director of quality control

Kite Pharma

<div><h3 class="jobSectionHeader"><b>Job Description</b></h3><p></p><p>
We&rsquo;re here for one reason and one reason only &ndash; to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We&rsquo;ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.</p><p></p><p>
Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.</p><p></p><p>
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.</p><h2 class="jobSectionHeader"><b><br>
Job Description</b></h2><p></p><p><br>
Everyone at Kite is grounded by one common goal &ndash; curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Join us in our mission!</p><p></p><p>
We are seeking a highly motivated individual to join us as an Associate Director, to lead Quality Control Analytical Tech Services group, reporting to the Senior Director, Quality Control in Frederick, MD. In this role, you will lead a group and work closely with the Senior Director and other Associate Directors on supporting commercial operations in CAR-T technology.</p><p>
You will work on complex projects involving <b>qPCR/ddPCR, Flow cytometry and cell-based bioassays </b>and lead <b>efforts in automation development for analytical assays</b>. You will have cross-functional interaction with personnel from other groups such as Quality Assurance, Analytical Development, Manufacturing, Material Management (MM) and Corporate teams.</p><p></p><p><b>
Position Responsibilities (include but not limited to):</b></p><ul><li><p>
Provide technical support, process trending and procedural updates</p></li><li><p>
Lead method validation and method transfers support continuous improvement, to support method/product/invalid trending, and to investigate laboratory/assay related findings.</p></li><li><p>
Lead and support method development, validations, and transfers</p></li><li><p>
Support laboratory investigations, deviations, CAPAs, change control as needed</p></li><li><p>
Assist in investigation, identify root cause for critical deviations and determine CAPA for QC as needed</p></li><li><p>
Establish data analytics to serve as metrics for monitoring trends in methods, products, and invalids</p></li><li><p>
Support incoming tech transfers from AD/PD as needed</p></li><li><p>
Author technical reports and protocols in support of cGMP activities</p></li><li><p>
Supervise, train, and mentor junior staff</p></li><li><p>
Create and/or revise procedures, SOPs, and test methods as needed</p></li><li><p>
Support equipment and software lifecyle process</p></li><li><p>
LIMS development and integration</p></li><li><p>
Provide technical expertise for AD/PD, QA, Regulatory, Manufacturing, and Supply Chain as needed</p></li><li><p>
Support and participate inspection readiness plans and participate during compliance audits (internal and external) and regulatory inspections.</p></li><li><p>
Follow technology changes, recommends new technologies, advises on technology purchases and implementation if appropriate.</p></li><li><p>
Additional duties as assigned.</p></li></ul><p></p><p><b>
Basic Qualifications:</b></p><ul><li><p>
Advanced scientific degree (i.e. MD, PharmD, PhD) and 2+ years&rsquo; experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment OR</p></li><li><p>
Master&rsquo;s Degree and 8+ years&rsquo; experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment OR</p></li><li><p>
Bachelor&rsquo;s Degree and 10+ years&rsquo; experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment OR</p></li><li><p>
High School Degree and 14+ years&rsquo; experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment</p></li></ul><p></p><p><b>
Preferred Qualifications:</b></p><p></p><ul><li><p>
Experience supervising/managing analytical labs within the biotechnology or pharmaceutical industry</p></li><li><p>
Well versed and experienced in bioanalytical methods working under GMP conditions.</p></li><li><p>
Deep experience in applying GMP in QC lab in conformance to US, EU and ROW standards.</p></li><li><p>
Experience in conducting investigations, writing deviations, implementing CAPA and initiating change controls.</p></li><li><p>
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211), Quality Control, GMPs, GLP</p></li><li><p>
Ability to effectively negotiate and develop collaboration within teams and amongst individuals.</p></li><li><p>
Demonstrated ability to create and maintain highly functioning teams.</p></li><li><p>
Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment</p></li><li><p>
Comfortable in a fast-pace small company environment with minimal direction and able to adjust workload based on changing priorities.</p></li></ul><p><br>
</p>The salary range for this position is: $165,495.00 - $214,170.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.<p></p><p>
For additional benefits information, visit:
</p><p>https://www.gilead.com/careers/compensation-benefits-and-wellbeing</p><p></p><ul><li>Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.</li></ul><p><br>
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA.</p><p></p><p>
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT<br>
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT</p><p><br>
Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.<br>
</p><p>Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.</p><p><br>
Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.</p><p></p><h2 class="jobSectionHeader"><b>
For Current Kite Pharma Employees and Contractors:</b></h2><p>
Please apply via the Internal Career Opportunities portal in Workday.</p></div><p></p>

