quality supervisor

Almarai - المراعي

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  <strong>
   The Company:
  </strong>
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  Founded in 1977, Almarai Company is the world&rsquo;s largest vertically integrated dairy company and the largest food and beverage manufacturing and distribution company in MENA. Headquartered in Riyadh, Almarai Company is ranked as the number one FMCG Brand in the MENA region and the market leader in all its categories across GCC, Egypt, and Jordan.Over five decades of sustainable growth, Almarai has consistently provided nutritious and healthy products to consumers of all ages, driven by its core principle: &ldquo;Quality you can trust.&rdquo;Almarai has expanded its product range to include, in addition to dairy products, juices and beverages, baked goods, poultry, infant formula, dates, fish and seafood, and bottled water, under more than 20 brands such as Almarai, L&rsquo;usine, 7DAYS, ALYOUM, Nuralac, Farm&rsquo;s Select, Ice Leaf, Almira, Seama, Oska, IVAL, Almara Pro, Premier Chef, Bakemart, and others. Almarai currently employs over 43,000 Quality Makers, across the GCC, Egypt &amp; Jordan. In 2025, Almarai reported net income of SAR 2.4 billion on sales of SAR 22 billion.
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  An aggressive expansion program together with acquisitions in new vertical markets have created an exciting opportunity to join a dynamic multinational team dedicated to furthering growth plans for the group.
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  <strong>
  </strong>
 </p>
 <p>
  <strong>
   About the Role:
  </strong>
 </p>
 <p>
  <u>
   Quality Supervisor - Alkharj
  </u>
 </p>
 <p>
  <br/>
 </p>
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  <strong>
   Core Purpose of the job:
  </strong>
 </p>
 <p>
  To maximize operations business performance by ensuring and confirming compliance to Almarai business/quality management systems across the operation division and its inputs.
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  <strong>
   Requirements:
  </strong>
 </p>
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  <strong>
   Potential candidates must meet the requirements mentioned below:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in food science or related discipline.
  </li>
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   Minimum 2-3 years of experience within the food industry.
  </li>
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   Experience in Packaging / Production.
  </li>
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   Formal ISO 9001:2008 and ISO 22000:2005 certified.
  </li>
  <li>
   Dairy, juice and processed cheese experience is preferrable.
  </li>
  <li>
   Proficient in Microsoft Office applications (Excell, Word, etc).
  </li>
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   Excellent verbal and written communication skills in both Arabic &amp; English.
  </li>
 </ul>
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  <br/>
 </p>
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  <strong>
   Almarai offers a competitive package, generous leave, medical coverage, discretionary bonus, training, and development etc.
  </strong>
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  <strong>
   This is a great opportunity to join a successful and expanding global business, offering an excellent remuneration and benefits package.
  </strong>
 </p>
</div>


