Quality Custom Distribution Jobs in Usa

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Power Distribution and Make Ready Designer (Remote) (Roanoke)
✦ New
Salary not disclosed
Description:


Power Distribution and Make Ready Designer

Overhead Utility Pole Design • Joint-Use Engineering • NESC-Compliant Make-Ready Work


Location: Roanoke, VA (Remote)


Are you an experienced Power Distribution Designer or Make-Ready Designer looking to support meaningful utility engineering projects? Join a team that values accuracy, collaboration, and long-term professional growth.


ABOUT THIS OPPORTUNITY
We are seeking skilled Make-Ready Designers (primary focus) and Power Distribution Designers to support engineering programs for major electric and telecom utilities. Ideal candidates bring demonstrated experience in overhead utility pole design, NESC application, clearance assessment, pole loading analysis, and construction package development. Useful design platforms include DDS, Katapult, O-Calc, GIS, MicroStation, AutoCAD, or client-specific drafting systems.


In this role, you will review field/walkout data, evaluate existing attachment conditions, model pole loading, determine make-ready requirements, and prepare accurate construction-ready deliverables. Applicants without utility pole design or distribution engineering experience will not be considered.


Note: This position is remote, but new hires must attend a 2-week paid, in-person orientation at our Perrysburg, OH headquarters.


WHAT YOU WILL DO
• Execute overhead distribution and make-ready design work orders while meeting quality, time, and budget expectations
• Apply established engineering design standards, NESC requirements, and internal processes
• Perform end-to-end make-ready, joint-use, and/or general distribution design
• Conduct permitting and easement research (pole ownership, ROW, property rights, approvals)
• Collaborate with team members to resolve design challenges and ensure accurate deliverables
• Use design software such as AutoCAD, MicroStation, DDS, PoleForeman, O-Calc, Katapult, or client systems
• Perform quality control reviews when required
• Support additional duties as assigned


TOP COMPETENCIES & SKILLS
Make-Ready Engineering, Joint-Use Design, Pole Loading Analysis, Utility Pole Design, Overhead Distribution Design, NESC Compliance, Utility Engineering, Pole Attachments, Make-Ready Construction, Aerial Design, Utility Coordination, Right-of-Way Permitting, Pole Replacement Design, Make-Ready Estimates, Field Survey Interpretation, CAD for Utility Design, GIS for Utility Design, Electrical Distribution Design, Utility Construction Standards, Telecommunications Make-Ready



Requirements:


WHAT WE’RE LOOKING FOR
High school diploma or equivalent required; an associate degree or higher in engineering, drafting, or a related field is preferred
Minimum 2 years of experience in make-ready engineering, joint-use design, or electric power distribution design (3+ years strongly preferred)
• Proven experience in utility pole design, including NESC application, clearance analysis, pole loading concepts, and preparation of construction-ready design packages
Proficiency with CAD or MicroStation; experience with DDS, Katapult, O-Calc, or similar utility design platforms is strongly preferred
• Solid understanding of power distribution construction practices, with the ability to learn utility-specific proprietary systems efficiently
• Must hold a valid driver’s license, maintain active auto insurance, and pass all required background, drug, and MVR screenings
Authorization to work in the United States is required
• Willingness to travel occasionally, including minimal overnight travel when project needs require
• Ability to work a standard Monday–Friday schedule aligned to Eastern Time, with Central/Mountain/Pacific adjustments as appropriate


PHYSICAL REQUIREMENTS
• Ability to work for extended periods using a computer keyboard, monitor, and telephone
• Ability to prepare and analyze data, review detailed information, and work with design tools requiring close vision, distance vision, color vision, peripheral vision, depth perception, and focus adjustment
• Ability to communicate effectively through oral and written channels


ABOUT SIGMA TECHNOLOGIES
Sigma Technologies is a growing engineering and design firm with 500+ team members across 30+ states. For over 25 years, we’ve supported major power and telecommunications utilities with work that directly impacts communities nationwide. Our core values — Safety, Honesty, Truth, and Decency — shape how we work and who we hire. We are TeamSigma™.


*To learn more about working at Sigma, view our video and career page.
* If you do not have Power Design experience, please refer to our other open positions: *While Designer openings are listed in multiple locations, you only need to apply to one, as they are remote roles.


WHAT WE OFFER
We want our Associates to stay healthy, happy, and secure. We offer a positive work environment with supportive coworkers, managers, and leaders, plus:

No-cost monthly healthcare plan option for employees
Competitive pay
• Medical, dental, and vision plans with up to 80% of the premium sponsored by Sigma
401(k) plan with matching contributions up to 5% of salary
Paid holidays, vacation, and sick time
Education and professional licensing assistance programs


This job advertisement is intended to outline the primary responsibilities and requirements of the role. It is not all-inclusive. Additional duties may be assigned as needed. This ad does not constitute an employment agreement, and job requirements may change based on organizational needs.


