4,899 Production Quality jobs in the United States

Production Quality Control 2nd Shift
Adecco is now hiring for one of the largest technology companies, and this is your chance to work with them in Ventura County!
Responsibilities:
· Visually inspect products throughout the stages of production to identify defective parts, component orientation errors, missing components, or wrong part insertion.
· Initial testing for product conformity.
· Assist others to provide an organized and clean workplace including: all areas of the plant, workstations, equipment, walkways, and break rooms using 5S procedures.
· Participation in and implementation of continuous improvement projects.
· Safely and efficiently meeting all production work requirements assigned to you by following operating procedures and work instructions.
· To produce the highest standard of quality products possible in accordance with the company's ISO 9001:2015 procedures.
· Other duties as assigned.
· Must adhere to all the company's safety requirements.
Perks:
· Weekly pay starting at $20 per hour.
· Competitive benefit options, after 1 week - medical, dental, and vision, options available
· FREE upskilling opportunities through the Aspire Academy
Our Aspire Academy offers 20+ online courses designed to help Adecco candidates and associates gain skills to take their careers to the next level - at your own pace. The mobile-friendly website is 100% FREE to access and has a dedicated support center to help YOU succeed. See how we can help you learn the fundamental, leadership, and/or industry-specific skills you need to secure a better future: Minimum 1-2 years experience in working in a manufacturing or industrial setting.
· Strong communication and reading skills.
· Possess strong organizational skills, a positive attitude and the ability to work well as a team.
· Ability to read and comprehend written instructions, as well as, comprehend verbal instructions and effectively communicate verbally.
· Strong computer skills
· Ability to self-start yet take orders as directed.
· Ability to move and lift up to 25 pounds. Ability to sit or stand as required to perform essential functions.
· Must be available to work assigned shifts and required overtime.
· **Clean room experience is a plus**
Shifts Available:
Shifts are available from **Monday - Friday, 2:00 pm - 10:30 pm with some overtime**
Click on Apply Now to be considered for this Assembler 2nd shift position in Ventura County or any related opportunities with Adecco
**Pay Details:** $20.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

** BR**
**Job Title:**
Meat Production Quality Control Supervisor
**Location:**
Performance Middendorf (0700)
**Job Description:**
**We Deliver the Goods:**
+ Competitive pay and benefits, including Day 1 Health & Wellness Benefits, Employee Stock Purchase Plan, 401K Employer Matching, Education Assistance, Paid Time Off, and much more
+ Growth opportunities performing essential work to support America's food distribution system
+ Safe and inclusive working environment, including culture of rewards, recognition, and respect
**Position Summary:**
Supervises, plans, coordinates and directs quality control program designed to ensure food safety consistent with established company and regulatory standards. Functions as a team member within the department and organization, as required, and performs any duty assigned to best serve the company
**Position Responsibilities:**
+ Supervise associates to include, but not limited to: staffing, training, coaching, performance management and problem resolution
+ Manage and control an effective quality assurance program
+ Assist with the monthly self-audit of the operation to determine the level of compliance with the good manufacturing practices (GMP), Hazard Analysis and Critical Control Point (HACCP), and company policies relating to food safety.
+ Manage and control effective quality assurance/food safety procedures and practices.
+ Ensure overall compliance with government food regulatory agencies and other applicable regulations, including state-specific regulatory programs
+ Manage and update the Food Safety Plan/ SQF program to ensure compliance with the most recent SQF standards
+ Prepare the facility to successfully achieve and maintain SQF Status
+ Performs other related duties as assigned.
**Req Number:**
BR
**Address Line 1:**
8600 Springdale Avenue
**Job Location:**
St Louis, Missouri (MO)
**Shift:**
1st Shift
**Full Time / Part Time:**
Full Time
**EEO Statement:**
Performance Food Group and/or its subsidiaries (individually or collectively, the "Company") provides equal employment opportunity (EEO) to all applicants and employees, regardless of race, color, national origin, sex, marital status, pregnancy, sexual orientation, gender identity, religion, age, disability, genetic information, veteran status, and any other characteristic protected by applicable local, state and federal laws and regulations. Please click on the following links to review: (1) our EEO Policy ( ; (2) the "EEO is the Law" poster ( and supplement ( ; and (3) the Pay Transparency Policy Statement ( .
**Required Qualifications:**
High School Diploma/GED or Equivalent Experience
1 - 3 Years
Quality control within foodservice industry and related regulatory compliance laws.
**Division:**
Performance Foodservice
**Job Category:**
Operations
**Preferred Qualifications:**
Bachelors
Food Science, Microbiology, Dairy Science, Chemistry, Biology or related area
3 - 5 Years
Quality control / management and supervisory experience
within foodservice industry.
**State:**
Missouri
**Company Description:**
Performance Foodservice, PFG's broadline distributor, maintains a unique relationship with a variety of local customers, including independent restaurants and hotels, healthcare facilities, schools, and quick-service eateries. A team of sales reps, chefs, consultants, and other experts builds close relationships with customers - providing advice on improving operations, menu development, product selection, and operational strategies. The Performance team delivers delicious food but also goes above and beyond to help independent restaurant owners achieve their dreams.
**Benefits:**
Click Here for Benefits Information (

