quality auditor

CCE Contracting & Construction Enterprises

<p>Key Responsibilities</p><ul><li>Develop and implement internal QA/QC audit plans and schedules.</li><li>Conduct periodic internal audits of quality management systems, processes, and project activities.</li><li>Verify compliance with approved quality plans, procedures, specifications, and contractual requirements.</li><li>Review quality records, inspection reports, test reports, material approvals, and non-conformance reports (NCRs).</li><li>Identify non-conformities, observations, and opportunities for improvement.</li><li>Prepare detailed audit reports and communicate findings to management and relevant stakeholders.</li><li>Monitor and verify the implementation and effectiveness of corrective and preventive actions.</li><li>Ensure compliance with applicable quality standards and organizational procedures.</li><li>Maintain audit records and documentation in accordance with established requirements.</li><li>Provide recommendations to enhance quality performance and continuous improvement.</li><li>Participate in management reviews and quality performance assessments as required.</li></ul><p>Minimum Qualifications</p><ul><li>Bachelor&rsquo;s Degree in Engineering, Quality Management, or a related discipline.</li><li>Certified Internal Auditor or ISO 9001 Internal Auditor/Lead Auditor certification.</li><li>Additional quality management certifications are preferred.</li></ul><p>Experience Requirements</p><ul><li>Minimum 10 years of experience in QA/QC auditing.</li><li>Proven experience auditing infrastructure and construction projects.</li><li>Experience in implementing and auditing Quality Management Systems.</li><li>Familiarity with contractor and consultant quality assurance processes.</li></ul><p>Skills &amp; Competencies</p><ul><li>Strong knowledge of Quality Management Systems (QMS) and ISO 9001 requirements.</li><li>Excellent auditing, analytical, and problem-solving skills.</li><li>Ability to prepare professional audit reports and technical documentation.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work independently and maintain objectivity and confidentiality.</li><li>Proficiency in Microsoft Office applications and document control systems.</li></ul><p>Reporting</p><ul><li>Reports audit findings, recommendations, and compliance status to project management and relevant stakeholders.</li><li>Supports management in ensuring continual improvement and compliance with quality requirements.</li></ul><p>Application Question(s):</p><ul><li>Your current location?</li><li>Are you able to relocate?</li><li>Are you working currently?</li><li>Your current salary?</li><li>Expected salary?</li><li>Is your Iqama valid?</li><li>Notice period (when you can join?)</li></ul><p>Work Location: In person</p>

Registered Internal Auditor (QA/QC)