Pay is commensurate with experience and education. Sigma is an equal opportunity employer and does not discriminate based on race, color, gender, sexual preference, gender identity, age, religion, national origin, disability, genetic information, veteran/military status, or any classification protected by law.


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Remote working/work at home options are available for this role.
temporary
Quality Safety Manager
Salary not disclosed
Griffith, IN 2 days ago

Quality Manager – Transportation & Logistics

Location: Griffith, IN (Hybrid / On-site preferred)


The Opportunity

A growing transportation company is seeking a proactive Quality Manager to lead the quality systems, security standards, and compliance roadmap. In this high-visibility role, you will bridge the gap between regulatory requirements and daily logistics, ensuring we meet the highest standards for our high-value freight customers.


Key Responsibilities

  • Lead QMS: Own, maintain, and optimize our Quality Management System (QMS).
  • Drive Compliance: Manage and achieve key industry certifications, including TAPA TSR-1, CTPAT, and FAST.
  • Incident Response: Lead root-cause analysis and CAPA for quality/security incidents.
  • Audit Management: Prepare for, support, and lead internal and external audits.
  • Collaboration: Partner with Safety, Operations, and Maintenance to enforce security controls and improve operational integrity.


What You Bring

  • Experience: 3+ years in quality, compliance, or logistics operations.
  • Technical Knowledge: Strong understanding of GDP/GxP, ISO 9001, and TAPA standards.
  • Regulatory Savvy: Familiarity with CTPAT, customs/security processes, and high-value shipment handling.
  • Soft Skills: Proven ability to manage documentation, lead audits, and communicate clearly under pressure.
Not Specified
Quality Control Associate
Salary not disclosed
Fremont, CA 2 days ago

Duties:

  • Primary responsibility is to execute routine Microbiology/Environmental monitoring, Raw Materials testing of bulk drug substance and drug product in a multi-product facility.
  • Executes Raw Material sampling, Microbiological compendial testing and sampling of clean rooms (as applicable).
  • Proficiency in 1-3 analytical methodologies.
  • Performs technical and quality review of data.
  • Responsible for routine lab maintenance work and quality and compliance activities.
  • Performs duties under supervision and according to standard operating and QC procedures.
  • Ensures that all data is organized and archived per appropriate workflows and SOPs.
  • Works with GMP and non-GMP databases to ensure all samples are received, logged, stored, distributed and tracked within defined timelines.
  • Interacts with Sample Management, QC laboratories and Raw Materials groups to prioritize samples, cross checks SOPs and protocols to ensure all samples have been received and distributed, troubleshoots discrepancies, and relays information back to line management to ensure all samples are tested per appropriate testing schedule.
  • Coordinates shipment of samples to contract labs and other testing site.
  • Maintain sampling and testing paper records, equipment logs and other controlled documentation.
  • Ensure accuracy and completeness of sampling and testing in LIMS system and/or test records.
  • Maintain cleanliness and orderliness of the labs.
  • Perform QC-related data entry.
  • Provides assistance to other group members as needed.
  • Responsible for transferring samples from cleanrooms to the labs.
  • Familiar with clean room gowning.


Skills:

  • 1-3 years of GMP lab and/or clean room experience.
  • Gowning and Aseptic techniques.
  • Pipetting skills.
  • Must be willing to work all shifts including weekend support if needed but primary work hours are during five days a week.


Education:

  • Bachelor’s Degree in a Scientific Discipline, preferably in Microbiology
Not Specified
Quality Assurance Quality Control Inspector
Salary not disclosed
Houston, TX 2 days ago

Quality Inspector

Overview

Join our client’s team as a QA/QC Inspector supporting a variety of construction projects. In this hands-on role, you will inspect installations, ensure compliance with project specifications, and maintain high-quality standards across electrical, civil, and structural work.


Why Work Here

  • Great company culture and atmosphere
  • Room to grow and learn


Key Responsibilities

  • Perform QA/QC inspections on assemblies, installations, and equipment
  • Implement project-specific Quality Plans and Inspection/Test Plans (ITPs)
  • Identify, document, and track deficiencies and corrective actions
  • Coordinate with Materials Management on non-conforming or damaged materials
  • Maintain Master Punch Lists and assemble QA/QC documentation packages
  • Inspect site preparation, foundations, concrete, structural steel, electrical cabling, substation/BESS equipment, and control buildings


Requirements & Qualifications

  • Post-secondary education in a related field
  • 3+ years of experience in Construction QA/QC or related construction roles
  • Strong technical document interpretation skills
  • Valid driver’s license and ability to travel to field sites