Our client is seeking a meticulous and experienced Production Quality Control Manager to lead their quality assurance efforts in a fully remote capacity. This role is essential for ensuring that all manufactured products meet stringent quality standards and customer expectations. You will be responsible for developing, implementing, and maintaining comprehensive quality control systems and processes, driving continuous improvement in product quality and manufacturing consistency, all while working remotely.

Responsibilities:

• Develop, implement, and maintain a robust Quality Management System (QMS) in accordance with relevant industry standards (e.g., ISO 9001).
• Establish and monitor key quality metrics (KPIs) and performance indicators for production processes.
• Oversee incoming material inspection, in-process quality checks, and final product testing procedures.
• Lead the root cause analysis of quality defects and implement effective corrective and preventive actions (CAPA).
• Develop and execute quality control plans for new product introductions and process changes.
• Train and mentor quality control personnel and production staff on quality standards and procedures.
• Conduct internal audits of manufacturing processes and systems to ensure compliance and identify areas for improvement.
• Manage non-conforming product disposition and maintain relevant documentation.
• Collaborate with R&D, Engineering, and Production teams to resolve quality issues and enhance product reliability.
• Stay current with regulatory requirements and industry best practices related to quality control.
• Utilize statistical tools and techniques for data analysis, process capability studies, and trend monitoring.
• Manage external supplier quality through audits and performance evaluations.
• Develop and maintain all necessary quality documentation, including procedures, work instructions, and records.
• Drive a culture of quality excellence throughout the organization.
• Effectively communicate quality status, risks, and improvement initiatives to management and cross-functional teams.

Qualifications:

• Bachelor's degree in Engineering (e.g., Industrial, Mechanical, Manufacturing), Quality Management, or a related field; advanced degree preferred.
• Minimum of 7 years of experience in quality control and assurance within a manufacturing environment.
• Proven experience in developing and implementing Quality Management Systems (QMS).
• In-depth knowledge of ISO 9001 standards and other relevant quality certifications.
• Proficiency in statistical analysis software (e.g., Minitab) and quality tools (e.g., FMEA, SPC, root cause analysis).
• Strong understanding of manufacturing processes and their impact on product quality.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional leadership, communication, and interpersonal abilities, particularly for remote team management.
• Ability to work independently, manage multiple priorities, and maintain high attention to detail in a remote setting.
• Experience with Lean Manufacturing and Six Sigma methodologies is highly desirable.
• Professional certification (e.g., ASQ Certified Quality Engineer, Certified Quality Manager) is a significant asset.
• Experience with supplier quality management.
• Commitment to continuous improvement and driving quality initiatives.

This remote position offers a pivotal role in shaping product quality and ensuring customer satisfaction for a growing manufacturing company.

