quality control microbiologist

Homemade Cuisine

<ul><li><b>You can WhatsApp us at 0345-200645 with your CV.</b></li><li><b>Duty Timings: 9 Hours, Monday-Saturday</b></li><li><b>Location: Chung, Multan Road, Lahore</b></li></ul><p>Homemade Cuisine, a gluten free foods company, is looking for a food microbiologist and quality control officer who can help perform the following functions at our factory site location:</p><ul><li>Conduct bioburden testing of food items, packaging material, raw material, and environmental samples to check for various strains of bacteria and other microorganisms.</li><li>Make sure our food traceability system is being implemented effectively by adding batch numbers and expiry labels to products, registering incoming raw material, conducting mock traceability exercises and following other requirements of the system such as creating records regularly for all daily production.</li><li>Creating lab reports, corrective action reports, root cause analysis reports, and other required documentation/forms as a part of our FSMS.</li><li>Maintain logs and records of all lab activities.</li><li>Maintain quality control checklists and regularly conducting rounds of the facility where food safety is actively audited in real-time.</li><li>Conduct internal audits and also aid in external audits such as ISO &amp; FSSC 22000.</li><li>Verifying the implementation of different PRPs including completion of startup checklists, changeover checklists, master sanitation schedules, wastage logs, and other food safety records.</li><li>Providing a direction for increasing the labs capabilities and strengthening our food safety processes + any recommendations.</li></ul><p>This role not only involves microbiological duties but also significant operational work centred around food traceability such as data entry and maintenance of batch records, batch labels, etc.</p><p>Job Type: Full-time</p><p>Pay: Rs45,000.00 - Rs50,000.00 per month</p><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Experience:</p><ul><li>Microbiology: 1 year (Required)</li></ul><p>Location:</p><ul><li>Lahore (Required)</li></ul><p>Work Location: In person</p>