Preferred Skills

  • Power systems experience (Substations, BESS, Transmission, Distribution)
  • Civil, structural, and electrical installation experience
  • Knowledge of concrete, piling, and earthworks
  • Familiarity with Bluebeam Revu or Procore
  • Trade certification or professional designation (preferred)
Not Specified
Quality Technician Supervisor (2233)
Salary not disclosed
Milwaukee, WI 6 days ago

Job Summary



Under the direction of the Quality Assurance Lab Supervisor, the Quality Technician Supervisor is responsible for overseeing day-to-day quality control activities and leading the technician team to ensure that all quality processes run smoothly. This position handles escalated quality issues, coordinates team schedules, supports training and development, ensures proper execution of quality processes, oversees team performance, and maintains compliance with established quality standards. The Lead also provides backup coverage for technical and administrative quality functions and plays a key role in fostering a culture of continuous improvement. This will be achieved while maintaining HellermannTyton's Quality and EHS certifications by supporting all corporate policies, procedures, work instructions and required documentation.



Essential Functions





  • Effectively manage outgoing and incoming shift transitions to understand any quality event escalations and maintain seamless Quality support across all shifts.

  • Lead shift meetings, communicate quality event escalations, hold tickets, and provide common quality focus across all shifts.

  • Set team priorities and assignments to align with priorities, production needs, and quality goals.

  • Work with the production team to develop a bench of qualified candidates to address daily staff shortages and maintain the designated staffing levels.

  • Monitor and approve escalation activities associated with Back Tracking, Red Stamp, and Hold Ticket processes to confirm the proper execution of the associated processes.

  • Support escalated quality concerns and coordinate with production and engineering for resolution.

  • Develop and manage employee schedules to ensure appropriate quality coverage to support production, including any necessary overtime.

  • Train new quality team members, provide necessary records, and support their ongoing development.

  • Continually monitor team performance, conduct process audits, reinforce good performance, identify opportunities for improvement, and support any necessary disciplinary actions.

  • Investigate escalated accountability concerns, determine the cause of the escalation, and work with team to provide actions / follow-up to resolve the issue.

  • Handle any employee relations concerns prior to the need for escalation.



Other Functions





  • Perform and/or supervise Hold Ticket, Backtracking, and Deviations processes

  • Support the "Red Bin" meeting, disposition decisions, and follow-up as needed

  • Perform "Red Stamp" reviews to confirm decision making and proper execution

  • Support the quality element of the daily huddle meeting as needed

  • Complete material certifications when needed



Success in this role will require





  • Proficient in MES, SQC PAC, and JDE systems.

  • Strong computer skills, including Microsoft Word and Excel.

  • Ability to read and interpret engineering drawings and blueprints.

  • Excellent communication and interpersonal skills for cross-functional coordination.

  • Highly organized, with strong recordkeeping and prioritization skills.

  • Strong math skills and high attention to detail.

  • Able to operate lab equipment and interpret testing results.

  • Demonstrated leadership ability with mentoring experience preferred.



What You'll Bring





  • Qualifications (skills, knowledge, experience)

  • High school diploma or equivalency, required.

  • 4+ years of experience in a quality assurance role in manufacturing or related industry.

  • Leadership or team coordination experience strongly preferred.

  • Must be able to lift, push, and pull up to 50 lbs.

  • Good vision and color identification required for inspections.

  • Ability to work non-standard hours and respond to shift demands.

  • Must be able to stand for 6-8 hours per shift.



Rev. 1.9.2026



COMP - 0003176

Not Specified
Senior Director of Quality Systems
✦ New
Salary not disclosed
Northfield 1 day ago
Job Summary Provides enterprise leadership for a central quality support organization that partners with multiple manufacturing locations to resolve complex quality and compliance issues, lead systematic remediation, CAPA execution, and strengthen manufacturing quality systems and processes.

This role is accountable for rapid, compliant problem resolution across sites while also driving longer-term capability building, standardization, and quality system maturity.

Manage people, projects, and priorities to address resource and operational challenges.

Direct and manage sites during FDA inspections and responses to observations.

Liaison with site operation management providing input and support to ensure Quality and Compliance requirements are being met.

Partners cross-functionally with manufacturing, engineering, regulatory, operations, corporate quality, to increase regulatory compliance.

Support Quality Systems related activities, analyze problems related to quality/regulatory information, and provide process structure and technical support in solving these problems.

Provide expertise, counsel and guidance to Quality leadership.

Manage the Quality data integrity for Medline products including but not limited to, sterile products, medical devices, pharmaceuticals, biologics, cosmetics, medical foods, and dietary supplements.

Job Description MAJOR RESPONSIBILITIES Lead personnel, activities, and resources for continuous Quality System improvement.

