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quality assurance specialist

Procter & Gamble

<div>Job Location
CAIRO OCT VI PLANT
Job Description
We&rsquo;re looking for a Central Quality Specialist to support our strategic operations and local management by ensuring full compliance with quality systems, regulations, and performance measures. 
Key Responsibilities<ul><li>
Lead the development, implementation, monitoring, and continuous improvement of one or more Quality Systems in accordance with internal policies and regulatory requirements.</li><li>
Balance quality standards with business performance objectives, ensuring efficient and compliant processes.</li><li>
Guarantee right-first-time project implementation, preventing critical or major quality issues.</li><li>
Execute and support both the global P&amp;G quality strategy and local regulatory requirements.</li><li>
Prioritize actions based on business needs and capacity, ensuring alignment with strategic goals.</li></ul>
Job Qualifications<ul><li>
BSc degree in Pharmacy or Science with (0-3) years of experience</li><li>
English fluency, spoken &amp; written</li><li>
Digital fluency, including AI, Data Analytics and Data Visualization skills</li><li>
Very good Microsoft Office skills</li><li>
Exceptional communication and teamwork skills</li><li>
Good Business Writing skills</li></ul>
ABOUT US
We produce globally recognized brands and we grow the best business leaders in the industry. With a portfolio of trusted brands as diverse as ours, it is paramount our leaders are able to lead with courage the vast array of brands, categories and functions. We serve consumers around the world with one of the strongest portfolios of trusted, quality, leadership brands, including Neurobion, Sangobion, Vicks, Always&reg;, Ariel&reg;, Gillette&reg;, Head &amp; Shoulders&reg;, Herbal Essences&reg;, Oral-B&reg;, Pampers&reg;, Pantene&reg;, Tampax&reg; and more. Our community includes operations in approximately 70 countries worldwide. 
Visit http://www.pg.com to know more.
We are an equal opportunity employer and value diversity at our company. We do not discriminate against individuals on the basis of race, color, gender, age, national origin, religion, sexual orientation, gender identity or expression, marital status, citizenship, disability, HIV/AIDS status, or any other legally protected factor.
Job Schedule
Full time
Job Number
R000146901
Job Segmentation
Entry Level</div>

Site Central Quality Specialist

Hikma Pharmaceuticals

<div>
 
 Duties &amp; Responsibilities:
 
 
 
 <ul>
 <li>
 Conducting regular investigations to guarantee that workers&rsquo; follow safety procedures as required
 </li>
 <li>
 Conducting quality audits as required to ensure compliance with GMP, Quality standards.
 </li>
 <li>
 Performing pre and post-production quality checks and providing related reports accordingly.
 </li>
 <li>
 Carrying out the issuance and weighing process of raw materials to guarantee the conformity of specifications to quality standards, approving the release of materials to production, as well as ensuring compliance of raw material storage with regulatory guidelines
 </li>
 <li>
 Ensuring compliance of plant conditions (Humidity, Temperature,&hellip;etc) with set guidelines
 </li>
 <li>
 Checking machine conformity to standards as well as ensuring periodic maintenance implementation
 </li>
 <li>
 Performing other duties related to the job as assigned by the direct supervisor
 
 
 
 </li>
 </ul>
 
 Job Requirements
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Pharmacy with grade Very good or Excellent
 </li>
 <li>
 Fresh graduate.
 </li>
 <li>
 Ability to work with a team and being an effective team member
 </li>
 <li>
 Good understanding in the QA processes and the Agile development process
 </li>
 <li>
 Knowledge of quality assurance terminology, methods, and tools
 </li>
 </ul>
</div>