Assoc Director, Quality Control

Amerikan Hastanesi

<div>
 <p>
  Stembio (a Koc Holding/Koc Healthcare company) is a cutting-edge cGMP laboratory specializing in the production and preparation of cellular products such as; Car-T/TILs, Mesenchymal Stem Cells (MSCs), exosomes, immunotherapy products, cord blood banking and tissue grafts. We are committed to delivering high-quality, regulatory-compliant cell therapy products through rigorous quality control and validation processes.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are seeking an experienced and strategic
  <strong>
   Head of Quality Control for Stembio
  </strong>
  to lead and oversee all quality control (QC) activities for our cell therapy products.
 </p>
 <p>
  <br/>
 </p>
 <p>
  This role is responsible for ensuring the accuracy, reliability, and compliance of QC testing, maintaining product integrity, and upholding regulatory and cGMP standards. The ideal candidate will have extensive experience in analytical testing, method validation, and laboratory operations, along with a proactive approach to continuous improvement and compliance.
 </p>
 <p>
  <br/>
 </p>
 <p>
  If you are passionate about quality control in advanced cell therapies and have the expertise to uphold the highest standards, we encourage you to apply!
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Advanced degree (PhD, or equivalent) in Biology, Biochemistry, Analytical Chemistry, or a related field.
  </li>
  <li>
   Minimum of 5 years of experience in Quality Control within preferably a GMP-regulated biopharmaceutical or cell therapy environment or Academia.
  </li>
  <li>
   Strong expertise in analytical techniques such as flow cytometry, PCR, ELISA, HPLC, and microbiological testing.
  </li>
  <li>
   Proven leadership experience, with the ability to manage and develop high-performing teams.
  </li>
  <li>
   Deep understanding of regulatory requirements (cGMP, TITCK, EMA, ICH) and industry best practices for QC.
  </li>
  <li>
   Excellent problem-solving skills, attention to detail, and a commitment to continuous improvement.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Lead and manage the Quality Control department, ensuring all testing activities meet regulatory, company, and cGMP standards.
  </li>
  <li>
   Oversee analytical, microbiological, and raw material testing to ensure product safety, efficacy, and consistency.
  </li>
  <li>
   Drive method validation, transfer, and optimization to support robust and reliable analytical processes.
  </li>
  <li>
   Collaborate with manufacturing, quality assurance, and regulatory teams to maintain product quality throughout the lifecycle.
  </li>
  <li>
   Ensure compliance with CGMP, TITCK, EMA, and other regulatory requirements through rigorous documentation, data integrity, and audit readiness.
  </li>
  <li>
   Manage laboratory operations, including equipment qualification, personnel training, and process improvements.
  </li>
  <li>
   Implement and oversee stability studies, environmental monitoring, and trending analysis to detect and prevent potential quality issues.
  </li>
  <li>
   Lead investigations and corrective actions for out-of-specification (OOS) results, deviations, and other QC-related issues.
  </li>
  <li>
   Stay current with industry advancements and regulatory changes to ensure the QC function remains best-in-class.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <u>
   Your personal data is processed for the purpose of receiving and evaluating your job application. You can find detailed information about your processed personal data and rights from the "Employee Candidate Clarification Text" under the "Human Resources" heading of our website.
  </u>
 </p>
 <p>
 </p>
</div>


