quality assurance tech

Formosa Plastics

Company Overview for Formosa Plastics Corporation, U.S.A.
 
Founded in 1978, Formosa Plastics Corporation, U.S.A. (Formosa Plastics) is a growing, vertically-integrated supplier of plastic resins and petrochemicals. With annual revenues of more than $5 billion, we employ over 2,800 people who operate 20 production units in six business divisions - Olefins, Polyolefins, Vinyl, Specialty Polyvinyl Chloride, Chlor-Alkali, and Oil & Gas.
 
Formosa Plastics offers a full line of polyvinyl chloride, polyethylene and polypropylene resins, caustic soda and other petrochemicals that deliver the consistency, performance and quality that customers demand. We market our polypropylene and polyethylene resins under the Formolene® tradename; we market our suspension PVC and specialty (dispersion) PVC resins under the Formolon® tradename. We also produce and sell caustic soda, ethylene dichloride, commercial bleach and hydrochloric acid.
 
We are committed to supplying the highest quality products and services to our customers, providing a safe and healthy workplace for our employees and contributing to the quality of life in the communities where we operate. This commitment is made possible through our dedicated people, consistent products, continued protection of the environment and ongoing investments in new product development, quality control systems and safe, modern and energy-efficient production facilities.
 
Formosa Plastics is a privately held company headquartered in Livingston, New Jersey. Our core business, producing plastic resins and petrochemicals, takes place at three wholly-owned chemical manufacturing subsidiaries located in Delaware City, Delaware, Baton Rouge, Louisiana and Point Comfort, Texas.
 
POSITION OBJECTIVE
 To perform laboratory testing to support process control, quality control, and finished product release, while ensuring compliance with approved methods, safety standards, and regulatory requirements.
 
II. MAJOR AREAS OF ACCOUNTABILITY
 1. Calibrate, operate, maintain, and troubleshoot laboratory instruments and equipment to ensure accurate and reliable results.
 2. Analyze raw materials, in-process samples, and finished products in accordance with approved methods and specifications.
 3. Perform quality control testing for process monitoring, additives, and final product release prior to shipment.
 4. Accurately document test results, calculations, and observations in a timely manner, ensuring data integrity and traceability.
 5. Enter analytical data into required systems and complete associated calculations and reports.
 6. Investigate, troubleshoot, and resolve analytical or equipment issues; coordinate repairs or corrective actions as needed.
 7. Complete and maintain all required QC, ISO, IATF, safety, and regulatory documentation.
 8. Ensure compliance with company policies, ISO/IATF standards, environmental, health and safety requirements, and applicable federal and state regulations.
 9. Participate in audits, inspections, daily NTG (Nothing Touching the Ground) checks, and operational clean sweep activities.
 10. Actively support pellet loss prevention, containment, cleanup, and proper disposal practices.
 11. Maintain a clean, organized, and safe laboratory and work environment following 6S or similar standards.
 12. Attend and actively participate in safety meetings, departmental meetings, and required training programs.
 13. Communicate results, issues, and trends effectively with operations, quality, and management teams.
 14. Support continuous improvement initiatives related to testing methods, efficiency, quality, and safety.
 15. Work outside normal business hours as required to support production or quality needs.
 16. Maintain regular, reliable attendance and professional conduct.
 17. Assist with inventory control of laboratory supplies, reagents, and standards as needed.
 18. Perform other duties as assigned to support laboratory and operational objectives.
 
