quality control systems manager

Primally Pure

<p><b>JOB DESCRIPTION</b></p><p><b>Quality Control Manager</b></p><p><b>Location: Murrieta</b></p><p><b>THE OPPORTUNITY</b></p><p>Primally Pure&rsquo;s Quality Manager is responsible for implementing and executing inspection, testing procedures, and evaluation methods to ensure our products meet the high standards our customers expect. This role is crucial in developing and enforcing programs, practices, and procedures that promote product quality and ensure compliance across all departments. The Quality Manager partners cross-functionally to ensure sitewide Good Manufacturing Practices (GMPs) are upheld, and is responsible for driving a culture of quality, accountability, and continuous improvement.</p><p>This role reports to the Sr. Quality Manager and is responsible for briefing management on quality performance metrics, issues, and opportunities for improvement. The Quality Manager also ensures all measurement tools are properly numbered and calibrated.</p><p><b>KEY RESPONSIBILITIES</b></p><ul><li>Manage and maintain sitewide Corrective Action and Preventive Action (CAPA) documentation</li><li>Lead root cause analysis to support resolution and continuous improvement initiatives</li><li>Develop and verify adherence to in-process quality checks during production runs</li><li>Track, monitor, and report on key quality metrics across departments</li><li>Create and deliver management briefs on quality performance and continuous improvement initiatives</li><li>Develop, review, and improve quality procedures and specifications for products and processes</li><li>Train team members on quality protocols, standards, and expectations</li><li>Communicate quality expectations and requirements to production teams and other departments</li><li>Identify opportunities to enhance the manufacturing process and ensure the production of high-quality goods</li><li>Conduct regular physical inspections of facilities and operations to ensure GMP compliance</li><li>Oversee and guide personnel responsible for quality oversight and compliance</li><li>Set raw material requirements and monitor supplier compliance</li><li>Supervise quality leads, technicians, and support staff, offering coaching and development</li><li>Ensure compliance with health and safety regulations and legal standards</li><li>Monitor product development procedures and intervene when deviations from standards occur</li><li>Inspect final products and approve or reject based on quality criteria</li><li>Maintain accurate documentation and conduct statistical analyses</li><li>Collect feedback, attend meetings, and support audits and inspections with required reporting</li></ul><p><b>IDEAL CANDIDATE CHARACTERISTICS</b></p><ul><li>Excellent communication and listening skills</li><li>Bachelor&rsquo;s degree in a science-based or business-related field</li><li>3+ years of experience in quality control, ideally in a production or manufacturing environment</li><li>Production or manufacturing experience preferred</li><li>Strong attention to detail, observation, and organizational skills</li><li>In-depth knowledge of quality procedures, legal standards, and GMPs</li><li>Proficiency in data analysis, statistical methods, and IT systems</li><li>Experience in business administration is a plus</li></ul><p>Job Type: Full-time</p><p>Pay: $110,000.00 - $120,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Application Question(s):</p><ul><li>Do you have experience in the Food, Cosmetics or Skin Care Quality manufacturing industry?</li></ul><p>Work Location: In person</p>

Quality Control Manager

L3 Inspection Services, LLC

<p><b>Long Term Project at Semiconductor Facility</b></p><p>Location: Sunnyvale, CA</p><p>Position Type: QC Manager (1099 Contract)</p><p>Duration: 6+ Months (Duration based on performance)</p><p>Compensation: Hourly Rate $80+/hour (DOE)</p><p>Per Diem: $1120/week</p><p><b>Job Description</b></p><p>Seeking an experienced Quality Control Manager (1099 Contract Position) to support a large semiconductor construction project in California, working directly with a major mechanical contractor. This role will be responsible for overseeing QA/QC activities associated with process piping installation (high purity), orbital welding, pressure testing, and inspection activities in accordance with ASME B31.3 and project-specific quality requirements.</p><p><b>Responsibilities</b></p><ul><li>Ensure piping fabrication and installation activities comply with ASME B31.3, project specifications, and approved procedures</li><li>Coordinate closely with the General Contractor and client project management team on quality expectations and issue resolution</li><li>Work directly with general contractor, mechanical contractor leadership including project managers, superintendents, welding foreman and craft.</li><li>Provide oversight and technical direction to client direct-hire and contract QC inspectors.</li><li>Oversee and support welder qualifications, welding procedure compliance, inspection planning, pressure testing and documentation compliance.</li><li>Support quality assurance efforts to meet client and regulatory requirements</li></ul><p><b>Qualifications</b></p><ul><li>AWS Certified Welding Inspector (CWI) certification preferred</li><li>VT Level Il certification acceptable based on relevant project experience</li><li>Strong knowledge of ASME codes, high-purity piping systems, orbital welding and bonding processes.</li><li>Proven ability to work directly with project management, construction supervision, and craft personnel</li><li>5+ years experience with semiconductor high purity process piping systems strongly preferred.</li></ul><p><b>Work Schedule</b></p><ul><li>Typical schedule: 10 hours per day, Monday through Friday</li><li>Occasional Saturday work may be required based on project demands</li><li>Project-based schedule with expected long-term duration</li></ul><p>Pay: From $80.00 per hour</p><p>Work Location: On the road</p>

