director of quality control

GoldBridge

<p>We are currently hiring a <b>Director of Quality Assurance</b> for a large industrial manufacturing company located in Leetsdale, PA. The Director of Quality will lead a team on QC/QA Managers &amp; Lab Technicians to ensure products meet company standards as well as client requirements to ensure complete client satisfaction through the implementation and/or improvement of Quality Control processes &amp; process/continuous improvement projects. This position is a full time, direct hire with a <b>starting salary up to $160,000 plus bonuses</b>, medical benefits, 401k, etc. In addition, this position will require extensive travel between Pittsburgh and their two manufacturing facilities in North Central Kentucky.</p><p>Additional Details:</p><ul><li>Implement &amp; maintain Quality Management Systems to ensure all products meet specifications and standards.</li><li>Lead continuous improvement projects to enhance quality and efficiency within the manufacturing processes.</li><li>Ensure ISO 9001 compliance and other regulatory standards.</li><li>Develop quality control plans for production processes and work with production &amp; engineering teams as well as suppliers &amp; customers to ensure quality standards are met throughout the manufacturing process.</li><li>Relocation assistance is available for this position*</li></ul><p>Job Type: Full-time</p><p>Pay: $125,000.00 - $160,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>Health insurance</li></ul><p>Work Location: In person</p>

Director of Quality Assurance

W.S. Badger Company, Inc.