III. QUALIFICATIONS
 A. TECHNICAL JOB CRITERIA
 1. Previous Related Experience Required
 High School diploma or equivalent with a minimum of eight hours of college-level chemistry; or an associate’s degree in Chemical Technology (Laboratory); or three years of industrial laboratory experience; or at least 15 consecutive months of experience in a Polyolefins, PVC, or Polymer Analysis laboratory.
 2. Technical Skills Required to Perform This Job
 <ul>
<li>Operation, calibration, preventive maintenance, troubleshooting, and basic repair of laboratory instruments</li>
<li>Wet chemistry techniques (titrations, dilutions, reagent preparation, standardization)</li>
<li>Sample preparation for raw materials, in-process, and finished products</li>
<li>Execution of routine analytical testing per approved SOPs</li>
<li>Basic method troubleshooting and verification</li>
<li>Routine calibration and calibration verification of lab equipment</li>
<li>Accurate data entry and calculation (ppm, ppb, %, dilution factors)</li>
<li>Use of LIMS or other electronic data systems (as applicable)</li>
</ul>
3. Education
 High school graduate or equivalent with a minimum of eight hours of college-level chemistry, or an associate’s degree in Chemical Technology (Laboratory) preferred.
 4. Other Certification/Training Required
 <ul>
<li>Will require training in Company Policies and Procedures after hire.</li>
<li>Current employees must meet all technical and safety training requirements for current position, as specified in the Master Training Plan.</li>
<li>Must participate in the following subject training and pass required certifications.</li>
</ul>
Check Out Our Benefits
 Health Coverage and Perks
 
Excellent medical, dental, and vision insurance plans
 
Flexible spending accounts for health, dependent care
 
Short-term Disability
 
Long-term Disability
 
Group Term Life, Dependent and
 Supplemental Life Insurance
 
Tuition Reimbursement
 ​​​​​​​
 Work/Life Balance
 
10 Paid Holidays
 
Paid Time Off for a balanced life
 (Vacation, Sick and Personal Time)
 
FlexTime Available
 
Competitive Compensation
 
Competitive salary, incentive/bonus, 401(k) plan with company match,
 Cash Balance, Pension Plan

LABORATORY SERVICES & QUALITY ASSURANCE LABORATORY TECH

Atilar Pharma

Job Description: Atilar Pharma is seeking a motivated and detail-oriented Quality Assurance Technician to support our quality systems and operations team. As a 503B outsourcing facility, maintaining the highest standards of product quality and regulatory compliance is at the core of everything we do. The Quality Assurance Technician will play an essential role in ensuring that our compounded sterile preparations meet all applicable USP, FDA, and cGMP requirements. If you are committed to quality and eager to contribute to a facility dedicated to patient safety, we encourage you to apply.Responsibilities&middot; Perform quality assurance reviews of batch records, logbooks, and production documentation to ensure accuracy, completeness, and cGMP compliance.&middot; Support environmental monitoring programs, including sample collection, trending, and reporting in accordance with USP &lt;797&gt; requirements.&middot; Conduct in-process and finished product inspections to verify adherence to established specifications and quality standards.&middot; Assist in the review and management of deviations, non-conformances, and out-of-specification results, supporting root cause analysis and CAPA documentation.&middot; Participate in the review and revision of SOPs, work instructions, and other controlled documents.&middot; Support internal audits and inspection readiness activities, ensuring documentation and facility practices are audit-ready at all times.&middot; Assist with the management of change control processes and stability programs. &middot; Collaborate with Operations, Pharmacy, and Validation teams to address quality issues and drive continuous improvement initiatives.&middot; Maintain accurate and organized quality records in compliance with regulatory requirements and data integrity standards.Qualifications&middot; Bachelor of Science degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific field required.&middot; Minimum of 3 years of quality assurance experience in a pharmaceutical, 503B outsourcing facility, sterile compounding, or cGMP-regulated environment.&middot; Working knowledge of cGMP regulations (21 CFR Parts 210/211), USP &lt;797&gt;, and FDA 503B guidance.&middot; Experience reviewing batch records, SOPs, and quality documentation in a regulated environment.&middot; Familiarity with deviation management, CAPA processes, and change control systems. &middot; Strong attention to detail with excellent organizational and documentation skills.&middot; Effective written and verbal communication skills with the ability to clearly convey quality findings to cross-functional teams.&middot; Ability to work both independently and collaboratively in a fast-paced, compliance-driven environment.&middot; Commitment to patient safety, data integrity, and a culture of continuous quality improvement.Compensation: Starting salary: $50,000 annuallyIf you meet the requirements and are interested in joining the Atilar Pharma team, please submit your resume and cover letter.Job Type: Full-timePay: From $50,000.00 per yearBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Paid time off</li><li>Parental leave</li><li>Tuition reimbursement</li><li>Vision insurance</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>USP, FDA, and cGMP Regulations: 3 years (Preferred)</li><li>Quality assurance: 3 years (Required)</li></ul>Ability to Commute:<ul><li>Houston, TX 77060 (Required)</li></ul>Work Location: In person

