quality control supervisor

SPIMACO

<div>
 Saudi Pharmaceutical Industries &amp; Medical Appliances Corporation (SPIMACO) is a Saudi Joint&ndash;Stock company with a fully paid-up capital of SR 1,200,000,000. It was established in 1986.
 
 
 SPIMACO identifies new opportunities to enrich its resources, capabilities and diversify its pharmaceutical products portfolio that will deliver maximum value to the patients and healthcare professionals.
 
 
 
 
 Job Details
 
 
 
 
 
 Job Title
 
 
 
 Quality Control Supervisor
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Check and evaluate the data of analytical reports of samples according to the laid down procedures
 </li>
 <li>
 Release, reject of products &amp; Materials based on the testing results.
 </li>
 <li>
 Maintain Quality Control Specifications and Methods (QCSM) to ensure their availability for analysis and ensure that these are followed by the analysts while carrying out the analysis.
 </li>
 <li>
 Prepare, review and check of Quality CSM&rsquo;s and ensures their conformance to the compendial and regulatory requirements, Comply with the Computerized Analytical Instrument Requirements(Audit trail, Security system and etc.)
 </li>
 <li>
 Schedule section activities to meet weekly Production schedule, product release requirements.
 </li>
 <li>
 Train the lab analysts to assure their qualification to perform analysis and Conduct training session for the lab staff for several related topics also conduct training for internal/external students. Maintain the records for reference.
 </li>
 <li>
 Prepare &amp; update SOPs (Standard Operating Procedure), WI (Work Instructions) and GTM&rsquo;s (General Test Methods) to make sure that these documents are used whenever applicable.
 </li>
 <li>
 Maintain Quality Control Specifications and Methods (QCSM) to ensure their availability for analysis. Ensure that these are followed by the analysts while carrying out the analysis.
 </li>
 <li>
 Maintain the Qualification (IQ/OQ/PQ)/Calibration and performance of the lab equipment such as UPLC , HPLC, UV , Dissolution , Disintegration, the tablets physical testing apparatus and etc.
 </li>
 <li>
 Create protocols for different types of Stability Studies (Validation, revalidation, scale-up, annual monitoring, change control, deviations, evaluation of supplier, verifications, shelf-life extension).
 </li>
 <li>
 Maintain inventory of in-house and compendial reference standards for use in the lab testing.
 </li>
 <li>
 Maintain the raw materials reference samples.
 
 
 </li>
 </ul>
 
 Required
 
 
 
 
 Job Requirements:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree in Chemistry, Pharma, Microbiology or related sciences.
 </li>
 <li>
 Minimum 7 years of experience in a similar role in a relevant industry.
 
 
 </li>
 </ul>
 
 Preferred
 
 
 
 <ul>
 <li>
 Master Degree in related field.
 </li>
 <li>
 3 years of experience as a supervisor or mid-management.
 
 
 </li>
 </ul>
 
 Language
 
 
 
 English -Proficient.
 
 
 Arabic &ndash; Working knowledge.
 
 
 
 
 Location
 
 
 
 
 Dammam
</div>

Quality Control, Supervisor

Ardagh Group

Role description: 
The Quality Control Supervisor is responsible for supervising the quality functions and personnel to ensure compliance with customer requirements and company specifications.
 
Responsibilities: 
Assist and serve as back-up to the Quality Control Manager as directed
 Interpret quality specifications and communicate to all applicable departments
 Maintain all pertinent records to adequately monitor quality performance and standards
 Review customer complaints with plant department to ensure corrective action measures are applied to prevent reoccurrence
 Supervise ware audits and report findings along with recommended corrective action plans.
 Interact with customers and customer service representative to solve problems and foster strong customer relations
 Oversee quality lab equipment calibrations and maintenance
 Manage lab supply inventory and ordering
 Manage the measuring of glass containers and provide reports
 Perform activities necessary for the effective management of the quality department by training and developing unionized workforce
 Establish and maintain a safe, sustainable, and healthy work environment
 Comply with environmental and food safety standards as set forth in plant policies and programs within the departmental responsibilities
 