Metallus

<p></p><div><p><b>Date: </b>Mar 19, 2026
</p><p><b>Location:</b> Canton, OH, Gambrinus Steel Plant (USA_GAMB STL), 44706
</p><p><b>Company: </b>Metallus
</p><div><div>Joining the Metallus team means becoming part of a legacy that dates back over a century. We are an industry leader, manufacturing the cleanest steel in the world for companies in the industrial, aerospace and defense, automotive, and energy markets.</div><br>
<div></div>
<div>
Relocation may be provided for this role.</div><div><br>
<b>
Purpose</b></div>
<div>
Defines and governs the Metallus Quality Management System to ensure business standards and processes meet ISO based, or equivalent, requirements and support consistent, scalable execution.</div><br>
<div></div>
<div>
Utilize expert knowledge of customer, industry, international quality standards, manufacturing processes, problem solving, lean tools, project management, and team facilitation to direct and assigned teams in setting goals, and strategic initiatives to better define and improve manufacturing and business process quality management systems so Metallus we fulfills the expectations of our markets, customers, and support the future growth of our business.<br>
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Leads and mentors teams and other associates in the business through both direct and indirect leadership, including setting clear expectations, priortizing work, and holding team members accountable for performance, in interpreting standard requirements and intent and translating them into terms that the business can understand and fulfill in the most cost effective, value-added manner consistent with our management, customer, and shareholder needs. This is done based on technical and subject matter expertise, in-depth understanding of quality systems and our overall business, and critical thinking that leads to optimal solutions which introduces the lowest impact and risk, but with enhanced value for our business from our management's perspective.<br>
<br>
Develops recommendations and leads internal process improvement and enhancement of quality systems. Leads, directs, or conducts audit assessments, performs statistical analysis and recommends process controls to improve all facets of business performance. Facilitates or leads quality problem-solving teams for systemic improvements. Evaluates performance and system health signals to create strategic proposals to management and senior management for initiatives to improve quality and business performance.</div><br>
<div></div>
<div>
This role has direct responsibility for building, developing, and leading a high performing quality systems team, ensuring appropriate capability, engagement, accountability, and succession to support current and future business needs.</div><br>
<div></div>
<div><b>
Responsibilities</b></div>
<ul>
<li>Evaluates business need and risk, guides and/or conducts extensive studies or pilots that effectively develop and/or apply new elements or customer specific requirements to the quality management system. Serves as a key quality system representative, on both the Quality Management System Team and assigned area(s) to ensure compliance to new or current quality system requirements.</li>
<li> Analyzes, interprets and recommends/applies quality system requirements to obtain and maintain customer and registrar approval of our quality system. This requires quality system expertise, business knowledge and the ability to interpret and communicate customer needs throughout relevant areas of the business and to obtain agreement in the business to meet these needs. Also recommends long term registration status goals to best position the business to meet its plan.</li>
<li>Leads, facilitates, and mentors direct reports and cross-functional teams others through the problem solving process to obtain deep root cause analysis and effective interplant corrective actions to fulfill and enhance quality management system processes and maintain the integrity of our corrective action system.</li>
<li>Determines best quality indices to use and mentors and develops team members others in quality system and performance analysis to focus quality efforts in the business on those things that directly contribute to meeting business goals and objectives. Analyzing and reporting of manufacturing information such as yield, cost of quality, complaints, CAR/PAR's, etc. to determine and recommend where to best apply resources for improvement of business results and to satisfy customers.</li>
<li>Able to apply and mentor others in the use of consistent and optimal statistical techniques, problem-solving, and other tools of quality (such as control plans, FMEA's, flow charts, graphical analysis, capability analysis, regression analysis, etc.). Maintenance of certifications of expertise in the field of quality such as the ASQ Certified Quality Auditor or Engineer designation. Leading the business in various applications of quality system principles such, as APQP.</li>
<li>Is an expert or administers the internal quality system audit process. Is a lead auditor for the process of quality system auditing and verification of corrective actions, either internally or at supplier facilities. Uses auditing skills, up to date knowledge of primary quality system standards, lead assessor training, lead assessor planning and control of audit teams, timely reporting of findings &amp; understanding of key control characteristics in the business. Performs consulting activities by recommending possible solutions to ensure compliance to stated requirements.</li>
<li>Leads and develops the quality system organization by owning talent management, performance accountability, and resource prioritization to ensure sustained capability, engagement, and execution of the quality management system in support of business objectives.</li>
<li>Initiates or provides key leadership for complex projects, including assigning resources, setting expectations, and ensuring accountability for results.</li>
<li>Effectively lead management of change initiatives both internally and those requiring customer approval.</li>
<li>Company and QS representative on customer audits critical to maintaining existing business and acquiring new business.</li>
<li>This role is both a senior technical contributor and a people manager, requiring the ability to balance hands on technical leadership with effective team leadership and talent development.</li></ul><br>
<div></div>
<div><b>
Minimum Qualifications</b></div>
<ul>
<li>Bachelor&rsquo;s Degree in engineering with 12 years of experience in quality management, quality systems, leading audits, managing compliance, or manufacturing.</li></ul><br>
<div></div>
<div><b>
Preferred Qualifications</b></div>
<ul>
<li>Bachelor&rsquo;s Degree in materials engineering with 15 years of experience in quality management, quality systems, leading audits, managing compliance, or manufacturing.</li></ul><div></div><div><br>
The company prohibits harassment or discrimination against any employee on the basis of any status protected by law, including, but not limited to, race, religion, color, national origin, ancestry, age, disability, genetic information, gender, sex or veteran status.</div></div></div><p></p>