Quality Supervisor

KoMiCo Phoenix LLC

<p><b>Quality Supervisor &ndash; KoMiCo Phoenix</b></p><p><b>Job Summary</b></p><p>KoMiCo Phoenix is seeking a detail-oriented and proactive <b>Quality Supervisor</b> to oversee daily quality assurance operations, final product inspections, and compliance with all Product Standard Operating Procedures (SOPs). This role is responsible for ensuring product Turn-Around-Time (TAT) goals are achieved, minimizing internal defects, and driving continuous improvement initiatives within the department.</p><p>The Quality Supervisor will manage QA document control to maintain ISO compliance, oversee equipment checklist completion, and generate end-of-day reports. This position also requires hands-on involvement in visual inspections and corrective action investigations.</p><p>The ideal candidate possesses strong organizational and leadership skills, a solid understanding of QA principles, and the ability to effectively train and mentor Cleanroom Technicians at all levels. Strong communication skills are essential for interacting with internal teams, customers, and vendors.</p><p><b>Compensation &amp; Benefits</b></p><ul><li><b>Salary Range:</b> $58,000 &ndash; $67,000 annually</li><li><b>Medical, Dental, and Vision Insurance</b></li><li><b>401(k) Retirement Plan</b></li><li><b>Paid Time Off (PTO)</b></li><li><b>Paid Holidays</b></li></ul><p><b>Key Responsibilities</b></p><ul><li>Ensure adherence to Product Standard Operating Procedures (SOPs)</li><li>Plan and execute daily and hourly tasks to meet TAT goals</li><li>Oversee final inspection processes to ensure product quality</li><li>Maintain and verify completion of daily equipment checklists</li><li>Drive continuous improvement initiatives to reduce defects and quality issues</li><li>Manage QA document control in compliance with ISO standards</li><li>Support and sustain 5S practices within the department</li><li>Prepare and deliver end-of-day reports and shift pass-downs</li><li>Perform additional duties as assigned</li></ul><p><b>Essential Duties</b></p><ul><li>Conduct visual inspections, including:</li><li>Cosmetic quality verification</li><li>Incoming and outgoing quantity checks</li><li>Part and serial number validation</li><li>Rejection reporting as needed</li><li>Train and mentor Cleanroom Technicians (Levels I, II, and Senior)</li><li>Ensure adherence to company safety policies and procedures</li><li>Reduce internal rework and delays</li><li>Coordinate and prioritize workflow to meet production demands</li><li>Lead corrective action investigations and reporting</li><li>Monitor and report employee time and attendance concerns</li></ul><p><b>Required Knowledge, Skills &amp; Abilities</b></p><ul><li>Proactive mindset with strong ownership of responsibilities</li><li>Ability to build and maintain professional relationships across departments, customers, and vendors</li><li>Intermediate proficiency in Microsoft Office</li><li>Strong organizational and multitasking skills</li><li>High attention to detail</li><li>Working knowledge of QA principles, inspection techniques, and testing procedures</li><li>Ability to identify materials and coatings including:</li><li>Ceramic</li><li>Stainless Steel (SS)</li><li>Titanium Silicon (TiSi)</li><li>Quartz</li><li>Various substrates and coatings</li></ul><p><b>Physical Requirements</b></p><ul><li>Full use of voice, vision, hearing, and mobility</li><li>Ability to navigate stairs, ladders, and confined spaces</li><li>Comfortable working in multiple environments (cleanroom, office, outdoors)</li><li>Ability to lift, push, and pull up to 50 pounds occasionally</li><li>Ability to bend, squat, sit, and stand for extended periods</li><li>Capable of performing repetitive motions (typing, writing, etc.)</li><li>Strict adherence to Environmental Health &amp; Safety (EHS) procedures</li><li>Understanding of the impact of non-compliance with operational and safety standards</li></ul><p>Benefits:</p><ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Application Question(s):</p><ul><li>Do you have at least 4 years of experience in quality assurance or a related field?</li><li>Do you have 3+ years of supervisory or leadership experience? </li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Work Location: In person</p>