<div><p>The Director of Quality supports the Badger Mission and Principles as the head of the Quality Unit. This role is responsible for company-wide quality governance, FDA regulatory compliance, and continuous improvement of the Quality Management System. This position ensures that quality systems and manufacturing operations remain compliant with FDA regulations, cGMP requirements, and internal standards across formulation, manufacturing, filling, packaging, warehousing, and supply chain operations. The Director of Quality partners closely with the Director of Operations and RDI leadership to support regulatory readiness and certification requirements, while maintaining independent authority for quality and product disposition decisions.<br>
</p><b>Essential Responsibilities:</b><b>Quality Leadership and Department Management -
</b><ul><li>Oversees all Quality functions, including Quality Assurance, Quality Control, Validation, and FDA compliance systems, ensuring alignment with company growth goals and regulatory requirements.</li><li>Drives quality strategy focused on compliance excellence, risk mitigation, right-first-time performance, and continuous improvement.</li><li>Establishes and maintains an effective, scalable Quality Management System (QMS).</li><li>Ensures manufacturing operations comply with FDA regulations, cGMP standards, OTC monographs, and internal quality requirements.</li><li>Partners with the Director of Operations to ensure smooth integration of quality systems within manufacturing, supply chain, and technical operations.</li><li>Collaborates with RDI Director to support regulatory submissions, certifications (e.g., NOP), and international requirements by ensuring quality systems and documentation meet applicable standards.</li><li>Establishes and monitors KPIs across Quality and in partnership with Operations to track batch release timeliness, deviation trends, CAPA effectiveness, audit readiness, and overall product quality.</li><li>Spearheads inspection readiness strategy and serves as primary Quality representative during FDA inspections and other audits, as required, confidently representing the organization in high-stakes regulatory interactions.</li><li>Prepares, reviews, and approves FDA inspection responses, corrective action plans, and executive communications related to compliance matters.</li><li>Communicates quality risks, compliance gaps, and mitigation strategies clearly and effectively to executive leadership and cross-functional stakeholders.</li><li>Anticipates and manages risks that could impact product quality, regulatory standing, or operational continuity.</li><li>Provides executive oversight of Quality systems for contract packagers and third-party manufacturers, ensuring compliance with FDA regulations, cGMP standards, and Badger quality requirements.</li><li>Owns the development and oversight of all Quality Agreements with critical suppliers, including contract packagers and third-party manufacturers, establishing clear quality accountability, regulatory expectations, performance standards, and risk management requirements.</li><li>Owns departmental resource planning and budgeting for the Quality Unit.</li><li>Ensures safe, ethical, and legally compliant quality practices consistent with Badger&rsquo;s mission and values.</li><li>Drives environmentally responsible quality practices aligned with Badger&rsquo;s sustainability commitments.</li></ul><b>
Quality Systems &amp; FDA Compliance Oversight-</b><ul><li>Provides governance and oversight for the Quality Management System, including:</li></ul><p>
o Document control</p><p>
o Batch record review and release</p><p>
o Deviation and investigation management</p><p>
o CAPA systems</p><p>
o Complaint handling</p><p>
o Supplier qualification
</p><p>o Validation programs (process, cleaning, equipment, IQ/OQ/PQ)</p><p>
o Training systems related to cGMP compliance</p><ul><li>Maintains ultimate authority for product disposition decisions.</li><li>Ensures effective escalation and resolution of quality events that may impact regulatory compliance.</li><li>Partners with RDI on certification and regulatory initiatives to ensure quality system alignment.</li><li>Ensures documentation, validation, and manufacturing controls support certification audits and regulatory commitments.</li></ul><b>
Cross-Functional Partnership &amp; Operational Integration-</b><ul><li>Partners closely with the Director of Operations to balance compliance requirements with operational efficiency.</li><li>Collaborates with Operations management to improve right-first-time performance, reduce nonconformances, and strengthen process capability.</li><li>Facilitates cross-functional root cause investigations involving Quality, Operations, and RDI.</li><li>Provides executive Quality oversight for new product launches, ensuring quality system readiness, validation compliance, and inspection preparedness prior to launch.</li><li>Supports new product introductions and technical transfer activities by ensuring quality system readiness and validation compliance.</li><li>Facilitates structured and professional communication between departments during investigations, audit responses, and significant compliance events to ensure alignment and timely resolution.</li><li>Provides clear, balanced guidance during high-pressure situations, including regulatory inspections, recalls, and significant quality events.</li><li>Represents the Quality Unit in Strategy Team meetings and other company leadership forums.</li></ul><b>
People Leadership Responsibilities-</b><ul><li>Oversees the QC Supervisor, QA Supervisor, QA Project Manager, and QA Validations Manager.</li><li>Models company mission and principles through day-to-day actions and strategic decisions, setting a standard for ethical, transparent, and purpose-driven direction.</li><li>Provides leadership, training, and guidance to Quality leaders and teams, cultivating a high-performing, collaborative, and mission-aligned workplace culture.</li><li>Upholds performance management processes, including conducting check-ins for new team members, facilitating Alignment Building Process meetings, managing complex performance issues with HR support, and making exit resolutions for Quality Unit staff.</li><li>Drives employee development, succession planning, and capability-building within the Quality organization.</li><li>Coaches' managers and supervisors on effective, inspection-ready communication during audits, investigations, and cross-functional interactions.</li><li>Resolves complex cross-functional conflicts and facilitates consensus among diverse stakeholders.</li><li>Makes critical independent determinations regarding product quality, compliance risk, and product disposition.</li><li>Balances multiple departmental and organizational priorities while maintaining regulatory compliance and quality integrity.</li><li>Fosters inclusive team environments by actively seeking diverse perspectives during discussions and decision-making processes.</li></ul><p></p><p>
Pay starting at $120,000; salary is commensurate to experience.</p><b><br>
Requirements</b><br>
<br>
<b>Education and Experience Required:</b><ul><li>Bachelor&rsquo;s degree in Chemistry, Microbiology, Engineering, Pharmaceutical Sciences, or related technical field (advanced degree preferred).</li><li>Minimum 7-10 years of progressive Quality leadership experience in a regulated OTC manufacturing environment.</li><li>Minimum 5 years of direct people management experience, including ownership of supervisors or managers within a regulated manufacturing environment.</li><li>Demonstrated experience leading FDA inspections and managing responses to regulatory observations.</li><li>Deep understanding of FDA regulatory requirements for OTC drugs and cosmetics.</li><li>Strong working knowledge of cGMP, 21 CFR 210/211, OTC drug monographs, validation requirements, and ISO standards.</li><li>Proven success overseeing and continuously improving Quality Management Systems in a regulated manufacturing environment.</li><li>Audit-level written and verbal communication skills, with the ability to represent the organization effectively in regulatory and executive settings.</li><li>Strong cross-functional collaboration, project management, budgetary, and analytical skills.</li><li>Experience with ERP/MRP systems and electronic quality management systems.</li></ul><p><br>
<b>Physical Requirements:</b>
<br>
Physical requirements for the job include but are not limited to prolonged periods sitting at a desk and working on a computer. Must be able to lift up to 15 pounds times. Employees should be able to perform the essential functions of the job with or without reasonable accommodations.</p><p><b>
EEO Statement:</b><br>
W.S Badger Company, Inc. is an equal opportunity employer, dedicated to the policy of non-discrimination in employment on any basis including race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family history), political affiliation, military service, marital status, hair texture or types, or other non-merit-based factors.</p><b><br>
Benefits</b><br>
<ul>
<li>Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401k, IRA)</li>
<li>Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li>
<li>Paid Time Off (Vacation, Sick &amp; Public Holidays)</li>
<li>Family Leave (Maternity, Paternity)</li>
<li>Short Term &amp; Long Term Disability</li>
<li>Wellness Resources</li></ul></div>

