Process Control Engineer Salary at Kinetics Inc BETA

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases. The Kyverna therapeutic platform leverages advanced T cell engineering to suppress and eliminate autoreactive immune cells at the origin of autoimmune and inflammatory diseases. Be at the forefront of cell therapy innovation by joining scientists, industry veterans and healthcare visionaries and help transform how autoimmune diseases are treated The role of Director, Manufacturing Sciences and Technology (MSAT), reports to the Senior Vice President, Manufacturing, Sourcing and Supply within the Technical Operations organization at Kyverna. This leadership role will provide technical oversight for core MSAT functions, including CDMO technical support, technology transfer, process monitoring, process validation, as well as regulatory submission authoring and review for cell therapy drug product and lentiviral vector man

HCLTech is looking for a highly talented and self- motivated Supplier Quality Engineer to join it in advancing the technological world through innovation and creativity. Job Title: Supplier Quality Engineer Job ID: 1494697BR Position Type: Full-time with HCLTech Location: Pleasanton, CA Role/Responsibilities Years of Supplier Development experience. Experience in working in New Product Introduction. Good experience in Component Qualification (plastics & sheet metal) Experience in Process Validations (IQ/OQ/PQ) Experience in Test Method Development and Validation. Experience in creating Incoming Inspection documentation (Component Specs, GD&T, Inspection Instructions, etc) Experience in handling Measuring/Inspection systems (MicroVu, Instron, CMM, etc.) Experience in Statistical data analysis Good communication skills Pay and Benefits Pay Range Minimum: $30.29 per hour Pay Range Maximum: $49.04 per hour HCLTech is an equal opportunity employer, committed to providing equal employment op

Hybrid position in Fremont RESPONSIBILITIES Review customer forecast and plan materials to support upcoming builds Work with engineering to manage and maintain accurate floorstock BOMs Track and process orders for equipment and supplies needed for manufacturing Manage vendor relationships and drive down material costs Summarize purchases into monthly / quarterly reports regarding stock levels by category and location Conduct regular review meetings with production to manage and control on hand inventory and aging Conduct risk assessments on supply trends, review and rebalance inventory Continuously improve procurement processes Document and maintain flowcharts of changes in process MINIMUM REQUIREMENTS Bachelor’s Degree or equivalent Minimum of 3-5 years in a procurement, program management, or supply chain role Proven ability to lead a cooperative effort among members of a team Must have good communication skills to work with multiple internal and external stakeholders Solid backgroun

Job Description Job Description Responsibilities: Excellent understanding of Quality Management Systems (QMS) and regulatory requirements in the medical device industry. Strong problem-solving skills with a focus on root cause analysis, CAPA, and continuous improvement. Ability to work collaboratively with cross-functional teams and communicate effectively at all levels of the organization. Proficient in the use of quality tools such as Six Sigma, PFMEA, and statistical process control (SPC). Requirements: Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or similar certifications. Minimum of 4-6 years of experience in quality assurance within the medical device manufacturing industry. Strong knowledge of validation protocol and other relevant medical device standards. Experience with process validation, risk management, CAPA, RFA, and validation protocols in a manufacturing environment.

Job Description Job Description JOB TITLE: Materials Production Planner LOCATION: Hayward, CA (onsite) PAY RANGE: $57.00 - $58.90/hr DURATION: 6 months TOP 3 SKILLS: JOB DESCRIPTION The Manufacturing Operations Logistics Planning team at drives the execution of all material procurement and build activities that support both the end-to-end manufacture and the maintenance of the Robotaxi fleet. We work cross-functionally and collaboratively with our internal partners to ensure everyone has what they need, when they need it. The primary role of the Materials Production Planner is to create, execute and monitor the attainment of all detailed Build Plans that support overall business goals. They will be responsible for maintaining version control, updating the PP master data that configures the SAP MRP system-logic, as well as maintaining accurate schedules and priorities to keep the whole MFG Ops team aligned and on-time. As a critical spoke in the wheel here at ***, this position will pro

Position Summary Reporting to the Senior Manager or Director of Quality, the Quality Engineer will have responsibility of ensuring that processes and products consistently meet established quality standards. While ensuring compliance to internal quality system and applicable regulations, the quality engineer will monitor and improve the quality of operational processes and outputs. His/her/their range of responsibilities will entail designing quality standards, inspecting materials, equipment, processes, and products, developing quality control systems, and determining corrective actions. Qualifications Bachelor's degree in engineering, biomedical engineering or related scientific discipline. 3-5 years’ experience working in manufacturing of finished medical device or related industry. Working knowledge of the FDA Quality System Regulation, ISO 13485, ISO 14971, and the EUMedical Device Directive. Lead auditor credentials for QSR, ISO, or MDSAP are desired (ASQ Certification preferred)

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

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