quality control expert

INNOVENT INTEGRATED SOLUTION FZ LLC

<div> Job Summary <div> The Quality Control (QC) Specialist will ensure that our products and services meet the highest quality standards through rigorous testing and evaluation. This role involves developing and implementing quality control procedures, conducting inspections, and collaborating with teams to resolve quality issues. The ideal candidate will have a keen eye for detail, strong analytical skills, and experience with quality control methodologies. They will be responsible for maintaining detailed records of quality control activities, conducting root cause analysis, and implementing corrective actions. This role is vital in ensuring customer satisfaction and maintaining our reputation for high-quality products. </div> </div> <div> What you'll do <div> <ul> <li>Develop and implement quality control procedures and standards.</li> <li>Conduct inspections and tests on products and services.</li> <li>Identify, document, and track defects and inconsistencies.</li> <li>Collaborate with development and production teams to resolve quality issues.</li> <li>Maintain detailed records of quality control activities.</li> <li>Conduct root cause analysis and implement corrective actions.</li> <li>Ensure compliance with industry standards and regulations.</li> <li>Train staff on quality control processes and best practices.</li> <li>Continuously improve quality control processes and procedures.</li> </ul> </div> </div> <div> Qualifications <div> <ul> <li>Bachelor s degree in Quality Management, Engineering, or related field.</li> <li>5+ years of experience in quality control or quality assurance.</li> <li>Strong knowledge of quality control methodologies and tools (e.g., Six Sigma, ISO standards).</li> <li>Excellent attention to detail and analytical skills.</li> <li>Strong communication and documentation skills.</li> <li>Ability to work collaboratively with cross-functional teams.</li> <li>Experience with quality control software and tools.</li> <li>Relevant certifications (e.g., Certified Quality Engineer) are a plus.</li> </ul> </div> </div> <div> <div> <div>Let's explore how Innovent can work with you!</div> <div>Please fill in the form with your details to book a meeting with our team.</div> </div> <div></div></div>

Quality Control (QC) Specialist

Texas Biomedical Research Institute

<div>We are seeking a Quality Control Specialist II to join our team. This position is responsible for performing detailed quality control reviews of research data, including non-GLP, GLP, and Animal Rule study records. The role also includes training QC personnel and assisting Study Directors with protocol development.
The Role:<ul><li>
Conduct comprehensive quality reviews of data and reports for completeness, accuracy, and compliance with minimal supervision.</li><li>
Prepare clear, concise QC Review Reports for Study Directors.</li><li>
Review and assess study-related processes and procedures.</li><li>
Support Study Directors with study protocol development and review.</li><li>
Assist during inspections by external monitoring authorities and study sponsors.</li><li>
Help identify and implement corrective and preventive actions in response to inspection findings.</li><li>
Meet regularly with Study Directors or Study Compliance Managers to report on study status, findings, and any compliance concerns.</li><li>
Train and mentor Quality Control Specialist I personnel.</li><li>
Serve as a key resource for quality-related issues across study teams.</li><li>
Maintain organized, accurate study documentation.</li><li>
Perform other quality control activities as assigned.</li><li>
Prepare and send QC correspondence and documentation as needed.</li></ul>
Our Ideal Candidate:
Education<ul><li>
Associate degree (60 semester hours) from an accredited institution required.</li><li>
Bachelor&rsquo;s degree preferred.</li></ul>
Experience<ul><li>
At least three years of experience reviewing preclinical research records for quality control.</li></ul>
Skills and Knowledge<ul><li>
Excellent written and verbal communication skills.</li><li>
In-depth knowledge of FDA regulations related to GLP (21 CFR Part 58), Animal Rule, and electronic records (21 CFR Part 11).</li><li>
Understanding of nonclinical/preclinical research protocols.</li><li>
Familiarity with medical and scientific terminology.</li><li>
Proficiency in Microsoft Word and Excel.</li><li>
Strong attention to detail, with excellent spelling, grammar, and punctuation.</li></ul>
Who We Are:
Join our incredible mission to pave the way for a world free from the fear of infectious disease!
Texas Biomedical Research Institute is pioneering and sharing scientific research to protect you, your families, and our global community from the threat of infectious diseases. Our scientific discoveries create breakthroughs in medical research to provide better overall global health.
Texas Biomed is the only independent, nonprofit infectious disease research institute in the U.S. to combine:<ul><li>
The highest-level biocontainment labs for infectious disease and biodefense research</li><li>
A federally designated National Primate Research Center</li><li>
More than 80 years of discoveries advancing diagnostics, vaccines and therapies</li><li>
An entrepreneurial culture and specialized expertise in regulated science required for FDA approval</li></ul>
What We Can Offer You:<ul><li>
Recognized as one of the San Antonio Business Journal&rsquo;s Best Places to Work in 2025.</li><li>
Awarded the 2024 Healthy Workplace Platinum Recognition by the San Antonio Business Group on Health (SABGH).</li><li>
Employee-centered culture with an emphasis on open communication, job empowerment and trust</li><li>
Comprehensive health, dental, vision, and life insurance plans for your family (and even your pets</li><li>
An incomparable employer funded retirement plan with 7% retirement funding starting day 1 (and increases upon years of service)!</li><li>
Generous paid time off, with 14 paid holidays including Winter Recess (paid week off the last week of December)</li><li>
On-site medical clinic, wellness incentives &amp; paid prescription drug resources to promote health management!</li><li>
On-site gym &amp; wellness programs!</li><li>
Flexible work arrangements for work-life balance!</li><li>
We offer a relaxed dress code so you can feel comfortable and be yourself at work.</li><li>
Dynamic learning environment with opportunities for professional development, mentorship, continuing education (tuition reimbursement) and leadership programs to help you thrive both personally and professionally.</li></ul>
We take pride in fostering a culture of respect, opportunity, and unity. Texas Biomedical Research Institute provides equal employment opportunities for all qualified employees and applicants without regard to race, color, sex, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.</div>