Quality Assurance Officer

HUHTAMAKI

<div><div>Enjoy a career, packaged with care, whilst helping protect food, people and the planet
</div><div>We are a key global provider of sustainable packaging solutions. We&rsquo;re on a mission to make all packaging recyclable, reusable, or compostable. Every day, we ensure the hygiene and safety of food and drink for people around the world. We are Huhtamaki.
</div><div>You could be part of our vision. Because it&rsquo;s our talented people that make it happen. Our people on the shop floor producing innovative, sustainable products. Our people in our offices delivering excellence for our customers every day. It&rsquo;s every one of us working together.
</div><div>We offer a place where you can feel safe, be supported, and make an impact so we can all focus on the future together.
</div>1. Ink Formulation &amp; Development
<ul><li>Formulate inks for various substrates (film, paper, foil) ensuring proper viscosity, color strength, drying properties, and adhesion.
</li><li>Adjust ink formulations based on print trials, customer specifications, or changes in raw material batches.
</li><li>Develop new ink systems or improve existing ones to enhance print quality and efficiency.
</li></ul>2. Quality Control &amp; Testing
<ul><li>Perform routine tests: color matching, viscosity, drying rate, gloss, and rub resistance.
</li><li>Monitor ink performance during machines' runs and troubleshoot issues such as color variation, smearing, or clogging.
</li><li>Maintain accurate records of ink batches tests, and corrective actions.
</li></ul>3. Lab &amp; Inventory Management
<ul><li>Supervise inventory of ink and additives stocks.
</li><li>Ensure proper storage, labeling, and safe handling of chemicals.
</li><li>Maintain lab equipment (k-bar, spectrophotometers, pumps, RK devices) and ensure calibration and upkeep.
</li><li>Ensure the ERP data entry is accurate and up to date.
</li></ul>4. Staff Supervision &amp; Training
<ul><li>Lead and train lab technicians in ink preparation, testing procedures, and safety protocols.
</li><li>Schedule shifts, assign tasks, and monitor performance to meet production deadlines.
</li></ul>5. Collaboration &amp; Communication
<ul><li>Work closely with machines' operators and production teams to ensure inks meet performance standards.
</li><li>Communicate effectively with quality assurance and management regarding issues, improvements, or customer feedback.
</li></ul>6. Safety &amp; Compliance
<ul><li>Enforce safety protocols, including chemical handling, storage, and disposal.
</li><li>Ensure compliance with environmental regulations regarding solvent emissions and waste management.
</li></ul>Join us. Help protect food, people and the planet .</div>

Ink lab supervisor

Unilever

<div><div>About Unilever 
With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people &ndash; we believe that when our people work with purpose, we will create a better business and a better world. 
 
At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don&rsquo;t believe in the &lsquo;one size fits all&rsquo; approach and instead we will equip you with the tools you need to shape your own future.</div>
Job Purpose 
The Site Quality Management role works focuses on factory operations, implementing, executing, improving and providing technical quality support to manufacturing site, Engineering, TIM (Technical Innovation Management) teams for Quality Management System (QMS) compliance, innovation execution, quality risk management and quality improvement.<div>
WHAT WILL YOUR MAIN RESPONSIBILITIES BE: 
<ul><li>Supports deploying of UL Quality strategy, governance and goals through specific Quality projects and targets.</li><li>Supports in enhancing and change mindset through trainings.</li><li>Ensure HACCP plans for the site are designed and operated to assure product safety</li><li>Supports ensuring compliance to product technology GMP requirements</li><li>Supports in Quality management for resolution of quality / consumer safety issues</li><li>Supports engineering studies to approve, evaluate or certify new or modified equipment capabilities (relative to quality attributes or performance) and identify specific design reviews for such aspects as hygienic design</li><li>Supports ensuring that quality requirements / considerations are managed for VIP changes</li><li>Supports changes to existing and new materials suppliers through activities that assure quality / hygienic control processes are in place and operating effectively, e.g. follow up on audit action plans</li><li>Supports ensuring that quality / hygiene control plans are established for production site changes or production capacity increases</li><li>Supports ensuring consumer safety and product quality in newly acquired Make sites by assessing compliance to UL Quality requirements and driving improvement plans to close gaps</li><li>Supports Quality Management System deployment and continuous improvement through support to WCM Quality Pillar and Virtual Sites</li><li>Supports resolving consumer/ customer product and package complaints and CRQS issues through analysis of care-line and CRQS audit information to identify improvements</li><li>Supports Factory Management with the Quality efforts to raise visibility and set priorities for Quality improvement</li><li>Determines quality improvement parameters by identifying statistical methods relevant to manufacturing processes.</li><li>Establishes statistical confidence by identifying sample size and acceptable error; determining levels of confidence.</li><li>Prepares reports by collecting, analyzing, and summarizing data; making recommendations.</li><li>Analyze quality performance utilizing using statistical and analytical tools and methods.</li><li>Implement methods to inspect, test and evaluate reliability, precision, reliability and accuracy of processes, products and production equipment.</li><li>Develop and establish quality procedures and systems for inspecting plans, quality trends, statistical plan price estimates and technical quality proposal plans.</li><li>Ensure process control documents adhere with set requirements.</li><li>Ensure on time processing of non-conforming components.</li><li>Assist disposition process by involving in failure analysis and suggest corrective actions as Material Review Board member.</li><li>Coordinate with suppliers and customers relating to quality trends, performance and corrective action.</li><li>Verify conformance and productivity of quality engineering system through supplier audits and surveys.</li><li>Initiate programs to enhance supplier performance.</li><li>Interact with product development committees to inspect and review engineering releases.</li><li>Review all product quality aspects like planning, manufacturing methods and process specifications.</li><li>Interact with manufacturing and engineering teams to optimize documentation related to quality and inspection checks.</li><li>Report and supply subassemblies as well as finish goods following Device Master Record.</li><li>Interact with Quality Control Packaging team to conduct Technician Training Program after evaluating Quality Inspections Techniques.</li><li>Assist manufacturing scrap performance evaluation and management.</li></ul></div><div>
Experiences &amp; Qualifications 
WHAT YOU WILL NEED TO SUCCEED 
<ul><li>1 &ndash; 3 Years of Experience in Quality related Field</li><li>Bachelor&rsquo;s degree in Engineering (Mechanical, Production, Chemical)</li><li>Experience in Manufacturing, FMCG is preferred</li></ul> 