**Production Quality Lead - Drive Excellence in Manufacturing!**
Chula Vista, San Diego, CA
PDS Tech Commercial | Honeywell
PDS Tech Commercial is seeking a **Production Quality Lead** to join our team supporting Honeywell Aerospace. In this role, you'll lead quality assurance efforts and oversee QA inspectors to ensure consistency throughout the manufacturing process and compliance with company and industry standards. You'll be instrumental in developing quality control procedures, mentoring staff, and fostering a culture of continuous improvement.
What You'll Do
+ Develop, implement, and monitor quality control processes and standards to ensure products meet specifications.
+ Conduct audits and inspections of raw materials, in-process materials, and final products.
+ Collect, analyze, and report quality-related data/KPIs to identify trends and improvement opportunities.
+ Lead root cause analysis for quality issues and implement corrective and preventative actions.
+ Train and mentor production staff on quality standards, inspection techniques, and best practices.
+ Maintain documentation for quality processes and reports.
+ Ensure compliance with company policies, industry regulations, and standards.
+ Collaborate with production, engineering, and management to resolve quality challenges.
What We're Looking For
**Required Qualifications**
+ College degree preferred OR 5 years of QA experience.
+ Knowledge of ISO9001 and QMS standards.
+ Proven leadership abilities.
+ Proficiency in Microsoft Office.
+ Strong analytical and problem-solving skills.
**Preferred Qualifications**
+ Knowledge of Minitab.
+ Familiarity with lean manufacturing tools.
+ Understanding of manufacturing processes and quality requirements.
+ **Bilingual in English & Spanish preferred.**
Pay & Schedule
+ Pay Rate: **$25/hour**
+ Overtime Pay: **$7.50/hour (1.5x rate)**
+ Shift: **1st Shift | 7:00am - 3:30pm**
Employment Requirements
+ **Drug test (including THC).**
+ **Background check.**
**Why Join Us?**
At PDS Tech Commercial, we value quality, leadership, and continuous improvement. When you join our team, you'll enjoy:
+ Opportunities for professional development and career advancement.
+ A collaborative, supportive work environment where your expertise makes a real impact.
**This position requires use of information or access to facilities subject to the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR). These regulations may limit access of controlled technologies: 1) to U.S. Persons, including U.S. Citizens, lawful permanent residents, and other narrow categories including refugees and asylees, or 2) to certain foreign nationals that have received an export license.**
**Pay Details:** 25.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

**Description:** Space is a critical domain, connecting our technologies, our security and our humanity. While others view space as a destination, we see it as a realm of possibilities, where we can do more- we can innovate, invest, inspire and integrate our capabilities to transform the future.
At Lockheed Martin Space, we aim to harness the full potential of space to cultivate innovation, reduce costs, and push the boundaries of what technology can achieve. We're creating future-ready solutions, focusing on resiliency and urgency through our 21st Century Security® vision. We're erasing boundaries and forming partnerships across industries and around the world. We're advancing spacecraft and the workforce to fuel the next generation. And we're reimagining how space can connect us, ensuring security and prosperity. Join us in shaping a new era in space and find a career that's built for you.
**As a Production Quality Engineer, you will support the Courtland Production. Your responsibilities will include:**
-Reviewing Engineering drawings and manufacturing work instructions
-Ensuring product compliance through accurate flow down of Program/Customer requirements and physical configuration audits
-Ensuring non-conformance's are accurately controlled, documented and dispositioned
-Trending Quality metrics and performing/leading root cause analysis and corrective action
-Helping resolve technical issues and communicating them back to the program and or Customer
-Helping dive process improvements and cost savings utilizing a continuous improvement mentality.
**Benefits of Employment:**
To promote the sharing of ideas, Lockheed Martin strives for a work environment that supports differences and big-picture thinking.
Our employees play an active role in strengthening the quality of life where we live and work by volunteering more than 850,000 hours annually. Here are some of the benefits you can enjoy:
-Medical
-Dental
-401k
-Paid time off
-Work/life balance
-Career development
-Mentorship opportunities
-Rewards & recognition
Learn more about Lockheed Martin's competitive and comprehensive benefits package.
**Basic Qualifications:**
**To be successful in this role you will need to possess the following requirements:**
- Interim Secret Clearance required
- Bachelor's degree from an accredited college in a technical discipline (e.g., engineering field) or equivalent discipline (e.g., math, physics, chemistry, etc.) or equivalent years of experience.
- Experience working in a Aerospace/Defense or related Manufacturing environment
- Knowledge of manufacturing/quality processes and documentation
- Demonstrated ability to comprehend and interpret drawings, work instructions, schematics, and specifications.
- Problem solving experience
**Desired Skills:**
- Lean Manufacturing experience (Green Belt/Black Belt Certification)
- Previous experience as an Material Review Board team member (MRB)
- Missile Assembly and Integration experience
- Program start up/development experience
- Experience working within a AS9100 certified quality system
- Experience running/managing projects that require cross functional support
- Audit experience
**Security Clearance Statement:** This position requires a government security clearance, you must be a US Citizen for consideration.
**Clearance Level:** Secret
**Other Important Information You Should Know**
**Expression of Interest:** By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings.
**Ability to Work Remotely:** Onsite Full-time: The work associated with this position will be performed onsite at a designated Lockheed Martin facility.
**Work Schedules:** Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits.
**Schedule for this Position:** 9x80 every other Friday off
**Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics.**
**The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration.**
At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work.
With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility.
If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs , and apply for roles that align with your qualifications.
**Experience Level:** Experienced Professional
**Business Unit:** SPACE
**Relocation Available:** No
**Career Area:** QA/Test and Inspection
**Type:** Full-Time
**Shift:** First

