supervisor quality control

DP World

<div>
 
 
 JOB PURPOSE
 
 
 
 To assist in supervising cargo examination operations with a strong focus on supporting quality assurance, minimizing damage, and contributing to process improvement. The Assistant Supervisor works closely with the Quality Foreman and Service Quality Supervisor to ensure cargo handling activities whether manual or equipment-based are conducted safely, efficiently, and in compliance with established procedures. Through regular inspections and hands-on support, this role helps maintain service standards, ensures proper documentation of quality checks, and promotes continuous improvement across cargo examination processes.
 
 
 
 
 
 
 KEY ACCOUNTABILITIES
 
 
 <ul>
 <li>
 Assist the Supervisor and Quality Foreman in overseeing cargo stripping, repacking, and lashing operations.
 </li>
 <li>
 Conduct regular spot checks during cargo examination activities to ensure compliance with handling procedures.
 </li>
 <li>
 Support in verifying proper handling of fragile, hazardous, and oversized cargo.
 </li>
 <li>
 Monitor equipment usage (e.g., forklifts, cranes) and report unsafe practices or malfunctions.
 </li>
 <li>
 Report deviations from SOPs and support in implementing corrective actions.
 </li>
 <li>
 Provide guidance and support to the quality team to maintain service standards.
 </li>
 <li>
 Deliver on-the-job coaching to labor teams on proper cargo-handling techniques.
 </li>
 <li>
 Participate in daily briefings to reinforce quality and safety priorities.
 </li>
 <li>
 Promote awareness of quality culture and customer service best practices.
 </li>
 <li>
 Ensure compliance with company policies, customs regulations, and health &amp; safety standards.
 </li>
 <li>
 Collaborate with operations teams to escalate and resolve quality-related issues.
 </li>
 <li>
 Contribute to SOP reviews and suggest improvements based on operational feedback.
 </li>
 <li>
 Maintain inspection logs and assist in preparing daily/weekly quality reports.
 </li>
 <li>
 Support in analyzing damage reports and assist in implementing preventive measures.
 </li>
 <li>
 Ensure repacking quality and secure lashing under supervision to minimize cargo damage.
 </li>
 <li>
 Coordinate with the Quality Foreman to optimize repacking and reduce excess cargo.
 </li>
 <li>
 Escalate exceptional cases and operational challenges to the Supervisor.
 </li>
 <li>
 Assist in training yard supervisors and foremen on quality procedures.
 </li>
 <li>
 Participate in audits of repacked and stripped containers.
 </li>
 <li>
 Support compliance with safety, environmental, and customs requirements.
 </li>
 <li>
 Assist in tracking and validating charges related to cargo examination and VAS.
 </li>
 <li>
 Ensure proper documentation and billing support for rendered services.
 </li>
 </ul>
 
 
 
 
 
 QUALIFICATIONS, EXPERIENCE AND SKILLS
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree or diploma in Logistics, Supply Chain, Quality Management, or related field.
 </li>
 <li>
 3&ndash;5 years&rsquo; experience in cargo handling operations, quality control, or terminal supervision.
 </li>
 <li>
 Strong knowledge of safe cargo handling techniques and equipment operation.
 </li>
 <li>
 Familiarity with customs examination processes and port terminal procedures is an advantage.
 </li>
 <li>
 Proven background in process improvement and lean management.
 </li>
 <li>
 Leadership and decision-making skills to drive quality initiatives.
 </li>
 <li>
 Excellent communication and coordination abilities.
 </li>
 </ul>
</div>

Assistant Supervisor - Service Quality

QuVa Pharma

<div>Our Supervisor, Calibration plays a vital role within our organization. Once you complete our training, your responsibilities will include the daily coordination and oversight of the Quva Calibration Program. This role serves as the technical subject matter expert (SME) for all calibrated equipment at the Quva facility and provides day-to-day supervision of calibration staff. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