Wilsonart International

<div><div><b>Win at Wilsonart</b></div><div><br>
At Wilsonart, we don&rsquo;t just make surfaces&mdash;we build careers. When you join our team, you become part of something bigger: a company driven by innovation, grounded in values, and powered by people who care.<br>
You&rsquo;ll be surrounded by teammates who take pride in their work and look out for one another. You&rsquo;ll have the chance to learn, grow and make a real impact. And you&rsquo;ll be part of a company that believes winning means helping you succeed at work and in life.</div><div><br>
Here, you&rsquo;ll win with:<br>
<b>Support that keeps you well</b><br>
<ul><li>Medical, dental, and life insurance</li><li>Company-paid short- and long-term disability</li><li>FSAs and dependent care options</li><li>Vision and legal benefits</li><li>Gym discounts and wellness clinics</li><li>Tuition reimbursement&mdash;for you and your dependents</li></ul><b>
Opportunities to grow</b><br>
<ul><li>Clear paths to promotion and internal mobility</li><li>Training, coaching, and mentorship</li><li>Development programs to support your goals</li></ul><b>
Time for what matters</b><br>
<ul><li>Paid vacation and holidays in your first year</li><li>A culture that respects work-life balance</li></ul></div><div><br>
We&rsquo;re looking for people who are ready to learn, ready to lead and ready to make a difference. If that sounds like you, you can win at Wilsonart.</div><div>
</div><div><b>
Product Quality Supervisor</b></div><div><br>
Administers the company&rsquo;s quality program within a defined department of the organization. Develops and implements techniques for ensuring the maintenance of quality levels. Support Wilsonart programs to ensure the integrity of all manufacturing processes and products: incoming material inspections, testing &amp; control; quality records review, conducting regular product audits, quality improvement initiatives, training, RCA/CAPA investigation of deviations and non-conformances, and support of ISO 9001 and similar programs. Performs other tasks as required.</div><div>
</div><div><b>
ESSENTIAL DUTIES AND RESPONSIBILITIES</b></div><div>
</div><div><ul><li>
Support Quality Management Systems including (Quality, Environmental, &amp; Safety)</li></ul></div><div><ul><li>
Maintain Quality Assurance culture; identify &amp; provides necessary training, coaching, performance evaluation, support and assistance; provides technical and functional guidance; delegates tasks to direct reports.</li></ul></div><div><ul><li>
Ensures that production records are complete, accurate, and in compliance</li></ul></div><div><ul><li>
Develop, analyze and implement quality procedures to improve product performance and reliability.</li></ul></div><div><ul><li>
Conducts periodic and special surveys of vendor&rsquo;s facilities to determine adequacy and capability of quality control and ability to comply with complete quality specifications.</li></ul></div><div><ul><li>
Develops and initiates standards for inspection, testing and evaluation.</li></ul></div><div><ul><li>
Directs workers engaged in testing products and tabulating data concerning materials, products or process quality and reliability.</li></ul></div><div><ul><li>
Assists in preparation, handling &amp; hosting regulatory or customer audits with Quality Compliance team</li></ul></div><div><ul><li>
 Support /Assist in any other quality-related activities; leads/facilitates quality improvement teams &amp; initiatives</li></ul></div><div><br>
<b>
ESSENTIAL DUTIES AND RESPONSIBILITIES</b></div><div><br>
<b>
ENTRY REQURIEMENTS</b></div><div><ul><li>
Knowledge of products manufactured.</li></ul></div><div><ul><li>
Skill in utilizing spreadsheets, process analysis, trends, Microsoft office,</li></ul></div><div><ul><li>
Project Management and databases.</li></ul></div><div><ul><li>
Ability to analyze problems and develop solutions.</li></ul></div><div><ul><li>
Ability to communicate well in oral and written forms at all levels of the organization.</li></ul></div><div><ul><li>
Self-motivated with the ability to meet objectives and customer expectations on multiple projects. Ability to manage multiple projects in a fast paced environment with a high level of accuracy.</li></ul></div><div><ul><li>
Ability to carry out tasks completely, efficiently and in a timely manner.</li></ul></div><div><ul><li>
Skill in mathematics.</li></ul></div><div><ul><li>
Knowledge of manufacturing process. Knowledge of chemical and physical principles.</li></ul></div><div>
</div><div><b>
MINIMUM REQUIREMENTS</b></div><div>
</div><div><b>
EDUCATION:</b><br>
Bachelor Degree Required</div><div>
Bachelor&rsquo;s degree in Chemistry, Engineering, Science, or a closely related field plus two years of experience. One additional year of experience may substitute for one year of required education with a maximum substitution of four years.<br>
<b>EXPERIENCE:</b><br>
2+ years</div><div>
Plus two years of experience. One additional year of experience may substitute for one year of required education with a maximum substitution of four years.</div></div>

Product Quality Supervisor

Bureau Veritas

<div><div><p>Purpose of Position</p><p><br>
A Project Quality Supervisor ensures that project deliverables meet established quality standards and compliance requirements.</p><p>
The position performs in line with the Bureau Veritas Quality Assurance System, including the BV Code of Ethics and the BV Group policy.</p><p></p><p><br>
 Major Responsibilities</p><ul><div><ul><li>
Manage a team of the project</li><li>
Review the audit report prior to the client submission
</li><li>Prepare a detailed execution and QHSE plan for the project
</li><li>Assure that the project deliverables have been submitted to client as per the agreed schedule
</li><li>Ensure project / client requirements are met and respected by the project team;</li><li>
Being the focal point of the project<br>
Coordinate with the client representative in order to collect the required data</li></ul></div></ul><p></p><p><br>
Qualification and Experience</p><p></p><ul><li><br>
BSr&rsquo;s in engineering + ISO 9001 lead auditor</li><li>10+ years proven experience in a QA/QC inspection services</li></ul><p><br>
Skills &amp; Qualities:</p><div><ul><li><br>
knowledge of international &amp; SEC standards along with construction, maintenance and material testing procedures</li></ul></div></div></div><p></p>