Looking for a new opportunity in the East Metro area? Hiring for a leading medical component manufacturer located in Vadnais Heights, MN. We are in search for a Quality Technician/ CMM Inspector on a day shift scheduled Monday- Friday (5am-3pm). What you will do as a Quality Technician:

Perform inspections as required, including first-piece and product inspections for Value Streams

Provide traceable verification by completing required inspection documentation for components, assemblies, and product lots

Evaluate returned goods to verify integrity at the request of the Material Review Board (MRB)

Maintain control of items in the inspection process

Train and provide feedback to associates on quality practices, acceptance criteria, and measurement techniques

Prepare reports and document test results and statistics

Retain records and inspection samples per company policy



What you need to be a Quality Technician:

~ 3-5 years of medical device or aerospace experience

~ Trained and practiced using inspection tools calipers, micrometers, drop indicators, & CMM.

~ Experience using ERP (Epicor) software system

~ For questions or additional details about the CMM Inspector/ Quality Technician position, please call/text us directly at or email company offers a comprehensive benefits package, including medical insurance options such as a High Deductible Health Plan (HDHP) with employer contributions to an HSA, PPO plans, and flexible spending accounts (FSA). You’ll also receive dental and vision insurance, employer-paid basic life insurance, and supplemental life insurance. Additional benefits include short-term and long-term disability coverage, a 401(k) plan with a 4% employer match, 120 hours of paid time off annually, and nine paid holidays. Employees also have access to an Employee Assistance Program (EAP) and an on-site gym.

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.
**Job Summary**
This position reports to the Site Head of Quality, and the person filling this role is responsible for partnering with functional stakeholders at the site level to ensure Quality performance and Compliance is designed into, and maintained, across all strategic initiatives, Operations, functional support organizations, and execution of GMP activities at the Rockville site. This position interacts regularly with key clients as well as interfaces with regulatory agencies during inspections. This position is responsible for overseeing all quality operations functions, including execution of environmental monitoring, sterility assurance, routine QC testing and deliver to stability testing, and the overall oversight and operation of the Quality Testing Lab. This position will also oversee timely batch lot disposition, timely investigation and CAPA related to deviations. The person filling this role will be responsible for the leadership, development and training of team members within their oversight as well as providing supportive leadership and strategic direction to operate with and maintain compliance to regulatory and industry quality standards in support of existing and new production processes.
Key Responsibilities and Duties:
+ Conceptualize, create and implement all Quality Production strategy and tactics for the site, in collaboration with other Quality, Operations, and Functional groups.
+ Develop and oversee the quality on the floor operations, including timely identification of deviations and corrective actions, and line clearances.
+ Develop and execute training and Management briefings at any technical or compliance level required on updates and regulatory requirements.
+ Regularly communicate with clients and participate in the Client quality reviews and other steering committees as required.
+ Guide Environmental Monitoring and Quality Lab Manager in identifying and maintaining services and timeframes to all internal and external clients.
+ Develop metrics and dashboard to show the effect Quality is having on the floor and in Production.
+ Supervise the QA Program leads, who are responsible for client communications during the production process, to ensure customer service and program KPIs are met successfully.
+ Provide leadership to and ensure necessary Quality oversight to areas within span of control.
+ Effectively model, demonstrate and live an employee-focused leadership style that prioritizes compliance, respectful and professional cross departmental collaboration, accountability, and the well-being, personal, and career development of each employee.
+ Effectively demonstrate and live the Charles River core values of Care, Lead, Own, and Collaborate.
+ Lead, coach and mentor individuals from all parts of the organization with varying levels of experience. Be a valued resource for the site in all matters related quality and compliance.
+ Perform all other related duties as assigned.
**Job Qualifications**
+ Minimum BS/BA Life Sciences or related field. An advanced degree in the life sciences is preferred, but not essential, based on experience
+ Minimum 8 years of experience in a biologics, pharmaceutical, medical device, or related industry. 10 years of experience is preferred
+ 5 years of experience with Environmental Monitoring and Assay Testing preferred
+ Minimum 5 to 7 years of managerial experience
+ Ability to maintain a high degree of accuracy and attention to detail
+ Ability to handle a fast-paced, multi-tasking environment, and prioritize effectively
+ Demonstrated project management skills
+ Demonstrated management and collaboration skills
+ Outstanding verbal and written communication skills
+ Complete competency with electronic document managements systems and other information management systems
+ Proficiency in Microsoft Office (Word, Excel, Outlook, etc.) is essential
+ Understanding/familiarity with relevant FDA, EMA, ICH, USP and EP guidelines and regulations associated with the quality control of biologic/cell therapies
+ Experience preferred with CDMO business and/or gene-modification modalities, cell-based gene therapies.
+ ISO Lead Auditor training, desirable
+ Certified Quality Engineer (ASQ), desirable
Compensation Data
The pay rate for this role is $150,000 - $176,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
**About Biologics Testing Solutions**
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.
**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
**Equal Employment Opportunity**
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit

**Job Description Summary**
**Job Description**
The Lead Production Quality Specialist will handle product quality review associated with the manufacturing process. This person will be responsible for departmental operations planning/execution or is focused on execution of professional activities within a technical discipline. Functions with some autonomy but guided by established policies or review of end results.
The job allows modification of procedures and practices covering work as long as the end results meet standards of acceptability (quality, volume, timeliness etc.).
Roles and Responsibilities
+ Approves recommendations for appointment and deletion of Certificated Repairman/Inspectors, and for application/revision to Repair Station Certificate
+ Liaison with the FAA CVG FSDO representative for such activities as periodic surveys, coordination of issuance and revisions to the Repair Station and Quality Control Manual for Repair Station Areas, and general administrative activities of the Repair Station operations
+ Maintains the Repair Station and Quality Control Manual and ensures the policies and procedures outlined within are followed
+ Maintains, as an attachment to, the Repair Station and Quality Control Manual a current roster of Key Personnel
+ Ensures that only FAA certified sources are used for contract maintenance, unless approved by the FSDO, and that inspection of items subcontracted to outside facilities is correctly performed prior to release for reassembly of the items/engines
+ Ensures that inspection tools and gages utilized in the Repair Station areas are maintained within calibration cycles and are adequate for the required measurements
+ Ensures that rejected, unserviceable, and/or non-airworthy parts are identified and tagged as such, and that such parts have been dispositioned for return to customer, mutilate and scrap, etc.
+ Ensures that current Service Manuals, instructions, and Service Bulletins are available to those Repair Station areas requiring such information
+ Provides oversight to ensure current technical data is available, nonconforming material processing is completed, shelf life and calibrated tooling programs are followed
+ Ensures preparation of historical file of Repair Orders, Build-Up Records, Inspection Records, and other informative data pertaining to maintenance or repair of the engine and/or components, with serial numbers of engines/parts correctly identified, and retention of such records for the prescribed period
+ Responsible for oversight of the repair station/facility scrap program
+ Provides audit support for customers, regulating authorities, and GE Aerospace's internal audit program
+ Provides technical expertise for non-standard or out-of-process maintenance efforts
+ Ensures timely closure of customer disruptions/escapes by providing effective root cause and corrective actions
+ Supports other GE Repair Stations with Quality investigations
+ Communicates directly with customers and maintains positive relationships
+ Manages customer complaints and provides feedback accordingly
+ Chairman for MRO Damage Investigation Committees
+ Completes Authorized Release Certificates for the FAA and other regulating authorities (FAA 8130-3, AAC-038, DA 8130, EASA Form 1, UK CAA Form 1, etc.)
Required Qualifications
+ Bachelor's degree from an accredited university or college (or a high school diploma / GED with at least 4 years of experience in Quality)
+ 3 years of Quality Experience
Desired Characteristics
+ FAA Repairman Certificate or meets minimum requirements per CFR Title 14 Part 65.101 to obtain Certificate
+ Humble: respectful, receptive, agile, eager to learn
+ Transparent: shares critical information, speaks with candor, contributes constructively
+ Focused: quick learner, strategically prioritizes work, committed
+ Leadership ability: strong communicator, decision-maker, collaborative
+ Problem solver: analytical-minded, challenges existing processes, critical thinker
GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness.
GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual.
#LI-KM1
_This role requires access to U.S. export-controlled information. Therefore, for applicants who are not U.S. lawful permanent residents, U.S. Citizens, or have been granted asylee or refugee status (i.e., not a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3), otherwise known as a U.S. Person), employment will be contingent on the ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government._
**Additional Information**
GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer ( . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
**Relocation Assistance Provided:** Yes
GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.