Unique Maritime Group

<div><p>Join Unique Group and Shape the Future of Engineering &amp; Technology Unique Group, a global leader in subsea technology and engineering, is driven by innovation and a commitment to excellence. Guided by our core values&mdash;Curious, Conscious, Committed&mdash;we encourage our team to break new ground in the subsea industry. Whether you&rsquo;re leading projects or driving innovation, your contributions will have a global impact. Join us and make your mark at Unique Group. Apply today!</p></div>
<br><div><div><h2 class="jobSectionHeader"><b>General Task Management</b></h2>
<ul><li>Manage all quality-related issues within the diving team (e.g. Internal, supplier, customer and customer warranty)</li>
<li>Identify root cause and instigate permanent corrective actions for product quality issues.</li>
<li>Work with internal and external stakeholders to resolve quality issues that arise as quickly and efficiently as possible to prevent compromising quality and safety standards.</li>
<li>Carry out product and process auditing.</li>
<li>Ensure control plans and associated documentation are implemented effectively and maintained.</li>
<li>Participate in cross-functional teams in the development of new products or changes related to current products in meeting customer requirements.</li>
<li>Contribute to continuous improvement activities.</li>
<li>Quality control of work by appropriate reviews</li>
<li>Support and lead process improvement activities</li>
<li>Write reports and present progress at project meetings and to clients.</li>
<li>Achieve goals within budget.</li>
 </ul><h2 class="jobSectionHeader"><b>People Management</b></h2>
<ul><li>Support groups of technicians and engineers</li>
<li>Provide guidance and necessary training to other team members</li>
 </ul><h2 class="jobSectionHeader"><b>Relationship Management</b></h2>
<ul><li>Support regular inspection meetings with representatives from appropriate departments to establish an action plan for improving build quality</li>
<li>Communicate efficiently throughout the shop floor and with own and customer&rsquo;s management</li>
<li>Liaise and communicate with other departments, customers, suppliers and other service providers</li>
</ul><h2 class="jobSectionHeader"><b>QHSSE</b></h2>
<ul><li>All activities must be executed in accordance with the company&rsquo;s Integrated Management System (IMS) to ensure compliance with the company&rsquo;s ISO accreditation.</li>
<li>Adhere to departmental &amp; interdepartmental business processes.</li>
<li>The employee shall adhere to all company Occupational Health &amp; Safety, Environmental, and Quality policies, procedures, and work standards.</li>
<li>The employee has the AUTHORITY to STOP WORK should an unsafe act or condition be observed to ensure compliance with OH&amp;S regulations and to achieve a ZERO HARM working environment.</li>
<li>There is an obligation on the employee to report such observations and interventions to the HSE Manager or Management</li>
</ul><h2 class="jobSectionHeader"><b>Knowledge, Skills &amp; Experience:</b></h2>
<ul><li>Bachelor&rsquo;s degree in engineering or related field plus at least 5 years&rsquo; experience in a Quality Management environment in similar role.</li>
<li>DIVING System IMCA Design auditor. (Strongly advantageous)</li>
</ul><h2 class="jobSectionHeader"><b>Further requirements:</b></h2>
<ul><li>Certified ISO Internal Auditor</li>
<li>Experience at working both independently and in a collaborative, collaborative environment is essential.</li>
<li>ISO Internal Auditor</li>
<li>Knowledge in Industrial Standards Such as IMCA, ASME, AWS, API</li>
<li>Knowledge in Classification Rules such as ABS, DNV, Lloyds BV Etc.,</li>
<li>Advanced proficiency in full MS Office suit</li>
<li>Deep knowledge of quality assurance terminology, methods, and tools</li>
</ul><p><b>Please forward your CV to </b><b>shibani.menon@uniquegroup.com</b></p>