Quality Control Specialist II

Hanwha Aerospace

<div>
 
 Soaring to the top 19th of the global defense industry ranking,
 
 Hanwha Aerospace
 
 is dedicated to provide state-of-the-art defense solutions for a safer future. Recognized by Times as one of the most influential companies of 2024,
 
 Hanwha
 
 has delivered not only defense solutions but has also embarked on industries of Aerospace, Maritime, and Space to provide a safer and more sustainable future for the world.
 
 
 
 
 
 🚀
 
 Join Hanwha Aerospace in our mission to protect people, the planet, and our future. Together, let&rsquo;s redefine innovation and shape the future of aerospace and defense.
 
 
 
 
 
 
 
 Job Overview
 
 :
 
 
 The employees will be responsible for ensuring that our products meet the highest quality standards through rigorous testing, inspection, and adherence to quality management systems such as ISO 9001.
 
 
 
 
 
 
 Responsibilities
 
 :
 
 <ul>
 <li>
 Conduct ISO 9001 training sessions for employees, focusing on auditor qualifications and understanding of quality requirements.
 </li>
 <li>
 Perform quality audits using tools such as process inspection, performance tests, and drawings to ensure compliance with quality standards.
 </li>
 <li>
 Collaborate with cross-functional teams to identify and resolve quality issues in a timely manner.
 </li>
 <li>
 Develop and implement quality control procedures and protocols to improve product quality and efficiency.
 </li>
 <li>
 Maintain accurate documentation and records of quality tests, inspections, and audits.
 </li>
 </ul>
 
 
 
 
 
 Requirements
 
 :
 
 <ul>
 <li>
 Major in Mechanical engineering
 </li>
 <li>
 Proficiency in Microsoft Word and Excel for documentation and data analysis.
 </li>
 <li>
 Strong attention to detail and analytical skills.
 </li>
 <li>
 Excellent communication and interpersonal skills. (in English)
 </li>
 </ul>
 
 
 
 
 
 Preferred Qualifications
 
 :
 
 <ul>
 <li>
 Certification in quality management or auditing.
 </li>
 <li>
 Knowledge of additional quality control tools and techniques.
 </li>
 <li>
 In-depth knowledge of ISO 9001 standards and quality management systems.
 </li>
 </ul>
 
 
 
 
 
 Benefits
 
 :
 
 <ul>
 <li>
 Competitive salary
 </li>
 <li>
 Opportunities for professional development and advancement.
 </li>
 <li>
 Dynamic and collaborative work environment.
 </li>
 </ul>
 
 
 
 
 #HanwhaAerospace #JoinOurTeam #CareerOpportunities #Innovation #GlobalTalentAcquisition
 
