s most advanced product technologies including, neuromodulation, implantable drug delivery, cardiac rhythm management, ventricular assist and interventional devices and delivery systems. We have the capabilities needed to bring products to full production, including assembly, packaging and testing, and in-house sterilization. Our employees have the expertise needed to design innovative devices, solve complex design challenges, and help bring our customers- devices to mar

This is an exciting opportunity to lead and manage digital quality and data integrity compliance within a cutting-edge biologics manufacturing facility. You will be responsible for overseeing 2 functional teams for Digital QA and Document Management QA up to 30 team members. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 720 KL total mammalian cell culture manufacturing capacity with commercial monoclonal antibody, mRNA vaccine and ADC manufacturing capabilities. Your roles and responsibility will include: Provide Oversight of the newly established Data Compliance group overseeing data integrity compliance efforts consistent with GMP and site Quality policies. Overseeing the DI framework and constituent policies, procedures, tools, and checklists governing DI and Computerized System Validation (CSV) that effectively establish data risk management stewardship and accountability throughout data and system life cycle

Meet is working with a clinical stage biotechnology company looking to hire an Associate Director of CGMP Quality Assurance. Reporting to the Head of Quality, you will be working with cross-functional teams to manage external vendors and CDMOs. The role involves providing quality support and contributing to the development of quality systems. Expertise in GMP and related regulations is required. RESPONSIBILITIES: Serve as the technical expert on CGMP-related regulations and guidelines, specifically for manufacturing, testing, and controls. Review and approve drug substance and drug product manufacturing, packaging, and labeling documents within defined timelines. Lead and support external quality activities, including batch record reviews, analytical method validations, tech transfers, deviations, quality agreements, supplier qualifications, and audits. Participate in CDMO team meetings, providing quality feedback and collaborating on complex investigations for the company's global pro