Minimum skills / qualifications: 
High School Diploma or equivalent
 Three years of experience in manufacturing quality
 Must be able to handle multiple tasks in a team-based environment
 Must have excellent presentation, interpersonal, and communication skills to interact effectively with management and outside customers
 Must have excellent problem-solving, planning, and organizational skills
 Must be proficient with Microsoft Office Suite
 
Preferred skills / qualifications: 
Undergraduate degree in math, engineering, or a related discipline
 Two years of experience leading in a manufacturing environment
 Prior experience working with SAP ERP
 Prior experience working with a quality management system
 Prior experience working in the glass container manufacturing environment
 Lean Six Sigma Green Belt Certification

Quality Control Supervisor

NutriCorp

Job Summary We are seeking a dynamic and detail-oriented Warehouse Quality Control Supervisor to lead our quality assurance efforts within the warehouse environment. In this role, you will oversee daily operations related to inventory accuracy, process improvements, and compliance with safety standards. Your leadership will ensure that all products are handled efficiently, accurately, and safely, supporting our commitment to excellence in logistics and distribution. This position offers an exciting opportunity to drive operational excellence while managing a dedicated team in a fast-paced warehouse setting.Key Responsibilities1. Product Inspection: Inspect and test products to ensure they meet the company&rsquo;s quality standards. This includes checking for defects and ensuring compliance with specifications.2. Defect Identification: Identify defects in products and recommend improvements to the production process to enhance quality and efficiency.3. Documentation: Maintain accurate records of inspections, tests, and quality control processes. Document any discrepancies and report them to management.4. Collaboration: Work closely with warehouse and supplier teams to address quality issues and implement corrective actions as necessary.5. Continuous Improvement: Participate in quality improvement initiatives and training programs to enhance quality control processes and ensure the highest level of product quality and customer satisfaction.Required Skills and Qualifications<ul><li>Strong attention to detail and ability to identify defects or non-conformities in products or materials</li><li>Previous experience in quality control or a related field is required.</li><li>Proven ability to communicate effectively with team members and management regarding quality issues and improvements.</li><li>Ability to use computer systems and software to input and analyze data related to quality control</li><li>Knowledge of quality control tools and techniques, such as statistical process control and root cause analysis</li><li>Excellent communication skills to work with other members of the warehouse team and provide feedback to suppliers and vendors</li><li>Flexibility and adaptability to work in a fast-paced environment with changing priorities and deadlines</li><li>Physical ability to stand, walk, and lift heavy objects as needed in a warehouse setting</li></ul>Pay: $65,000.00 - $80,000.00 per yearPeople with a criminal record are encouraged to applyWork Location: In person