Director of Quality

ICON plc

<div>Asset Quality Lead- Remote<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Director Quality Assurance to join our diverse and dynamic team. As a Director Quality Assurance at ICON, you will play a pivotal role in ensuring the quality and compliance of clinical trials, interpreting regulatory requirements, and contributing to the advancement of innovative treatments and therapies.</div><div><br>
What you will be doing</div><ul><li>
Leading the development and implementation of quality assurance strategies and processes to support clinical trial activities.</li></ul><ul><li>
Conducting comprehensive quality assessments and audits to ensure compliance with regulatory standards and guidelines.</li></ul><ul><li>
Collaborating with cross-functional teams to identify and address quality issues and implement corrective actions as needed.</li></ul><ul><li>
Providing expert guidance and support to staff regarding quality assurance policies, procedures, and best practices.</li></ul><ul><li>
Contributing to the continuous improvement of quality management systems and documentation.</li></ul><div><br>
Your profile</div><ul><li>
Bachelor's degree in Life Sciences, Pharmacy, or related field; advanced degree preferred.</li></ul><ul><li>
Minimum of 10 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry, with significant experience in a leadership role.</li></ul><ul><li>
Extensive knowledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations).</li></ul><ul><li>
Strong analytical and problem-solving skills, with the ability to identify and resolve complex quality issues.</li></ul><ul><li>
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders.</li></ul><div></div><div>
Nous recherchons actuellement un(e) Directeur(trice) Assurance Qualit&eacute; pour rejoindre notre &eacute;quipe diversifi&eacute;e et dynamique. En tant que Directeur(trice) Assurance Qualit&eacute; chez ICON, vous jouerez un r&ocirc;le cl&eacute; dans la garantie de la qualit&eacute; et de la conformit&eacute; des essais cliniques, dans l&rsquo;interpr&eacute;tation des exigences r&eacute;glementaires et dans la contribution au d&eacute;veloppement de traitements et th&eacute;rapies innovants.</div><div>
Vos responsabilit&eacute;s</div><ul><li><div>
Diriger le d&eacute;veloppement et la mise en &oelig;uvre des strat&eacute;gies et des processus d&rsquo;assurance qualit&eacute; afin de soutenir les activit&eacute;s li&eacute;es aux essais cliniques.</div></li><li><div>
R&eacute;aliser des &eacute;valuations qualit&eacute; compl&egrave;tes et des audits afin de garantir la conformit&eacute; aux normes et directives r&eacute;glementaires.</div></li><li><div>
Collaborer avec des &eacute;quipes transverses afin d&rsquo;identifier et de r&eacute;soudre les probl&eacute;matiques qualit&eacute; et de mettre en place des actions correctives si n&eacute;cessaire.</div></li><li><div>
Fournir des conseils d&rsquo;expert et un accompagnement aux &eacute;quipes concernant les politiques, proc&eacute;dures et bonnes pratiques en assurance qualit&eacute;.</div></li><li><div>
Contribuer &agrave; l&rsquo;am&eacute;lioration continue des syst&egrave;mes de management de la qualit&eacute; et de la documentation associ&eacute;e.</div></li></ul><div>
Votre profil</div><ul><li><div>
Dipl&ocirc;me universitaire (Licence ou &eacute;quivalent) en sciences de la vie, pharmacie ou domaine connexe ; dipl&ocirc;me sup&eacute;rieur souhait&eacute;.</div></li><li><div>
Minimum de 10 ans d&rsquo;exp&eacute;rience en assurance qualit&eacute; dans l&rsquo;industrie pharmaceutique, biotechnologique ou au sein d&rsquo;une CRO, avec une exp&eacute;rience significative dans un r&ocirc;le de leadership.</div></li><li><div>
Connaissance approfondie des exigences et directives r&eacute;glementaires encadrant les essais cliniques (par exemple ICH-GCP, r&eacute;glementations FDA).</div></li><li><div>
Solides comp&eacute;tences analytiques et en r&eacute;solution de probl&egrave;mes, avec la capacit&eacute; d&rsquo;identifier et de r&eacute;soudre des probl&eacute;matiques qualit&eacute; complexes.</div></li><li><div>
Excellentes comp&eacute;tences en communication et en relations interpersonnelles, avec la capacit&eacute; de collaborer efficacement avec des &eacute;quipes transverses et des parties prenantes.</div></li></ul><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Director, Quality Assurance

