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Quality Control Lead

Ingersoll Rand

Salt Lake City, Utah • Today

Full-time

Fiber Field Technician / Quality Control / South Georgia

Motion Recruitment Partners, LLC

Remote or Alpharetta, Georgia • Today

Easy Apply

Full-time

Fiber Field Technician / Quality Control / North Georgia

Motion Recruitment Partners, LLC

Remote or Alpharetta, Georgia • Today

Easy Apply

Full-time

BIM/VDC Engineering Services Specialist - QA/QC (Waterworks)

Ferguson Enterprises, LLC

Remote or Springfield, Virginia • Today

Full-time

USD 4,799.70 - 9,075.00 per month

Data Center QA/QC Specialist - Site Inspector

Motion Recruitment Partners, LLC

Remote or Amarillo, Texas • Today

Easy Apply

Full-time

Oncology Clinical Data Quality Lead

US Venture, Inc.

Remote or Texas • Today

Full-time

USD 94,500.00 - 157,500.00 per year

Oncology Clinical Data Quality Lead

McKesson Corporation

Remote or Texas • Today

Full-time

USD 94,500.00 - 157,500.00 per year

Lead Data Quality Engineer

EPAM Systems

Remote • Today

Full-time

Sr / Lead Quality Assurance Consultant - Pharma industry

People Force Consulting Inc

Remote • Today

Easy Apply

Third Party, Contract

Engineering Intern - Substation Protection & Control

Qualis LLC

Farmington, Utah • Today

Full-time

Lead Engineer - Protection & Control

Qualis LLC

Remote or Palm Beach Gardens, Florida • Today

Full-time

USD 130,000.00 - 180,000.00 per year

Epic Beaker Multiple Roles Build Analyst OR Interface OR Data Innovations Analyst OR Readiness OR Flex Analysts

Tech Pro Inc.

Remote • Today

Contract

$70 - $75

Transmission Line Engineer (Mid, Senior, & Lead)

Leidos

Remote • Today

Full-time

USD 73,450.00 - 132,775.00 per year

Transmission Line Engineer

Leidos

Remote • Today

Full-time

USD 73,450.00 - 132,775.00 per year

Job Details

Skills

FLSA
ISO 13485
QA Management
Scheduling
Workflow
QMS
Manufacturing Engineering
Logistics
Purchasing
Testing
Security Clearance
Process Control
Enterprise Resource Planning
5S
Interviewing
Training
ROOT
Auditing
Documentation
Risk Management
FMEA
Teaching
Inspection
Communication
Microsoft Windows
Medical Devices
Manufacturing
Management
Regulatory Compliance
Attention To Detail
Multitasking
Work Ethic
Collaboration
Reporting
Productivity
Mechanical Engineering
System Integration Testing
Quality Control
Quality Assurance

FLSA
ISO 13485
QA Management
Scheduling
Workflow
QMS
Manufacturing Engineering
Logistics
Purchasing
Testing
Security Clearance
Process Control
Enterprise Resource Planning
5S
Interviewing
Training
ROOT
Auditing
Documentation
Risk Management
FMEA
Teaching
Inspection
Communication
Microsoft Windows
Medical Devices
Manufacturing
Management
Regulatory Compliance
Attention To Detail
Multitasking
Work Ethic
Collaboration
Reporting
Productivity
Mechanical Engineering
System Integration Testing
Quality Control
Quality Assurance

Summary

POSITION: Quality Control Lead

DEPARTMENT: Quality

REPORTS TO: Site Quality Manager

FLSA STATUS: Non-exempt

JOB DESCRIPTION:

The Quality Lead is responsible for overseeing inspection activities to ensure compliance with regulatory requirements, internal quality standards, and customer specifications. The Quality Lead demonstrates a strong knowledge of the ISO 13485 and 21 CFR 820 requirements. The Quality Lead interacts professionally with company management, internal departments, and customers on Quality related tasks. This position also manages and maintains day-to-day scheduling and workflow of the Quality Inspectors. They also support the management team by conducting training, performing troubleshooting, managing the daily shipment schedule, and generally supporting the QC department and Quality functions to ensure compliance with the company's QMS requirements and established processes.