Motivate and engage the team and others around the operational excellence vision and ensure execution.

Advises leadership to ensure the QMS for assigned departments are in compliance as measured by FDA/ISO/internal audits.

Collaborate with cross-functional teams to deploy quality processes and systems.

Consult and provide guidance to business partners.

Partners with other applicable leaders to ensure a strategic approach to any regulatory audit and related responses.

Partners with other applicable leaders to ensure a strategic approach to any regulatory audit and related responses Prepare and deliver Customer presentations Oversee critical Quality systems projects and team that identify, lead and drive opportunities to improve quality systems and develop long-term strategies that support the success of the business.

Review and determine the application of various system compliance regulations.

Ensure compliance to global regulatory requirements with internal procedures.

Identify risk and compliance opportunities.

Train and coach personnel and cross-functional teams to deliver optimal results.

Management responsibilities include: Typically manages through multiple Managers Provide leadership and management to one or more major departments of an operating unit or to a department that has systemwide accountability Strategic, tactical and operational planning (12 + months) for the function or department Direct budgetary responsibility for one or more departments, functions or major projects/programs Interpret and execute policies for departments/projects; develop, recommend and implement new policies or modifications to existing policies Hiring staff, recommending pay increases, performing performance reviews, training and development of staff, estimating personnel needs, assigning work, meeting completion dates, interpreting and ensuring consistent application of organizational policies MINIMUM JOB REQUIREMENTS Education Bachelor’s degree in technical or scientific discipline Work Experience Knowledge of Food and Drug Administration (FDA), Quality System Regulations (QSR) and International Organization of Standardization (ISO).

Proficiency in Microsoft Suite.

Position requires travel up to 20% of the time for business purposes (within state and out of state).

Knowledge / Skills / Abilities Job Title: Sr Dir Quality Systems Job Code: 62398 MINIMUM JOB REQUIREMENTS Experience leading people and cross functional teams through quality change and continuous improvement.

Experience hosting FDA/ISO GMP inspections and regulatory meetings.

Experience writing, reviewing, and managing FDA responses Experience with quality systems development and implementation.

Experience with Medical Device Design Controls, CE technical File Requirements, and 510K submissions.

Experience in the Medical Device, Pharmaceutical industry, cosmetic, combination product industry.

Experience hosting FDA/ISO GMP inspections.

Proficiency in analyzing and reporting data to identify issues, trends, or exceptions to drive improvement of results and find solutions.

Demonstrated ability to control and coordinate team priorities, concurrent projects, competing priorities and critical deadlines.

Position requires travel up to 25% of the time for business purposes (within state, out of state and/or internationally).

PREFERRED JOB REQUIREMENTS Work Experience 8 years or more of managerial experience preferred.

10 years or more of related experience in Medical Device, Pharmaceutical, Food, Cosmetic, or Personal Products industries preferred.

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position: $203,000.00
- $305,000.00 Annual The actual salary will vary based on applicant’s location, education, experience, skills, and abilities.

This role is bonus and/or incentive eligible.

Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average.

For a more comprehensive list of our benefits please click here .

For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

We’re dedicated to creating a Medline where everyone feels they belong and can grow their career.

We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best.

Explore our Belonging page here .

Medline Industries, LP is an equal opportunity employer.

Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.
Not Specified
Quality Engineer I, Quality Ops (Wayne, NJ)
🏢 Getinge
Salary not disclosed
Wayne, NJ 4 days ago


With a passion for life



Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.



Are you looking for an inspiring career? You just found it.



Job Overview


The Quality Engineer I Quality Operations specializes in Quality Operations, and is responsible for overseeing and improving the quality of manufacturing processes, ensuring compliance with regulatory requirements, and driving continuous improvement initiatives to enhance product quality and customer satisfaction. You will play a key role in ensuring that our manufacturing operations meet the highest standards of quality and efficiency while adhering to relevant regulations and industry best practices.