 What the Supervisor, Calibration Does Each Day:
<ul>
<li>Provide overall leadership and supervision of the site calibration program and calibration staff</li>
<li>Manage all calibration and calibrated equipment maintenance activities</li>
<li>Perform and/or oversee verification, qualification, calibration, and maintenance of laboratory equipment and instruments</li>
<li>Continuously evaluate calibration practices and calibrated equipment maintenance</li>
<li>Manage the preventive maintenance program for all calibrated equipment</li>
<li>Minimize calibrated equipment downtime by tracking, trending, and reporting key performance metrics</li>
<li>Adjust, repair, and troubleshoot instruments</li>
<li>Coordinate instrument calibration, certification, and re-certification with external standards laboratories</li>
<li>Serve as the technical subject matter expert for calibration-related issues</li>
</ul>
Our Most Successful Supervisor, Calibration:
<ul>
<li>Has a sense of urgency, accountability and resourcefulness (e.g., work in changing environment)</li>
<li>Is a self-starter and independent learner</li>
<li>Promotes active listening with team members; Contributes appropriately to conversations; Has strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization</li>
<li>Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform</li>
</ul>
Minimum Requirements for this Role:
<ul>
<li>Associate&rsquo;s degree required; bachelor&rsquo;s degree preferred</li>
<li>5+ years overall in calibration/metrology instrumentation&mdash;ideally in pharmaceutical or other regulated manufacturing</li>
<li>18+ years of age</li>
<li>Able to successfully complete a drug and background check</li>
<li>Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas</li>
</ul>
Any of the Following Will Give You an Edge:
<ul>
<li>3 years leading teams, training technicians, or coordinating schedules and projects</li>
<li>Experience with Good Manufacturing Practices (cGMP), documentation controls, and audit readiness is highly valued</li>
<li>Proficiency in calibrating instruments used in pharma manufacturing&mdash;such as: Pressure, temperature, flow, level, pH transmitters; Electrica instruments (multimeters, oscilloscopes, signal generators)</li>
</ul>
Benefits of Working at Quva:
<ul>
<li>Set, full-time, consistent work schedule</li>
<li>Comprehensive health and wellness benefits including medical, dental and vision</li>
<li>401k retirement program with company match</li>
<li>22 paid days off plus 8 paid holidays per year</li>
<li>Occasional weekend and overtime opportunities with advance notice</li>
<li>National, industry-leading high growth company with future career advancement opportunities</li>
<li>The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions</li>
<li>Range: $74,766 - $102,817 Annually</li>
</ul>
About Quva:

Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma&rsquo;s multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva&rsquo;s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.

Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is &ldquo;at will.&rdquo;

California Consumer Privacy Act (CCPA) Notice for Applicants and Employees</div>

Supervisor, Calibration

SG Allied Businesses Ltd

Location: B-40 SG Allied Businesses Limited SITE KarachiCompany: SG Allied Businesses LimitedEmployment Type: Full-timeSalary: PKR 100,000 &ndash; 150,000 (based on experience)Experience: Minimum 2 yearsAge: 28 years and aboveJob DescriptionWe are looking for a Quality &amp; Compliance Supervisor(Cleanroom) to manage and supervise aseptic laboratory operations. The selected candidate will be responsible for handling autoclave operations and performing inoculation work under laminar flow hoods, ensuring strict hygiene and contamination-free procedures.Key Responsibilities<ul><li>Operate and monitor autoclaves for sterilization of media, tools, and materials</li><li>Perform inoculation and culture handling under laminar flow hood</li><li>Supervise cleanroom hygiene, gowning, and aseptic protocols</li><li>Ensure proper sterilization cycles, documentation, and log maintenance</li><li>Identify and prevent contamination issues</li><li>Train and guide junior lab staff in cleanroom best practices</li><li>Maintain SOP compliance and laboratory discipline</li></ul>Required Skills &amp; Qualifications<ul><li>Hands-on experience working in a cleanroom or aseptic lab environment</li><li>Practical knowledge of laminar flow hood operations</li><li>Experience handling autoclaves (loading, cycles, safety)</li><li>Understanding of aseptic techniques and contamination control</li><li>Background in microbiology, biotechnology, mycology, or related field (preferred)</li><li>Ability to supervise staff and enforce laboratory standards</li></ul>Preferred Experience<ul><li>Mushroom spawn lab, tissue culture lab, or microbiology lab experience</li><li>Familiarity with SOPs, batch records, and lab documentation</li></ul>Job Type: Full-timePay: Rs100,000.00 - Rs150,000.00 per monthWork Location: In person

Quality & Compliance Supervisor (Cleanroom)

