Quality Engineer Salary at Stats Perform BETA

Job Description Job Description · Looking for a more senior quality professional preferably with the following experience / skills. - 4 year degree with ~ 5years experience in a quality function. · Quality Experience working in pharma, medical device or related life sciences industry with cGMP / GDP manufacturing environment preferred. · Ability to effectively manage smaller projects and day to day activities to meet timelines for regular job functions. · Supplier Quality Experience with supplier quality metrics, performance monitoring, Supplier CAPA or any combination of the experience is preferred. · Skills needed to be successful in position: Able to use sharepoint cloud based systems. - Knowledge of and previous use of word tools and excel. · Knowledge of cGMP/ GDP and working in a heavily regulated manufacturing-related environment. Good interpersonal skills to work with individuals from another company to achieve tasks and goals. - Ability to complete tasks independently with min

Company Federal Reserve Bank of Kansas City When you join the Federal Reserve-the nation's central bank-you'll play a key role, collaborating with leading tech professionals to strengthen and protect our economic, financial and payments systems. We dedicate more than $1 billion to technology each year to support the Federal Reserve and our economy, and we're building a dynamic and diverse team for our future. Bring your passion and expertise, and we'll provide the opportunities that will challenge you and propel your growth-along with a wide range of benefits and perks that support your health, wealth, and life. What we Do: Federal Reserve Financial Services (FRFS) delivers a suite of payments services to financial institutions via FedLine Solutions, Fedwire Funds and Securities, the National Settlement Service (NSS), FedCash1, FedACH, Check Services, and the FedNow Service. FRFS operates as a fully integrated organization with groups dedicated to operations, technology, product and in

Responsibilities and Requirements: Software Quality Engineer. Experience in Software Quality Assurance and hands on software validation experience. Experience in regulated industry needed: Pharma or Med device. Experience in ISO13495, CFR 820, 21 CFR Part 11, HIPAA, Data Privacy, GDPR, NIST cybersecurity Framework, FDA Computer System Validation Guidelines, FDA Computer System Assurance. Complete validation of the software which includes creating and identifying all deliverables starting from Risk classification requirements, design development, testing test protocols, OQ/OQ, traceability matrix and summary documents. There will be coordination needed with multiple teams. So, they must be able to communicate clearly and identify the risks proactively. They must raise the requests wherever there is potential of issue and delay that may impact the project deliverable in timely completion. Must have experience working in a matrixed environment. FDA submission experience will be a plus. No

Job Description Job Description This position ensures that the quality related engineering needs of the organization are met. Responsibilities include compliance and risk analysis, process validation, pFEMA’s, IQ, OQ, PQ and PPQ validation, CAPA and etc. Position works in collaboration with operations, supply chain, and new product development teams. Position Description/Responsibilities: Lead in supporting compliance for medical device manufacturer in ID/Traceability throughout supply chain, well documented and executed Acceptance Activities, Non-conforming material management, Packaging/Labeling control, Production/Process controls, Process Validation. Risk Assessments, project meetings, pilot builds, First Article Inspections, and Post Market Risk Management Designs and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and/or production equipment. Design and execution of pFEMA’s, IQ, OQ, PQ and PPQ validation Corrective a

Job Description Job Description Qualifications: • Understand the inspection equipment accuracy and repeatability required for use during product verification. • Has the ability to interpret customer drawings, parts lists and BOM’s, including GD&T expertise. • Good Reporting Skills, including support of the Quality Management System (QMS). • Has the ability to communicate with customer representatives (quality and engineering) to address concerns and assist with solving job-related problems, as applicable to quality. • Can organize and prioritize job related duties. • Has the ability to mentor quality technicians and shop personnel by sharing job related information provided by the customer. Duties & Expectations: • Create balloon drawings utilizing company provided (DISCUS) software. • Create First Article Inspection Reports for all required parts using an AS9102 format and provide them to customers for review and approval. • Create Designated Inspection Points for final inspections an

ESOP Employee Stock Option - Employee Owned Company Company moving to brand new building by next year! About Our Client Our client, an employee-owned custom plastic injection molding company established in the late 1960s, specializes in serving the automotive and medical industries. Renowned for their expertise in injection molding, rapid prototyping, and value-added services, they offer a supportive and collaborative environment. This Quality Engineer position provides a chance to enhance your skills under the guidance of seasoned quality leaders. Job Description The Quality Engineer will be responsible for the following: Over 3 years of experience as a Quality Engineer or 4 years of experience with PPAP Solid expertise in PPAP processes Proficient in measuring processes using SPC Experience in supporting audits Collaborate directly with customers to discuss reports and non-conformances Lead corrective actions utilizing Root Cause Analysis techniques Please apply below, if you're resu

Job Title: Quality Engineer Location: Rolling Meadows, IL Salary: $70,000-$80,000 LHH Recruitment Solutions is currently seeking a Quality Engineer to join our client's organization in the Rolling Meadows, IL area. Key Responsibilities: Develop and maintain quality standards for processes, materials, and products. Oversee product testing and data collection on quality and reliability. Conduct internal and external audits. Monitor supplier performance. Investigate and resolve quality issues. Write and review standard operating procedures. Conduct root cause analysis and implement corrective actions. Design and specify inspection and testing methods. Develop quality control policies and procedures. Manage production part approval processes. Qualifications: Bachelor's degree in engineering or a related field. Relevant manufacturing experience. Experience in supplier quality and development. Strong communication skills. Familiarity with quality control methodologies and tools. Benefits: Co

Sr. Quality Engineer Bloomingdale, IL (http://maps.google.com/maps?q=333+Munroe+Drive+Bloomingdale+IL+USA+60108) Job Type Full-time Description OVERVIEW Cadrex is seeking a Sr. Quality Engineer who is responsible for developing, implementing, and maintaining quality systems and processes to ensure compliance with industry standards and customer requirements. This role requires a thorough understanding of quality engineering principles, excellent problem-solving skills, and the ability to work collaboratively with cross-functional teams. The ideal candidate will have a strong background in quality assurance within a manufacturing environment and a commitment to continuous improvement. KEY RESPONSIBILITIES + Develop, implement, and maintain quality systems and procedures to ensure compliance with ISO standards, industry regulations, and customer requirements + Conduct root cause analysis and implement corrective and preventive actions to address quality issues and non-conformances + Lead