This is an entry level position and is generally intended for individuals who have limited to some level of assembly and/or Inspection experience. The position is responsible for the performance of routine mechanical inspections per the technical documentation provided using pre trained/determined methods to determine product acceptability. Works with moderate independenc

The Associate Director of Quality Sterility Assurance and Aseptic Controls is recognized as having expertise in the principals and application of sterile processing technologies and providing technical support for manufacturing of cell and gene therapy programs within cGMP manufacturing. This role will partner with stakeholders to define strategies for microbial control a

Develops, modifies, applies, and maintains quality standards for products and processes. Provides diverse and complex statistical information for quality improvement by determining and applying testing methods and criteria. Responsible to guide technical evaluations, analysis, and related data acquisition processes to ensure division quality objectives are achieved. RESPO

Reporting to the Quality Manger, the Quality Coordinator provides hands on quality assurance, inspection, problem solving, and root cause corrective actions of manufactured components. In this dynamic role, the QC will review and troubleshoot internal & external audit findings related to prevention and closure. This role interacts consistently across multiple areas, assis

Hands on quality assurance, inspection, problem solving, root cause corrective actions of manufactured components. Internal & external audit findings prevention and closure Site Quality assurance initiative support & Starpoint facilitation Essential Functions Plan, schedule, and coordinate quality functions, such as, authorize to returns, customer rework, nonconformance m

Responsible for verification of purchased and in house manufactured products to ensure conformance to process and product requirements. Such verification can include inspection, test and audit functions or some combination thereof. II. MINIMUM KNOWLEDGE, EDUCATION AND SKILL REQUIREMENTS High school graduate or equivalent. 1 3 years' experience in Quality Control or Manufa

Reporting to the Quality Manger, the Quality Coordinator provides hands on quality assurance, inspection, problem solving, and root cause corrective actions of manufactured components. In this dynamic role, the QC will review and troubleshoot internal & external audit findings related to prevention and closure. This role interacts consistently across multiple areas, assis

Hands on quality assurance, inspection, problem solving, root cause corrective actions of manufactured components. Internal & external audit findings prevention and closure Site Quality assurance initiative support & Starpoint facilitation Essential Functions Plan, schedule, and coordinate quality functions, such as, authorize to returns, customer rework, nonconformance m

Physical Demands and Working Conditions This role routinely uses standard office equipment such as computers, phones, scanners, etc. Position can be hybrid 3 days in office, 2 days remote, or 100% remote for a candidate who has experience working 100% remotely Some travel may be required We are interested in a qualified candidate who is eligible to work in the United Stat

Benchmark provides comprehensive solutions across the entire product lifecycle, leading through its innovative technology and engineering design services, leveraging its optimized global supply chain, and delivering world class manufacturing services. The industries we serve include commercial aerospace, defense, advanced computing, next generation telecommunications, com

At Getinge we have the passion to perform Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge, our passion is to secure that every person and community have access to the best possible care, offering hospitals and life science institutions products and solutions that aim to improve clinical res

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary The QA Associate I, Raw Materials is responsible for pr

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary The QA Associate I, Raw Materials is responsible for pr

During product development, this role participates in guiding the design for quality, manufacturability and producibility, while ensuring project quality plans are compliant to the customers' requirements and applicable standards and regulations. After the initial design and development is complete, transitioning the product to manufacturing is a critical aspect of this r

During product development, this role participates in guiding the design for quality, manufacturability and producibility, while ensuring suppliers and processes are capable of meeting requirements and applicable standards and regulations. After the initial design and development is complete, transitioning the product to manufacturing is a critical aspect of this role. Yo