Quality Systems Manager

Grifols

<div></div><div><div><div><div><div><p>Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.</p></div></div><div><br>
<div></div>
</div><br>
</div></div><div>We&rsquo;re Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!</div><br>
<div></div>
<div>
If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a <b>QUALITY SYSTEMS MANAGER</b>! Please read on ...</div><br>
<div></div>
<div><b>
APPLICATION DEADLINE: </b>APRIL 12, 2026</div><br>
<div></div>
<div><b>
Job Title: </b>QUALITY SYSTEMS MANAGER</div>
<div><b>
Estimated Salary Range: </b><b>$62,500.00 - $93</b><b>,500.00</b> per year, depending on training, education, and experience. This position is eligible to participate in up to 20% of the company bonus pool.</div>
<div><b>
Relocation Assistance! </b>This position is eligible for relocation assistance of up to $20K!</div><br>
<div></div>
<div><b>
Summary:</b></div>
<div>
Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.</div><br>
<div></div>
<div><b>
Primary Responsibilities for Role:</b></div>
<ul>
<li>Maintains oversight of the center&rsquo;s quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties.</li>
<li>Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance.</li>
<li>Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained.</li>
<li>Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks.</li>
<li>Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required.</li>
<li>Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations.</li>
<li>Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product.</li>
<li>Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness.</li>
<li>Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment.</li>
<li>Performs a review of the documentation of unsuitable test results and unit lookback information.</li>
<li>Performs a review of donor adverse event reports and the applicable related documents.</li>
<li>Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file.</li>
<li>Performs employee training observations to ensure staff competency prior to releasing employees to work independently.</li>
<li>Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance.</li>
<li>Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities.</li>
<li>Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues.
</li><li>Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented.
</li><li>Holds monthly Quality Meeting to communicate status updates and manage action outcomes.</li><br>
</ul>
<div></div><div><b>Other Responsibilities for Role:</b></div>
<ul>
<li>Leads projects and initiatives as requested.</li><br>
</ul>
<div></div><div>This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.</div><div><br>
</div><div><b>Job Requirements:</b></div>
<div><b>
EDUCATION:</b></div>
<ul>
<li>Bachelor of Science degree or equivalent.</li>
<li>Certified and proficient in quality and compliance.</li>
</ul>
<div><b>EXPERIENCE:
</b></div><ul><li>Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment.</li>
</ul><ul><li>Experience with plasma or whole blood.</li>
</ul>
<div><b>EQUIVALENCY:
</b></div><div>Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor&rsquo;s degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate&rsquo;s degree with 6 years of experience, or a Master&rsquo;s degree with 2 years of experience.</div>
<div><b>
KNOWLEDGE, SKILLS &amp; ABILITIES:
</b></div><div>Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.</div><br>
<div></div>
<div><b>
Occupational Demands:</b></div>
<div>
Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32*, miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.</div><br>
<div></div>
<div>
&ldquo;We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers.&rdquo;</div><br>
<div>
</div><div>#BiomatUSA