Food Microbiologist & QC/QA Officer

State of Kansas

<p></p><div><div><div><h1 class="jobSectionHeader"><b>Important Recruitment Information for this vacancy</b></h1><div><h2 class="jobSectionHeader"><b>
Job Posting closes:</b><b> May 21st, 2026</b></h2><h2 class="jobSectionHeader"><b>
Required documents uploaded by:</b><b> May 21st, 2026</b></h2></div><p></p><p><b><br>
Kansas Department of Health and Environment:
</b></p><p>Our agency is led by Secretary Janet Stanek, who was appointed by Gov. Kelly in Dec 2021. KDHE is comprised of three divisions: Public Health, Environment, and Health Care Finance (which includes the State&rsquo;s Medicaid program, KanCare). We are the only agency in the nation to have these three entities under one roof which allows us to take a holistic approach to improving and protecting the health and well-being of all Kansans.</p><p>
Verification of identity and employment eligibility to work in the United States is required by federal law. For a list of acceptable documents that establish these criteria, please refer to the federal Form I-9. <b>KDHE does not provide sponsorships for this position.</b></p><p><b>
E-Verify:</b> Kansas Department of Health and Environment (KDHE) participates in E-Verify and will provide the federal government with your I-9 information to confirm that you are authorized to work in the U.S. For additional information regarding E-Verify, please click here. For additional information regarding Immigrant and Employee Rights (IER) please click here.</p><p><i>
http://www.kdhe.ks.gov/</i></p><p></p><p><b>
About the Position</b></p><ul><li><b>
Who can apply:</b> Anyone (External)</li><li><b>
Classified/Unclassified Service: </b>Unclassified</li><li><b>
Full-Time/Part-Time: </b>Full-Time</li><li><b>
Regular/Temporary: </b>Regular</li><li><b>
Work Schedule: </b>Monday-Friday, 8am-5pm (Flexible schedules available)</li><li><b>
Eligible to Receive Benefits: </b>Yes</li><li><b>
Veterans' Preference Eligible: </b>Yes</li><li><b>
Sponsorship:</b> KDHE does not provide sponsorship for this position.</li></ul><p></p><p><b>
Compensation:</b></p><ul><li><b>
Pay Range:</b><ul><li><b>
Microbiologist I - </b>$28.18 per hour</li><li><b>
Microbiologist II - </b>$29.20 per hour</li><li><b>
Microbiologist III - </b>$30.22 per hour</li><li><b>
Microbiologist IV - </b>$31.25 per hour</li></ul></li><li><i>Salary can vary depending upon education, experience, or qualifications.</i></li></ul><p></p><p><b>
Employment Benefits</b></p><p><b>
Comprehensive medical, mental, dental, vision, and additional coverage</b></p><p><b>
Sick &amp; Vacation leave</b></p><p><b>
Work-Life Balance programs: parental leave, military leave, jury leave, funeral leave</b></p><p><b>
Paid State Holidays (designated by the Governor annually)</b></p><p><b>
Fitness Centers in select locations</b></p><p><b>
Employee discounts with the </b><b>STAR Program</b></p><p><b>
Retirement and deferred compensation programs</b></p><p></p><p><br>
Visit the Employee Benefits page for more information&hellip;</p><p></p><p><b>
Position Summary &amp; Responsibilities</b></p><p><b>
Position Summary:</b></p><p>
The position (K0231118)</p><p>
A minimum of a bachelor&rsquo;s degree is required for this role as it is a requirement set by EPA.</p><p>
Serve as testing personnel (high and moderate complexity testing), as defined by CLIA, for bacteriology and mycobacteriology areas. Perform technical duties in the identification of bacteria and report results in an accurate and timely manner. Bacteriology testing involves laboratory isolation of bacterial pathogens from human clinical samples and identification of cultures using biochemical analysis, microscopy, matrix-assisted laser desorption ionization time-of-flight spectroscopy (MALDI-ToF), PCR, and serological tests. Mycobacteriology testing involves isolation and identification of mycobacteria using culture, fluorescent microscopy, MALDI-ToF, and nucleic acid amplification. As delegated, assist with the evaluation and implementation of new and alternative test methods for bacteriology and mycobacteriology areas.</p><p>
Assist with accessioning of samples and the processing of clinical specimens and cultures as needed. Help track consumables to ensure that supplies and reagents are maintained and ordered as needed. Ensure measures for safety are practiced and completed, including trash pickup, keeping lab benches clean, and restocking supplies. Perform quality control tests and maintain related records. Prepare and update written standard operating procedures and test methods as necessary to reflect current technology and methods. Participate in appropriate proficiency testing programs. Once eligible, serve as general supervisor or technical supervisor, as defined by CLIA, for applicable testing services and carry out the duties assigned to those roles.</p><p><b>
Job Responsibilities may include but are not limited to the following:</b></p><p>