KEY ROLE AND RESPONSIBILITIES:

Partner with departmental peers in manufacturing, engineering, logistics, purchasing, maintenance, and QC to monitor and ensure compliance with the quality assurance program established by the company.
Coordinate and manage daily schedules and work assignments of Quality Inspector personnel.
Lead the QC department in daily activities, such as visual and dimensional inspection, quality testing, Device History Record (DHR) review, and others as assigned.
Review and approve inspection records, nonconformance reports, and related documentation.
Cooperate with and act professionally with coworkers and managers.
Meet Flexan standards for quality, cleanliness, and productivity.
Follow all procedures for cleanroom operation, cleanroom attire, and contamination control.
Follow all Flexan procedures for traceability, line clearance, process control, safety, and housekeeping.
Accurately input data into ERP system daily (including clock in time, work orders worked on, operation worked on, indirect work performed, quantities of parts produced and quantities of parts that are deviated).
Participate in 5S activities and follow 5S procedures.
Conduct on-boarding and on-the-job training for new employees as needed.
Participate in interviewing candidates for inspection roles, assessing technical skills, and cultural fit.
Work closely with the Quality Manager to provide objective feedback and recommendations for development plans, training needs, and performance evaluations for inspection personnel.
Manage and maintain Flexan's quarantine locations and ensure proper disposition of parts/materials.
Assist with root cause investigations driven through nonconformance reports (NCs) and CAPAs.
Assist with internal and external audits, providing inspection-related documentation and evidence of compliance.
Assist in risk management activities including preventive actions, pFMEA and Control Plans.
Assist in the development of Dimensional, Quality Control, and other process sheets or work instructions.
Work with Engineering to develop vision system measurement teaching files for dimensional inspection.
Lead the execution of Gage R&Rs and other validation activities within the QC department.
Perform dimensional and visual inspections.
Identify opportunities to improve inspection processes, methods, and reduce defects.

MINIMUM QUALIFICATIONS:

Excellent interpersonal and communication skills, both written and verbal, and presents well at all levels of the organization.
Works well independently and in a team environment, can lead people that are not direct reports, strong goal setting, follow up, organization and prioritization skills, and excellent attention to detail.
Strong computer skills and familiar with Microsoft Windows applications.
Medical Device Manufacturing environment experience preferred.
Demonstrable ability to analyze a wide variety of information and data to assist management decisions regarding potential risks that may impact product or compliance status.
Strong attention to detail and ability to multitask.
Good work ethic (comes to work and returns from lunch and breaks on time, works hard to reach work standards, tries to minimize waste)
Team player that gets along well with others (respectful of supervisors and co-workers, helps others by offering assistance and ideas when appropriate)
Able to recognize and address both good and sub-standard performance (praise excellent performance and cooperation, recognize and immediately discuss any safety issues, identify and report interpersonal and attitude problems, recognize and either immediately stop or report any incidences of misuse of tools and equipment)
Is proactive in identifying potential problems or opportunities to increase productivity and quality, decrease waste and improve morale.
Follows through on tasks and projects as assigned.
Demonstrates all corporate values:
- We think and act like owners.
- We are bold in our aspirations while moving forward with humility and integrity.
- We are committed to making our customers successful.
- We foster inspired teams.

PHYSICAL DEMANDS AND WORK ENVIRONMENT:

The employee is required to work in a cleanroom environment and is expected to follow the guidelines and rules for working in the cleanroom. This includes following the gowning procedures, covering hair in a hairnet, and wearing personal protective equipment as appropriate.
While performing the duties of this position, the employee is frequently/occasionally exposed to moving mechanical parts.
The employee is occasionally required to sit, climb, balance, stoop, kneel, crouch, or crawl.
The employee is frequently required to lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds.

PandoLogic. Keywords: Quality Control / Quality Assurance Manager, Location: Salt Lake City, UT - 84105

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: pandfeed
Position Id: 604618636
Posted 14 hours ago

Fitment

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Job Details

Skills

FLSA
ISO 13485
QA Management
Scheduling
Workflow
QMS
Manufacturing Engineering
Logistics
Purchasing
Testing
Security Clearance
Process Control
Enterprise Resource Planning
5S
Interviewing
Training
ROOT
Auditing
Documentation
Risk Management
FMEA
Teaching
Inspection
Communication
Microsoft Windows
Medical Devices
Manufacturing
Management
Regulatory Compliance
Attention To Detail
Multitasking
Work Ethic
Collaboration
Reporting
Productivity
Mechanical Engineering
System Integration Testing
Quality Control
Quality Assurance