</div><div><div><div><div><b>Job Category: </b>Operations
</div><div><b>Job Type: </b>Full Time
</div><div><b>Job Location: </b>Sharjah United Arab Emirates</div></div></div></div></div>

Quality Inspector

ANSWER CONSULTING

<div><h2 class="jobSectionHeader"><b>A day in this role</b></h2><p>
You start by reviewing current procedures and building a risk-based audit plan aligned to AS 9100. By mid-morning, you&rsquo;re on the production floor comparing product appearance, composition, and functionality to drawings, customer specifications, and regulatory expectations. After lunch, you coach auditors, assign audit scopes, and observe practices in-process. You wrap the day by updating the QMS training course you own&mdash;complete with a knowledge-check quiz&mdash;then document findings, confirm corrective and preventive actions are effective, and prepare insights for senior leadership. Along the way, you stay current on industry regulations and standards so our system never falls behind.</p><h3 class="jobSectionHeader"><b>
What you&rsquo;ll do</b></h3><ul><li>
Develop and implement AS 9100 audit plans that reflect internal procedures and regulatory needs.</li><li>
Execute audits to plan, from opening meetings through closure and verification activities.</li><li>
Define and maintain product conformity criteria aligned to drawings, customer requirements, and applicable regulations.</li><li>
Evaluate processes and outputs for quality in appearance, composition, and performance.</li><li>
Lead and delegate work to audit team members; oversee execution and follow-up.</li><li>
Train employees on quality standards, procedures, and QMS best practices.</li><li>
Ensure products consistently meet customer and industry benchmarks.</li><li>
Document nonconformities, drive robust corrective actions, and verify their effective implementation.</li><li>
Author clear, data-driven audit reports and present results to senior management.</li><li>
Continuously monitor evolving regulations and standards to keep the QMS current.</li></ul><h3 class="jobSectionHeader"><b>
What you bring</b></h3><ul><li>
Bachelor&rsquo;s degree in business management, quality management, or a related field&mdash;or an equivalent blend of education and experience.</li><li>
5+ years as a quality auditor across AS9100, ISO 9001, ISO/IEC 17025, and/or ISO 14001 within a related industry.</li><li>
Formal AS 9100 auditor training completed through an accredited AS 9100 regulatory/oversight body.</li><li>
Proficiency with quality management software and the Microsoft Office Suite.</li><li>
Post-secondary coursework in Aerospace preferred.</li><li>
ASQ certification is advantageous.</li><li>
Deep knowledge of industry standards, exceptional attention to detail, and strong leadership, organization, and communication skills.</li></ul><h3 class="jobSectionHeader"><b>
Core capabilities</b></h3><ul><li><b>
Language:</b> Read and comprehend straightforward instructions, short correspondence, and memos.</li><li><b>
Reasoning:</b> Apply general understanding to carry out detailed written and verbal instructions; resolve issues with a limited number of concrete variables in standardized situations.</li><li><b>
Mathematics:</b> Perform addition, subtraction, multiplication, and division using whole numbers, fractions, and decimals.</li><li><b>
Technical literacy:</b> Interpret detailed blueprints, shop travelers, and engineering sketches.</li></ul><h3 class="jobSectionHeader"><b>
Tools &amp; references</b></h3><ul><li><b>
Tools:</b> Laptop computer, copiers.</li><li><b>
Materials:</b> Existing procedures, policies, and current industry, regulatory, and statutory documents as needed.</li></ul><h3 class="jobSectionHeader"><b>
Apply now</b></h3><p>
https://evoportalus.tracker-rms.com/GlobalConductor/apply?jobcode=13081</p><h3 class="jobSectionHeader"><b>
You should be proficient in:</b></h3><ul><li>
AS9100</li><li>
AS9100 Experience</li></ul></div>