Stembio - Head of Quality Control

Confidential Company

<ul><li>Develop, implement, and maintain the corporate Quality Management System (QMS) in line with international standards (e.g., ISO 9001).</li><li>Define the company&#x27;s quality policy, objectives, and strategic goals.</li><li>Lead and mentor a team of QA/QC Managers, Engineers, and Inspectors across various projects.</li><li>Report directly to senior management on the performance of the QMS and opportunities for improvement.</li><li>Establish and enforce standard operating procedures (SOPs) for all key construction processes (e.g., concrete pouring, welding, MEP installations, finishing works).</li><li>Develop and control project-specific Quality Control Plans (QCPs) and Inspection & Test Plans (ITPs).</li><li>Ensure all quality records are properly maintained and readily retrievable for audits and project close-outs.</li><li>Review project contracts, specifications, and drawings to identify all quality requirements.</li><li>Participate in pre-construction meetings to establish quality expectations with clients, designers, and subcontractors.</li><li>Vet and approve the quality systems of key subcontractors and suppliers.</li><li>Oversee all on-site and off-site quality control inspection and testing activities.</li><li>Ensure materials and equipment received on site are as specified and properly stored.</li><li>Monitor workmanship to ensure compliance with approved methods and standards.</li><li>Manage the Non-Conformance Report (NCR) process, ensuring timely identification, documentation, and resolution of defects.</li><li>Chair regular quality coordination meetings with project teams and subcontractors.</li><li>Plan and conduct internal audits of projects and company processes.</li><li>Serve as the primary point of contact for external audits (client, third-party, certification bodies).</li><li>Analyze quality performance data (e.g., NCR rates, rework costs) to identify trends and root causes.</li><li>Implement Corrective and Preventive Action (CAPA) plans to address systemic issues.</li><li>Foster a culture of continuous improvement and quality excellence throughout the organization.</li><li>Ensure full compliance with local, state, and federal building codes and regulations.</li><li>Stay abreast of the latest industry standards, construction methodologies, and best practices.</li></ul>

