procurement specialist

assurance & compliance analyst Jobs in Giza

assurance & compliance analyst

compliance support specialist Jobs in Giza

compliance support specialist

customer success specialist

field & product quality improvement supervisor Jobs in Giza

field & product quality improvement supervisor

quality assurance specialist

EVA Pharma

<div><p>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
</p><p></p><h3 class="jobSectionHeader"><b>Job Summary</b></h3><p>
We are seeking a passionate and talented <b>Quality Compliance Senior Specialist / Supervisor</b> to join our dynamic team.</p><p>
The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.</p><p></p><h3 class="jobSectionHeader"><b><br>
Key Responsibilities</b></h3><ul>
<li>Handling of deviations according to the current procedure including initial assessment, root cause investigation, root cause identification, and proposal of corrective &amp; preventive actions.</li>
<li>Handling of changes within the site according to Change Management SOP along with the associated follow up of actions.</li>
<li>Implement Product Quality Review procedure and follow up of QMS CAPA closure and effectiveness check.</li>
</ul><p><b>Requirements</b></p><ul><li>
Bachelor&rsquo;s degree in Pharmaceutical Sciences.</li></ul><ul>
<li>2-4 years of experience in a similar position with proven track record in passing regulatory inspections.</li>
<li>Excellent communication and interpersonal skills, Result-oriented personality with team working ability &amp; resilience.</li>
<li>Fluency in spoken &amp; written English is required, Excellent knowledge of Microsoft Office Professional (word, Excel, PowerPoint, MS Outlook).</li></ul></div>

Quality Compliance Senior Specialist

<div><p>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.</p><p><b><br>
Job Summary</b><br>
We are seeking a passionate and talented <b>Compliance Support Specialist</b> to join our dynamic team.
</p><p>The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.</p><p></p><p><b>
Key Responsibilities:
</b></p><ul><li>Conduct regular field audits of commercial activities, including HCP visits, promotional events, cycle meetings, and new launches.</li>
<li>Monitor the distribution, use, and storage of promotional materials based on the company's strategy and policies.</li>
<li>Identify areas of risk and improvement, delivering insightful solutions based on live monitoring activities.</li>
<li>Audit digital tools and platforms, including sales trends, field force visits, and activities.</li>
<li>Audit the third-party and vendors engaged in commercial operations.</li></ul><p><br>
</p><p><b>Requirements</b></p><ul><li>
Bachelor&rsquo;s Degree in Pharmaceutical Sciences.
</li></ul><ul><li>1-2 years of experience in a pharmaceutical field auditing.</li>
<li>Strong analytical, observation, and reporting skills.</li>
<li>High ethical standards, attention to detail, and confidentiality.
</li><li>Good Communication and interpersonal skills.</li></ul></div>

Compliance Support Specialist

Alorica

<div>
 <p>
  At Alorica, we deliver insanely great customer experiences for the world&rsquo;s best-known brands. As a leading provider of customer experience (CX) solutions, we specialize in digital customer care, customer relationship management, and back-office support across a wide range of industries &mdash; from tech and healthcare to finance, retail, and communications.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   A BRIEF OVERVIEW
  </strong>
 </p>
 <p>
  Under general supervision, conducts audits, analyzes reports and communicates quality trends, variances, strategies and provides coaching feedback relative to both quality scans and CSAT surveys.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   YOUR DAY-TO-DAY
  </strong>
 </p>
 <ul>
  <li>
   Provides complete, accurate and timely entry of data into a database system.
  </li>
  <li>
   Checks accuracy and relevance of input and output data.
  </li>
  <li>
   Reports on information contained in the database to internal clients, according to a standard format.
  </li>
  <li>
   Performs data analysis, including evaluating data to determine whether or not the data is valid, and identify patterns and trends based on a variety of quality control procedures.
  </li>
  <li>
   Produces standard and ad hoc reports based on data contained in a database.
  </li>
  <li>
   Pulls coaching/transaction metrics weekly and provides to the client.
  </li>
 </ul>
 <p>
  &middot;
 </p>
 <p>
  <strong>
   WHAT YOU BRING TO THE TABLE!
  </strong>
 </p>
 <ul>
  <li>
   Advanced English level (B2 in CEFR) and excellent communication skills (oral and written).
  </li>
  <li>
   Organizational, time management, analytical thinking and presentation skills. Detail-oriented and Results-Oriented.
  </li>
  <li>
   Strong knowledge to identify behaviors during a call, and to identify serious violations in customer policies, required.
  </li>
  <li>
   Microsoft Office package intermediate proficiency. Capable to work on-site. Schedule flexibility, including AM/PM shifts during training.
  </li>
 </ul>
 <p>
 </p>
</div>