Job Responsibilities and Essential Duties



  • Develop, implement, and maintain quality control processes and procedures for manufacturing operations to ensure compliance with regulatory requirements and industry standards.
  • Establish and monitor key performance indicators (KPIs) to assess manufacturing quality and identify opportunities for improvement.
  • Participate/ Lead validation and verification activities for manufacturing processes, equipment, and software systems to ensure they meet quality and regulatory requirements.
  • Develop/ review validation protocols, execute validation studies, and analyze data to ensure process robustness and reliability.
  • Ensures through Design Transfer activities the Device Master Records (DMRs) contents are developed, controlled, and maintained leading to Risk based Manufacturing Control Plans.
  • Support/ Investigate and resolve Out of Tolerance events identified during equipment/ instrument calibrations.
  • Investigate product nonconformances, conduct root cause analysis, and implement corrective and preventive actions (CAPA).
  • Track and monitor CAPA effectiveness to ensure issues are resolved and prevented.
  • Support the Health and Hazard Evaluation process by gathering required data and performing in-depth analysis prior to sharing the information with the Field Action Committee.
  • Implement corrective and preventive actions (CAPAs) to address root causes and prevent recurrence of quality issues.
  • Facilitate risk management activities related to manufacturing processes, identifying, and mitigating risks to product quality, safety, and efficacy.
  • Implement risk-based decision-making processes to prioritize quality activities and allocate resources effectively.
  • Lead and support continuous improvement projects aimed at enhancing manufacturing processes, reducing defects, and optimizing productivity.
  • Utilize quality tools and methodologies, such as Six Sigma, Lean Manufacturing, and Statistical Process Control (SPC), to drive process optimization and waste reduction.
  • Ensure compliance with applicable regulations, including FDA Quality System Regulation (QSR), ISO 13485, and other international standards.
  • Support both internal and external audits as an SME for Production & Process Controls and presents records of activities related to Design Transfer for New Product Development and Design Changes.


Minimum Requirements



  • Bachelor's degree in engineering, Science, or other related field is required.
  • Six Sigma Green Belt or other applicable certifications are a plus.
  • Minimum 1 year experience in Quality or Engineering.
  • Experience in a medical device or pharmaceutical industry.
  • Experience with Class III disposable and/or Electro-Mechanical medical devices is preferred.
  • Knowledge and understanding of the US Food and Drug Administration (FDA) 21 CFR 820, ISO 13485, ISO 14971, EU MDD, and EU MDR. Knowledgeable on specific requirements for Design Controls and Risk Management is preferred.
  • Knowledge of application & selection of Sampling Plans, to support Risk based Manufacturing Controls Plans.
  • Project management and leadership experience is desirable.
  • Knowledge of Microsoft Office Products such as Word, Excel, or equivalent software applications.


Required Knowledge, Skills and Abilities



  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.
  • Proficiency in quality tools and methodologies (e.g., Six Sigma, FMEA, Gage R&R).
  • Ability to work effectively in a cross-functional team environment.
  • Ability to review and understand technical standards and their requirements for products.
  • Lead improvement initiatives, either independently or as part of cross-functional teams

The base salary for this the position is a minimum salary of $87,000 and a maximum of $90,000 with 8% annual bonus



About us



With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.



Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

Not Specified
Senior Vice President, Quality and Safety
Salary not disclosed
Buffalo, NY 2 days ago
Job Description & Requirements

Senior Vice President, Quality and Safety

StartDate: ASAP

Senior Vice President, Quality and Safety

Catholic Health

Buffalo, NY

The Opportunity

Catholic Health, an integrated health system in Buffalo, New York, announces an exceptional opportunity for an accomplished nurse leader to serve as its Senior Vice President, Quality and Safety.

Reporting directly to the Executive Vice President, Chief Nursing Officer, the SVP Quality and Safety is responsible for the overall management of an experienced broad-based team charged with monitoring, reporting, educating and inspiring devotion to excelling in internal and external quality metrics for the entire enterprise with the goal of attaining and sustaining top decile performance. The SVP serves as the system liaison and senior executive for all Quality and Patient Safety collaborative initiatives with the acute care hospitals, service lines, continuing care division and homecare ministries to promote integration and alignment in an effort to improve the quality and safety outcomes across the continuum, thereby improving the patient's overall experience.

The SVP will provide leadership and guidance for the executive leaders' education and development and lead the efforts for quality improvement education, training and coaching of all Catholic Health staff. The SVP will be responsible for establishing a strategic framework for achieving the institution's goals with relation to medical care quality, education quality, research quality and patient safety. Additionally, the SVP will play a critical role in system and Catholic Medical Partners initiatives regarding population health management, quality improvement, clinical practice standardization. The SVP will also foster a culture of safety, champion high reliability and the magnet journey in addition to other cross functional activities.

The Ideal Candidate:

- A master's degree with clinical major required.
- Current registration with the New York State Education Department as a Registered Professional Nurse or ability to quickly obtain will be required.
- Minimum of 10 years of progressive quality and safety management experience in an acute care setting.
- Experience in an academic medical center and/or progressive health system of significant size and complexity preferred.
- Experience establishing and monitoring appropriate process and outcome measures for key initiatives using a systems perspective; evaluating the processes by which clinical care and patient services are delivered.
- Experience working with informatics, metrics, and performance improvement.
- Demonstrated change management skills in a complex environment.
- An inspirational leader that motivated colleagues and staff throughout the organization by clearly articulating a compelling vision for the future, making courageous decisions, following through with commitments, and demonstrating an unrelenting passion for CH mission and performance.
- Experience with tracking, reporting, and improving key quality and safety metrics.
- Experience with Lean Six Sigma methodologies.