HRI Private Limited

<p><b>Key Responsibilities:</b></p><ul><li>Develop, implement, and monitor quality control systems and procedures</li><li>Ensure compliance with ISO and other applicable quality standards</li><li>Supervise in-process and final product inspections</li><li>Lead internal and external audits</li><li>Analyze quality data and drive continuous improvement initiatives</li><li>Handle customer complaints and implement corrective and preventive actions (CAPA)</li><li>Train and manage the QC team to maintain high performance standards</li></ul><p><b>Eligibility Criteria:</b></p><ul><li>Bachelor&rsquo;s degree in a relevant discipline</li><li>5&ndash;7 years of relevant experience in Quality Control, preferably in the packaging industry</li><li>Strong knowledge of quality management systems and regulatory compliance</li><li>Proven leadership, analytical, and reporting skills</li></ul><p>Interested candidates may send their updated CVs to <b>careers@hri.com.pk</b> mentioning <i>&ldquo;Manager &ndash; Quality Control&rdquo;</i> in the subject line.</p><p>Job Type: Full-time</p><p>Pay: Rs150,000.00 - Rs200,000.00 per month</p><p>Work Location: In person</p>

Manager – Quality Control

Trango Tek

<p><b>About Us:</b></p><p>Libermann International is a Family-owned business which originates, manufactures and markets high end quality and advanced textile apparels &amp; gloves for versatile industries, solvating it with the power of Rise to Quality<b>. </b>For more than last three decades, company has experienced rapid growth in import/export volumes, human capital, turnover as well as revenues. At present, company possesses 4 manufacturing plants, an independent environmental friendly tanning house, advanced knitting and dying unit, robotic Vinyl TPRs production facility, robotic cutting and up to 20 stitching floors. Nizam Son's is market leader within Workwear garments in Pakistan and among the prestigious manufacturers in Asia Pacific.</p><p><b>Website:</b> https://www.nizamsons.com/page/about-us.html</p><p><b>Job Description:</b><br/>The <b>Executive &ndash; Quality Control</b> is responsible for ensuring that all products meet the company&rsquo;s strict quality standards and customer specifications. This role involves monitoring quality control processes, supervising inspections, analyzing data, and leading initiatives to continuously improve product quality and compliance across all manufacturing stages.</p><p><b>Responsibilities:</b></p><ul><li>Supervise quality control operations during production to ensure adherence to product and process specifications.</li><li>Conduct detailed inspections and testing of raw materials, in-process goods, and finished products to ensure compliance with quality standards.</li><li>Maintain accurate documentation of inspection findings, test results, and corrective actions.</li><li>Identify non-conformities, lead root-cause analysis, and implement effective corrective and preventive actions.</li><li>Collaborate with production, planning, and quality assurance teams to resolve quality issues and improve process consistency.</li><li>Ensure compliance with customer requirements, internal policies, and relevant international standards.</li><li>Participate in internal and external audits and prepare quality reports for management review.</li><li>Contribute to continuous improvement initiatives aimed at reducing defects and enhancing product reliability.</li></ul><p><b>Qualifications &amp; Skills:</b></p><ul><li>Bachelor&rsquo;s degree in Textile Engineering, Quality Management, or a related discipline.</li><li>4&ndash;6 years of experience in Quality Control within the textile or apparel manufacturing sector.</li><li>Strong understanding of inspection techniques, sampling methods, and quality standards.</li><li>Proficiency in MS Office and familiarity with quality documentation and reporting tools.</li><li>Excellent attention to detail, problem-solving, and communication skills.</li></ul><p>Job Types: Full-time, Fresher</p><p>Ability to commute/relocate:</p><ul><li>Sialkot Gpo: Reliably commute or willing to relocate with an employer-provided relocation package (Required)</li></ul><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Experience:</p><ul><li>Quality: 5 years (Required)</li></ul><p>Work Location: In person</p>