Warehouse Quality Control Supervisor

hims & hers

<div>Hims &amp; Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health &amp; wellness challenges and innovating on their solutions, we&rsquo;re making better health outcomes easier to achieve.
Hims &amp; Hers is a public company, traded on the NYSE under the ticker symbol &ldquo;HIMS.&rdquo; To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company&rsquo;s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.<h3 class="jobSectionHeader">
About the Role</h3>
We are seeking a detail-oriented and hands-on Quality Control Supervisor to join our Quality team at our large-scale, sterile compounding pharmacy. Reporting to the Quality Control Manager, you will play a vital role in ensuring our products meet the highest standards of safety, efficacy, and regulatory compliance. This position is ideal for someone with a strong foundation in pharmaceutical or compounding environments who thrives on the production floor and is passionate about continuous quality improvement.
You will be directly involved in overseeing in-process and final product inspections, supporting compliance initiatives, and mentoring quality control staff on day-to-day operations and procedures.
This position requires working onsite at our Mesa, AZ facility.<h3 class="jobSectionHeader">
You Will</h3><ul><li>
Supervise a team of quality control specialists.</li><li>
Supervise and execute in-process and final product inspections across various stages of the compounding and visual inspection process.</li><li>
Ensure raw material and product compliance through quality checks and documentation reviews.</li><li>
Support the Quality Control Manager in investigations for non-conformances, deviations, and customer complaints.</li><li>
Conduct and document equipment verifications and assist in calibration schedules (e.g., balances, pH meters).</li><li>
Help implement and sustain compliance with USP &lt;795&gt; and applicable cGMP practices.</li><li>
Assist with internal audits, third-party inspections, and maintain audit readiness.</li><li>
Maintain accurate records of inspections, results, and quality metrics for reporting purposes.</li><li>
Train, coach, and mentor the operation and pharmacy team members on quality control procedures and standards.</li><li>
Participate in drafting and revising SOPs, work instructions, and related documents.</li></ul><h3 class="jobSectionHeader">
You Have</h3><ul><li>
Minimum 3 years of experience in quality control or assurance, preferably in a sterile compounding or pharmaceutical manufacturing environment.</li><li>
Strong understanding of USP &lt;795&gt; , USP &lt;797&gt;, USP &lt;800&gt; standards and cGMP practices.</li><li>
Associate's or Bachelor&rsquo;s degree in Chemistry, Microbiology, Biology, Quality Management, or a related field (preferred).</li><li>
Excellent attention to detail, with strong documentation and communication skills.</li><li>
Proficiency in Microsoft Office (Word, Excel, Outlook) and Google platform applications; experience with MRP/ERP systems is a plus.</li><li>
Experience in regulated environments (FDA 21CFR 210/211 knowledge a plus).</li><li>
Ability to manage multiple tasks simultaneously, with strong time management and organizational skills.</li><li>
A Pharmacy Technician license or willingness to obtain one within the first six months of employment (we cover costs and will help you obtain your trainee hours).</li></ul><h2 class="jobSectionHeader">
Our Benefits (there are more but here are some highlights):</h2><ul><li>
Competitive salary &amp; equity compensation for full-time roles</li><li>
Unlimited PTO, company holidays, and quarterly mental health days</li><li>
Comprehensive health benefits including medical, dental &amp; vision, and parental leave</li><li>
Employee Stock Purchase Program (ESPP)</li><li>
401k benefits with employer matching contribution</li></ul>
Conditions of Employment:
<ul><li>This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required.</li><li>
This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR).</li><li>
Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs.</li><li>
Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs.</li></ul>
We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply&mdash;even if you're not sure if your background or experience is a perfect match.
Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.
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.
Hims &amp; Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims &amp; Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.
To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.</div>