</div><div>#CB
</div><div>#GrifolsJobs
</div><div>#Plasma
</div><div>#app
</div><div>#LI-Onsite</div>
<div>
#Indeed</div><br>
<div></div>
<p><b>COMPENSATION AND BENEFITS:</b></p>
<p>
The estimated pay scale for the <b>QUALITY SYSTEMS MANAGER </b>role based in <b>Colorado Springs, CO</b> is <b>$62,400.00 - $93,500.00</b><b> per year</b>. Additionally, the position is eligible to participate in up to <b>20%</b> of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!</p>
<p><b>
THIRD PARTY AGENCY AND RECRUITER NOTICE:</b></p>
<p>
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.</p>
<p><b>
EEO:</b></p>
<p><b>
GRIFOLS </b><b>provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.</b></p>
<p></p>
<p><b>Location: NORTH AMERICA : USA : CO-Colorado Springs</b></p>
<div><b>
Center Address: </b>3776 Airport Rd, Colorado Springs, CO 80910</div>
<div><b>
Contact:</b> Alex S. Contreras, <i>Senior Talent Acquisition Partner </i>&ndash; (213) 219-5494 | acontreras@grifols.com</div><br>
<p></p>
<p>
Learn more about Grifols</p>
<ul>
<li>Follow us on<b> Facebook:</b> https://www.facebook.com/grifolsplasma1940/
</li><li>Follow us on<b> LinkedIn:</b> https://www.linkedin.com/company/grifols/
</li><li>Follow us on <b>Instagram:</b> https://instagram.com/grifolsplasma_us</li></ul><br>
<div>
</div><div>To find more jobs with<b> Grifols:</b> https://grifols.jobs</div>
<div>
Or Text GRIFOLS to<b> 833-233-7621</b></div></div>

Quality Systems Manager for Plasma Center

Robar Enterprises

<div><p>We are looking for a <b>QC Manager</b> to lead our quality department. You will be responsible for ensuring every piece of steel leaving our facility meets project specifications, AWS D1.1 welding codes, and AISC certification standards. Unlike traditional QC roles, we require a manager who is tech-forward, someone who can leverage <b>Tekla </b>to track inspections and manage non-conformance reports (NCRs).</p><p><b>
Key Responsibilities</b></p><ul><li><i>
Quality Management System (QMS):</i> Act as the primary lead for our AISC Certification audits. Maintain, update, and enforce the shop Quality Manual.</li><li><i>
Visual &amp; Dimensional Inspection:</i> Oversee fit-up and final weld inspections.</li><li><i>
Welding Oversight:</i> Manage the Welding Procedure Specifications (WPS) and ensure all welders are currently certified (WPQR) for the processes being used.</li><li><i>
Material Traceability:</i> Ensure 100% traceability of heat numbers and Material Test Reports (MTRs) from receiving through to the finished product.</li><li><i>
NDT Coordination:</i> Coordinate third-party Non-Destructive Testing (NDT) including Ultrasonic (UT), Magnetic Particle (MT), and Radiographic (RT) testing as required by the contract.</li><li><i>
Digital Integration:</i> Champion the use of mobile tablets on the shop floor for real-time QC signoffs within the Tekla ecosystem to eliminate paper-trail lags.</li></ul><p><b>
Required Skills &amp; Qualifications</b></p><ul><li><i>
Certification:</i> Current AWS Certified Welding Inspector (CWI) status is required.</li><li><i>
Experience:</i> Minimum 5&ndash;7 years in structural steel fabrication.</li><li><i>
Tekla Proficiency:</i> Ability to navigate Tekla to pull dimensions, check piece marks, and verify bolt patterns.</li><li><i>
Regulatory Expert:</i> Deep understanding of AISC 360 (Specification for Structural Steel Buildings) and AWS D1.1.</li><li><i>
Leadership:</i> Proven ability to halt production when quality is compromised and coach shop personnel on corrective actions.</li></ul><p><b>
If you are passionate about maintaining the highest quality standards in structural fabrication and have a proven track record in quality control management, we encourage you to apply for this exciting opportunity.</b></p></div>