</div>

Quality Control

Gasket & Seal Fabricators

Gasket and Seal Fabricators (GSF) is a 48 year old manufacturing company that cuts custom gaskets in the Midwest. GSF also owns Seal Tite Corporation, expanding our sealing solutions and elastomer expertise.Our customers&mdash;including some of the world&rsquo;s most sophisticated manufacturers&mdash;depend on us for consistent quality, accurate documentation, and reliable delivery. We are expanding our Quality team to support both facilities and ensure continued excellence.GSF is a stable company with long, trusted customer relationships - we were deemed an essential business during COVID. We put people first in our organization and pride ourselves in being an enjoyable place to work with a great culture.Position OverviewWe are seeking a Quality Control Specialist who will play a key role in strengthening product quality, supporting our customers, and ensuring consistent standards across both GSF and Seal Tite operations. This position will work hands-on with our production teams, maintain essential quality documentation, and help drive continuous improvement throughout the organization. The role includes regular travel between our Sauget and St. Louis facilities to support inspections, collaboration, and alignment of quality processes.Responsibilities will include:Inspection &amp; Measurement<ul><li>Perform incoming, in-process, and final inspections on gaskets, seals, and converted materials.</li><li>Use calipers, micrometers, gauges, optical comparators, and other measurement tools to verify dimensions.</li><li>Confirm compliance with engineering drawings, tolerance requirements, and customer specifications.</li></ul>Quality &amp; Compliance Documentation<ul><li>Prepare and maintain REACH/ROHS declarations, material compliance statements, and customer-required documentation.</li><li>Manage and issue Country of Origin, Certificate of Conformance, and traceability documents.</li><li>Support AS9100-compliant documentation, including process controls, calibration records, and audit readiness.</li><li>Assist with PPAP and First Article Inspection (FAI) packets when required.</li></ul>Material Rejections &amp; Corrective Actions<ul><li>Process non-conforming materials, issue NCRs, quarantine product, and coordinate rework/disposition.</li><li>Initiate and track corrective and preventive actions (CAPA).</li><li>Work closely with Production and Purchasing to resolve supplier-related quality issues.</li></ul>Performance &amp; Reporting<ul><li>Maintain On-Time Delivery (OTD) reports and quality performance metrics.</li><li>Support customer scorecards and internal performance dashboards.</li><li>Monitor trends in rejections, defects, and delivery performance and suggest improvements.</li></ul>Standards &amp; Audit Support<ul><li>Support compliance with AS9100 and ISO 9001 standards across GSF and Seal Tite operations.</li><li>Manage the companies' Quality Manuals and coordinate required audits and inspector site visits.</li><li>Assist with internal audits, process evaluations, and continuous improvement projects.</li></ul>Skills and Qualifications<ul><li>1&ndash;3 years of quality control or inspection experience in a manufacturing environment.</li><li>Ability to read and interpret engineering drawings, blueprints, and technical documentation.</li><li>Strong understanding of measurement tools (calipers, micrometers, comparators, gauges).</li><li>Experience with material certifications, compliance paperwork, or customer documentation requirements.</li><li>Excellent attention to detail, communication skills, and organization.</li></ul>Preferred<ul><li>Working knowledge of AS9100 standards and audit processes.</li><li>Familiarity with PPAP, FAI, SPC, CAR, NCR.</li></ul>Additional Details<ul><li>Hours: 5:45am &ndash; 4:00pm M-Th</li><li>In-person</li></ul>Benefits<ul><li>Health Insurance</li><li>Life Insurance</li><li>Disability Insurance</li><li>Workers Compensation</li><li>401k with Corporate Matching</li><li>Paid Vacation</li><li>Paid Holidays</li><li>Paid Sick Days</li><li>Birthday Time Off</li><li>Free snacks + and other employee benefits!</li></ul>If you are looking to grow your career long-term with a stable, yet evolving company&hellip;we look forward to meeting you.Job Type: Full-timePay: $28.00 - $34.00 per hourExpected hours: 40 per weekBenefits:<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 sick time</li><li>Paid time off</li><li>Vision insurance</li></ul>People with a criminal record are encouraged to applyWork Location: In person

Quality Control Specialist

Thermo Fisher Scientific

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
Job Description
About the Company
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies &amp; Services makes it easier for customers.
Responsibilities:<ul><li>
Responsible to carry out analysis on analytical instruments like HPLC, GC, ICP, GCMS etc.</li><li>
Responsible to analyse and interpretate the analytical data basis customer requirement on Window based tools</li><li>
Process knowledge of chemical testing, Analytical work, basic trouble shooting, method preparation/validation, handling and calibration of instrument like HPLC, GC, ICP, GCMS etc.</li><li>
Responsible to maintain and carry out chemical analysis basis ISO/NABL standards 17025 and 17034.</li><li>
Responsible for good laboratory practice in Quality control lab.</li><li>
Perform analysis and reporting of raw materials, packing materials, Finished products, in-process and routine analysis.</li><li>
Preparation of volumetric solutions, reagents, buffer solutions, indicator and maintain its records.</li><li>
Perform standardization of volumetric solutions.</li><li>
Preparation of Quality control SOP&rsquo;s.</li><li>
Responsible to be self aware of Safety and Quality compliance and adhere to set compliance norms.</li></ul>
Experience and Skill Sets:<ul><li>
B.Sc. Chemistry with five years experience</li><li>
M.Sc in Analytical / Inorganic chemistry with three years experience</li><li>
The role needs good communication, presentation skill &amp; solution-oriented approach.</li></ul>
Benefits: 
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! 
At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds have a unique story to tell. 
ThermoFisher is committed to crafting a diverse work environment that values and respects individuals.</div>

Quality Control Executive

Atlanta Flooring Design Centers, Inc.