 Serve as a point of contact for the Bureau of Epidemiology and Public Health Informatics during foodborne outbreaks and other disease investigations relating to the Diagnostic Microbiology lab. Collaborate with other units to ensure PCR and other molecular testing of outbreak samples is completed. As delegated, prepare shipments of outbreak specimens to the CDC and other laboratories as necessary. Maintain current packing and shipping certification for Category A and B infectious substances</p><p>
In the event of a natural or man-made event, work through extended shifts to help testing personnel maintain a 24 hour, 7 day a week testing period. Assist and support staff members carrying out the Laboratory Response Network protocols for the analysis of suspect materials and the confirmation of environmental or clinical specimens, as part of the bioterrorism program.</p><p></p><p><b>
Qualifications</b></p><ul><li><b>
Education</b>:<ul><li>
Bachelor&rsquo;s degree in microbiology, biology, chemistry, biochemistry, or other related field. Must have at least 24 semester hours of science that include 6 semester hours of Biology, 6 semester hours of Chemistry, and 12 semester hours of chemistry, biology, or medical technology in any combination.</li></ul></li><li><b>
Licensing &amp; Certification:</b><ul><li>
Valid Driver's License - Incumbent is required to have and maintain a valid driver's license when operating a state vehicle, a private vehicle, or a rental vehicle for the benefit of the State.
</li></ul></li><li><b>Minimum Qualifications:
</b><ul><li><b>Microbiologist I</b><ul><li>
Bachelor&rsquo;s degree in microbiology, biology, chemistry, biochemistry, or other related field. Must have at least 24 semester hours of science that include 6 semester hours of Biology, 6 semester hours of Chemistry, and 12 semester hours of chemistry, biology, or medical technology in any combination.</li></ul></li><li><b>
Microbiologist II</b><ul><li>
Bachelor&rsquo;s degree in microbiology, biology, chemistry, biochemistry, or other related field. Must have at least 24 semester hours of science that include 6 semester hours of Biology, 6 semester hours of Chemistry, and 12 semester hours of chemistry, biology, or medical technology in any combination.</li><li>
AND 1+ years of experience in a clinical laboratory setting.</li><li>
AND must be a general supervisor (as defined by CLIA) within 6 months of hire.</li></ul></li><li><b>
Microbiologist III</b><ul><li>
Bachelor&rsquo;s degree in microbiology, biology, chemistry, biochemistry, or other related field. Must have at least 24 semester hours of science that include 6 semester hours of Biology, 6 semester hours of Chemistry, and 12 semester hours of chemistry, biology, or medical technology in any combination.</li><li>
AND 4+ years of experience in a clinical laboratory setting.</li><li>
AND must be a technical supervisor (as defined by CLIA) within 6 months of hire or be cross-trained into an additional laboratory unit.</li><li>
AND must be a member of an APHL community of practice that is relevant to their laboratory work.</li></ul></li><li><b>
Microbiologist IV</b><ul><li>
Bachelor&rsquo;s degree in microbiology, biology, chemistry, biochemistry, or other related field. Must have at least 24 semester hours of science that include 6 semester hours of Biology, 6 semester hours of Chemistry, and 12 semester hours of chemistry, biology, or medical technology in any combination.</li><li>
AND 10+ years of experience in a clinical laboratory setting.</li><li>
AND must be a technical supervisor (as defined by CLIA) within 6 months of hire.</li><li>
AND must be a member of an APHL community of practice that is relevant to their laboratory work.</li><li>
AND must be assigned writing, tracking, and reporting responsibilities for a health grant project related to their work.</li></ul></li></ul></li><li><b>
Preferred Qualifications:
</b><ul><li>Master&rsquo;s degree in microbiology, biology, chemistry or biochemistry.</li><li>
PhD in microbiology, biology, chemistry or biochemistry.</li><li>
ASCP certification in Microbiology or Medical Technician</li><li>
Word, Excel, PowerPoint, Access</li><li>
Proofreading, editing, attention to detail</li><li>
Experience in working under BSL-3 laboratory conditions.</li><li>
Six months experience in the lead role for microbiology testing services in a CLIA regulated lab</li><li>
Experience in identifying bacteria, mycobacteria, or fungi</li><li>
One year experience in a clinical Microbiology laboratory</li><li>
12 semester hours of chemistry, biology, or medical technology in any combination</li><li>
24 semester hours of science that include 6 semester hours of Chemistry, 6 semester hours of Biology</li></ul></li><li><b>
Post-Offer, Pre-employment Requirements:
