Perform incoming and final quality control inspections to support Manufacturing and Operations quality for all NanoString instruments following latest Incoming Specifications Update incoming inspection specifications and procedures as required, in collaboration with other affected departments. Record non conformances and support in conducting root cause investigations. Ma

Perform incoming and final quality control inspections to support Manufacturing and Operations quality for all NanoString instruments following latest Incoming Specifications Update incoming inspection specifications and procedures as required, in collaboration with other affected departments. Record non conformances and support in conducting root cause investigations. Ma

The Quality Assurance Associate II is responsible for supporting the NanoString Quality Management System (QMS) process. Primarily responsibilities will include creating and modifying standard operating procedures, Quality Assurance (QA) product release, administration of change management and document control processes, and auditing. Ensure consistent implementation, imp

Support Manufacturing and Operations in navigating the Quality System including SCARS, nonconformances, deviations, change requests, CAPAs, and validations. Monitor SCARS, nonconformances, deviations, complaints, and trends to identify and recommend corrective and / or preventive actions. Conduct root cause investigations and analyses of issues as assigned. Conduct risk a

The Quality Assurance Associate II is responsible for supporting the NanoString Quality Management System (QMS) process. Primarily responsibilities will include creating and modifying standard operating procedures, Quality Assurance (QA) product release, administration of change management and document control processes, and auditing. Ensure consistent implementation, imp

Company Description At Coffman Engineers, we serve as both prime consultant and sub consultant on projects large and small, including commercial, retail, institutional, government, industrial, and project/construction management. Incorporated in 1979, we have employees in more than 20locations serving clients across the United States and overseas. To meet client objectives

Supervising and coordinating various projects at the airport, warehouse or named location, for safety and quality control of client's high value, and high importance products. Create, coordinate, and complete shipments of goods between company and clients. Coordinate with off site logistics locations, clients, and vendors to meet deadlines and track all shipments. Process

Act as a System Administrator that manages all aspects of this system including user access and periodic reviews for the Document Management System (DMS), the LMS, and CAPA. Perform document management activities in the electronic document management system for controlled documents throughout its lifecycle (e.g. SOPs, Policies, Work Instructions, Forms). Design and develo

Continue to develop a Palantir wide QMS that lives under ISO 9001 and drives consolidation of process documentation and promotes process consistency at Palantir. Author and ensure implementation of approved procedures across the organization, setup non conformance and CAPA processes to monitor deviations and management reporting. Establish inter departmental relationships

What success looks like in this role Conduct internal and external investigations into potential or actual violations of compliance policies, laws, or regulations, and recommend appropriate corrective actions and remedial measures. Build relationships with the association relations and HR teams as well as technical subject matter experts throughout the company to ensure a

Excellent working knowledge on pharmacovigilance and drug safety regulations (ICH, GxP) Work to streamline and optimize business processes based on industry best practices. Generate listings from the safety database, both standard reports and ad hoc queries. Conduct peer review of safety database queries for accuracy and completeness of the results. Coordinate safety syst

The Support Quality Manager leads the Smartsheet Support team's quality program. You understand the business metrics and are able to summarize holistic quality performance, identify solutions, and implement the necessary actions needed to improve performance and customer experience. You will maintain a continuous closed loop improvement process with Support training, oper

Implements and supports project HSE plans, regulatory requirements, and other safe work practices. Identifies, evaluates, develops and delivers project specific HSE training. Implements district HSE communication strategies on projects. Recognizes, evaluates, and advises on hazard identification. Leads and conducts project HSE inspections and monitors the quality and effe

Bio Rad is looking for a Quality Control Specialist II to support Bio Rad's commitment to quality and safety by testing raw material and in process commercial Quality Control testing. As a part of our Quality Control team, you'll apply your science knowledge in testing BioPlex for assay component raw materials, bulks, fills and finished kits tested according to FDA/ISO re

As the Bio Rad Quality Manager, you will provide direct leadership for your team. You attend cross function meetings representing Quality Assurance to ensure the effectiveness of the Seattle Operations site Quality Management System. You will manage the Change Management Board, Validation Review Boards, training program, Management Review and site quality initiatives. Rev