Key Skills: 
<ul><li>Strong Communications skills</li><li>Problem solving skills</li><li>Managing Conflict</li><li>Managing &amp; Leading Change</li></ul></div>
Unilever is an organization committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bringing their &lsquo;Whole Self&rsquo; to work and this includes you! Thus, if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.
Unilever is an organisation committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bringing their &lsquo;Whole Self&rsquo; to work and this includes you! Thus if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.</div>

Quality Engineer

Axios International

<div>Position: Patient Care Specialist 
Position Purpose 
The Patient Care Specialist plays a vital role in supporting and managing Patient Support Programs, ensuring that patients receive timely, compassionate, and professional assistance throughout their treatment journey. 
The Patient Care Specialist serves as a trusted advocate and a caring voice, ensuring no patient lives their patient support program journey alone. From coordinating services to providing guidance and quality care, the Patient Care Specialist brings clarity, transparency, guidance, direction, education, and awareness to the patient support program journey. Whether in the field or the office, every action is taken to make each patient&rsquo;s experience convenient and compliant. 
At its core, this role is about removing barriers to care and ultimately expanding access strategies around the globe, so patients have the chance to receive and maximize the medical benefits and support they deserve.<div> 

 Duties and Responsibilities 
<ul><li>Assist the line manager and assigned program team in effectively managing Patient Support Program(s) by liaising with key stakeholders.</li><li>Ensure timely enrolment of eligible patients in accordance with defined workflow and program timelines.</li><li>Educate and coordinate with patients to facilitate a seamless enrollment process aligned with program procedures.</li><li>Maintain accurate, complete patient files, prepared for timely submission in line with project standards.</li><li>Accompany team members on visits to healthcare providers, pharmacies, or patient support sites to support program implementation.</li><li>Ensure patients receive their medications efficiently and without delay.</li><li>Prepare and maintain regular reports on program performance, including patient numbers, services provided, and quality assurance metrics, in collaboration with the team.</li><li>Maintain and update electronic records related to patient data and quality assurance.</li><li>Participate in and complete all required training, including product training, pharmacovigilance, and any other client-provided or Axios-mandated trainings.</li><li>Report any adverse events or product complaints in line with client requirements and Axios Standard Operating Policies and Procedures (SOPPs).</li><li>Perform administrative duties related to program operations and general office support.</li><li>Utilize Axios&rsquo; Patient Management System (PMS) exclusively for all program activities.</li><li>Ensure a solid understanding and consistent application of international standards and relevant Axios policies and procedures.</li><li>Comply with all applicable laws, regulations, Axios Code of Conduct, and internal SOPPs.</li><li>Promote awareness of escalation protocols for any deviations or non-compliance issues.</li><li>Support governance and operational monitoring activities across all Axios programs.</li><li>Provide guidance, training, and ongoing support to subordinates and newly onboarded team members to ensure smooth integration and performance.</li><li>Liaise with external stakeholders to ensure clear, effective, and professional communication.</li><li>Monitor and maintain performance KPIs by analyzing reports and implementing action plans to meet established standards</li><li>Collaborate with various internal divisions to ensure alignment</li><li>Ensure proper utilization of all provided digital platforms for both internal and external usage</li><li>Conduct quality assurance and monitoring procedures for Patient Safety Data reporting</li><li>Perform additional duties as assigned by your line manager</li></ul></div> 