Quality Control Supervisor , Sterile

<div>Hims &amp; Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health &amp; wellness challenges and innovating on their solutions, we&rsquo;re making better health outcomes easier to achieve.
Hims &amp; Hers is a public company, traded on the NYSE under the ticker symbol &ldquo;HIMS.&rdquo; To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company&rsquo;s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.
We are seeking a detail-oriented and hands-on Quality Control Supervisor to join our Quality team at our large-scale, non-sterile compounding pharmacy. Reporting to the Quality Control Manager, you will play a vital role in ensuring our products meet the highest standards of safety, efficacy, and regulatory compliance. This position is ideal for someone with a strong foundation in pharmaceutical or compounding environments who thrives on the production floor and is passionate about continuous quality improvement.
You will be directly involved in overseeing in-process and final product inspections, supporting compliance initiatives, and mentoring quality control staff on day-to-day operations and procedures.
This position requires working onsite at our Gilbert, Arizona, facility.<h3 class="jobSectionHeader">
You Will</h3><ul><li>
Supervise and execute in-process and final product inspections across various stages of the compounding process.</li><li>
Ensure raw material and product compliance through quality checks and documentation reviews.</li><li>
Support the Quality Control Manager in investigations for non-conformances, deviations, and customer complaints.</li><li>
Conduct and document equipment verifications and assist in calibration schedules (e.g., balances, pH meters).</li><li>
Help implement and sustain compliance with USP &lt;795&gt; and applicable cGMP practices.</li><li>
Assist with internal audits, third-party inspections, and maintain audit readiness.</li><li>
Maintain accurate records of inspections, results, and quality metrics for reporting purposes.</li><li>
Train, coach, and mentor production and pharmacy team members on quality control procedures and standards.</li><li>
Participate in drafting and revising SOPs, work instructions, and related documents.</li></ul><h3 class="jobSectionHeader">
You Have</h3><ul><li>
Minimum 3 years of experience in quality control or assurance, preferably in a non-sterile compounding or pharmaceutical manufacturing environment.</li><li>
Strong understanding of USP &lt;795&gt; standards and cGMP practices.</li><li>
Associate's or Bachelor&rsquo;s degree in Chemistry, Biology, Quality Management, or a related field (preferred).</li><li>
Excellent attention to detail, with strong documentation and communication skills.</li><li>
Proficiency in Microsoft Office (Word, Excel, Outlook); experience with MRP/ERP systems is a plus.</li><li>
Experience in regulated environments (FDA 21 CFR 210/211 knowledge a plus).</li><li>
Ability to manage multiple tasks simultaneously, with strong time management and organizational skills.</li></ul>
A Pharmacy Technician license or willingness to obtain one within the first six months of employment (we cover costs and will help you obtain your trainee hours).<h3 class="jobSectionHeader">
Our Benefits (there are more but here are some highlights):</h3><ul><li>
Competitive salary &amp; equity compensation for full-time roles</li><li>
Unlimited PTO, company holidays, and quarterly mental health days</li><li>
Comprehensive health benefits including medical, dental &amp; vision, and parental leave</li><li>
Employee Stock Purchase Program (ESPP)</li><li>
401k benefits with employer matching contribution</li><li>
Offsite team retreats</li></ul>
Conditions of Employment:
<ul><li>This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required.</li><li>
This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR).</li><li>
Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs.</li><li>
Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs.</li></ul>
We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply&mdash;even if you're not sure if your background or experience is a perfect match.
Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.
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.
Hims &amp; Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims &amp; Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.
To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.</div>

Quality Control Supervisor, Non-Sterile

New Enterprise Stone & Lime Co., Inc.