Quality Assurance Technician

Morrison Healthcare

<div><ul><li>We are hiring immediately for a full time QUALITY ASSURANCE TECHNICIAN position.</li><li>
Location: Fresh and Ready - 3201 Fulling Mill Road, Middletown, PA 17057. Note: online applications accepted only.</li><li>
Schedule: Full time schedule. Days and hours may vary based on business needs. Includes weekends, holidays, and extended hours. Further details upon interview.</li><li>
Requirement: Previous food safety and quality assurance experience in a food manufacturing facility is required.</li><li>
Pay Range: $18.00 per hour to $20.00 per hour. 
<ul><li>Internal Employee Referral Bonus Available</li></ul></li></ul>
Please note that employees in this role will work in a temperature-controlled environment with exposure to cold conditions for extended periods of time.
We Make Applying Easy! Just text JOB to 75000 &amp; search for the requisition ID number 1532198 .
The advertised program is a conversational recruiting assistant that helps you apply to jobs with Compass Group. Message frequency varies. Message and data rates may apply. Text STOP to opt out or HELP for help. Terms and conditions: http://olivia.paradox.ai/moSkg
Application Deadline: applications are accepted ongoing until all openings are filled for this position. If an applicant is declined due to the position being filled, they may still be considered for future opportunities and are always welcome to reapply.
Diversity of thought and inclusion for all is what drives our success - we invite you to start your journey with us today!<div><div><div><h2 class="jobSectionHeader">
Job Summary</h2>
</div><div>
SUMMARY:
Under general supervision and according to the established policies and procedures, conducts quality assurance audits, space inspections, shop inspections, mechanical space inspections, room and area inspections and department evaluations.
Incumbent is guided by thorough knowledge of computer software system for quality program, word processing, data management, supervision, and basic building system knowledge.
ESSENTIAL DUTIES AND RESPONSIBILITIES:<ul><li>
Plans, organizes, and controls functions of computerized Quality Assurance programs in maintenance operation.</li><li>
Prepare, set-up system, and maintain computerized Quality Assurance program and schedule all inspections, audits and evaluations as per established matrix.</li><li>
Conduct all inspections, audits, and evaluations as per the established matrix. Investigate all complaints regarding quality issues.</li><li>
Operates and maintains Cleantelligent software system and all other data, hardware software systems related to the departments operation.</li><li>
Support performance improvement and safety activities.</li><li>
Audit, research, gather data and prepare reports on quality assurance and day-to-day operations.</li></ul>
Performs a variety of duties:<ul><li>
Responds to emergencies at the facility as directed.</li><li>
Submits ideas on continuous quality improvement.</li><li>
Takes minutes and participates in committees as required.</li><li>
Must be able to drive a motorized vehicle on a daily basis</li><li>
Performs related and other department duties as required.</li></ul>
QUALIFICATIONS:
<ul><li>Associates Degree in an Engineering or Business Field, and 5 years&rsquo; of experience in the maintenance field with a demonstrated skill in one trade and a good understanding of other trades through work experience at similar institutions, or;</li><li>
High School Diploma/GED and 10 years&rsquo; experience in the maintenance field, with a demonstrated skill in one trade and a significant understanding of other trades acquired through work experience at similar institution/s, and;</li><li>
The ability to read, comprehend and transmit complicated detailed instructions in writing and orally.
</li><li>Effective written (spelling/grammar) skills, computer proficient (Microsoft Office, specifically proficiency in Excel &amp; Word etc.) Database management, accounting, and knowledge of various office equipment/systems.
</li></ul></div></div></div>Associates at Fresh &amp; Ready Food Group are offered many fantastic benefits.
Full-time and part-time positions offer the following benefits to associates: Retirement Plan, Associate Shopping Program, Health and Wellness Programs, Discount Marketplace, Identity Theft Protection, Pet Insurance, Voluntary Benefits, including Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Legal Services, and Choice Auto and Home Program
Full-time positions also offer the following benefits to associates: Medical, Dental, Vision, Life Insurance/AD, Disability Insurance, Commuter Benefits, Employee Assistance Program, Flexible Spending Accounts (FSAs)
Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws. For positions in Washington State, Maryland, or to be performed Remotely, click here or copy/paste the link below for paid time off benefits information.
https://www.compass-usa.com/wp-content/uploads/2023/08/2023_WageTransparency_FreshIdeas.pdf
About Compass Group: Achieving leadership in the foodservice industry
Compass Group is an equal opportunity employer. At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law.
Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity.
Certain positions may require Florida Level 2 background screening. Details: https://info.flclearinghouse.com/
Applications are accepted on an ongoing basis.
Fresh and Ready Foods maintains a drug-free workplace.</div>

