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Working under the direction of the Manufacturing Engineering Manager, this individual will support new process development, equipment installation and validation, facility/layout optimization, process characterization, capital projects, and continuous improvement initiatives . The engineer will work closely with Design Engineering, Quality, Production, Tool & Die, and Maintenance to ensure manufacturing processes meet cost, quality, productivity, and schedule requirements .

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Nesco Resource, LLC

Manufacturing Engineer

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CONTRACTOR

FEED

The specific compensation for this position will be determined by several factors, including the scope, complexity, and location of the role, as well as the cost of labor in the market; the skills, education, training, credentials, and experience of the candidate; and other conditions of employment. Successfully placed or hired candidates would only be asked for banking details after accepting an offer from us during our official onboarding processes as part of payroll setup.

HOUR

Pinnacle Technical Resources

Service Engineer (Data Center)

If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

Medtronic

Senior Supplier Quality Engineer

If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

Medtronic Plc

If you enjoy working in a collaborative, fast-paced environment where your ideas drive innovation and continuous improvement, this role offers the chance to grow your career while making a meaningful impact on the future of energy. This is an opportunity to collaborate across engineering, supply chain, and manufacturing teams while working closely with suppliers to drive quality excellence.

Hitachi

Sr. Supplier Quality Engineer

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Supplier Quality Engineer II

This is an exciting opportunity to partner with cross functional teams and suppliers worldwide, driving quality excellence, continuous improvement, and patient focused outcomes while supporting a global quality strategy. Join Smith+Nephew as a Supplier Quality Engineer in Memphis, Tennessee, where you will play a critical role in ensuring supplier quality and compliance across our medical device operations.

The Group has a history dating back 160 years to the family enterprise of Thomas James Smith who opened a small pharmacy in Hull, England in 1856. On his death in 1896, his nephew Horatio Nelson Smith took over the management of the business.

Thomas James Smith black and white photograph
Image: Thomas James Smith

A few days after the declaration of World War 1 in 1914, Horatio Nelson Smith (the nephew of the company founder T. J Smith) met with an envoy of the French President in London. The company was awarded a contract to supply £350,000 of surgical and field dressings, to be delivered in five months.

By the late 1990s, Smith & Nephew had expanded into being a diverse healthcare conglomerate with operations across the globe, including various medical devices, personal care products and traditional and pioneering woundcare treatments.

In 1998, Smith & Nephew announced a major restructuring to focus management attention and investment on three business units — wound management, endoscopy and orthopaedics — which offered high growth and margin opportunities.

Smith & Nephew was incorporated and listed on the London Stock Exchange in 1937 and in 1999 the Group was also listed on the New York Stock Exchange.

In 2001, Smith & Nephew became a constituent member of the FTSE-100 index in the UK. This means that Smith & Nephew is included in the top 100 companies traded on the London Stock Exchange measured in terms of market capitalisation.

Today, Smith & Nephew is a public limited company incorporated and headquartered in the UK and doing business in many countries around the world.

Smith & Nephew Plc

Supplier Quality Engineer

Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs. Applying ISO and QSR requirements to processes and procedures for Highridge Medical and outside suppliers; Working with suppliers on new product introduction to insure that quality and performance requirements are fulfilled.

Highridge Inc

Senior Quality Engineer II

The Quality Engineer II provides Quality Engineering support to Manufacturing, Engineering, Quality Control /Quality Assurance, and Process Development teams to ensure that products are manufactured with a high level of quality, while being in compliance with regulations governing medical device manufacturing. Generates, analyzes, and presents reports on quality related Key Performance Indicators (KPI) such as line yields, final release, supplier performance and customer experiences to internal product improvement teams.

Bioventus

Quality Engineer II

Perform other duties as assigned in support of ongoing business activities which include but are not limited to: the ISO-9001 program, daily and routine manufacturing and QC inspection issues, and lean manufacturing initiatives, internal audits, customer and supplier visits or field assessments, testing issues or general QA/QC procedural matters. • Confer with engineering, and technical personnel to resolve manufacturing and testing problems, such as product or systems malfunctions, manufacturing defects, supplier related nonconformances, and incomplete test data.

Hyosung HICO

Quality Engineer

Collaborate with appropriate plant floor and engineering support personnel to execute/facilitate/analyze the first article or first piece inspection at relevant production operations to ensure planned process steps, controls, and outcomes are fully executable or need further improvement. Collaborate with MEs, the Programming team, and others with relevant machining and set-up experience to understand the alignment of features to process steps and execute/facilitate inspection criteria development for plant floor operations.

Engineered Medical Systems

Launch Quality Engineer

Maintains professional and technical knowledge by attending educational workshops, reviewing publications, establishing industry networks, benchmarking state-of-the-art practices, maintaining American Society for Quality certification, and/or participating in other professional associations. Communicates and educates Value Stream Team on matters requiring specialized knowledge of quality functions, i.e., Production Approval Process (PPAP),Advanced Product Quality Process (APQP), and document control.