Aerospace QMS Lead Auditor (AS9100)

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
First Shift (Days)<p></p><p><b>
Environmental Conditions</b></p>
Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)<p></p><p><b>
Job Description</b></p><p></p><p>
At Thermo Fisher Scientific team, you&rsquo;ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe and delivering COVID-19 solutions. As the world leader in serving science, with the largest investment in R&amp;D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.</p><h2 class="jobSectionHeader"><b>
Location/Division Specific Information</b></h2><p><b>
This is an on-site role based at our Detroit, Michigan campus,</b> supporting our Biologicals and Chemicals Division. The Detroit Site maintains ISO 13485 Quality Management System (QMS) certification, manufacturing peptones and other fine chemicals used in bioproduction and culture media.</p><h2 class="jobSectionHeader"><b>
Discover Impactful Work:</b></h2><p>
The Quality Specialist II will have various responsibilities within Quality Assurance to support product release activities, ensuring on-time delivery to customers as well as initiatives for maintaining compliance to the QMS.</p><h2 class="jobSectionHeader"><b>
A day in the Life:</b></h2><ul><li>
Complete Quality record reviews including, but not limited to, batch history records, equipment and calibration documentation, QC records, and shipping records.</li><li>
Support timely delivery of products to customers through lot release (raw materials and manufactured product) and preparation of certificates of analysis</li><li>
Respond to compliance-related customer inquiries in a timely manner, including but not limited to preparing certificates of origin and other regulatory documents, supplier questionnaires</li><li>
Maintain Quality records according to Thermo Fisher Scientific policies and procedures</li><li>
Maintain the site&rsquo;s Quality Systems&rsquo; compliance to ISO 13485:2016 standards and regulatory requirements and policies as applicable.</li><li>
Support the execution of the site's training program</li><li>
Support internal and external audits and ensure compliance with site and industry standards</li><li>
Assist in completion of various QMS requirements, including but not limited to quality management reviews, change management including document change control, and customer notifications.</li><li>
Other projects will be assigned as various business needs arise</li></ul><h2 class="jobSectionHeader"><b>
Keys to Success:</b></h2><h2 class="jobSectionHeader"><b>
Education</b></h2><ul><li>
A Bachelor's Degree is required. A science major preferred.</li></ul><h2 class="jobSectionHeader"><b>
Experience</b></h2><ul><li>
Minimum of 2 years' experience in a Quality Assurance function in an ISO 13485 environment. Familiarity with the life sciences industry is desired.</li><li>
Record review and/or auditing experience; ASQ CQA or ISO 13485 Lead Auditor or Internal Auditor certifications preferred but not required.</li><li>
Familiarity with enterprise software systems including ERPs, electronic document control systems, CAPA and training software packages.</li></ul><h2 class="jobSectionHeader"><b>
Knowledge, Skills, Abilities</b></h2><ul><li>
Strong critical thinking skills, with a close attention to detail and history of good judgment</li><li>
Proven ability to prioritize work according to urgency and impact, with good time management skills</li><li>
Driven and resourceful, with minimal to moderate direction required</li><li>
Proficiency in MS Office tools (e.g. Word, Excel, PowerPoint) and comfortable with learning and using new software programs</li><li>
Strong technical writing skills</li><li>
Proven ability to work in a team and matrixed environment</li></ul><h2 class="jobSectionHeader"><b>
Benefits</b></h2><p>
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!</p><p></p><p>
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.</p><h2 class="jobSectionHeader"><b>
Apply today! http://jobs.thermofisher.com</b></h2><p>
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.</p><h2 class="jobSectionHeader"><b>
Accessibility/Disability Access</b></h2><p>
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.</p><ul><li>This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.</li></ul></div><p></p>