QUALITY ASSURANCE TECHNICIAN (FULL TIME)

FireKing Bakery

The PM Quality Assurance Technician is responsible for monitoring and ensuring that all products manufactured by Fireking Baking Company are safe for consumption and are top quality. The position consists of verifying product safety, quality, weights, shapes, size, and reporting all deviations to management. Shift is from 6pm - 3AM.Essential Functions:<ul><li>Responsible for enforcing GMPs</li><li>Responsible for enforcing and adhering to company policy and procedures</li><li>Responsible for monitoring product shelf-life test, weight checks, scale verifications, thermometer verification, QA Holds, Raw Material Inspections and Finished Product Inspection.</li><li>Responsible for documenting and reporting all deviations to the line lead, line supervisor, QA Supervisor, Director of QA, or production management.</li><li>Assist the Quality Supervisor / Director of Quality with quality or food safety projects.</li><li>Monitors CCP&rsquo;s to ensure the company&rsquo;s HACCP program is being followed for food safety.</li><li>Responsible for incoming ingredient inspection.</li><li>Ensures compliance with local and federal regulatory requirements throughout the manufacturing facility.</li><li>Other duties may apply</li></ul>Job Qualifications:1. Good reading and writing skills2. Bilingual preferred (English, Spanish, Portuguese)3. Must have good communication skills4. Available to work on different shift when neededTraining:1. Annual training in GMP procedures, Safety, Food Safety, Allergens, HACCP, and Sanitation &amp; Hygiene.Job Type: Full-timeBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Health insurance</li><li>Paid time off</li></ul>Schedule:<ul><li>8 hour shift</li><li>Monday to Friday</li><li>Night shift</li></ul>Work Location: In person

PM Quality Assurance Technician

Argen Corporation

<div>
 
 Monday &ndash; Friday, 7:00 am - 3:30 pm
 
 
 
 
 About the Opportunity
 
 
 
 
 Maintains and improves the quality systems in accordance with the requirements of MDSAP, ISO, FDA, QSR, and Argen policies. Executes activities concerned with development, implementation, maintenance, and continuous improvement of Argen&rsquo;s quality system.
 
 
 
 
 In this role, the successful candidate will:
 
 
 
 <ul>
 
 <li>
 Aids in the preparation of regulatory documentation for domestic and international product registrations and secures appropriate regulatory documentation including device licenses, device listings, permits, and import/export certificates.&nbsp;
 </li>
 
 <li>
 Ensures compliance to applicable regulatory standards and internal procedures.&nbsp;
 </li>
 
 <li>
 Supports design and development activities for new product development, including regulatory submissions.&nbsp;
 </li>
 
 <li>
 Test Method Documents (TMs, TM Validation Protocols, TM Validation Reports) pFMEAs.&nbsp;
 </li>
 
 <li>
 Performs ongoing quality activities on current products to improve product designs and/or manufacturing processes including participation in NCM, Complaint, and CAPA investigations, supplier activities and actions as necessary.&nbsp;
 </li>
 
 <li>
 Assists in maintenance and improvement of the Quality System with guidance of QA Management, including internal audits, external audits, and quality improvement activities.&nbsp;
 </li>
 