Parker is the global leader in motion and control technologies, precisely engineering solutions for customers around the world. Capabilities Parker’s engineering expertise spans the core motion technologies – electromechanical, hydraulic and pneumatic – will a full complement of fluid control systems; software and electronic controls; filtration systems; and instrumentation and sealing technologies. The motion and control industry supports nearly all finished goods on the market today. We’re committed to helping our customers achieve higher levels of productivity. You can’t see the engineering in our products, but every day you experience the results of our work, on virtually everything that moves. Global Strengths With operations in more than 46 countries around the world, Parker offers many career paths and opportunities for advancement. We offer a number of hands-on training programs that enables new hires to quickly get up to speed and begin contributing to Parker’s success immediately. In addition, employees are encouraged to actively participate in professional and industry- related organizations. Company facts With annual sales exceeding $10 billion, Parker is the world’s leading diversified manufacturer of motion and control technologies and systems, providing precision- engineered solutions for a wide variety of commercial , mobile, industrial and aerospace markets. Parker has increased its annual dividends paid to shareholders for 54 consecutive years, among the top five longest- running dividend-increase records in the S&P 500 index. For more information, visit the company’s website at <a target="_blank" href="http://www.parker.com">http://www.parker.com</a> , or its investor information site at <a href="http://www.phstock.com" target="_blank">http://www.phstock.com</a> <br/

Parker Hannifin Corp

POSITION OBJECTIVE: Assists the Quality Assurance and Regulatory Affairs Manager in regulatory compliant company-wide quality assurance department that provides all research, support, product development, and quality assurance functions required along with accurate specifications, service, and delivery of product to our customers. Associate's degree or equivalent from an accredited two-year college/technical school, or higher will be considered, plus 2-4 years of quality assurance engineering experience in a medical device manufacturing environment; or equivalent combination of education and experience.

Inteplast Group Corp

6Q02 - Quality - QAEN - QUALITY ASSURANCE ENGINEER

BS degree in Computer Science, Electrical, Mechanical or Industrial Engineering or relevant discipline plus 3 years of experience including a combination of 2+ years in manufacturing, 3+ years in quality control and 3+ years in a leadership position or equivalent combination of experience. Hyve Solutions is a leader in the data center solutions industry, designing, manufacturing, and delivering custom Server, Storage, and Networking Solutions to the world’s largest Cloud, social media, and Enterprise companies.

Hyve Solutions

Quality Engineer (First Shift)

BS degree in Computer Science, Electrical, Mechanical or Industrial Engineering or relevant discipline plus 3 years of experience including a combination of 2+ years in manufacturing, 3+ years in quality control and 3+ years in a leadership position or equivalent combination of experience. Able to work as business needs require which may include long days, occasional evenings and weekends, and travel to all manufacturing and warehouse locations, for business meetings or training.

Quality Engineer III

YEAR

Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability. Direct and facilitate investigations and the corresponding preventative actions and corrective actions that result from abnormal results, customer complaints, quality inquiries, and other quality performance indicators.

CONMED Corp

Bioventus Inc

Must possess at least two (2) years of experience with each of the following: DMAIC methodology; Minitab, DOE, SPC, Variable Gage R & R, ANOVA, t-test, regression analysis, Process Capability, and Confidence & Tolerance interval analysis; Product and Process risk utilizing FMEA and ISO 14971, A3 thinking, PDCA, 5 Why's, and Ishikawa (Fishbone); QMS process, CTQ identification, FDA 21 CFR Part 820, ISO 13485, and GDP; IQ/OQ/PQ, CAPA and RCA; PSUR, CER and TD files as per EU MDR and global requirements; and PPAP, CP, PF, MR for transfer projects. Utilize design development, analysis and statistical tools including Minitab, and statistical methods including DOE (Design of Experiments), SPC (Statistical Process Control), Variable Gage R & R (Reliability and Repeatability), ANOVA (analysis of Variance), t-test, regression analysis, Process Capability, and Confidence & Tolerance interval analysis.

Quality Engineer Jobs in Memphis, TN

Manufacturing Engineer Nesco Resource, LLC

Service Engineer (Data Center) Pinnacle Technical Resources

Senior Supplier Quality Engineer Medtronic

Senior Supplier Quality Engineer Medtronic Plc

Sr. Supplier Quality Engineer Hitachi

Supplier Quality Engineer II Medtronic

Supplier Quality Engineer II Medtronic Plc

Supplier Quality Engineer Smith & Nephew Plc

Senior Quality Engineer II Highridge Inc

Quality Engineer II Bioventus

Quality Engineer Hyosung HICO

Launch Quality Engineer Engineered Medical Systems

Quality Engineer Parker Hannifin Corp

6Q02 - Quality - QAEN - QUALITY ASSURANCE ENGINEER Inteplast Group Corp

Quality Engineer (First Shift) Hyve Solutions

Quality Engineer III Hyve Solutions

Quality Engineer II Hyve Solutions

Quality Engineer II CONMED Corp

Quality Engineer II Bioventus Inc

Sr. Design Quality Engineer Medtronic Plc

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