Project Quality supervisor

Coating Place, LLC

<div><p><b>**New Hires eligible for $2,000 Sign-On Bonus!**</b></p><div>
1st Shift - 8am to 5pm, Monday through Friday</div><div></div><p><b><br>
Position Overview:</b></p><p>
The Quality Supervisor/Manager is responsible for providing leadership and oversight of the quality function, including quality assurance and quality control laboratory function. This position has supervisory responsibility and oversees direct reports supporting quality systems, laboratory testing, and continuous improvement initiatives. Ensures compliance with regulatory requirements applicable to Animal Health nutritional products under 21 CFR Part 507.</p><p><b>
Essential Job Functions:</b></p><ul><li>
Provide oversight and leadership of the Quality function, including Quality Assurance and Quality Control laboratory activities, and maintaining quality systems.</li><li>
Supervises and develops direct reports, ensuring appropriate training, performance management, and accountability.</li><li>
Ensures compliance with applicable regulatory requirements, including 21 CFR Part 507 Current Good Manufacturing Practice (CGMP) and Hazard Analysis and Risk-Based Preventive Controls for Food for Animals, as well as FDA and state feed regulations.</li><li>
Oversees development, implementation, and maintenance of the site Food Safety Plans in accordance with 21 CFR Part 507 Subpart C, including leading or supporting Preventive Controls Qualified Individual (PCQI) responsibilities.</li><li>
Leads or participates in hazard analysis activities, food safety activities, and ensures appropriate preventive controls are implemented and maintained.</li><li>
Ensures compliance with supply chain program requirements under 21 CFR Part 507.</li><li>
Provides oversight of laboratory operations including sampling, testing, specifications, data review, equipment calibration, and product disposition decisions.</li><li>
Reviews and approves quality documentation including procedures, specifications, laboratory methods and forms, master batch reports, and Certificates of Analysis as applicable.</li><li>
Ensures appropriate control, disposition of nonconforming materials and finished products, including investigation, root cause analysis, and implementation of corrective and preventive actions (CAPA).</li><li>
Coordinates and manages client and regulatory inspections, including FDA and state feed regulatory audits, and leads drafting responses to findings.</li><li>
Develops, monitors, and reports quality system metrics.</li><li>
Ensures labeling compliance with FDA and applicable state feed laws.</li><li>
Supports food safety programs, including recordkeeping, internal audits, regulatory documentation, and maintaining document control systems as needed.</li><li>
Follows all company quality and safety policies and procedures.</li><li>
Other duties as assigned.</li></ul><p><b>
Education/Skills/Knowledge Required:</b></p><ul><li>
Bachelor&rsquo;s degree in a scientific discipline or related field preferred.</li><li>
Minimum 5-10 years of experience in quality assurance or quality control within Animal Health, animal food, feed, or other regulated manufacturing environment.</li><li>
Minimum 2 to 5 years supervisory or leadership experience preferred.</li><li>
PCQI certification or willingness to obtain certification preferred.</li><li>
Knowledge of quality management systems and regulatory requirements for animal nutritional products.</li><li>
Strong written, verbal, and interpersonal communication skills.</li><li>
Strong organization skills and attention to detail.</li><li>
Proficiency with Microsoft Office applications.</li></ul><p><b>
Competitive Benefits:</b></p><ul><li>
Friendly work environment.</li><li>
Medical, Dental, Vision, Life, AD&amp;D, and Disability Insurance.</li><li>
Pre-tax 401(k) and after-tax Roth 401(k) contribution options with company matching up to 5%.</li><li>
Generous Paid-time Off - Accrue up to 17 days of PTO within the 1st year.</li><li>
Tuition Reimbursement Program.</li></ul></div>