<div>
 <p>
  <strong>
   Company Overview:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Dar, the founding member of the Sidara group, is an international multidisciplinary consulting organization specializing in engineering, architecture, planning, environment, project management, facilities management, and economics. Sidara operates in 60 countries with 20,500 professionals, Dar connects people, places, and communities through innovative solutions to the world's most complex challenges. We deliver projects from inception through completion, embracing challenges to empower communities worldwide. Learn more at
  <strong>
   www.dar.com
  </strong>
  .
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Our Vision and Values:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  We aspire to be the chosen home of those with a gift for crafting solutions that empower people and an unwavering passion for learning and innovation. Our core values shape our culture and guide our decision-making. We are committed to:
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Excellence
  </li>
  <li>
   Responsibility
  </li>
  <li>
   Empowerment
  </li>
  <li>
   Connectivity
  </li>
  <li>
   Courage
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Role Overview:
  </strong>
 </p>
 <p>
  To oversee and manage all quality assurance and quality control activities within the Maintenance and Operation project, ensuring that all services, maintenance works, and operational activities comply with project specifications, quality standards, and client requirements.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Develop, implement, and monitor the Quality Management System (QMS) for the project.
  </li>
  <li>
   Ensure all maintenance and operational activities comply with quality standards, project specifications, and contractual requirements.
  </li>
  <li>
   Conduct regular quality inspections and audits of maintenance works and services.
  </li>
  <li>
   Review and approve method statements, inspection plans, and quality documentation.
  </li>
  <li>
   Monitor contractor performance and ensure compliance with quality procedures.
  </li>
  <li>
   Identify non-conformities and ensure corrective and preventive actions are implemented.
  </li>
  <li>
   Coordinate with project teams and contractors to ensure quality objectives are achieved.
  </li>
  <li>
   Prepare and submit quality reports and performance evaluations to project management.
  </li>
  <li>
   Ensure compliance with health, safety, and environmental standards related to maintenance activities.
  </li>
 </ul>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Mechanical Engineering.
  </li>
  <li>
   Minimum 20 years of experience, including experience in maintenance and operation projects.
  </li>
  <li>
   Strong knowledge of Quality Assurance and Quality Control systems and standards.
  </li>
  <li>
   Experience in quality management within large infrastructure or facilities maintenance projects.
  </li>
  <li>
   Professional certifications such as ISO 9001 Lead Auditor or Quality Management certifications are preferred.
  </li>
 </ul>
 <p>
 </p>
</div>