 <li>
 Assists Engineering in the preparation and execution of verification and validation protocols and verification and validation test reports for new products and changes to current products.&nbsp;
 </li>
 
 <li>
 Participates in Hazard Assessment, Failure Mode and Effect Analysis, and risk management analysis, as required, for new and current products.&nbsp;
 </li>
 
 <li>
 Plans and participates in internal and external audits as required.&nbsp;
 </li>
 
 <li>
 Aids in the evaluation of customer complaints for regulatory compliance and adherence to product claims.&nbsp;
 </li>
 
 <li>
 Assists in manufacturing NPI activities.&nbsp;
 </li>
 
 <li>
 Creates SOP&rsquo;s and update exiting SOP&rsquo;s.&nbsp;
 </li>
 
 <li>
 Reviews and approves Device History Records for finished device release as required.&nbsp;
 </li>
 
 <li>
 Serves as a technical resource for technicians, assemblers, and other Argen personnel.
 </li>
 
 <li>
 Other duties as assigned.
 </li>
 
 </ul>
 
 
 
 What does it take to be successful?
 
 
 
 <ul>
 
 <li>
 Bachelor&rsquo;s degree in Quality Engineering, Quality Assurance, Biomedical Engineering or an equivalent degree from an accredited institution is required or equivalent experience in quality system such as ISO 13485, 21CFR820&nbsp;
 </li>
 
 <li>
 Preferred working knowledge of ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD)R Sch3.&nbsp;
 </li>
 
 <li>
 Demonstrated understanding of required standards / regulations impacting medical devices&nbsp;
 </li>
 
 <li>
 Team-oriented professional with good interpersonal skills who is hands-on with a high energy approach to work&nbsp;
 </li>
 
 <li>
 Ability to communicate ideas and information clearly, effectively, and frequently (verbal and written)&nbsp;&middot;&nbsp;Ability to prioritize and execute tasks in a timely manner without direct supervision&nbsp;
 </li>
 
 <li>
 Knowledge of PFM, Crown and Bridge applications and their use in the dental lab is a plus
 </li>
 
 </ul>
 
 
 
 Our Awesome Benefits!
 
 
 
 
 Working for a growing innovative company like Argen means exciting opportunities for training and learning, career development and advancement from only the best in the dental industry. With all that hard work, Argen is committed to ensuring the welfare of its employees and provides an amazing benefit package that includes:
 
 
 <ul>
 
 <li>
 Health Plans
 </li>
 
 <li>
 Dental Plans
 </li>
 
 <li>
 Vision Plan
 </li>
 
 <li>
 401k with Employer Match
 </li>
 
 <li>
 Paid Time Off and Paid Holidays
 </li>
 
 <li>
 Employee Events
 </li>
 
 <li>
 Wellness Programs
 </li>
 
 <li>
 Discounts for home, travel, entertainment, relaxation that includes Mobile phone service, Technology, Airline and Hotel, Theater/Theme Park tickets, Restaurants and so much more!
 </li>
 
 </ul>
 
 
 
 &nbsp;EOE/M/F/Vet/Disabled VEVRAA Federal Contractor
 
</div>

Almarai - المراعي

<div>
 
 
 QA Technician | Saudi Arabia, Jeddah
 
 
 
 
 
 
 
 
 The Company:
 
 
 
 
 
 
 
 
 
 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.
 
 
 
 
 
 
 About the role:
 
 
 
 To handle RDNCNs and investigate minor QA related issues in the area of warehouse, transport, workshop and yard operation.
 
 
 
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Manage and follow up on Reefer Delivery Non‑Compliance Notifications (RDNCN) raised by the Sales Division.
 </li>
 <li>
 Conduct regular Good Hygiene Practice (GHP) audits across the Transportation &amp; Logistics (T&amp;L) operations.
 </li>
 <li>
 Perform Pre‑Requisite Program (PRP) verifications in line with quality and food safety standards.
 </li>
 <li>
 Support the maintenance and updating of QA databases, including GHP audit records, training logs, and QA monitoring sheets through data collection and verification.
 </li>
 <li>
 Assist in the preparation of weekly and monthly KPI reports.
 </li>
 <li>
 Monitor Non‑Conformance Notices (NCNs) and ensure timely follow‑up and closure of corrective actions with relevant stakeholders.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Requirements:
 
 
 <ul>
 <li>
 Diploma holder in any science discipline.
 </li>
 <li>
 1 Year of working experience in quality function in FMCG environment
 </li>
 <li>
 English Fluency
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 
 Almarai offers a competitive package, generous leave, medical coverage, discretionary bonus, training, and development etc.
 