Executive - Quality Control (Apparel)

HITT Contracting

<div><p><i>Every day, our team members do amazing things in pursuit of our shared purpose to build trust with our clients, partners, subcontractors, and teammates. No matter your background, education, or career path, if you share our vision to create extraordinary experiences, you belong </i><b><i>at HITT </i></b><i>.
</i></p><p></p>Senior Associate, Quality Control
<p></p><h1 class="jobSectionHeader"><b>Job Description:<br>
</b></h1><p></p><p>The Senior Associate, Quality Control is a intermediate position that is responsible for developing and implementing a quality control program for small and mid-sized projects. This includes preparatory and initial meetings, inspections of the installations, and supporting the Site Ops Teams with issue/punch list resolution. The Senior Associate, Quality Control will assist the Quality Control Manager in supporting our Site Ops Team in the execution of our Quality Control Program (QCP). In addition, the Senior Associate, Quality Control will execute the QCP (if needed) for multiple projects and will act as a liaison between the client and HITT&rsquo;s Site Ops team.
</p><p></p><p><b>Responsibilities
</b></p><ul><li><p>Work with the QCS Management Team and Associate, Quality Control on miscellaneous QC tasks
</p></li><li><p>Participate in the Planning Phase of the QCP by meeting with HITT&rsquo;s Site Ops Team to align project expectations for the Quality Control Program
</p></li><li><p>Develop a list of features of work (FOW) for each project and tie them to the project schedule
</p></li><li><p>Develop site-specific QC Programs for small to mid-level projects and submit to the QC Senior Manager and QC Manager for final review
</p></li><li><p>Develop Preparatory and Initial meeting agendas and inspection templates for each FOW
</p></li><li><p>Execute four phases of control (Planning, Preparatory, Initial and Inspections) for each FOW with the subcontractors, vendors, and client(s) and perform all required meetings for mid-sized to more complex projects
</p></li><li><p>Inspect incoming materials for submittal compliance and ensure that they are properly stored
</p></li><li><p>Oversee HITT&rsquo;s Superintendents inspections for each FOW and perform inspections as needed during the ongoing installation and record any deficiencies found
</p></li><li><p>Schedule and monitor third party inspections and tests and collect documentation
</p></li><li><p>Incorporate safe work practices across the QCP
</p></li><li><p>Document and track all QC documentation including all required third party inspections and test reports
</p></li><li><p>Proactively notify responsible parties, including the QC team, of deficiencies and non-conformance issues
</p></li><li><p>Provide weekly status reports with updated progress, status, and a QC observation spotlight to the QC Manager
</p></li><li><p>Attend all HITT progress meetings and client-based meetings and provide status on all QC activities
</p></li><li><p>Interface with the client and their representatives to provide status on project QC activities and to receive any feedback on our QC program
</p></li><li><p>Track deficiencies and rework items to final resolution enforcing effective and timely corrective actions
</p></li><li><p>Coordinate QC support for startup and commissioning documentation with the MEP Services team
</p></li><li><p>Assist HITT&rsquo;s MEP Services team to complete equipment inspections on the field if needed
</p></li><li><p>Interface with the project manager and superintendent to align QC deliverables
</p></li><li><p>Develop final punch list with the Site Ops Team and oversee the project closeout process
</p></li><li><p>Complete any QC tasks and deliverables provided by the Manager, Quality Control
</p></li></ul><p></p><p><b>Qualifications
</b></p><ul><li><p>Active certification with the Army Corps of Engineers- Construction Quality Management for Contractors or an inactive certification that needs to be refreshed within 3 months of hire
</p></li><li><p>OSHA-30 certification or within 3 months of hire
</p></li><li><p>Motivated self-starter familiar with the QC process including developing a site-specific QC Program and establishing the 4 phases of control
</p></li><li><p>Is proficient with the use of Procore and/or Cx Alloy for QC documentation
</p></li><li><p>Ability to communicate effectively with the HITT Project Team and our clients
</p></li><li><p>Adequate knowledge in the CSA and MEP disciplines
</p></li><li><p>Adequate knowledge of building codes, NFPA-70E, and the NEC.
</p></li><li><p>Proficient with Microsoft Office Suite software (Word, Excel, Powerpoint, and Outlook)
</p></li><li><p>Excellent written and verbal skills
</p></li><li><p>Proficient document control skills
</p></li></ul><p></p><p><b><i>HITT Contracting is an equal opportunity employer. We are committed to hiring and developing the most qualified individuals based on job-related experience, skills, and merit. All employment decisions are made without regard to race, color, religion, sex, national origin, age, disability, veteran status, or any other protected characteristic. We value a respectful, inclusive workplace where everyone has the opportunity to succeed. HITT Contracting maintains a drug-free workplace, consistent with applicable local, state, and federal laws.</i></b></p></div>