Quality Supervisor/Manager

INCOG BioPharma Services

<div><p>Working closely with the Director of Quality, the Quality Supervisor will serve as an integrated quality leader with accountability spanning both Quality Assurance Operations and Quality Control activities. This role is instrumental in championing INCOG&rsquo;s Quality Mindset and fostering a culture of efficiency, attention to detail, and on-time delivery across manufacturing and laboratory functions.</p>
<p>
The Supervisor will need to successfully navigate and identify operational and quality gaps in both the manufacturing environment and the QC laboratory setting. They will bring a balanced technical depth across GMP manufacturing oversight, contamination control, and laboratory testing operations &mdash; ensuring seamless alignment between QA and QC functions in support of compliant, inspection-ready operations.</p>
<p>
The Quality Supervisor will exemplify excellent interpersonal skills and develop productive, customer-centric working relationships with subordinates, colleagues, customers, suppliers, and partners. The Supervisor will demonstrate excellent written and oral communication skills, with the ability to clearly and concisely articulate complex issues to a range of audiences. The Supervisor will thrive in a team environment but will also work autonomously, leveraging strong self-management and organizational skills. They will value process owners and subject matter experts and will possess a demonstrated ability to influence positive outcomes without direct reporting authority.</p>
<p><b>
This role supervises Weekend shift personnel (Friday&ndash;Sunday). Two shifts are available: Days (7:00 AM&ndash;7:30 PM) and Nights (7:00 PM&ndash;7:30 AM). Candidates must demonstrate availability and flexibility for occasional support outside of their standard shift hours.</b></p><p><b><br>
Essential Job Functions</b></p>
<ul><li>
Recruit, build, and lead an integrated QA Operations team; train and maintain an engaged workforce competent in the theory and application of quality processes across aseptic drug product manufacturing.</li><li>
Maintain an on-floor presence to coach, mentor, and enforce rigorous quality work standards; prioritize and coordinate QA resources to balance production timelines with product quality assurances.</li><li>
Lead development of room/line clearance processes for formulation, aseptic filling, and inspection/packaging areas; train QA personnel on gowning requirements, contamination controls, aseptic line operations, and equipment applications and verifications.</li><li>
Lead QA strategy in partnership with Operations for on-floor batch record review and correction; establish an ongoing state of readiness for rapid decision-making in the evaluation of deviating events, product segregation requirements, and implementation of initial corrective actions.</li><li>
Partner with EH&amp;S and Operations management to communicate safety expectations, assess safety behaviors, practice positive intervention, and enforce best practices aligned to SOPs, compliance requirements, and site goals.</li><li>
Provide technical support, oversight, and team leadership for QC Chemistry, Microbiology, and QC Technical Services; oversee daily QC activities to ensure testing and data review is completed within appropriate timeframes.</li><li>
Deliver daily expectations and assignments to QC personnel; provide in-lab support as needed for routine and on-demand testing.</li><li>
Develop QC team members through mentorship to analysts and data reviewers; communicate with Quality Control Leadership on team performance.</li><li>
Support deviation investigations, laboratory investigations, and CAPA implementation spanning both manufacturing and laboratory quality events; develop and improve current processes to maintain and control general QC functions.</li><li>
Conduct laboratory walk-throughs to ensure inspection readiness and cGMP compliance across all QC laboratory operations.</li><li>
Continuously evaluate processes and procedures across QA and QC functions to create a productive environment while maintaining the highest possible quality standards; ensure all work is carried out in accordance with regulatory requirements, cGMP, and SOPs.</li><li>
Influence the accomplishment of company-wide and team goals; inspire team members while consistently modeling ALP values in all interactions.</li></ul><br>
<p><b>
Special Job Requirements</b></p>
<ul><li>Bachelor's Degree required; Science discipline preferred (Chemistry, Biology, Biochemistry, Microbiology, or related field).</li></ul>
<ul><li>Minimum of 5 years of cGMP experience in biopharma or a similarly regulated industry, including at least 2 years in a Quality Assurance capacity.</li></ul>
<ul><li>Working knowledge of QC Microbiology and/or Chemistry, GxP principles, CAPA/investigation management, data/document review, and relevant quality and regulatory requirements.</li></ul>
<ul><li>Working knowledge of contamination controls, manufacturing processes, and output quality across automated and non-automated systems, including associated data integrity requirements.</li></ul>
<ul><li>Demonstrated experience making risk-based decisions to ensure product quality.</li></ul>
<ul><li>Knowledge of aseptic techniques and processing.</li></ul>
<ul><li>Strong communication and relationship-building skills across all levels of the organization, including operations, quality, and business leadership.</li></ul><p><b><br>
Additional Preferences</b></p>
<ul><li>Advanced Degree.</li></ul>
<ul><li>Certification(s) in Risk Management, Quality Process Analysis, Technical Writing, and/or Quality Investigation.</li></ul>
<ul><li>Hands-on experience with aseptic manufacturing Quality, including isolator based processing.</li></ul>
<ul><li>3 to 5 years of demonstrated working knowledge of GMP laboratory operations (QC Chemistry and/or Microbiology).</li></ul>
<ul><li>2+ years of experience as a people leader or supervisor.</li></ul>
<ul><li>First-hand experience participating in and/or hosting operational floor inspection tours related to Quality Assurance.</li></ul>
<ul><li>Experience building processes and procedures.</li></ul>
<ul><li>Experience with Continuous Improvement, Six Sigma, and/or Lean principles.</li></ul><p><b><br>
Additional Information about INCOG BioPharma Services</b></p>
<p><i>
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.</i></p>
<p><i>
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.</i></p>
<p><i>
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.</i></p>
<p><i>
By submitting your resume and details, you are declaring that the information is correct and accurate.</i></p></div>