The Organization

Catholic Health ("the System"), based in Buffalo, New York, is one of upstate New York's leading and largest integrated health care systems. The System serves a population of approximately 1.5M people in Erie County, New York, and neighboring counties. With more than 9,000 employees, a 1,600-member medical staff, and net patient service revenue of more than $1.1B, this dynamic health care system provides a comprehensive network of high quality advanced medical care, primary care, post-acute care, and senior services. These programs and services are provided across four member hospitals, multiple ambulatory care sites, four skilled nursing facilities, three home care agencies, a PACE (Program of All-inclusive Care for the Elderly) program, and community-based behavioral health services spanning 74 access points across the full continuum of care.

The Location

Buffalo, New York is located on the eastern side of Lake Erie near Niagara Falls and the Canadian border. As the second-largest city in New York State, Buffalo has more than one million people living in its metropolitan area. Coined the nickname "The City of Good Neighbors," Buffalo is notorious for its friendly residents and welcoming sense of community. With its growing population and diverse culture, it is understandable how Buffalo has become such a desirable location for young professionals and families.

Considered to be one of the best places to live in New York, many people are moving to Buffalo for its affordability, education opportunities, and employment options. Providing its residents with a mixture of urban and suburban living, Buffalo knows how to blend big-city perks with all the conveniences of suburban life.

Compensation Range: The base salary range for this position is $275,000 to $300,000 annually. In addition, a leader may be eligible for other benefits, including but not limited to health insurance coverage, retirement benefits, and bonuses. The total compensation for the finalist selected for this role will be determined based on various factors, including but not limited to scope of role, level of experience, education, accomplishments, internal equity, budget, and subject to Fair Market Value evaluation. The base salary range listed above is a good faith determination of potential base compensation at the time of this job advertisement and may be modified in the future.

Nominations are greatly appreciated and may be sent to:

Rachael Burns, Vice President

Ellen Lockhart, MD, Principal

Heather Van Hecke, Consultant

Physician and Leadership Solutions - Executive Search

AMN Healthcare

#BESRecruitment

#LI-HV3

Facility Location
Nestled on the banks of Lake Erie and at the southern end of the Niagara River, Buffalo is New York's second largest city right behind the Big Apple. Cultures blend in this waterfront city known for its culinary delights and friendly inhabitants who welcome newcomers with open arms. Discover the unique urban and historical neighborhoods that add to the city's charm and character, or spend some time relaxing at one of the 20 parks found around town.

Job Benefits

About the Company

At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable.

Quality, Quality Services, Performance Improvement, Performance Management, Clinical Effectiveness, Accreditation, Outcomes Management, Regulatory Compliance
Not Specified
Manager of Quality Assurance
Salary not disclosed
Houston, TX 2 days ago
GENERAL SUMMARY

The Manager of Quality Assurance is responsible for overseeing the Quality Department to ensure compliance with ISO 9001 standards and company quality objectives. This role manages quality staff, supports manufacturing operations, and drives continuous improvement initiatives. Key responsibilities include maintaining quality systems, leading audits, supporting new product introductions, managing corrective actions, and monitoring supplier performance. The Manager of Quality Assurance also develops training and reports on quality metrics, and manages departmental resources to improve product quality, customer satisfaction, and overall business performance. This is a working manager role requiring the incumbent to both lead the quality function and directly perform hands-on quality engineering and assurance activities as the business needs dictate.

PRINCIPAL DUTIES AND RESPONSIBILITIES (ESSENTIAL FUNCTIONS)

  • Manage the quality department, directing the work of quality technicians to satisfy the quality requirements for the current business and future business improvement.
  • Develop and execute annual quality goals and objectives that align with overall company goals and long-range strategy plans.
  • Assure that the Quality System is active and the ISO 9001 registration is maintained with minimal audit findings. This includes the many aspects including management reviews, internal audits, risk assessment and those outlined below.
  • Provide technical support to manufacturing through the Quality Team.
  • Participate in any new product introduction or product change projects, assuring that all requisite quality characteristics and requirements are met.
  • Maintain accurate calibration of all measuring instruments and any tools that require such calibration.
  • Actively direct the corrective action system for customer complaints/returns, internal processes as well as purchased product and material.
  • Work with Mfg. Engineering and Maintenance; develop and guide documented evidence of machine and process capability.
  • Develop training and education for the business in key aspects of quality, including the quality department and new hires.
  • Lead Receiving Inspection and assist in driving the Supplier Quality Program to improve overall Supplier performance.
  • Provide management with measurements of our product, process and customer/supplier quality and recommendations for both remedial as well as preventive measures to be taken with alternatives, costs, resources, timing and risk and benefit analysis.
  • As part of business planning, lead the development of quality plans and improvement plans that have a positive impact on the overall cost of quality.
  • Manage resources, including budgets, expense recommendations and capital appropriations to ensure effectiveness of the quality system and improve overall gross margins.