Quality Specialist II

Zoetis

<div><p><b>Quality Liaison
</b></p><p><b>Louisville Lab
</b></p><p></p><p><b>Summary:
</b></p><p>The Quality Liaison is responsible for driving Non-Conforming Event (NCE) management and conformance to ZRL Quality checklists and policies for their location, as well as providing coordination for local Document Control. The primary focus is on investigating NCEs and Opportunities for Improvement (OFIs), developing and implementing Corrective/Preventative Actions (CAPAs), and supporting the quality team in driving continuous improvement. This role serves as a subject matter expert in quality systems, supports staff training of quality requirements, tools and initiatives, and collaborates with Lab Operations, Medical, Operations Support, and other supporting department teams. Additionally, this position will be responsible for project managing the quality assessment activities, participating as an auditor in Quality Assessments, and leading the lab in OFI resolution. The Quality Liaison utilizes the MediaLab web-based Quality Management System platform for daily operations and serves an administrator for this software. This role is also responsible for compiling and analyzing quality metrics for quality scorecards for their location.
</p><p></p><p><b>Job Duties:
</b></p><p>&middot; Oversee and project manage Non-Conforming Event Management for site. Collaborate with local management and subject matter experts to investigate and resolve Quality Improvement Tickets (QITs). Apply structured root cause analysis techniques (such as 5 Whys, Fishbone Diagram, etc.) to accurately identify underlying issues, work with departmental and local leaders to develop and implement corrective/preventive actions (CAPAs), and, when appropriate, include Return on Investment (ROI) analysis using the Cost of Poor Quality calculator.
</p><p>&middot; Conduct periodic comprehensive and weekly focused audits to maintain continuous quality conformance to ZRL checklist requirements for patient safety and assessment readiness. Coordinate onsite audits for location, participate in other ZRL Quality Assessments as required, and project manage and participate in the resolution of findings through Opportunity for Improvement (OFI) QITs.
</p><p>&middot; Act as the site&rsquo;s Document Control specialist, ensuring all documents are properly managed and compliant, and maintaining an up-to-date local SOP manual for use during system downtime.
</p><p>&middot; Deliver training to staff on Quality related programs, tools, philosophies and processes. Serve as subject matter expert to answer questions around document control, NCEs, good documentation practices, temperature monitoring, quality assessment program and quality related topics to ensure consistent compliance and excellence.
</p><p>&middot; Manage the Man Overboard (MoB) program for location by overseeing the Man Overboard program. Coordinate the searches for missing samples using MoB form, ensuring each incident is documented as a Quality Improvement Ticket (QIT) to facilitate tracking through resolution, remediation and corrective action development.
</p><p>&middot; Generate and communicate local quality metrics to inform Management Review KPI feedback.
</p><p>&middot; Contribute to other quality improvement projects and fulfill other duties as assigned.<br>
</p><p></p><p><b>Education/Experience:<br>
</b></p><p></p><p>Minimum Requirements:
</p><p>&middot; Requires an Associate&rsquo;s degree in science or related discipline or equivalent combination of experience and/or education.
</p><p>&middot; Minimum of two (2) years on the bench in a veterinary or clinical laboratory. Must possess an understanding of most service lines and departments offered by the ZRL network to include accessioning, chemistry, hematology, histology, microbiology, parasitology, urinalysis and cytology.
</p><p>Preferred Experience:
</p><p>&middot; Previous experience in laboratory Quality Management.
</p><p>&middot; Experience with Non-conforming Event Management, Internal Auditing, and/or Document Control.
</p><p>&middot; Experience with MediaLab.
</p><p>&middot; MLS/MT/MLS/CLS and/or Relevant ASQ Certification.<br>
</p><p></p><p><b>Technical Skills Required:
</b></p><p>&middot; Proficient in the use of the Microsoft Office suite, including Excel, Outlook, Word and Powerpoint.
</p><p>&middot; Strong analytical and troubleshooting abilities, and a flexible, adaptable approach to shifting priorities and new challenges
</p><p>&middot; Ability to apply established organizational policies to make decisions with minimal supervision.
</p><p>&middot; Excellent written and oral communication skills.
</p><p>&middot; Ability to work within a team and as an individual contributor in a fast-paced, demanding, and changing environment.
</p><p>&middot; Candidate must possess flexibility to respond to constantly changing conditions and priorities.
</p><p>&middot; Self-directed - can work with little supervision on most tasks.
</p><p>&middot; Excellent organization, prioritization, and time management skills &ndash; can work effectively under pressure.
</p><p>&middot; Exceptional attention to detail.
</p><p>&middot; (Preferred) Advanced skills utilizing Excel, Power BI and/or other software to generate and analyzer reports pertaining to metrics, raw data, and other role related tasks.<br>
</p><p></p><p><b>Physical Position Requirements:
</b></p><p>&middot; Able to work hours on a computer and tolerate computer screens
</p><p>&middot; Ability to travel domestically up to 5%.
</p><p>&middot; Some irregular hours as needed to collaborate with Lab Operations teams.
</p><p>Routine responsibilities may include standing and/or walking for extended periods of time.<br>
</p><p></p>Full time<br>
<p></p>Regular<br>
<p></p>Colleague<br>
<p></p><p>Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
</p><p></p><p>Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.<br>
</p><p></p><p><b><i>Notice: </i></b><i>Zoetis Recruiters will contact candidates via email from an address ending in </i><b><i>@zoetis.com </i></b><i>and may also initially connect with candidates through </i><b><i>LinkedIn </i></b><i>, including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that does not come from </i><b><i>@zoetis.com </i></b><i>, please treat it as suspicious. For your security, do not reply, click links, open attachments, share personal or financial information, or send money in response to unexpected or questionable recruitment communications.<br>
</i></p><p></p>Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of &ldquo;@zoetis.com&rdquo;. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.</div><p></p>