Pall

<div>Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Pall Corporation, one of Danaher&rsquo;s 15+ operating companies, our work saves lives&mdash;and we&rsquo;re all united by a shared commitment to innovate for tangible impact.
You&rsquo;ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher&rsquo;s system of continuous improvement, you help turn ideas into impact &ndash; innovating at the speed of life.
As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper&mdash;everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation.
Learn about the Danaher Business System which makes everything possible.
The Quality Control Inspection Supervisor is responsible for planning and managing inspection workflows to meet labor, material, quality, and schedule objectives. The supervisor also oversees the Quality Control inspection team, providing direction, coordination, and leadership to ensure timely and cost-effective inspection activities that support production requirements.
This position reports to the site Sr. Quality Manager and is part of the Aerospace quality department located in New Port Richey, FL and is an on-site role.
This position requires access to export-controlled commodities, technical data, technology, software, and services. U.S. citizenship, U.S. legal permanent resident status, protected person status, or U.S. Government export authorization is required. Any offer of employment is contingent upon Pall obtaining the necessary employment visa and export authorization, including, if required, an export license from the applicable U.S. government agency.
In this role, you will have the opportunity to:<ul><li>
Work closely with internal value streams, external customers, and regulatory bodies to ensure products are fully compliant and meet all customer and Pall requirements and expectations.</li><li>
Apply your knowledge of quality management, Lean principles, and continuous improvement methodologies while coaching, mentoring, and developing inspectors to ensure consistent performance and adherence to quality standards and regulatory requirements.</li><li>
Integrate Danaher Business System (DBS) into quality inspection including updating charts (Visual Management tools), report inspection yield metrics and activities, team goals and countermeasures to management during Daily Management meetings, and associate training.</li><li>
Manage associate performance and development including recognition, feedback, corrective / disciplinary actions, training, and developmental processes, and daily attendance.</li><li>
Coordinate with customer source inspectors and government source inspectors, when needed, to ensure no impact on production schedules.</li><li>
Maintain departmental training matrix and ensure redundant coverage for all customers that require source and FAA inspection.</li></ul>
The essential requirements of the job include:<ul><li>
Bachelor&rsquo;s degree in quality or an engineering discipline.</li><li>
A minimum of 5 years of quality control experience in a regulated industry. (i.e. Aerospace or Automotive)</li><li>
A minimum of 2 years of leadership experience supervising a team of six or more individuals performing inspection-related activities.</li><li>
Skilled in the use of inspection tools and equipment. (i.e. calipers, micrometers, height gauges, comparators, and other precision instruments)</li><li>
Knowledgeable in AS9100/AS9102/AS9110 &ndash; Aerospace Quality Management System Requirements</li><li>
Knowledgeable in interpreting complex engineering part drawings &amp; Geometric Tolerancing (GD&amp;T).</li></ul>
Travel, Motor Vehicle Record &amp; Physical/Environment Requirements:<ul><li>
Less than 5% travel is expected for this position.</li><li>
Must have a valid driver&rsquo;s license with an acceptable driving record</li><li>
Ability to lift, move or carry equipment up to 30 lbs.</li><li>
Bend, sit and/or stand for long periods of time</li></ul>
It would be a plus if you also possess previous experience in:<ul><li>
ASQ certification in quality</li><li>
AS9100 lead auditor</li></ul>
Pall Corporation, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it&rsquo;s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
At Pall we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Pall can provide.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid.
#LI-LCS
Join our winning team today. Together, we&rsquo;ll accelerate the real-life impact of tomorrow&rsquo;s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.</div>

Quality Control Inspection Supervisor

Jadex

Alltrista Plastics LLC, is a subsidiary of Jadex Inc., and is a leading manufacturer in high-volume, precision injection molded parts. The company designs and manufactures with proprietary engineering processes and extensive manufacturing capabilities, from five (5) locations worldwide. From the first spark of an idea, through the design of the mold to the actual manufactured product, Alltrista Plastics focuses all efforts on delivering innovative plastic solutions. The company’s core markets include Consumer Products, Medical/Healthcare, Personal Care, Health & Beauty, Caps & Closures, and Packaging.
 