 
 
 
 
 This is a great opportunity to join a successful and expanding global business, offering an excellent remuneration and benefits package.
 
</div>

MMI Industrial & Steel

<div>Job Posting: Quality Assurance / Quality Control Manager
MMI Industrial &amp; Steel is thrilled to announce an opening for the position of Quality Assurance / Quality Control Manager. This pivotal role is designed for a dedicated and technically skilled individual who is passionate about upholding the highest quality standards in industrial construction. As a Quality Assurance / Quality Control Manager at MMI Industrial &amp; Steel, you will assume full-time responsibilities in a hands-on, field-based setting. Please note, this is not a remote job and will require presence on-site to manage and oversee project quality effectively.
The QA/QC Manager is responsible for developing, implementing, and enforcing our comprehensive quality protocols across various high-stakes projects. These projects typically involve complex industrial, semiconductor, data center, and high-tech construction initiatives. The successful candidate will bring expertise and a meticulous approach to ensure all work aligns impeccably with our company standards, contractual obligations, relevant codes, and client expectations.
Responsibilities
Develop, tailor, and oversee the implementation of project-specific QA/QC plans and procedures.<ul><li>
Lead the coordination and execution of inspection protocols across all stages of the project to ensure compliance with quality standards.</li><li>
Manage and direct project teams, subcontractors, and QA/QC personnel towards achieving contractual quality requirements.</li><li>
Organize and guide quality assurance planning meetings, promoting proactive engagement among diverse project stakeholders.</li><li>
Ensure all inspection and testing activities are conducted in accordance with established standards and project schedules.</li><li>
Monitor, evaluate, and report on quality performance metrics, instituting necessary corrective actions to remedy any deviations.</li><li>
Facilitate robust documentation processes, ensuring all quality records and reports are accurate, timely, and compliant with regulatory demands.</li><li>
Act as the primary company representative in quality matters during client interactions, audits, and regulatory reviews.</li><li>
Implement continuous improvement strategies, identifying opportunities to enhance quality outcomes across projects.</li><li>
Empower and mentor QA/QC team members through organized training sessions, fostering a culture of quality and precision.</li></ul><h3 class="jobSectionHeader">
Requirements</h3><ul><li>
Bachelor&rsquo;s degree in Construction Management, Engineering, Industrial Technology, or a related field.</li><li>
At least 5-10 years of proven experience in a QA/QC role within the industrial or high-tech construction sectors.</li><li>
Strong leadership skills and prior experience managing quality assurance teams and complex projects.</li><li>
Comprehensive knowledge of quality management systems, relevant construction standards, and regulatory compliance.</li><li>
Proficiency in key software such as Procore, Bluebeam, SharePoint, and Microsoft Office Suite.</li><li>
Exemplary communication skills, capable of effectively articulating quality standards and expectations to multiple stakeholders.</li><li>
Detail-oriented with a commitment to accuracy in all areas of responsibility including inspections, documentation, and reporting.</li><li>
Ability to manage multiple projects and priorities in a dynamic, fast-paced environment.</li><li>
Preferred additional qualifications: CWI, CQC, OSHA, or similar certifications.</li><li>
Experience in fostering continuous improvement and leading root cause analysis within quality-focused initiatives.</li></ul></div>

Quality Assurance / Quality Control Manager

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LABORATORY SERVICES & QUALITY ASSURANCE LABORATORY TECH

Quality Assurance Technician

QUALITY ASSURANCE TECHNICIAN (FULL TIME)

PM Quality Assurance Technician

Quality Assurance Technician

Quality Assurance Technician

Quality Assurance / Quality Control Manager