Quality Supervisor, Weekend Shift

<div><p>PPG's Aerospace Business is looking for a <b>Senior Quality Assurance Supervisor</b> to join our team in Grand Prairie! In this role you will be responsible for leading and executing quality assurance activities across aerospace manufacturing operations. You will ensure compliance with AS9100, customer, and internal requirements while driving a strong culture of continuous improvement, product conformity, and regulatory integrity. You will also provide day‑to‑day direction to quality inspectors and technicians and serve as a key interface with Manufacturing, Engineering, Supply Chain, and external auditors.</p><p></p><p>
You will work onsite at our Grand Prairie, TX facility and report to the Senior Aerospace Production Quality Manager.</p><p></p><p><b>
Key Responsibilities</b></p><ul><li><p>
Supervise, coach, and develop Quality Inspectors and Technicians to ensure consistent application of aerospace quality standards.</p></li><li><p>
Ensure compliance with AS9100, ISO 9001, and customer‑specific aerospace requirements.</p></li><li><p>
Maintain and enforce Quality Management System (QMS) procedures, work instructions, and inspection plans.</p></li><li><p>
Support internal, customer, and third‑party audits; ensure timely closure of corrective actions.</p></li><li><p>
Ensure proper execution of incoming, in‑process, and final inspections for aerospace products.</p></li><li><p>
Review and disposition nonconforming material in accordance with approved procedures.</p></li><li><p>
Lead investigative efforts for quality escapes, defects, and customer complaints.</p></li><li><p>
Approve or support MRB (Material Review Board) activities and decisions.</p></li><li><p>
Lead root cause analysis using structured methods (e.g., 5‑Why, Fishbone, FMEA)Drive corrective and preventive action (CAPA) effectiveness.</p></li><li><p>
Analyze quality metrics (scrap, rework, defects, audit findings) and identify improvement opportunities.</p></li><li><p>
Partner with Manufacturing, Engineering, and Supply Chain to reduce variation and improve process capability</p></li></ul><p></p><p><b>
Qualifications</b></p><div><ul><li><p>
Bachelor's degree in Engineering, Quality, Manufacturing, or related technical field or equivalent experience.</p></li><li><p>
5+ years of quality experience in aerospace manufacturing or regulated production environments.</p></li><li><p>
2+ years of supervisory or lead experience.</p></li><li><p>
Proficiency in inspection techniques, GD&amp;T, and quality tools.</p></li><li><p>
Data‑driven problem‑solving and decision‑making ability.</p></li><li><p>
Only U.S. Citizens, Green Card holders, and political asylees or refugees are eligible to apply.</p></li></ul></div><p></p><p>
#LI-Onsite</p><p></p><p><b>
About us:</b></p><p>
Here at PPG we make it happen, and we seek candidates of the highest integrity and professionalism who share our values, with the commitment and drive to strive today to do better than yesterday &ndash; everyday.</p><p></p><p><b>
PPG: WE PROTECT AND BEAUTIFY THE WORLD&trade;</b></p><p>
Through leadership in innovation, sustainability and color, PPG helps customers in industrial, transportation, consumer products, and construction markets and aftermarkets to enhance more surfaces in more ways than does any other company. To learn more, visit www.ppg.com and follow @ PPG on Twitter.</p><p></p><p>
At PPG we use AI in the hiring process to make the process more efficient. AI tools do not make hiring decisions. You can learn more by going to https://careers.ppg.com/us/en/candidate-resources.</p><p></p><p>
PPG provides equal opportunity to all candidates and employees. We offer an opportunity to grow and develop your career in an environment that provides a fulfilling workplace for employees, creates an environment for continuous learning, and embraces the ideas and diversity of others. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, color, creed, religion, national origin, age, disability status, marital status, veteran status, sexual orientation, gender identity or expression. If you need an adjustment due to a disability, please email recruiting@ppg.com.</p><p></p><p>
PPG values your feedback on our recruiting process. We encourage you to visit Glassdoor.com and provide feedback on the process, so that we can do better today than yesterday. Benefits will be discussed with you by your recruiter during the hiring process.</p><p>
PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply.<br>
<br>
Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.</p></div>

Aerospace Senior Quality Supervisor

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