<div>
Relationships 
<ul><li>Work closely with the Line Manager and program team members.</li><li>Work with the related divisions of Axios.</li><li>Maintain ongoing and frequent communication with Axios staff.</li><li>External Partners.</li></ul></div><div> 
Competencies 
<ul><li>Application of job knowledge.</li><li>Concern for order and quality.</li><li>Adaptability and flexibility.</li><li>Dependability.</li><li>Teamwork.</li></ul></div><div> 
 Educational Background and Experience 
<ul><li>A degree in a Scientific or healthcare-related field is preferred</li><li>Hands-on experience in a healthcare or scientific field or NGO is ideal</li><li>Experience in data monitoring and management is an advantage.</li><li>Experience coordinating and handling logistics/supply chain is a plus</li><li>Experience in customer service management</li></ul></div> 


Benefits of working with Axios include: 
<ul>
<li>Paying fair market value</li>
<li>Annual performance-based bonus (based on role, levels, and contract)</li>
<li>Premium Private health insurance</li>
<li>Career progression aligned with a competency framework . Humanitarian Impact: Contribute to patient support programs that make a meaningful difference in patients lives.</li>
<li>Learning Exposure: Expand your expertise through hands-on experience in global health initiatives and patient-focused programs.</li></ul><div> 
Job Circumstances 
<ul><li>The position is based in our regional office, and it does entail frequent travel to Clients and partners, which may be outside your designated region.</li><li>Flexibility in ability to travel as well as working hours is essential.</li></ul></div></div>

Patient Care Specialist (Egypt)

PepsiCo

<div>
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Performing internal audits on production areas &amp; warehouses.
 </li>
 <li>
 Participate in Food Safety, Food Defense &amp; Hold &amp; Release teams.
 </li>
 <li>
 Implementing of AIB, FSSC &amp; requirements.
 </li>
 <li>
 Preparation for Management review meeting annually.
 </li>
 <li>
 Follow up on Implementation of the integrated pest management system.
 </li>
 <li>
 Enforce operation to comply with the pre-requisite programs.
 </li>
 <li>
 Participate in Develop, review, and validate HACCP, food defense &amp; food fraud studies.
 </li>
 <li>
 Review the SOPs that may impact food safety.
 </li>
 <li>
 Prepare the training plans, materials, and exams.
 </li>
 <li>
 Review the sanitation programs of lines and areas and follow up execution.
 </li>
 <li>
 Follow up the PEM activities of the site, follow up the sampling process, review the testing results and call EMRT for meeting to take the necessary actions.
 </li>
 <li>
 Control the MOH and control spending along the year.
 </li>
 <li>
 Participate in investigation of incidents relative to FS, review the needed actions, follow up on the action plan and modify the preparedness for emergencies&rsquo; plan.
 </li>
 <li>
 Keeping the site prepared for the AIB, FSSC &amp; NFSA audits any time.
 </li>
 <li>
 Participate in inspection plan in the site (monthly internal AIB, internal FSSC audit, daily inspection), and outside the corresponding site (cross audits and audit the expected partners when needed).
 </li>
 <li>
 Review the action plans prepared by/with the different departments and determine the weak planned actions to be addressed to the site heads.
 </li>
 <li>
 Achieve AIB Target
 </li>
 <li>
 Sustain FSSC audit and QAS without major NC
 </li>
 <li>
 Sustain NFSA whitelist. complete 100% of action plan
 </li>
 <li>
 Contribute to distributors and trade audits to conduct audits as per shared plan
 </li>
 <li>
 Prepare for the external FSSC22000 audit and develop an action plan for the findings.
 </li>
 <li>
 Issuing the needed PRs and POs.
 </li>
 <li>
 Contribute to pick up a pest controller for the site, review the IPM program suggested by the contractor, follow up the execution, and develop analysis system for trends and raw data
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in science, Agriculture, Food Technology, or any relevant field.
 </li>
 <li>
 2-3 years of Quality &amp; Food safety experience in FMCGs.
 </li>
 <li>
 Very good English language is required.
 </li>
 </ul>
</div>

