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

About us Cognex is the largest, most successful and recognized global player in industrial machine vision! We are a financially strong, international company with no debt and have been in business for over 40 years. Using advanced optics, image sensors and artificial intelligence software Cognex vision and ID systems capture an image then analyze it to make sense of what'

The Opportunity Avantor, a Global Fortune 500 company is looking for a dedicated Quality Engineer II to optimize our Avantor Fluid Handling organization. This Devens, MA based role is full time, on site. If you have quality engineering experience let's talk! Minimum Education Highschool diploma with 7 + years equivalent work experience. Bachelor's degree preferred. Requir

Environmental Health & Safety (EHS) Intern Job Locations 50 minutes ago (5/9/2024 7 01 PM) Job ID 2024 10603 Posted Date Operations Job Location US MA Company Overview We are a world class team of professionals who deliver next generation technology and products in robotic and autonomous platforms, ground, soldier, and maritime systems in 50+ locations world wide. Much of

Design and development of equipment, processes, and control systems, used for production and assembly of cell encapsulation devices. Manage the evaluation and selection of new equipment/technologies or modifications to existing systems to consider new processing technologies. Support ongoing optimization and improvement in equipment/systems/processes for long term robustn

Facilitate root cause investigations and developing corrective and preventive measures. Carry out the effectiveness controls. Monitor and track measures and CAPA phases. Ensure complete and adequate documentation of the CAPA. Manage and moderate CAPA team meetings. Provide guidance and direction of the CAPA systems Body of Knowledge. Provide subject matter expertise, lead

GLAUKOS ENGINEERING DOCMENTATION SPECIALIST II (BURLINGTON, MA) How will you make an impact? We are seeking a meticulous and detail oriented Engineering Documentation Specialist to join our team. The ideal candidate will be responsible for ensuring the accuracy, completeness, and compliance of all documentation related to our processes and products. This role requires pro

Ensures that the packaging line runs productively following all Packaging Operations SOPs and cGMPs Completes appropriate paperwork Monitors product from the line for accuracy and ensures proper packing procedure is utilized for shipment Complies with company policies and procedures and maintains regular work attendance Follows safety rules, SOP's and cGMP guidelines Main

In the Quality Control Lead role, you will assume responsibility for managing the QC activities that are pivotal in ensuring the quality and compliance of our new emerging therapy services. This includes the new GMP Phase 1 clinical production facility in Marlborough MA with the focus on novel modalities including allogenic stem cell, cell and gene therapy, extracellular v

Quality Assurance Analyst IT Prod Mgmt 0 && !infoField.enableCommand"> Job Tracking ID 512272 878258 0 && !infoField.enableCommand"> Job Location 0 && !infoField.enableCommand"> Job Level Any 0 && !infoField.enableCommand"> Level of Education BA/BS 0 && !infoField.enableCommand"> Job Type Full Time/Regular 0 && !infoField.enableCommand"> Date Updated 05/01/2024 0 && !info

Lead the development and continuous improvement of high performance optical coatings; Develop coating processes for e beam / IAD to improve yield and performance; Design optical thin film coatings for VIS and NIR products; Provide recipe development, parameter optimization and process documentation; Use characterization equipment to understand film uniformity and performa

Coordinate and perform day to day activities related to performance improvement, patient safety, risk management, patient satisfaction, and hospital accreditation. Regulatory compliance activities include audits and investigations, developing and shepherding action plans, and conducting related educational programs. Key Responsibilities Safety occurrence reporting system

Genesis10 is currently seeking a Quality Assurance Engineer working a contract with our client onsite in the healthcare industry in their Westborough, MA location. Summary The Quality Assurance Engineer is responsible for providing manufacturing and/or engineering process support in accordance with documented procedures and practices. The Quality Assurance Engineer is res

The Site EHS Specialist I will manage field personnel to ensure compliance with EHS policies, programs, procedures and legislative standards. Will communicate and contribute to the development of site based programs, conduct onsite EHS audits and inspections, and provide recommendations for improving EHS performance and creating a NO HARM culture. Will ensure all personne

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. 3 5 years' experience in Quality Control or in a m