Quality Control Director

CORDENPHARMA

<p></p><div><h2 class="jobSectionHeader"><b>CordenPharma </b><b>is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical, and biotech companies manufacture medicines with the ultimate goal of improving people&rsquo;s lives.</b></h2><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids &amp; Carbohydrates, Injectables, Highly Potent &amp; Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being.</b></h2><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
Our People Vision</b></h2><h2 class="jobSectionHeader"><b>
We strive for excellence. We share our passion. Together, we make a difference in patients' lives.</b></h2><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
SUMMARY</b></h2><h2 class="jobSectionHeader"><b>
This role will have responsibility for Quality Systems and Compliance Management including Deviation, CAPA, and Change Control Quality oversight, Master Control oversight, Supplier Quality Management (SQM), Document Control and Document Management, Regulatory Inspections and Client Audit oversight, and Quality Metrics. The Associate Director of Quality Systems and Compliance will lead monthly Quality Management Review (QMR) and will drive Quality and Site Metrics for the Colorado Corden site.</b></h2><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
ESSENTIAL DUTIES AND RESPONSIBILITIES</b></h2><div>
Include the following. Other duties may be assigned.</div><div></div><div><br>
<ul><li>
Oversight of Deviations (Quality Systems)</li><li>
Oversight of CAPAs (Quality Systems)</li><li>
Oversight of the Change Control Program</li><li>
Oversight of Master Control</li><li>
Oversight of Regulatory Inspections and Client Audits (oversee Quality Compliance Manager)</li><li>
Oversee Document Control and Document Management</li><li>
Oversee Supplier Quality Management (SQM)</li><li>
Organize and lead monthly Quality Management Review (QMR)</li><li>
Drive compliance and gap assessments for Corporate Standards</li><li>
Drive and provide regular metrics updates to the Leadership Team and site</li><li>
Participate in Global Corden Quality Systems discussions</li><li>
Exceptional Management Skills</li><li>
Exceptional Communication Skills (both written and verbal)</li><li>
Strong Quality and Regulatory knowledge</li><li>
Ability to transform and drive improvement to systems and organizations</li></ul></div><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
LEADERSHIP &amp; BUDGET RESPONSIBILITIES</b></h2><h2 class="jobSectionHeader"><b>
Provide strong leadership to the organization and be able to collaborate well cross-functionally. Provides guidance, and partners with the Head of QA and QC to stay within budget and determine budget requirements year over year.</b></h2><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
SAFETY &amp; ENVIRONMENTAL RESPONSIBILITIES</b></h2><div>
Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
QUALITY RESPONSIBILITIES</b></h2><div>
Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC&rsquo;s Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company.</div><div></div><div><br>
cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
QUALIFICATIONS</b></h2><div>
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
EDUCATION and/or EXPERIENCE</b></h2><div>
BA or BS (scientific degree preferred) from a four-year university ; and 15 years of related experience; or equivalent combination of education and experience. Strong Quality background and experience is a must</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
LANGUAGE SKILLS</b></h2><div>
Ability to read, analyze, and interpret general business periodicals, professional</div><div>
journals, technical procedures, or governmental regulations. Ability to write reports,</div><div>
business correspondence, and procedure manuals. Ability to effectively present</div><div>
information and respond to questions from groups of managers, clients, customers,</div><div>
and the public.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
MATHEMATICAL SKILLS</b></h2><div>
Ability to work with mathematical concepts such as probability and statistical</div><div>
inference. Ability to apply concepts such as fractions, percentages, ratios, and</div><div>
proportions to practical situations.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
REASONING ABILITY</b></h2><div>
Ability to add, subtract, multiply, and divide in all units of measure, using whole</div><div>
numbers, common fractions, and decimals. Ability to compute rate, ratio, and</div><div>
percent, and to draw and interpret bar graphs.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
CERTIFICATES, LICENSES, REGISTRATIONS</b></h2><div>
None.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
PHYSICAL DEMANDS</b></h2><div>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><div></div><div><br>
While performing the duties of this job, the employee is regularly required to sit; work with hands; and talk or hear. The employee is occasionally required to stand; walk; reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include the ability to adjust focus.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
WORK ENVIRONMENT</b></h2><div>
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><div></div><div><br>
While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles and noise typical of an office environment.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
CORE COMPETENCIES</b></h2><div>
These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.</div><div></div><div><br>
<ul><li>
Leadership and deep knowledge of the concepts (above described as responsibilities)</li><li>
Governance and decision making regarding regulatory compliance and operational knowledge of API manufacture</li><li>
Effective in prioritizing workloads, resolution of issues based on compliance, and scientifically documented risk</li><li>
Excellent customer service skills</li><li>
Business acumen to drive successful customer experience while meeting business targets from a Quality perspective</li><li>
Good written and oral communication skills</li><li>
Computer skills with intermediate ability to use Microsoft Office Suite</li><li>
Strong planning, implementation, and follow-up skills</li><li>
Good facilitation skills and ability to interact with colleagues from all levels of the organization</li><li>
High analytical capabilities</li></ul></div><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
SALARY</b></h2><div>
Actual pay will be based on your skills and experience</div><div></div><h2 class="jobSectionHeader"><b><br>
BENEFITS</b></h2><ul><li>
401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service</li><li>
Accident Plan</li><li>
Critical Illness Insurance</li><li>
Dental Insurance</li><li>
Disability Insurance</li><li>
Employee Assistance Program</li><li>
Flexible Spending Account</li><li>
Health Insurance PPO/HSA</li><li>
Hospital Indemnity Plan</li><li>
ID Theft Protection</li><li>
Life Insurance</li><li>
Paid Parental Leave</li><li>
Tuition Reimbursement</li><li>
Wellness Program</li><li>
Vacation &ndash; Three Weeks 1st Year</li><li>
Vision Insurance</li></ul><h2 class="jobSectionHeader"><b>
EQUAL OPPORTUNITY EMPLOYER</b></h2><div><i>
Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.</i></div><p></p><p><br>
This post will expire November 24, 2025</p></div>