<div><div><div><div><div>Employment Status:
</div><div>Full-Time (&gt;30 hrs/wk)</div>
</div>
</div></div><div>New Enterprise Stone &amp; Lime Co., Inc (NESL) is currently hiring a Quality Control Supervisor (AGG &amp; HMA). This position is responsible for supporting Aggregate and HMA QC Technicians. The QC Supervisor will conduct a variety of tests on AGG &amp; HMA products to verify adherence to standards set by PennDOT, NYSDOT, NYS Thruway Authority, City of Buffalo, and other municipal authorities. This position will support NESL under the direction of the Regional QC Manager, focusing on the safety of coworkers, product quality, cost efficiencies, and industry best practices.
The annual salary is $85,000 and candidates maybe be considered for a higher rate based upon experience.<div>
Quality Control Supervisor (AGG &amp; HMA) - What Will You Do? 
<ul><li>Drive innovation across operations by leveraging data, collaboration, and lean methodologies to enhance product quality, optimize inventory, and achieve sustainable cost reductions&mdash;while empowering teams to continuously improve the customer experience</li><li>Supervise a small group of QC Technicians, under the guidance the Regional QC Manager.</li><li>Complete all necessary documentation/record-keeping requirements for PennDOT, NYSDOT, and NESL.</li><li>Assist QC Technicians to ensure that AGG and HMA products are produced to the highest industry standards. This includes collaborating with Plant Superintendents on production and escalating any specification issues to the Regional QC Manager as needed.</li><li>Maintain an open line of communication with local, state, and federal materials personnel to stay up to date on changing specifications and regulations.</li><li>Communicate with the sales team to understand job specifications both before and during the bidding process.</li><li>Ensure that all personnel, equipment, and labs maintain required certifications.</li><li>Record results of inspections and report findings of inspections if the required specifications are not met.</li><li>Collect, record, and process any material certifications required for products.</li><li>Input mix designs and test results into specified QC process management system.</li><li>Assist in the hiring of QC personnel.</li><li>Perform other duties as assigned.</li></ul></div><div>
Qualifications? 
<ul><li>Bachelor&rsquo;s Degree in Geology, Engineering, Construction Management, or related field is preferred.</li><li>Minimum of five (5) years of experience in the Construction Materials Industry. QC experience in AGG, HMA or Concrete is preferred.
</li><li>Ability to build professional relationships with leaders and external networks.</li><li>Must have strong interpersonal, verbal, and written communication skills.</li><li>Must be able to work in a fast-paced environment and handle multiple tasks simultaneously.</li><li>Must possess strong attention to detail, good organizational skills with the ability to ensure accurate work.</li><li>Ability to work independently but as part of a team concept.</li><li>Flexibility and the ability to operate under stressful, time-sensitive deadlines.</li><li>Proficient in Microsoft Office (Word, Outlook, Excel, PowerPoint) and related database systems.</li><li>Valid driver&rsquo;s license and compliant with NESL driving standards.</li></ul></div><div>
Why Apply? 
<ul><li>Competitive Benefit Package - Medical, Vision, Dental, 401k, Vacation, Life Insurance &amp; more</li><li>Career Growth - We pride ourselves in developing Coworkers and promoting from within.</li><li>Stable Industry - Our materials are in high demand year over year.</li></ul></div> 
</div><div><div><div><div>What Is a NESL Career<ul><li>
BUILD AMERICA - Our work goes directly toward rebuilding America's infrastructure</li><li>
Contribute to a sustainable future improving the lives of people and communities we serve.</li><li>
Collaborate in an open culture where sound values and dedicated people come together for greater results.</li><li>
Thrive in a people-driven family owned company with countless opportunities to learn and grow.</li></ul>
NESL is a privately held family-owned company, priding itself on being Pennsylvania&rsquo;s largest construction materials producer/supplier and not to mention, leader in heavy highway construction. Founded in 1924, NESL boasts over 1,800 coworkers helping To Build America From the Ground Up! Headquartered in New Enterprise, PA, our footprint encompasses 57 quarries, 3 sand deposits, 33 hot mix asphalt plants, 21 fixed and portable ready mix concrete plants and 1 lime distribution center throughout PA and Western NY.
And&hellip;we are GROWING!
New Enterprise Stone &amp; Lime Co., Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristics protected by law. New Enterprise Stone &amp; Lime Co., Inc. is a background screening, drug-free workplace.
All qualified applicants are encouraged to apply.</div></div></div></div></div>

Quality Control Supervisor (AGG & HMA)

Siemens

<div>Here at Siemens, we take pride in enabling sustainable progress through technology. We do this through empowering customers by combining the real and digital worlds. Improving how we live, work, and move today and for the next generation! We know that the only way a business thrive is if our people are thriving. That&rsquo;s why we always put our people first. Our global, diverse team would be happy to support you and challenge you to grow in new ways. Who knows where our shared journey will take you?
Transform the everyday with us

We are looking for a Quality Control Supervisor for 2nd shift. This position will be based at our new facility in Fort Worth, TX. This opportunity is essential towards maintaining quality of high custom and sophisticated products for Electrical Products while supervising 10-20 team members.