SC QC Associate - Food Safety - October Plant

<div><div>Enjoy a career, packaged with care, whilst helping protect food, people and the planet
</div><div>We are a key global provider of sustainable packaging solutions. We&rsquo;re on a mission to make all packaging recyclable, reusable, or compostable. Every day, we ensure the hygiene and safety of food and drink for people around the world. We are Huhtamaki.
</div><div>You could be part of our vision. Because it&rsquo;s our talented people that make it happen. Our people on the shop floor producing innovative, sustainable products. Our people in our offices delivering excellence for our customers every day. It&rsquo;s every one of us working together.
</div><div>We offer a place where you can feel safe, be supported, and make an impact so we can all focus on the future together.
</div><h3 class="jobSectionHeader">About Huhtamaki
</h3>At Huhtamaki, we are committed to protecting food, people, and the planet. We provide innovative and sustainable packaging solutions to customers around the world. Join our team and be part of a purpose-driven organization that values innovation, responsibility, and continuous improvement.
<h3 class="jobSectionHeader">Role Summary
</h3>We are seeking a detail-oriented and resourceful Procurement &amp; Logistics Specialist with strong market awareness and international sourcing capabilities. The ideal candidate will have experience in managing procurement operations, coordinating with planning and logistics teams, and driving cost-effective sourcing strategies in alignment with business needs.
<h3 class="jobSectionHeader">Key Responsibilities
</h3>Market &amp; Supplier Research:
<ul><li>Conduct market research across local and international markets as assigned by the Marketing Coordinator.
</li><li>Identify and evaluate new suppliers; support supplier mapping and cross-trading initiatives within the group.
</li><li>Monitor market trends, innovations, and competitor activities relevant to packaging and raw materials.
</li></ul>Procurement Coordination:
<ul><li>Collaborate with the planning and logistics teams to place, track, and manage purchase orders.
</li><li>Maintain and update supplier information and contract details in the ERP system.
</li><li>Ensure compliance with procurement policies and quality standards.
</li><li>Support continuous improvement in sourcing processes and cost optimization.
</li></ul>Data Management &amp; Reporting:
<ul><li>Create and maintain supplier and customer data, including accurate address and contact information.
</li><li>Compile sales and purchasing data, perform statistical analyses, and prepare regular reports for leadership.
</li><li>Communicate market intelligence and procurement performance updates to the Regional Manager and other stakeholders.
</li></ul>Quality &amp; Compliance:
<ul><li>Adhere to the Quality Assurance system and contribute to the development of procedures and internal controls.
</li><li>Ensure all procurement activities align with company policies and sustainability goals.
</li></ul><h3 class="jobSectionHeader">Candidate Requirements
</h3>Education &amp; Experience:
<ul><li>Bachelor's degree in Business, Supply Chain, Engineering, or a related field.
</li><li>Minimum of 3 years&rsquo; experience in procurement and/or logistics, preferably in an industrial or packaging environment.
</li><li>Experience in local and international sourcing , and a strong understanding of supplier management.
</li></ul>Skills &amp; Competencies:
<ul><li>Fluent in English (spoken and written).
</li><li>Proficient in Microsoft Excel, PowerPoint , and other MS Office tools.
</li><li>Hands-on experience with ERP systems (SAP, Oracle, etc.).
</li><li>Strong communication and negotiation skills.
</li><li>Analytical mindset with the ability to manage multiple priorities under pressure.
</li><li>Collaborative team player with a proactive, learning-oriented attitude.
</li></ul><h3 class="jobSectionHeader">Why Join Us?
</h3>Be a part of a company that is passionate about protecting the future through sustainable packaging solutions. You&rsquo;ll work with a global team, contribute to meaningful projects, and grow within a purpose-driven organization.
Join us. Help protect food, people and the planet .</div>

Sourcing Specialist

Explore 177+ Quality assurance specialist in Giza this May. Find roles across top companies and apply now to boost your career.