</b><ul><li>Kansas Tax Clearance Certificate: A valid Kansas Tax Clearance Certificate is a condition of employment for all employees of the State of Kansas. Applicants (including non-residents) who receive a formal job offer for a State job, are required to obtain a valid Tax Clearance within ten (10) days of the job offer. A Tax Clearance can be obtained through the Kansas Department of Revenue who reviews individual accounts for compliance with Kansas Tax Law. If you have a missing tax return(s) or you owe taxes to the State of Kansas, please know that the Kansas Department of Revenue will work with you. The Kansas Department of Revenue can set you up on a payment plan to receive a Tax Clearance so you can get a job working for the State of Kansas. The Kansas Department of Revenue can be contacted at 785-296-3199. Kansas Department of Revenue - Tax Clearance Frequently Asked Questions</li></ul></li></ul><p></p><p><b>
Recruiter Contact Information</b></p><p><b>
Name:</b> Kyle Sanders</p><p><b>
Email:</b> <b>kyle.sanders@ks.gov</b></p><p><b>
Mailing Address:</b> 1000 SW Jackson St. Suite 580 Topeka, KS 66612</p><p></p><p><b>
Job Application Process</b></p><ul><li><b>
First Sign in or register as a New User.</b></li><li><b>
Complete or update your contact information on the Careers&gt; My Contact Information page. *This information is included on all your job applications.</b></li><li><b>
Upload required documents listed below for the Careers&gt; My Job Applications page. *This information is included on all your job applications.</b></li><li><b>
Start your draft job application, upload other required documents, and Submit when it is complete.</b><ul><li><b>
Manage your draft and submitted applications on the Careers&gt; My Job Applications page.</b></li></ul></li><li><b>
Check your email and My Job Notifications for written communications from the Recruiter.</b><ul><li><b>
Email &ndash; sent to the Preferred email on the My Contact Information page</b></li><li><b>
Notifications &ndash; view the Careers&gt; My Job Notifications page</b></li></ul></li></ul><p><b><i>
Helpful Resources at </i></b><i>jobs.ks.gov</i><b><i>:</i></b><i> &ldquo;How to Apply for a Job &ndash; Instructions&rdquo; and &ldquo;How to Search for a Job &ndash; Instructions&quot;</i></p><p></p><p><b>
Required Documents for this Application to be Complete</b></p><p><b>
Upload these on the Careers - My Job Applications page</b></p><p>
Transcripts</p><p>
DD214 (if you are claiming Veteran&rsquo;s Preference)</p><p><b>
Upload these on the Attachments step in your Job Application</b></p><ul><li>
 Resume</li><li>
Cover Letter</li></ul><p><b><i>
Helpful Resources at </i></b><b><i>jobs.ks.gov</i></b><b><i>: &ldquo;How, What, &amp; Where do I Upload Documents&rdquo;</i></b></p><p></p><p><b>
How to Claim Veterans Preference</b></p><p>
Veterans' Preference Eligible (VPE): Former military personnel or their spouse that have been verified as a &quot;veteran&quot;; under K.S.A. 73-201 will receive an interview if they meet the minimum competency factors of the position. The veterans' preference laws do not guarantee the veteran a job. Positions are filled with the best qualified candidate as determine by the hiring manager.</p><p>
Learn more about claiming Veteran&rsquo;s Preference</p><p></p><p><b>
How to Claim Disability Hiring Preference</b></p><p>
Applicants that have physical, cognitive and/or mental disabilities may claim an employment preference when applying for positions. If they are qualified to meet the performance standards of the position, with or without a reasonable accommodation, they will receive an interview for the position. The preference does not guarantee an applicant the job, as positions are filled with the best qualified candidate as determined by the hiring manager.</p><p>
Learn more about claiming Disability Hiring Preference</p><p><b>
PLEASE NOTE</b>: The documentation verifying a person's eligibility for use of this preference should <b><i>not </i></b>be sent along with other application materials to the hiring agency but should be sent directly to OPS. These documents should be sent either by fax to (785)296-7712, scanned and emailed to Gustavo.Victoriano@ks.gov, or can be mailed/delivered in person to:</p><p>
ATTN: Disability Hiring Preference Coordinator<br>
Office of Personnel Services<br>
Landon State Office Building<br>
900 SW Jackson, Rm 401<br>
Topeka, KS 66612</p><p></p><p><b>
Equal Employment Opportunity</b></p><p>
The State of Kansas is an Equal Opportunity Employer. We value diversity, equity, and inclusion as essential elements that create and foster a welcoming workplace. All qualified persons will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, political affiliation, disability or any other factor unrelated to the essential functions of the job.</p><p>
If you wish to identify yourself as a qualified person with a disability under the Americans with Disabilities Act and would like to request an accommodation, please address the request to the agency recruiter.</p></div></div></div><div></div>