EDUCATION AND EXPERIENCE


  • A bachelor's degree in quality or an engineering discipline.
  • 10 years of pertinent experience in a manufacturing-based business.


KNOWLEDGE, SKILLS AND ABILITIES


  • Knowledge of quality methods, tools and instruments.
  • Strong background with ISO 9000 quality system requirements.
  • Strong problem solving skills.
  • Ability to develop and implement training for part measurement/inspection, quality systems and TQM methods.
  • Excellent communication skills.
  • Computer skills including Microsoft Word, Excel, Power Point at a minimum.
  • General knowledge of safety and environmental requirements in a manufacturing environment.


PHYSICAL DEMANDS


  • Physical demands are typical of an office position including extended periods of sitting, extensive use of a personal computer and telephone.
  • Position requires movement around the facilities.
  • Occasional handling of material and components


WORKING CONDITIONS

Normal manufacturing and office environment. When working occasionally in some shop areas, personal protection equipment (PPE) will be recommended and/or required (safety shoes, safety glasses w/side shields, hearing protection, face shield, gloves, apron and boots). Must have the ability to support extended business hours to meet customer business needs.

DISCLAIMER

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

QUALITY

Quality encompasses all aspects of DeZURIK, Inc.'s business, and every team member shares the responsibility to prevent the occurrence of any nonconformity relating to product, process, and the quality system. All team members have an obligation to identify and record any such nonconformity, and, through designated channels, initiate and recommend solutions.

SALARY AND BENEFITS

DeZURIK offers a competitive base salary in the $98,221 to $122,776 range, based on experience and qualifications, along with annual bonus opportunities tied to performance.

Beyond pay, our market-leading benefits are designed to support your wellbeing. These include medical, dental, vision, and life insurance, as well as short- and long-term disability coverage. DeZURIK also provides a health savings account with company match, a retirement plan for employer contributions through Vanguard, and access to the Granite Assistance Fund for support when it's needed most. We value time for rest and personal growth, offering generous paid time off, including volunteer time off and paid holidays.

Please note: Sponsorship is not available for this role.

#LI-JW1
Not Specified
Director Quality Engineering
Salary not disclosed
Lexington, KY 2 days ago

It All Starts with Our People

As the leader in automotive preventive maintenance, Valvoline has a proven track record of growth. We continue to invest in our people, processes, and technology to strengthen our ability to efficiently deliver Quick, Easy, Trusted service across all our stores – every day. We're not just in the car business; we're in the people business. And we're looking for humble, hungry, and smart people to help us shape the future of mobility. If you're hungry to drive change and seek a dynamic, collaborative environment that fuels both personal and professional growth, you've found your place with us.

Our highest priority is creating a welcoming workplace with team members from a wide variety of diverse backgrounds and experiences.


How You'll Make a Difference

Valvoline has a rewarding opportunity as a Director, Quality Engineering. In this role, you’ll be a strategic and hands-on leader who will drive the transformation of quality across our technology organization. This leader will be responsible for building and scaling a modern Quality Engineering function that goes beyond traditional QA, with ownership spanning QA environments, test automation, AI-enabled quality practices, quality governance, best practices, and the establishment of a Quality Engineering Center of Excellence (COE).


The ideal candidate will bring a strong blend of leadership, technical depth, operating model design, and change management, with the ability to embed quality throughout the software development lifecycle. This role will partner closely with Engineering, Product, Architecture, Infrastructure, Security, and Delivery teams to create a scalable, efficient, and forward-looking quality strategy that supports speed, reliability, and business growth.


Key Responsibilities


Quality Engineering Strategy & Leadership

  • Define and lead the enterprise Quality Engineering vision, strategy, and roadmap aligned to Valvoline’s broader technology and business priorities.
  • Shift the organization from traditional testing approaches to a modern quality engineering model focused on prevention, automation, continuous validation, and measurable quality outcomes.
  • Establish quality as a shared responsibility across product, engineering, and delivery teams while maintaining strong governance and standards.
  • Lead, mentor, and grow a high-performing team of quality engineers, automation engineers, and QA leaders.


QA Center of Excellence (COE)

  • Build and operationalize a Quality Engineering Center of Excellence (COE) to define frameworks, standards, tooling, reusable assets, and governance processes.
  • Create enterprise-wide best practices for test design, automation, environment strategy, defect management, release readiness, and quality metrics.
  • Standardize quality processes across portfolios while allowing for flexibility based on product and platform needs.
  • Develop playbooks, templates, training, and maturity models to improve quality capability across teams.