Associate Dir., Quality Systems and Compliance

Soar Software Development Company

<div><p><b>About us:</b></p><p>
Soar is a global fintech startup that specializes in financing and investment. Currently headquartered in Saudi Arabia, Soar is growing throughout the region with a mission to help people achieve their financial goals with innovative financial and property investment solutions and tools through its multi-purpose platform, designed to offer a simple and seamless user experience.</p><p></p><p>
Role Summary:</p><p>
As the QA Director at SOAR, you will be responsible for leading, mentoring, and scaling a team of quality assurance professionals. You will define and implement comprehensive QA strategies, ensuring our mission-critical applications are robust, reliable, and performant. This is a leadership role for someone who thrives under pressure, can track progress with precision, and makes timely, effective decisions that directly impact our success</p><p></p><p><b>
.</b></p><p><b>
Key responsibilities:</b></p><ul>
<li>
<b>Team Leadershi</b>p: Lead, manage, and mentor a team of QA engineers to increase overall productivity and output. Foster a culture of excellence, accountability, and continuous improvement.</li>
<li><b>Strategy &amp; Proces</b>s: Develop and execute a scalable QA strategy, defining best practices and processes across the entire software development lifecycle.</li>
<li><b>Progress Trackin</b>g: Establish key performance indicators (KPIs) and metrics to track team progress, project health, and product quality. Report on these metrics to leadership on a regular basis.</li>
<li><b>Decision-Makin</b>g: Make quick, informed, and correct decisions under pressure, ensuring that quality gates are maintained without hindering release schedules.</li>
<li><b>Quality Assuranc</b>e: Oversee the design, development, and execution of comprehensive test plans, test cases, and automation scripts for our web and mobile applications.</li>
<li><b>Cross-Functional Collaboratio</b>n: Work closely with product management, engineering, and DevOps teams to ensure quality is a shared responsibility and is integrated into every stage of development.</li>
<li><b>Risk Managemen</b>t: Proactively identify potential quality risks and create mitigation plans to ensure the stability of the application.</li>
</ul><p></p><p><b>
Qualifications &amp; Skills:</b></p><ul>
<li>
Proven experience ( 7+ years) in a QA management or leadership role, preferably within a fintech, proptech, or other mission-critical software environment.</li>
<li>Strong leadership skills with a track record of building and managing high-performing teams.</li>
<li>Expertise in a variety of testing methodologies (functional, regression, performance, security, etc.) and a deep understanding of the full software development lifecycle.</li>
<li>Experience with test automation frameworks and tools.</li>
<li>Exceptional problem-solving abilities and the capacity to make sound, data-driven decisions quickly.</li>
<li>Excellent communication skills, with the ability to articulate complex technical issues to both technical and non-technical stakeholders.</li>
<li>Demonstrated ability to work effectively in a fast-paced and high-pressure environment.</li></ul></div>

Director of Quality Assurance

National Foods Limited

<div>
 At National Foods Limited, we are on a journey of growth and on building our most valuable assets which include our brands, financial strength, global presence, and our unbridled commitment to becoming a truly sustainable and a renowned company in the world.
 <br/>
 <br/>
 <ul>
  <li>
   JOB PURPOSE To ensure the quality and consistency of NFL production processes, identify areas for improvement, and contribute to a culture of excellence in food manufacturing
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Accountabilities &amp; Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Monitor and assess various stages of the production process, from raw material intake to finished product packaging, to ensure compliance with quality standards and specifications
  </li>
  <li>
   Perform chemical tests to assess chemical properties in accordance with NFL standards and record the results in the control logbook
  </li>
  <li>
   Conduct routine quality inspections of production lines, equipment, and product samples, identifying any deviations from established quality control factors
  </li>
  <li>
   Investigate and analyse process-related deviations or quality issues, identifying root causes and collaborating with cross-functional teams to implement corrective and preventive actions
  </li>
  <li>
   Maintain comprehensive documentation of standard operating procedures (SOPs), work instructions, and quality control protocols related to production processes
  </li>
  <li>
   Prepare and distribute reports summarising process quality performance, highlighting key metrics, and recommending improvements
  </li>
  <li>
   Identify opportunities for process improvement, increased efficiency, and enhanced product quality
  </li>
  <li>
   Implement continuous monitoring and process control measures to prevent quality deviations and optimise process performance
  </li>
  <li>
   Collaborate with the procurement team and GMS team to ensure the timely creation of purchase orders (POs) and the availability of materials
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Qualifications &amp; Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in relevant discipline with 3-5 years of experience
   <br/>
   <br/>
  </li>
 </ul>
 Or
 <br/>
 <br/>
 <ul>
  <li>
   Postgraduate degree in relevant discipline with 1-2 years of experience
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Location:
  <br/>
  <br/>
 </strong>
 FIEDMC, Faisalabad, Paksitan.
 <br/>
 <br/>
 National Foods Limited provides equal employment opportunity (EEO) to all persons regardless of age, color, origin, physical or mental disability, race, religion, creed, gender, marital status, status with regard to public assistance or any other characteristic protected by federal, state or local laws.
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QA/QC Executive

