Director, Quality Salary at Kvi BETA

Are you ready to make a significant impact in the fight against cancer? This clinical-stage targeted oncology company, is on a mission to develop groundbreaking therapies designed to improve outcomes for cancer patients. With an innovative pipeline that includes antibody-drug conjugates (ADCs) and targeted radioligand therapies, this company is at the forefront of oncology advancements. We are looking for a Senior Manager/Associate Director, Quality Assurance to join our team and play a pivotal role in ensuring the highest quality standards for our Small Molecule and ADC portfolio. This is a unique opportunity to collaborate with industry-leading experts and contribute to the development of first- and best-in-class targeted therapies. Desired Skills and Experience Demonstrated track record of third-party supplier management. Experience managing quality oversight for development products. Demonstrates initiative and proactively provides collaborative support to the internal and external

Job Description Job Description Position Summary: Under general supervision and reporting to the Director of Quality Operations, the CMM Programmer is responsible for the day-to-day operation of a CMM to ensure that products meet quality standards and specifications. Essential Functions: The essential functions include, but are not limited to the following: Set up and run existing programs, perform alignment, and daily calibration and understand basic program commands and datum structure Prepare inspection reports and maintain files of inspection documents. Review inspection records received for compliance Maintain inspection and measuring equipment Prepare and coordinate Non-Conformance Reports (NCRs) for nonconforming parts. Performs other duties as assigned Knowledge: CMM Programming skills in a variety of programming languages; such as: PCDMIS, CALYPSO, or other programming languages Performing FAI’s – AS9102 Hand measurement tools Other inspection devices such as: 3D scanners, FAR

Skilled as a Preparator/Art Handler, and interested in part time opportunities with SAM? SAM's Museum Design & Production department maintains a pool of On Call Preparators to support fluctuating needs at different times throughout the year. Should you want to join our Preparator Talent Pool for consideration for future On Call openings, please submit your resume here. When we find ourselves in need of additional On Call Preparator talent, we'll reach out to this Talent Pool to gauge interest and availability. Curious if this position might be the right fit for you? Read on for the position details! Preparator/Art Handler, On Call ROLE OVERVIEW:The On Call Preparator/Art Handler supports the Museum Design & Production department in art handling and gallery preparation of temporary and permanent installations, and ongoing gallery maintenance. FLSA STATUS: Non-Exempt REPORTS TO: Director of Design & Installation COMPENSATION: $26.00 / hour WORK SCHEDULE: The schedule for this On Call rol

Company Overview Immunome is a clinical-stage targeted oncology company committed to developing first- and best-in-class targeted therapies designed to improve outcomes for cancer patients. We are advancing an innovative portfolio of therapeutics, drawing on leadership that previously played key roles in the design, development, and commercialization of cutting-edge targeted cancer therapies, including antibody-drug conjugate therapies (ADCs.) Our most advanced pipeline programs are varegacestat (formerly AL102), a gamma secretase inhibitor which is currently in a Phase 3 trial for treatment of desmoid tumors, IM-1021, a ROR1 ADC with an active IND, and IM-3050, a FAP-targeted radioligand, which is the subject of an IND expected to be submitted in the first quarter of 2025. Our pipeline also includes IM-1617, IM-1335, and IM-1340, all of which are preclinical ADCs pursuing undisclosed targets with expression in multiple solid tumors. Position Summary The Senior Director/Director of Cli

Description Innovation is at the core of what we do. We believe that by removing and reducing the barriers that prevent people from taking their medications, we can help customers conveniently get the medications they need, when they need them and take them as prescribed. We have provided customers with the ability to find transparent and simple pricing, receive 24/7 customer service support, and have their meds delivered to their doorsteps while creating programs and products that embody our mission and position ourselves in becoming the worlds safest and fastest online pharmacy. Amazon Pharmacy is seeking an industry proven and detail-oriented Pharmacy Process Engineer to support the Pharmacy Operations Excellence team. As a process engineer, you will act as an operational leader to drive process stabilization, standardization, and continuous improvement for the pharmacy fulfillment center network. Your role is essential to establish best in class network performance across all proce

Director/Senior Director Quality Assurance & Regulatory Affairs Will serve as the Head of QA/RA and Quality Management Representative reporting to a COO. Scope: Quality Engineering & QMS + Regulatory Affairs strategy, 510K submissions and international registrations. Lead a team of Quality Engineers & Regulatory Specialists (5-10 Direct Reports) **Need a good mix of Quality & Regulatory experience (not just strong in one and light in the other). Class II Medical Device products: plastic Injection molded components and mechanical/electro-mechanical systems. This is an On-Site position, with some flex-hybrid days that can be worked from home. No fully-remote or commuting candidates please. Must either reside in the Seattle area, or be willing to relocate. The company has been around over 10+ years, and has multiple products on the US Market. They have a new device to be launched in the US and OUS later this summer/fall. Requirements: BS Degree in an engineering or scientific discipline 1

Do you have an eye for quality? Are you skilled in identifying problems and troubleshooting solutions? Do you feel compelled to make things right? Are you interested, and/or have a background, in mechanics or engineering? Headquartered in Redmond, Washington, Data I/O is a global company with subsidiary offices in Munich, Germany and Shanghai, China and the leading provider of device programming systems and solutions for memory devices. We are currently seeking a full-time Quality Assurance Specialist to ensure product quality on the manufacturing floor. In this role, you will report directly to the Director of Quality, assisting them in identifying and correcting quality issues, while alerting production leaders and team members to quality issues. Additional responsibilities include, but are not limited to: Validating all product has undergone thorough testing and conforms to cosmetic and engineering specifications. Scheduling internal audits of production capability and ensure qualit

Job Description Job Description Job Description Summary- Responsible for the leadership, strategic direction, and management of the day-to-day activities of all Performance Improvement/Quality and Risk Management program, including accreditation, infection prevention and control, employee health screening, patient safety, risk management, compliance, credentialing, coordination of regulatory and accreditation compliance survey, and all other quality related activities. Key Essential Functions and Accountabilities of the Job Develops and maintains the structure of the Quality and Accreditation Management division and fosters cross-disciplinary, cross-department, and cross-jurisdictional relationships. Develops and manages the SEARHC Performance Improvement/Quality Management program; leads and integrates quality improvement beyond the clinical setting to all divisions. Formulates, analyzes and implements Performance Improvement policies, programs and procedures in alignment with SEARHC