Microbiologist III

Indiana University

<p></p><div><div><div><div><div><div><div>Faculty Posting for Evansville MLS Program<br>
<br>
The Medical Laboratory Science (MLS) Division in the Department of Pathology and Laboratory Medicine at the Indiana University School of Medicine is recruiting for a faculty position in Evansville, Indiana. The MLS Division&rsquo;s ideal candidate is a Generalist with experience working as an MLS in a clinical laboratory as chemist and immunohematologist. However, other areas of expertise or specialization will be considered (Clinical Chemist with experience working as an MLS in a clinical laboratory, Immunohematologist with experience in a clinical or reference blood bank laboratory, or Medical Microbiologist with experience in clinical bacteriology, mycology, parasitology, serology, and/or virology laboratories).<br>
</div><div>The MLS program started in 1936 and has been operating continuously in Indianapolis since its inception. The program expanded in August 2024 with the launch of a second location at the IU School of Medicine&rsquo;s campus in Evansville, Indiana. The program maintains full accreditation through NAACLS (National Accrediting Agency for Clinical Laboratory Science).<br>
</div><div><b>Responsibilities:</b><br>
</div><ul><li>Teaching classroom, laboratory, clinical courses, and online courses at the undergraduate and graduate levels</li>
<li>Participation in MLS recruitment and admissions activities</li>
<li>Scholarly activity in photomicroscopy, teaching and learning, or other endeavors that support the department</li>
<li>Service to the department, school, and university</li>
<li>Administrative duties including admissions and onboarding processes, scheduling, ordering of supplies and other tasks as directed</li>
<li>Develop a service record at the campus, state, and national levels.</li></ul><p></p><div><br>
</div><div>
<b>Our Ideal Candidate:</b><br>
</div><ul><li>Must have an interest in pursuing an academic career at an academic health center</li>
<li>Will have excellent interpersonal and teaching skills</li>
<li>Has strong analytical abilities</li>
<li>Has enthusiasm for both teaching and the scholarship of teaching and learning</li>
<li>Generalist with experience in a clinical chemistry laboratory and additional experience in immunohematology</li></ul><div><br>
</div><div>
<b>Additional Information:</b><br>
</div><ul><li>This is a 12-month faculty position.</li>
<li>Academic rank and track commensurate with education and experience.</li>
<li>Infrequent travel to the Indianapolis MLS program or travel for recruitment opportunities may be required.</li>
<li>Application materials should include a letter of interest, a current curriculum vitae, names/contact information for three references. The letter of interest should include key motivation for application, a statement of teaching philosophy, and a summary of qualifications and experience.</li></ul><div><br>
</div><div>
<b>Minimum Qualifications:</b><br>
</div><ul><li>Bachelor&rsquo;s degree</li>
<li>MLS (ASCP) or equivalent certification</li>
<li>Master&rsquo;s degree or higher. Candidates who do not possess a master&rsquo;s degree or higher will be required to complete a degree within 3 years of appointment.</li>
</ul><div>
<br>
<b>Preferred Qualifications:</b>
</div><ul><li>Two years of teaching experience at the college/university level</li>
<li>Experience in evidence-based and innovative teaching practices</li>
<li>Curriculum design or management/supervisory experience</li>
<li>Strong commitment to high-quality teaching</li>
</ul><div>
<br>
<b>IUSM</b><br>
IU School of Medicine is committed to being a welcoming campus community and we seek candidates whose research, teaching, and community engagement efforts contribute to robust learning and working environments for all students, staff, and faculty. We invite individuals who will join us in our mission to improve health equity and well-being for all throughout the state of Indiana.</div></div>
</div><br>
<div><div><b>Basic Qualifications</b></div>
<div><div><b>Minimum Qualifications:</b><br>
</div><ul><li>Bachelor&rsquo;s degree</li>
<li>MLS (ASCP) or equivalent certification</li>
<li>Master&rsquo;s degree or higher. Candidates who do not possess a master&rsquo;s degree or higher will be required to complete a degree within 3 years of appointment.</li><br>
<p></p>
</ul><div>
<br>
<b>Preferred Qualifications:</b></div><div><br>
</div><ul>
<li>Two years of teaching experience at the college/university level</li>
<li>Experience in evidence-based and innovative teaching practices</li>
<li>Curriculum design or management/supervisory experience</li>
<li>Strong commitment to high-quality teaching</li>
</ul></div>
</div><br>
<div><div><b>Department Contact for Questions</b></div>
<div><div>For more information on the position, please contact:<br>
<br>
Nicholas Brehl, M.Ed. MLS (ASCP)CM</div><div>
Assistant Professor of Clinical Pathology and Laboratory Medicine</div><div><b>
nbrehl@iu.edu</b></div></div>
</div><br>
<div><div><b>Additional Qualifications</b></div>
</div><br>
<div></div><div><div><b>Special Instructions</b></div>
</div><br>
<div></div><div><div><b>Priority Application Review Deadline</b></div>
</div><br>
<div></div><div><div><b>Expected Start Date</b></div>
</div><br>
<div></div><div><div><b>Posting Number</b></div> <div>IUSM-02432-2026</div></div></div></div></div></div>