Quality Liaison

Pratt Industries

<div><p><b>SUMMARY</b></p>
<p>
Responsible for auditing activities associated with quality control specifications and auditing operating procedures.</p>
<p>
</p><p><b>DUTIES AND RESPONSIBILITIES</b></p>
<ul>
<li>Work safely at all times, be aware of surroundings and understand and comply with Pratt Industries Safety rules, operating procedures, and help hold co-workers responsible for safety related items. Participate in our safety program-Eyes on Safety.
</li><li>Follow at all times GMPs (Good Manufacturing Processes)</li>
<li>Learn and comply with Pratt Industries quality procedures and policies. Stop bad quality from leaving the facility to the Customer. Catch it on the front end of manufacturing the product. Strong attention to detail for poor quality; prevent bad quality being sent to customer.
</li><li>Superior time management skills and must be self-driven and self-motivated. Excellent attendance is a must.</li>
<li>Must have outstanding organizational skills and attention to detail is must.</li>
<li>Ability to solve practical problems: ability to interpret verbal and written instructions.</li>
<li>Multi-tasking; ability to work with various challenges and deal with a variety of situations</li>
<li>Ability to read, comprehend and interpret operating instructions, training and procedure manuals.</li>
<li>Excellent communication skills; able to speak effectively to employees, managers, customers</li>
<li>Excellent listening skills; ability to provide positive and corrective feedback</li>
<li>Will be very involved in the complaint process for internal and external customers; entering, tracking, receiving complaint issues and resolutions to complaints or root cause analysis</li>
<li>Ability to perform process audits</li>
<li>Data entry</li>
<li>Management and control of documents (safety, training and quality)</li>
<li>Control of non-conforming supplier defects and returns</li>
<li>Management of sorting and reworks</li>
<li>Management of weekly KPI's and/or compliances with CAR (corrective action reports).</li>
<li>Responsible for PAR (Preventive Acton Reports)</li>
<li>Must be able to work overtime as necessary, sometimes on short notice.
</li><li>Additional duties may be assigned by management.</li>
</ul>
<p></p><p><b>Requirements</b></p>
<ul>
<li>Computer literacy.</li>
<li>Previous Quality experience in a Manufacturing environment
</li><li>High school graduate or equivalent with related college degree and/or technical courses or associate (two-year) college degree.</li>
<li>Minimum of one years of experience in a related field and knowledge of LEAN manufacturing, ISO, Six Sigma preferred, OSHA or Safety related field.</li>
</ul>
<p></p><p><b>LANGUAGE SKILLS</b></p>
<ul>
<li>Able to read and follow instructions; quality, safety, job packets</li>
</ul>
<p><b>MATHEMATICAL SKILLS</b></p>
<ul>
<li>Able to read a tape measure with speed and accuracy.
</li><li>Able to calculate figures and amounts such as percentages, measurement, volume and rate.
</li><li>Able to apply concepts of high school math.</li>
</ul>
<p><b>REASONING ABILITY</b></p>
<ul>
<li>Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
</li><li>Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.</li>
</ul>
<p></p><p><b>PHYSICAL DEMANDS
</b></p><ul><li>Employee is regularly required to walk and talk and hear.
</li><li>The employee is frequently required to stand; use hands to finger, handle, or feel; and reach with hands and arms. The employee is occasionally required to sit.
</li><li>Vision requirements include: close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.</li>
<li>Candidate must be able to lift up to 50 pounds.</li>
</ul>
<p><b>WORK ENVIRONMENT
</b></p><ul><li>While performing the duties of this job, the employee is regularly exposed to moving mechanical parts.
</li><li>The employee is frequently exposed to wet and/or humid conditions.
</li><li>The employee is occasionally exposed to high, precarious places; fumes or airborne particles; and vibration.
</li><li>The noise level in the work environment is usually loud.</li>
</ul>
<p><b>This is a 2nd shift position-Hours are 3:00 p.m. to 11:00 p.m. Training will be on 1st shift but then will be moved to 2nd shift once training is complete.
</b></p>Requirements:
<p>Pratt is America's 5th largest corrugated packaging company and the world's largest, privately-held 100% recycled paper and packaging company, with more than 10,000 highly-skilled, green-collar employees dedicated to the environment and sustainability.</p>
<p>
</p><p>We provide careers where employees' needs are met first. At Pratt, you can find pride in your work, benefits built around your life and a culture focused on helping you learn, grow and thrive.
</p><p></p><p><b>BENEFITS</b></p>
<ul>
<li>Insurance benefits-first of the month after hire date</li>
<li>Paid holidays from day one</li>
<li>401(k) with match at 3 months.</li>
<li>Paid vacation at 6 months.</li>
<li>Tuition reimbursement at one year.</li>
<li>Stability in an organization that has continued to outpace growth of the entire industry.</li>
<li>Excellent benefits package including medical, dental, STD, and a HDHP with HSA.</li></ul></div>

Quality Technician-2nd shift

HanmiGlobal Saudi

<div><p>HanmiGlobal Saudi is looking for a diligent and detail-oriented <b>Quality Inspector</b> to ensure that the products and services delivered meet the prescribed quality standards and specifications. The Quality Inspector will be responsible for conducting inspections, identifying defects, and ensuring compliance with quality guidelines throughout the production and construction process.</p><b>
Key Responsibilities</b><ul><li>
Perform regular inspections of materials, equipment, and workmanship to verify compliance with quality standards.</li><li>
Review project specifications, drawings, and applicable codes to ensure consistency with deliverables.</li><li>
Identify, document, and report non-conformances and deficiencies promptly.</li><li>
Coordinate with project teams to implement corrective actions and ensure resolution of quality issues.</li><li>
Maintain accurate and detailed inspection records and prepare quality reports.</li><li>
Assist in final quality audits and participate in continuous improvement initiatives.</li><li>
Ensure adherence to health, safety, and environmental standards during inspections.</li></ul><br>
<b>
Requirements</b><br>
<ul><li>
Bachelor&rsquo;s degree or diploma in Engineering or relevant technical field.</li><li>
Minimum 7 years of experience in quality inspection or control in the construction sector.</li><li>
Strong knowledge of quality standards, inspection techniques, and relevant codes.</li><li>
Ability to read and interpret technical drawings and specifications.</li><li>
Attention to detail with excellent observational and reporting skills.</li><li>
Good communication and interpersonal skills.</li><li>
Familiarity with safety standards and quality management systems is preferred.</li></ul></div>

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