You&rsquo;ll make an impact by:
<ul>
<li>Leading the In Process Quality Control Team; assigning tasks, providing mentorship, training, and ensuring that work is completed efficiently, on time, and performed in compliance with safety protocols, company policies and regulatory requirements.</li><li>
Testing and inspecting Low Voltage Switchgear and Switchboards to applicable standards (i.e. UL1558, UL891, IEEE, etc)</li>
<li>Use multi meter and electrical theory to verify power readings and circuit design to ensure proper wiring and operation.</li>
<li>Use Hipot, test card, hand tools, specialized software (i.e. Siemens WinPM, Step 7, MicroWin, WinCC Flexible, SAP, etc.) and various other tools to aid in testing and inspecting.</li>
<li>Perform inspection/audit of mechanical and electrical assemblies.</li>
<li>Maintain and input records or reports related to testing/inspecting activities.</li>
</ul>
You&rsquo;ll win us over by having the following qualifications:
Basic Qualifications:
<ul>
<li>2+ years in a supervisory role in a manufacturing facility.</li><li>
Bachelor's degree or equivalent work experience with High School diploma/GED.</li>
<li>Strong leadership and time management skills, understanding of management approaches for work direction, motivation, talent development and performance management.</li><li>
Proficient in Microsoft Office products.</li><li>
Legally authorized to work in the United States on a continual and permanent basis without company sponsorship.</li> 
</ul>
Preferred Qualifications:
<ul>
<li>2+ years in capacity of engineering or quality functions for power distribution equipment.</li><li>
2+ years exposure to electrical components or knowledge of electrical components.</li>
<li>Knowledge of prevailing codes (UL1558, UL891, UL508).</li>
<li>Knowledge of power distribution components (breaker, relays, communication devices).</li>
<li>Associates degree or technical training in area of responsibility</li>
</ul>
You&rsquo;ll benefit from:
<ul><li>Siemens offers a variety of health and wellness benefits to our employees. Details regarding our benefits can be found here: https://www.benefitsquickstart.com/siemens/index.html</li>
<li>The pay range for this position is $49,350.00 - $84,600.00. The actual wage offered may be lower or higher depending on budget and candidate experience, knowledge, skills, qualifications and premium geographic location.</li>
</ul>
Create a better #TomorrowWithUs

About Siemens:

We are a global technology company focused on industry, infrastructure, transport, and healthcare. From more resource-efficient factories, resilient supply chains, and smarter buildings and grids, to sustainable transportation as well as advanced healthcare, we create technology with purpose adding real value for customers.

Siemens Corporation is a U.S. subsidiary of Siemens AG, a leading technology company focused on industry, infrastructure, transport, and healthcare. From more resource-efficient factories, resilient supply chains, and smarter buildings and grids, to cleaner and more comfortable transportation as well as advanced healthcare, the company creates technology with purpose adding real value for customers. By combining the real and the digital worlds, Siemens empowers its customers to transform their industries and markets, helping them to transform the everyday for billions of people. Siemens also owns a majority stake in the publicly listed company Siemens Healthineers, a globally leading medical technology provider shaping the future of healthcare. In fiscal 2023, which ended on September 30, 2023, the Siemens Group USA generated revenue of $19.9 billion and employs approximately 45,000 people serving customers in all 50 states and Puerto Rico.

Our Commitment to Diversity, Equity, and Inclusion:
We value your unique identity and perspective. We are fully committed to providing equitable opportunities and building a workplace that reflects the diversity of society. Come bring your authentic self and create a better tomorrow with us. Learn more about our commitment to DEI here.

Protecting the environment, conserving our natural resources, fostering the health and performance of our people as well as safeguarding their working conditions are core to our social and business commitment at Siemens. They are an integral part of our Business Conduct Guidelines and our corporate strategy.
#Ll-DG1 #siemenstradesperson #SiemensMFGcareer #MFGFortWorthTX #MFGTX
$68,830 $117,994</div>

Quality Control Supervisor - 2nd Shift

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