Lakeside Industries Inc.

<div><p><b>Quality Control Intern &ndash; Summer 2026</b></p>
<p><i>
Location: Portland, OR</i><br>
<i>Company: Lakeside Industries, Inc.</i><br>
<i>Internship Duration: 10&ndash;16 Weeks (Summer)</i><br>
<i>Department: Quality Control</i></p><br>
<p></p>
<p><b>
About Us:</b></p>
<p>
We are a family-owned and operated company, proudly serving the Pacific Northwest. Our team is dedicated to quality, safety, and innovation in every project we take on. As we continue to grow, we&rsquo;re looking for a motivated <b>Quality Control Intern</b> to join our team for the summer.</p><br>
<p></p>
<p><b>
Position Overview:</b><br>
As a Quality Control Intern, you will work alongside our QC engineers and technicians, field supervisors, and paving crews to gain hands-on experience with <b>asphalt testing, material inspection, and compliance standards</b>. This role is ideal for students interested in civil engineering, construction management, or materials science.</p><br>
<p></p>
<p><b>
Key Responsibilities:</b></p>
<ul><li>
Assist in asphalt density training</li><li>
Opportunity to work with aggregate and mix testing</li><li>
Participate in mix design formulation basics</li><li>
Interaction with other departments including Risk &amp; Safety and Operations</li></ul><br>
<div></div>
<p><b>
Qualifications:</b></p>
<ul><li>
Currently pursuing a degree in Construction Management, Civil Engineering, or closely related field</li><li>
Experience in Microsoft Office Suite of tools</li><li>
Excellent attention to detail and organizational skills</li><li>
Strong communication skills and ability to work in a team environment</li><li>
Ability to have fun while working hard</li></ul><br>
<p></p>
<p><b>
What We Offer:</b></p>
<ul><li>
 Hands-on field and lab experience in the paving industry</li><li>
 Mentorship from experienced QC professionals and engineers</li><li>
 Exposure to real construction projects and industry standards</li><li>
 Competitive hourly pay</li><li>
 Opportunities to return for future internships or full-time roles</li></ul><br>
<p></p>
<p><b>
Wage and Benefits:</b></p>
<p>
The pay rate for this position is $22.00 hour to $26.00 hour depending on experience, education, and qualifications.</p>
<p>
Lakeside Industries, Inc. seasonal employees participate in state run paid sick, medical and family leave programs, and have access to our company sponsored employee assistance program. Interns working beyond 90 days, may have the option to participate in our 401(k)-retirement plan.</p><br>
<p></p>
<p><b>
How to Apply:</b><br>
Please submit your application to https://lakesideindustries.com/job-openings/</p><br>
<p></p>
<p><i>
Join us this summer and help build the roads and infrastructure that keep communities moving.</i></p><br>
<p>
</p><p><i>Lakeside Industries is an equal opportunity employer committed to diversity and inclusion for our workforce and will consider any qualified applicant without regard to race, color, creed, gender, religion, age, marital status, national origin, sexual orientation, disability, veteran, or any other protected status.</i></p></div><p></p>

Intern-Quality Control Portland OR

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