Automation & Tooling

  • Define and execute an enterprise test automation strategy across UI, API, integration, data, regression, performance, and end-to-end testing.
  • Drive adoption of scalable automation frameworks and ensure integration with CI/CD pipelines and DevOps practices.
  • Evaluate, select, and optimize quality tools and platforms to improve speed, coverage, traceability, and reporting.
  • Increase automation efficiency and effectiveness by implementing reusable components, common libraries, and engineering best practices.


AI-Enabled Quality Engineering

  • Lead the adoption of AI and intelligent automation within quality engineering, including opportunities such as:

test case generation

intelligent defect triage

predictive risk analysis

self-healing automation

release quality insights

test optimization and prioritization

  • Assess emerging AI capabilities and define practical use cases that improve quality outcomes, team productivity, and speed to market.
  • Partner with engineering and architecture leaders to ensure AI solutions are implemented responsibly, securely, and at scale.


QA Environments & Test Data Management

  • Own the strategy for QA environments, including environment planning, availability, stability, governance, and optimization.
  • Partner with infrastructure and platform teams to improve environment readiness, reduce bottlenecks, and support parallel delivery.
  • Establish strong processes for test data management, environment provisioning, and integration dependency coordination.
  • Drive improvements in environment monitoring and readiness reporting to reduce delays and improve release confidence.


Governance, Metrics & Best Practices

  • Define and implement quality KPIs, SLAs, dashboards, and scorecards to provide visibility into quality performance, automation maturity, defect trends, release risk, and environment health.
  • Set standards for quality gates, entry/exit criteria, defect leakage reduction, root cause analysis, and continuous improvement.
  • Build a culture of measurable quality and operational discipline through governance routines, audits, and executive reporting.
  • Ensure best practices are embedded into agile delivery, DevSecOps, and release management processes.


Sourcing & Vendor Management

  • Define the sourcing strategy for quality engineering capabilities, including the right balance of internal talent, strategic partners, and offshore/onshore vendor models.
  • Lead vendor evaluation, selection, governance, and performance management related to quality engineering and testing services.
  • Optimize spend, capability, and service quality across external partners while ensuring alignment to Valvoline standards and delivery expectations.
  • Build workforce strategies that support both immediate delivery needs and long-term capability development.


Cross-Functional Partnership

  • Partner with Product, Engineering, Infrastructure, Security, Architecture, and PMO leaders to embed quality into planning, design, development, and release processes.
  • Influence senior stakeholders on quality investments, transformation priorities, and operating model improvements.
  • Support mission-critical initiatives by ensuring strong quality planning, risk management, and execution.


What You’ll Need to Succeed

Qualifications

  • 10+ years in software quality engineering
  • 5+ years leading enterprise QA teams
  • Experience in high-volume retail, omnichannel, or consumer-facing environments strongly preferred
  • Deep experience with:

Automation frameworks (Selenium, Cypress, Playwright, etc.)

API testing tools

CI/CD tools

Performance testing tools (JMeter, LoadRunner, etc.)

  • Experience leading QA in Agile/SAFe or hybrid environments
  • Experience using agentic tools for test development and integrating work with agentic code development (ie: Github Copilot, Claude code)
  • Proven track record reducing defect escape rates


Leadership Competencies

  • Enterprise systems thinker
  • Data-driven decision maker
  • Builder of scalable processes
  • Collaborative but boundary-setting partner
  • Comfortable operating in fast-paced retail cycles
  • Must be authorized to work in the U.S.


We Take Care of the WHOLE You

  • Health insurance plans (medical, dental, vision)
  • HSA and flexible spending accounts
  • 401(k)
  • Incentive opportunity*
  • Life insurance
  • Short and long-term disability insurance
  • Paid vacation and holidays*
  • Employee Assistance Program
  • Valvoline Instant Oil Change discounts
  • Tuition reimbursement*
  • Adoption assistance*

*Terms and conditions apply, and benefits may differ depending on position.


Your Path to Valvoline

Valvoline provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.


Join us in revolutionizing the automotive aftermarket industry while enjoying competitive benefits, a supportive work culture, and opportunities for advancement. Apply now and become an integral part of our journey at Valvoline.


The Company endeavors to make its recruitment process accessible to any and all users. Reasonable accommodations will be provided upon request to applicants with disabilities to facilitate equal opportunity throughout the recruitment and selection process. Please contact Human Resources at 1.833.VVV.Report or email to make a request for reasonable accommodation during any aspect of the recruitment and selection process. The contact information is for accommodation requests only; do not use this contact information to inquire about the status of applications.

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