Assistant/Associate/Professor of Clinical Pathology & Laboratory Medicine

Centerre Construction

<p><b>Overview</b><br/>Join our dynamic team as a Commercial Construction Quality Control (CQC) Manager, where you will lead the three-phase quality assurance and inspection processes for a commercial construction project at Mesa Verde National Park in Southwestern Colorado. This pivotal role ensures that all construction activities meet rigorous quality standards, contractual obligations, and safety regulations. As a CQC Manager, you will drive continuous improvement, uphold compliance, and collaborate closely with project teams to deliver exceptional results on time and within scope. Your expertise will help shape the success of large-scale construction initiatives, fostering a culture of excellence and precision on this project.</p><p><b>Duties</b></p><ul><li>The Construction Quality Control Plan will include three phases of controls, to be managed by the CCQ, for each definable feature of the project's work. The three phases of control are the Preparatory Phase, the Initial Phase, and the Follow-Up Phase.</li><li>Develop and implement comprehensive quality control plans tailored to each construction project, ensuring alignment with contractual requirements and industry standards.</li><li>Conduct detailed quality inspections at various stages of construction to verify compliance with design specifications, codes, and safety protocols.</li><li>Collect, analyze, and document data related to construction quality metrics, identifying trends and areas for improvement.</li><li>Oversee construction site activities to ensure adherence to quality control procedures, including materials testing and workmanship evaluations.</li><li>Collaborate with project managers, contractors, and subcontractors to resolve quality issues promptly and effectively.</li><li>Review contracts and technical documentation to confirm scope accuracy and compliance with quality standards.</li><li>Maintain meticulous records of inspections, non-conformance reports, corrective actions, and compliance documentation for audit readiness.</li></ul><p><b>Experience</b></p><ul><li>Proven experience in construction site management with a focus on quality control or inspection roles within commercial construction projects.</li><li>Must have completed the USACE Contract Quality Control Course with the issued Certificate.</li><li>Prior experience working as the CQC Manager on $10M+ size federal projects, or prior work for the federal government in their Quality Control program, is required.</li><li>Strong understanding of construction management principles, including contract administration, project coordination, and preparing CQC plans</li><li>Demonstrated ability to perform detailed analysis of construction processes and identify root causes of quality issues.</li><li>Familiarity with construction inspection techniques, materials testing procedures, and relevant safety regulations.</li><li>Excellent data collection skills coupled with the ability to interpret quantitative information for decision-making purposes.</li><li>Prior experience overseeing multiple projects simultaneously while maintaining high standards of quality assurance.</li><li>Effective communication skills to facilitate collaboration among diverse project teams and stakeholders. Join us in delivering top-tier commercial construction projects by ensuring every detail meets our high-quality standards!</li></ul><p>Pay: $90,000.00 - $130,000.00 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>Relocation assistance</li><li>Vision insurance</li></ul><p>Work Location: In person</p>

