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Mechanical Support
Engineering Economics, Inc.
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- $38.46 to $54.8 USD / hour
Hands-on technical experience through internships, technician roles, trade programs, military service, facility operations, maintenance, or field-based project work.
Added 1 min ago
CO
Health Instructional Assistant
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- $21.7 to $23.93 USD / hour
…materials and implementing the student’s Individualized Education Program (IEP). Assist students with personal hygiene and self-help skills. Perform and/or assist with specialized health…
Added 1 min ago
Client Experience Supervisor
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Added 2 mins ago
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Signal and Communication Engineer III
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Saint Louis, MO
Bi-State Development is an eligible employer for the Public Service Loan Forgiveness (PSLF) program
Added 3 mins ago
TH
Guest Services Representative - Lakecrest Hotel
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- $14 to $16 USD / hour
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Added 3 mins ago
FM
HVAC Sales Representative
FIRSTCALL MECHANICAL GROUP LLC
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…business partners and each other as family, within a culture of service and accountability, where we do the right thing because it is the right thing to…
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…create solutions and change lives. To fulfill this, the Reentry Program Specialist will assist participants in the reentry and Transition Employment Opportunity (TEO) Program, a 16-week,…
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REENTRY PROGRAM SPECIALIST
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Customer Service Representative
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Finance Assistant I (FT)
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Patient Service Representative II
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Conflicts Analyst
McDermott Will & Schulte LLP
NY
…successful career and a rich life. That’s why our benefits program supports your physical, emotional, mental, and financial health, with an emphasis on work-life…
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BH
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Service Arrangements Representative 1
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- $26 to $29 USD / hour
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Added 10 mins ago
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Columbus Sanitation - Maintenance Rep - Part time
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Coghlin Companies

Quality Engineer II

West Boylston, MA, United States

$85,000 to $110,000 USD / year

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Job details

Pay: $85,000 to $110,000 USD / year
Posting language: English
Posted: Feb 8, 2021

Original job description

The Quality Engineer II will support all compliance activities throughout the organization at Cogmedix.

Responsibilities:

Under the direction of the Quality Engineering Manager, the Quality Engineer II will:

Lead by example and promote the criticality of strict compliance adherence at Cogmedix.
Lead in the training of personnel, including customers and suppliers on workmanship and quality standards.
As part of the Cogmedix team, assure all outgoing product is manufactured in a compliant manner.
Support process qualification/validation and new product introduction processes.
Development and execution of Control Plans.
Build strong rapport with customers and suppliers through generating data and presenting quality metrics to meet or exceed mutually defined expectations. The metrics shall include First Pass Yield (FPY), Nonconformance, Martial Review Board trends, On Time Delivery and other metrics as required by the customer. The metric support will be based on customer requirements but may include weekly, monthly or quarterly business reviews.

Review device history records for quality approval as needed.

Complaints, CAPAs
Under the direction of the Quality Engineering Manager, help manage the Customer Complaint and CAPA systems.
Propose, review and implement approved Corrective and Preventive actions.
Collaborate with all internal groups and customers to help determine root cause of customer issues, Complaints, and CAPAs using various techniques including but not limited to Reenactment, PFMEA, Control Plans, Five Whys, Ishikawa (fishbone) Diagrams, Pareto Analysis, etc.
Provide oversight of all containment activities associated with potentially discrepant material identified through the Nonconforming Material, CA, and Compliant processes.
Collaborate with customer to help determine root cause of customer issues.

QC Inspection:

Provide oversight to the Quality Control inspection process for assigned product lines.
Proven skills as a Trainer for new QC Inspection resources, as well as training all QC inspection specialist when changes are made to affected processes.
Development and maintenance of quality inspection plans.

Under direction of the Quality Management, provide support in the form of review and approval for Redline and Engineering Change Notifications (ECN’s) processing.

Suggest improvements to ECN/ECO process that lead to improved efficiency, accuracy, and quality.
Meet or exceed established ECO implementation performance metrics.
Assist in the development and execution of supplier quality plans.
Frist Article Review and Approval
Contribute to the ongoing assessment of current and potential suppliers.
Lead continuous supplier improvement through collection of data and performing statistical analysis.

Production Quality:

As needed, assist Manufacturing Engineers (ME’s) with manufacturing compliance issues, taking appropriate action within the Cogmedix Quality System.
Responsible for communication of quality related issues to the production team. This communication should be documented in the form of Quality Alerts.
As the quality representative on the product Success Team, review and approve all RMA’s within Omnify.
Development and maintenance of Quality Forms, and QC Procedures, as needed, for assigned product lines.
Work with ME’s, assembly, production and test to identify trends, propose, and implement corrective actions.
Collaborate with Program Managers (PM’s) and ME’s to develop optimal work order routings.
Collaborate with Supply Chain, PM’s and Operations on the Material Review Board (MRB) process.
During the Scaled Product Launch (SPL) provide Quality support to the success team. As new products are transferred to Cogmedix support Co-Build activities to ensure that inspection points are clearly defines and understood.
As part of the product success team any qualification of the manufacturing will require quality review and approval of Validation Protocols and Reports.
Performs other responsibilities as directed.

Essential Requirements:

Positive attitude, self-motivator, and tenacious follow up required.
Superior customer service attitude.
Excellent teamwork, communication, and interpersonal skills.
Bachelor’s degree, preferably in a science or engineering discipline. Significant and applicable professional experience may be considered in lieu of certain educational requirements.
Strong electro-mechanical orientation.
Proven experience in ISO-13485 certified required and cGMP organizations preferred.
5 years professional experience in medical subassembly and finished device manufacturing required. 6 to 10 years preferred.
Certified Quality Engineer (CQE) preferred.
Proven problem solver.
Knowledge of IPC 610 and 620 standards required. Certified training beneficial.
Advanced Level Skills in MS Word and Excel such as keyboard short cuts, creating macros and forms, table techniques, working with images and text, pivot tables.
Advanced Level Skills in MS Visio such as creating Visio diagrams, creating custom styles and templates, cross functional flow charts, linking drawings to other MS applications, working with data, custom reports, and exporting is valuable.
Standing for prolonged periods of time.
Ability to lift up to 30 pounds.

Note: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and/or skills required of all personnel so classified.

Cogmedix is an Equal Opportunity Employer. Cogmedix does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

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Jobs in the United States