Senior Associate, Quality Control

Continental Print & Pack (Pvt) Ltd

<p>This position will be responsible to carry out and assist in day-to-day operations of the QA &amp; QC function while simultaneously ensuring products meet quality and efficiency standards as per assigned deadlines</p><p><b>Responsibilities:</b></p><ul><li>Check &amp; review all QC parameters as per requirement before production, during production &amp; after production and ensure all results are within specifications.</li><li>Conduct Inspection of all incoming materials such as cores, cartons, inks, solvents and films.</li><li>Make sure all dimensions and requirements of material should be according to the supplier&rsquo;s COA.</li><li>Conduct ink testing which involves checking (viscosity, specific gravity &amp; solid content) to ensure ink quality and performance.</li><li>Responsible for making shades for every new job as per customer provided sample or Epson.</li><li>Carry out lab test for Raw material, semi-finished and finished material as per requirement.</li><li>Documents results of testing and analyze data.</li><li>Perform Bonding and Sealing Strength inspections for Semi-finished and Finished goods.</li><li>Operate X-Rite Spectrophotometer to control Shade variations and perform new color/ink shades development as per requirement.</li><li>Operate &amp; maintain laboratory equipment such as Tensile Machine, Heat sealer, Leak Tester, etc. to evaluate product durability, sealing efficacy and integrity.</li><li>Observing and reporting any kind of process deviation to immediate supervisors and QAQC manager.</li><li>Communicate with supplier regarding complaints and align visits if needed.</li><li>Documents inspection results by completing reports and logs, summaries and inputs data into quality data base.</li><li>Maintain sample retention system as per Company Policy.</li><li>Follow Company Policies, procedures, HSE, food safety protocols and core processes as defined by the organization within daily working routine.</li><li>Performs other duties and tasks as allocated by A.M QA/QC and above in the reporting line.</li></ul><p><b>Qualification &amp; Experience:</b></p><ul><li>Thorough knowledge of Food Safety, Halal Food Management Systems &amp; Quality Management Systems.</li><li>1-2 years of relevant work experience in the same field.</li><li>Technical understanding of quality parameters and equipment &amp; machines.</li><li>Strong organizational skills with excellent attention to details.</li><li>Good writing, analytical and problem-solving skills.</li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

QA/QC Executive

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