Commercail Construction Quality Control (CQC) Manager

ELECTRICAL POWER PRODUCTS

<div>Description:
<p><b>
Reports To</b></p><p>
The Quality Control Supervisor will report to the Quality Assurance Manager.</p><p></p><p><b><br>
Job Summary</b></p><p>
This is an exciting entry-level front-line supervisory role responsible for the day-to-day supervision and execution of quality inspection activities. The Quality Control Supervisor provides direct supervisory leadership to Quality Control Inspectors to ensure product compliance, safe work practices, and adherence to established quality standards.</p><p>
The Quality Control Supervisor oversees inspection activities across multiple quality gates&mdash;including Steel, Paint, Mounting, Wiring, Enclosure, and Special Projects&mdash;and is accountable for shift-level manpower planning, daily priority setting, and communication of quality issues and risks. Success in this role requires strong organization, structured planning, and the ability to lead through clear expectations, accountability, and consistent floor presence in a fast-paced manufacturing environment.</p><p><b>
Responsibilities and Duties</b></p><ul><li>
Supervise and direct Quality Control personnel to meet daily production and Ready-to-Ship (RTS) goals across all assigned quality gates.</li><li>
Develop and execute daily and weekly manpower plans aligned to workload and staffing requirements.</li><li>
Assign work, set priorities, and monitor inspection execution to ensure compliance with quality standards and procedures.</li><li>
Coach, train, and evaluate Quality Control employees, providing regular feedback and performance documentation.</li><li>
Maintain the quality training schedule and versatility matrix to ensure adequate skill coverage per shift.</li><li>
Reinforce a strong quality culture by holding employees accountable to standards, ownership, and continuous improvement expectations.</li><li>
Participate in Quality Improvement Board meetings and support initiatives to reduce Defects Per Unit (DPU).</li><li>
Communicate daily priorities, quality risks, nonconformances (Fixems), and engineering alerts to cross-functional stakeholders.</li><li>
Manage Quality Control equipment needs, including preventive maintenance coordination and calibration tracking.</li><li>
Approve and manage timekeeping, attendance, and performance evaluations for direct reports.</li><li>
Serve as a visible safety leader, enforcing all safety rules and procedures during inspection activities.</li><li>
Lead initial containment actions and root cause discussions for quality issues within the department.</li><li>
Perform inspection activities as needed to support production flow and staffing gaps.</li><li>
Perform other related duties as assigned.</li></ul>
Requirements:
<p><b>
Skills &amp; Abilities</b></p><ul><li>
Strong organizational and prioritization skills with the ability to manage multiple workflows and shifting priorities.</li><li>
Demonstrated experience in a front-line supervisory role with accountability for people, performance, and results.</li><li>
Clear and effective verbal and written communication skills.</li><li>
Working knowledge of structured problem-solving and root cause analysis.</li><li>
Ability to make sound decisions in a fast-paced manufacturing environment.</li><li>
Strong interpersonal skills with the ability to enforce standards while maintaining positive working relationships.</li><li>
Proficiency with standard computer applications and manufacturing systems.</li></ul><p><b>
Qualifications</b></p><ul><li>
Bachelor&rsquo;s degree in Engineering, Industrial Technology, Business, or a related field is preferred.</li><li>
2&ndash;3 years of experience in quality control, inspection, or manufacturing operations.</li><li>
Prior experience with direct employee supervision is highly preferred.</li><li>
Equivalent combination of education and experience will be considered.</li></ul><p><b>
Physical Requirements</b></p><ul><li>
Continuous speaking, hearing, and visual effort, including close and distance vision and depth perception.</li><li>
Frequent standing, walking, bending, crouching, kneeling, reaching, and handling.</li><li>
Regular lifting and moving up to 40 lbs independently.</li><li>
Occasional lifting of 50&ndash;100 lbs with assistance.</li><li>
Exposure to typical manufacturing environments, including noise, machinery, and production hazards.</li><li>
Ability to stand and walk for extended periods.</li><li>
Ability to safely climb ladders.</li></ul></div>