<div>The Quality Control Specialist will build and maintain good working relationships with our building contractors and field supervisors, communicate concerns and issues effectively with installers and ensure that we provide the highest quality of service to our new home builder clients while controlling costs. He or she works with subcontractors to maintain high quality job standards, conduct field audits and job site/safety inspections. He/She will be responsible for completing minor repairs on occasion. This role works with mobile technology such as a company-owned iPad and iPhone for reporting and communication purposes. 
 
Candidates for this position must have previous experience in wood, carpet, vinyl or tile flooring. He or she must have strong interpersonal skills and a talent for working with variety of personalities. Good written communication skills, time management, professional dress, speech, and behavior are all required for this position. Verbal fluency in both English and Spanish is highly preferred, but is not required. Local travel is required in this position, but very little-to-no overnight travel should be expected. The candidate must have reliable transportation, as Quality Control Specialists are required to drive their own vehicle for work. A vehicle allowance as well as a fuel card will be included with the compensation package.
RESPONSIBILITIES:<ul><li>
Works with subcontractors to maintain high quality job standards</li><li>
Conducts field audits and job site/safety inspections</li><li>
Makes repairs onsite as necessary</li><li>
Address customer concerns and issues, escalating them as necessary for job completion and customer satisfaction</li><li>
Respond to builder and/or post-sale customer concerns regarding warranty issues, repairs, and material or quality issues</li><li>
Communicates with installers to insure clear understanding of job specifications and installation requirements to maintain high quality job standards</li><li>
Work with account representatives in various departments to insure that complete and proper information is provided for work assignments</li><li>
Other duties as assigned</li></ul>
BENEFITS:<ul><li>
Bi-weekly payroll via direct deposit</li><li>
Eligible to participate in group health, dental &amp; vision insurance plans after 60 days full-time employment</li><li>
Supplemental life, accident, cancer and short-term disability insurance available after 60 days full-time employment</li><li>
Retirement Plans: Employee Stock Ownership Plan and 401(K) with match</li><li>
Paid Time Off (PTO) from first day of employment</li></ul><ul><li>
Previous experience in flooring operations and/or construction highly preferred</li><li>
Experience with using iPhone and iPad</li><li>
Reliable vehicle that can be used for work</li><li>
Able to lift up to 50 pounds</li><li>
Able to bend, kneel, squat, stand and lift heavy objects as needed</li><li>
Must have satisfactory Motor Vehicle Report (MVR)</li><li>
Must have reliable vehicle to drive for work</li></ul></div>

Meraj limited

About the Company: Meraj Limited is a leading manufacturer of specialized vehicles, firefighting equipment, and engineering solutions. We are dedicated to delivering innovation, reliability, and the highest quality standards in every product we produce.Key Responsibilities:<ul><li>Inspect incoming materials, fabricated parts, and assemblies according to company quality standards.</li><li>Perform PDI (Pre-Delivery Inspection) of specialized vehicles and equipment.</li><li>Conduct inspection of fabrication, welding, paint, and hydraulic systems to ensure compliance with drawings, specifications, and quality procedures.</li><li>Verify welding quality, paint thickness, and finishing standards.</li><li>Inspect hydraulic assemblies, fittings, and functional operations.</li><li>Monitor in-process and final inspection stages across departments.</li><li>Prepare and maintain inspection reports and documentation.</li><li>Identify non-conformities and coordinate corrective actions with concerned departments.</li><li>Support continuous improvement and ensure adherence to company safety and quality standards.</li></ul>Requirements:<ul><li>DAE (Mechanical / Automotive ) or equivalent qualification.</li><li>3&ndash;5 years of experience in quality inspection, preferably in vehicle manufacturing or fabrication industry.</li><li>Hands-on experience in fabrication, welding, paint, and hydraulic system inspection is mandatory.</li><li>Strong knowledge of inspection tools, gauges, and measurement techniques.</li><li>Good communication and reporting skills.</li><li>Attention to detail and commitment to high quality standards.</li></ul>Job Type: Full-time Experience: 3&ndash;5 years (Required) Education: DAE (Mechanical / Automotive)How to Apply: Interested candidates can apply through Indeed or email their updated CV to Careers@merajlimited.com with the subject line &ldquo;QC Inspector &ndash; Application&rdquo;.Job Type: Full-timeWork Location: In person

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