Position Summary
 Responsible for the day-to-day quality support for the manufacturing function and the supervision of the quality department inspection staff.
 Primary Functions
 <ul>
<li>Reviews reports from each shift and reports discrepancies to appropriate personnel.</li>
<li>Sends complete and accurate inspection and certification data to the customer and maintains Good Manufacturing Practices.</li>
<li>Understands and utilizes statistical tools and techniques to further enhance the prevention-based quality system.</li>
<li>Assures that all non-conforming materials are properly identified, isolated, and dispositioned and that any necessary corrective actions are adequately communicated, implemented, and monitored for effectiveness.</li>
<li>Reviews each new or existing job on a period basis to ensure that customer requirements are continually satisfied and helps to identify and implement any necessary corrective actions.</li>
<li>Monitors the calibration program, updates the database as required, and ensures all test and measurement equipment is calibrated in accordance with procedures.</li>
<li>Assists the quality manager with the implementation of quality initiatives, new or revised policies and procedures, corrective actions and helps to monitor resulting data for effectiveness.</li>
<li>Ensures training is in place and effective for new hires within the quality department.</li>
<li>Provides ongoing training to subordinates to ensure continued growth and improvement in all aspects of their responsibilities.</li>
<li>Provides timely completion and submission of performance reviews and evaluations for subordinates along with recommendations for corrective actions and promotion potential.</li>
<li>Provides counseling and disciplinary actions both verbal and written when required.</li>
<li>Maintains enforcement of and compliance with policy and procedures to ensure that the results conform to planned and/or desired results and to assure a safe working environment is maintained.</li>
<li>Manages the corrective action activity (internal, external, and supplier) by coordinating input from the various manufacturing teams to provide continuous improvement of our daily activity and to provide prompt and accurate responses to our customers in potentially difficult situations.</li>
<li>Supports the development, daily use, and long-term improvements of the ISO 9001 system and cGMP requirements through internal audits, process monitoring, and creative thinking.</li>
</ul>
Key Qualifications
 <ul>
<li>Associates degree or equivalent in related field. Bachelor’s Degree preferred.</li>
<li>Background in ISO certified manufacturing environment.</li>
<li>Hands on experience as a Quality Technician, a Quality Systems Technician, or a Quality Department supervisor/manager.</li>
<li>Three to five years processing injection molding or related experience preferred.</li>
<li>Thorough understanding of quality standards and systems including Statistical Process Control.</li>
</ul>
Physical Requirements
 The conditions herein 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 essential job functions. Please refer to the Physical Job Description, which is contained as a separate document, for more detail.
 
Environment: Normal manufacturing environments; work with machinery and media in or around confined spaces; exposure to chemicals, grease and oils.
 Physical: Sufficient physical ability to perform heavy lifting and carrying; reaching, kneeling, crawling, climbing; standing for moderate periods of time.
 Vision: See in the normal visual range with or without correction; vision sufficient to read computer screens and printed documents.
 Hearing: Hear in the normal audio range with or without correction.
 Other: Ability to work overtime or occasionally on weekends with short notice.
 
Jadex Inc and its Businesses do not discriminate in employment based on race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status, military service, or other non-merit factor.

Alltrista - Supervisor, Quality

HRI Private Limited

Key Responsibilities:<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>Eligibility Criteria:<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>Interested candidates may send their updated CVs to careers@hri.com.pk mentioning &ldquo;Manager &ndash; Quality Control&rdquo; in the subject line.Job Type: Full-timePay: Rs150,000.00 - Rs200,000.00 per monthWork Location: In person

Manager – Quality Control

Key Responsibilities:<ul><li>Conduct in-process and final product inspections</li><li>Monitor production activities to ensure adherence to quality standards</li><li>Record and report inspection results</li><li>Identify defects and coordinate corrective actions</li><li>Maintain quality documentation and reports</li></ul>Eligibility Criteria:<ul><li>Intermediate or Bachelor&rsquo;s degree</li><li>Minimum 2 years of relevant experience, preferably in the packaging industry</li><li>Basic knowledge of quality inspection procedures and documentation</li><li>Attention to detail and good reporting skills</li></ul>Interested candidates may send their updated CVs to careers@hri.com.pk mentioning &ldquo;Inspector &ndash; Quality Control&rdquo; in the subject line.Job Type: Full-timePay: Rs50,000.00 - Rs100,000.00 per monthWork Location: In person

Inspector – Quality Control

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