Quality Control Supervisor

Concrete Concepts ( Pvt ) Ltd

<p>A well-reputed concrete products manufacturing company require the services of experienced and competent <b>Manager &ndash; Quality Control</b> for its production unit located in <b>Hattar (KPK), near Taxila</b>.</p><p><b>Position:</b> Manager &ndash; Quality Control</p><p><b>Location:</b> Hattar Industrial Area, KPK</p><p><b>Qualification:</b></p><ul><li>Diploma of Associate Engineering (DAE) in Civil</li></ul><p><b>Experience:</b></p><ul><li>Minimum <b>15 years of relevant experience</b> in the <b>concrete manufacturing industry</b></li></ul><p><b>Key Responsibilities:</b></p><ul><li>Manage and oversee all quality control operations within the production unit</li><li>Ensure products meet required standards, specifications, and compliance requirements</li><li>Develop and implement quality assurance procedures and testing protocols</li><li>Monitor raw materials and finished products for consistency and quality</li><li>Conduct inspections, audits, and prepare quality reports</li><li>Coordinate with production teams to resolve quality-related issues</li></ul><p>Job Type: Full-time</p><p>Pay: Up to Rs100,000.00 per month</p><p>Work Location: In person</p>

Manager Quality Control

Omada Rail Systems

<div><ul><li><b>Permanent Contract
</b></li></ul><ul><li><b>Mid-Senior Level
</b></li></ul><ul><li><b>Riyadh
</b></li></ul><ul><li><b>Technical Engineering</b></li></ul></div>
<br><div><p><b>About Us</b></p><p><br>
Egis is an international player active in architecture, consulting, construction engineering and mobility services. We create and operate intelligent infrastructures and buildings that respond to the climate emergency and contribute to more balanced, sustainable and resilient territorial development. Operating in 100 countries, Egis puts the expertise of its 19,500 employees at the service of its clients and develops cutting-edge innovations accessible to all projects. Through its wide range of activities, Egis is a key player in the collective organization of society and the living environment of citizens all over the world.</p><p>
With 3,500 employees across 8 countries in the Middle East, Egis has delivered over 700 complex development projects, stimulating economic growth and enhancing quality of life. Ranked among the top ten firms in the Middle East by Engineering News Record (ENR), Egis is committed to sustainable development. The Group&rsquo;s operations in the Middle East are built on strategic acquisitions and a deep understanding of local market conditions. Egis&rsquo; long history of providing comprehensive engineering, consulting, and project management services makes it a trusted partner for regional governments, investors, and developers.</p><p><b><br>
About the Role</b></p><p><br>
We are seeking a highly organized and efficient Document Control Manager to join our team in Riyadh, Saudi Arabia. The successful candidate will be responsible for overseeing the organization's document management systems, ensuring compliance with industry standards, and optimizing document workflows.</p><ul><li>
Develop, implement, and maintain document control policies and procedures</li><li>
Manage the organization's document management system, ensuring proper storage, retrieval, and version control of all documents</li><li>
Coordinate with various departments to ensure timely document updates and revisions</li><li>
Conduct regular audits to ensure compliance with industry standards and regulations</li><li>
Train staff on document control procedures and best practices</li><li>
Implement and oversee quality control processes for all managed documents</li><li>
Analyze document workflows and propose improvements to increase efficiency</li><li>
Collaborate with IT department to maintain and upgrade document management software</li><li>
Prepare reports on document control activities and metrics for management review</li><li>
Ensure proper archiving and retention of documents in accordance with company policies and legal requirements</li></ul><p><b><br>
What do we need from you</b></p><br>
<ul><li>
Bachelor's degree in Business Administration, Information Management, or related field</li><li>
PMIS experience is mandatory</li><li>
Minimum of 15 years of experience in document control, preferably rail projects experience.</li><li>
Proficiency in document management systems and Microsoft Office Suite</li><li>
Strong knowledge of quality control processes and workflow optimization</li><li>
Experience with database management and data analysis</li><li>
Familiarity with industry standards and regulations related to document control</li><li>
Knowledge of ISO 9001 or similar quality management systems</li><li>
Excellent organizational and time management skills</li><li>
Strong attention to detail and ability to maintain accuracy in a fast-paced environment</li><li>
Effective communication and interpersonal skills</li><li>
Project management experience</li><li>
Certifications in document management or quality control (preferred)</li></ul></div>

Document Control Manager

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