Quality Control & Assurance Manager

Batchelor & Kimball

<div><p>Headquartered in Conyers, Georgia, Batchelor &amp; Kimball takes pride in partnering with our clients to deliver excellent results from engineering and construction to operations and maintenance. We offer design/build and turnkey construction services, including teaming with selected subcontractors for electrical and general construction. If you are looking to grow your career and thrive in a team environment, then we invite you to apply for this position.<br>
<br>
</p><p></p><br>
<p>There&rsquo;s not a lot of BS here, and not a lot of turnover. Good people work at Batchelor &amp; Kimball. We&rsquo;re good at our jobs, and good to each other. We have high expectations because the work is challenging, but we know the most valuable thing about the work is the people who do it. If this sounds like a good fit for you, we&rsquo;d like to meet you!</p><p></p><p><br>
We are seeking a Quality Control Manager for our facility in Stillwater, OK that will provide Quality Management (QM) related services. In this role, you will be involved in daily operations to plan and execute QM operations; also, in resolving complex issues to meet QM expectations while assisting management with scheduling and budgets. As the QA/QC Manager, you will frequently be working with the construction crews on our job sites. You will be the main point of contact with internal and external individuals at all management levels, and you will be responsible for project QM successful outcomes.
<br>
<br>
<b>Job Responsibilities/Accountabilities:</b></p>
<ul>
<li>Ensure a safe working environment is maintained at all times.</li>
<li>Manage inspector resources including third party and direct-hire quality inspectors.</li>
<li>Provide overall project-wide oversight on quality and requirements compliance matters on QA/QC functions. Monitor construction activities and review materials and equipment delivered to the project for adherence to specifications, coordinating lists, punch list items, observations and logs.</li>
<li>Manage company risk and understand all aspects of contract documents.</li>
<li>Manage ASME/AWS/IPC/AWWA/UPC code related welding projects.</li>
<li>Work with preconstruction, field supervision and other teams to ensure the project is set up to support the quality management needs of the program.</li>
<li>Establishes metrics to identify trends for inspections, non-conformances root causes and corrective/preventive actions per the ISO 9001 Quality Standard.</li>
<li>Ensure that Quality is maintained on site in relation to all affected aspects of the project.</li>
<li>Responsible for recognizing and implementing change orders as it relates to quality.</li>
<li>Collaborate with clients, engineers, technicians, managers, and other project stakeholders to achieve project objectives, work with and support engineers, technicians, and other project managers across multiple disciplines.</li></ul><br>
<p><br>
<b>Supervisory /Budgetary / External communications responsibility</b></p>
<ul>
<li>This an individual contribution role. The incumbent will be responsible for communicating with internal employee as well as third party companies and the IT team at EMCOR.</li></ul><br>
<p><br>
<b>Knowledge, skill and ability requirements (minimum competencies required for job performance)</b></p>
<ul>
<li>Ability to speak clearly and exercise good judgment.</li>
<li>Ability to work under pressure.</li>
<li>Ability to work remote locations.</li>
Ability to travel and move &lt;<li>- delete depending on project location.</li>
<li>Able to create a collaborative team environment.</li>
<li>ASME,AWS, IPC,AWWA,UPC welding experience.</li>
<li>Ability to read, comprehend, and interpret technical literature/writing and plans.</li>
<li>Ability to define problems, assess options and make appropriate recommendations.</li>
<li>Ability to distinguish between shades of color.</li>
<li>Competence and confidence in public speaking/presentations.</li>
<li>Self-driven desire to learn, become competent, and succeed in field.<br>
</li>
<li>Good verbal and written communication with the ability to train and mentor.</li>
<li>Exudes a professional demeanor.</li>
<li>Good analytical skills and ability to generate creative solutions.</li>
<li>Ability to perform well and meet expectations in a fast-paced environment.</li>
<li>Good interpersonal skills.</li>
<li>Ability to coordinate project activities relating to Quality and monitor progress to successfully reach project goals.</li>
<li>Ability and willingness to demonstrate ethical behavior and a high level of integrity.</li>
<li>Ability to balance team and individual responsibilities.</li>
<li>Ability to cooperatively work with others.</li></ul><br>
<p><br>
<b>Prior work experience and educational requirements</b></p>
<ul>
<li>Minimum 15 years&rsquo; experience in the construction industry with a contractor engaged in general building construction.</li>
<li>Prior experience with welding to include certification in code stamp.</li>
<li>Knowledge of a wide range of construction materials, methods, and techniques.</li>
<li>Combination of high school diploma with QC experience and certifications will be considered.</li>
<li>Proficient in MS-based software including Word, Excel, Outlook.</li>
<li>Proficient with QA/QC systems, platforms, and technologies that allow for tracking, metrics and reporting. Cx Alloy, Procore, Autodesk Construction Cloud, BIM 360, Project Sight etc.</li>
<li>OSHA 10 or 30-hour certification.</li></ul><br>
<p><br>
<b>Physical Demands</b></p>
<ul>
<li>The physical demands are those of a typical construction site, including some field travel:</li>
<li> Ability to lift 50 lbs. as necessary when performing necessary duties.</li>
<li>Work from heights (ladder access and usage)</li>
<li>Work outside during all types of weather</li></ul><br>
<p><br>
NOTE: This job description is not intended to be all-inclusive. The duties described may be changed or reassigned at the discretion of management, and the employee may be required to perform duties that are not listed in the job description.</p></div><p></p>

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