FLSA
ISO 13485
QA Management
Scheduling
Workflow
QMS
Manufacturing Engineering
Logistics
Purchasing
Testing
Security Clearance
Process Control
Enterprise Resource Planning
5S
Interviewing
Training
ROOT
Auditing
Documentation
Risk Management
FMEA
Teaching
Inspection
Communication
Microsoft Windows
Medical Devices
Manufacturing
Management
Regulatory Compliance
Attention To Detail
Multitasking
Work Ethic
Collaboration
Reporting
Productivity
Mechanical Engineering
System Integration Testing
Quality Control
Quality Assurance

Summary

Partner with departmental peers in manufacturing, engineering, logistics, purchasing, maintenance, and QC to monitor and ensure compliance with the quality assurance program established by the company.
Coordinate and manage daily schedules and work assignments of Quality Inspector personnel.
Lead the QC department in daily activities, such as visual and dimensional inspection, quality testing, Device History Record (DHR) review, and others as assigned.
Review and approve inspection records, nonconformance reports, and related documentation.
Cooperate with and act professionally with coworkers and managers.
Meet Flexan standards for quality, cleanliness, and productivity.
Follow all procedures for cleanroom operation, cleanroom attire, and contamination control.
Follow all Flexan procedures for traceability, line clearance, process control, safety, and housekeeping.
Accurately input data into ERP system daily (including clock in time, work orders worked on, operation worked on, indirect work performed, quantities of parts produced and quantities of parts that are deviated).
Participate in 5S activities and follow 5S procedures.
Conduct on-boarding and on-the-job training for new employees as needed.
Participate in interviewing candidates for inspection roles, assessing technical skills, and cultural fit.
Work closely with the Quality Manager to provide objective feedback and recommendations for development plans, training needs, and performance evaluations for inspection personnel.
Manage and maintain Flexan's quarantine locations and ensure proper disposition of parts/materials.
Assist with root cause investigations driven through nonconformance reports (NCs) and CAPAs.
Assist with internal and external audits, providing inspection-related documentation and evidence of compliance.
Assist in risk management activities including preventive actions, pFMEA and Control Plans.
Assist in the development of Dimensional, Quality Control, and other process sheets or work instructions.
Work with Engineering to develop vision system measurement teaching files for dimensional inspection.
Lead the execution of Gage R&Rs and other validation activities within the QC department.
Perform dimensional and visual inspections.
Identify opportunities to improve inspection processes, methods, and reduce defects.

MINIMUM QUALIFICATIONS:

Excellent interpersonal and communication skills, both written and verbal, and presents well at all levels of the organization.
Works well independently and in a team environment, can lead people that are not direct reports, strong goal setting, follow up, organization and prioritization skills, and excellent attention to detail.
Strong computer skills and familiar with Microsoft Windows applications.
Medical Device Manufacturing environment experience preferred.
Demonstrable ability to analyze a wide variety of information and data to assist management decisions regarding potential risks that may impact product or compliance status.
Strong attention to detail and ability to multitask.
Good work ethic (comes to work and returns from lunch and breaks on time, works hard to reach work standards, tries to minimize waste)
Team player that gets along well with others (respectful of supervisors and co-workers, helps others by offering assistance and ideas when appropriate)
Able to recognize and address both good and sub-standard performance (praise excellent performance and cooperation, recognize and immediately discuss any safety issues, identify and report interpersonal and attitude problems, recognize and either immediately stop or report any incidences of misuse of tools and equipment)
Is proactive in identifying potential problems or opportunities to increase productivity and quality, decrease waste and improve morale.
Follows through on tasks and projects as assigned.
Demonstrates all corporate values:
- We think and act like owners.
- We are bold in our aspirations while moving forward with humility and integrity.
- We are committed to making our customers successful.
- We foster inspired teams.

PHYSICAL DEMANDS AND WORK ENVIRONMENT:

The employee is required to work in a cleanroom environment and is expected to follow the guidelines and rules for working in the cleanroom. This includes following the gowning procedures, covering hair in a hairnet, and wearing personal protective equipment as appropriate.
While performing the duties of this position, the employee is frequently/occasionally exposed to moving mechanical parts.
The employee is occasionally required to sit, climb, balance, stoop, kneel, crouch, or crawl.
The employee is frequently required to lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds.

PandoLogic. Keywords: Quality Control / Quality Assurance Manager, Location: Salt Lake City, UT - 84105

Dice Id: pandfeed
Position Id: 604618636
Posted 14 hours ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

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