Quality Assurance Associate

Grifols Egypt for Plasma Derivatives (GEPD)

<div>
 <strong>
  Job Description:
  <br/>
  <br/>
 </strong>
 Responsible for ensuring that operational systems and processes comply with local and international regulations, as well as internal company standards.
 <br/>
 <br/>
 The role involves managing and improving operational processes related to change control, deviation management, and continuous improvement within the donor center and/or plasma logistic center.
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 <br/>
 This position ensures compliance with industry regulations and company policies while enhancing operational efficiency through effective system oversight and process optimization.
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 <strong>
  Key responsibility
  <br/>
  <br/>
 </strong>
 <strong>
  Deviation and CAPA Management:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Follow the approved deviation management and CAPA system, involving appropriate stakeholders for investigation and closure.
  </li>
  <li>
   Proactively identify root causes of deviations and implement corrective and preventive actions to reduce their occurrence.
  </li>
  <li>
   Monitor and analyze deviation trends to identify areas for improvement and implement strategies to minimize the number and impact of deviations.
  </li>
  <li>
   Work closely with cross-functional teams to ensure timely closure of deviations, reducing the overall time taken for resolution.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Change Control Management:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Coordinate and oversee the implementation of operational change control processes.
  </li>
  <li>
   Work closely with cross-functional teams to ensure changes are documented, reviewed, and executed efficiently.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Process Improvements:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Identify and lead continuous improvement initiatives in operational processes to enhance efficiency and quality.
  </li>
  <li>
   Maintain and optimize systems used for tracking and managing deviations and change controls.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Documentation Standardization:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Develop and implement standardized documentation practices to ensure consistency and compliance across all operational processes.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Collaboration and Training:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Serve as a key liaison between operations and other departments regarding process management.
  </li>
  <li>
   Provide training and guidance to employees on operational compliance and system updates.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Key Process Indicators
 <strong>
  :
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Compile all information related to the different processes referred to key process indicators established for plasma supply chain areas.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Other duties as assigned.
 <br/>
 <br/>
 <strong>
  Academic Experience Required
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in engineering, Health-related Sciences, or a related field.
  </li>
  <li>
   Knowledge of Quality Management Systems.
  </li>
  <li>
   Knowledge of current Good Manufacturing Practices (cGMP).
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Professional Experience Required
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Minimum of 2 years of related experience in GMP Quality Systems.
  </li>
  <li>
   Minimum of 5 years of professional experience in the pharmaceutical, biotech, or regulated manufacturing industries.
  </li>
  <li>
   Experience with GMP regulations, deviation handling, and change control processes.
  </li>
  <li>
   Familiarity with CAPA investigations and operational excellence methodologies.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Computing Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Knowledge of Microsoft Office applications (Word, Excel, PowerPoint, Outlook).
  </li>
  <li>
   Experience with electronic quality management systems such as SAP-QM, TrackWise, Veeva, or similar platforms.
  </li>
  <li>
   Ability to analyze data and generate reports using database management tools.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Personal Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Strong problem-solving and analytical skills.
  </li>
  <li>
   Excellent organizational and time management abilities.
  </li>
  <li>
   Effective communication and collaboration with cross-functional teams.
  </li>
  <li>
   Ability to work independently and manage multiple tasks in a fast-paced environment.
  </li>
  <li>
   Strong integrity and commitment to quality and compliance.
  </li>
  <li>
   Excellent interviewing, listening, and observation skills in order to obtain the information needed to fully grasp and document a process.
  </li>
  <li>
   Demonstrated ability to organize work and keep comprehensive substantiating records.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Languages
  <br/>
  <br/>
 </strong>
 Proficiency in English and Arabic (professional-level reading, writing, and communication required).
</div>


Operations Technical Specialist - Al Haram

PepsiCo

<div>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <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

ELCO

<div><div>Ariston Group is a global leader in sustainable thermal comfort that offers a unique, extensive range of solutions for climate comfort, water heating and air handling, as well as components and burners. Listed on Euronext Milan since November 2021, in 2024 the group reported over 2.6-billion-euro revenues, with over 10,000 employees, direct presence in 40 countries in 5 continents, 28 production sites and 28 research and development centers. The group demonstrates its commitment to sustainability through the development of renewable and high efficiency solutions, such as heat pumps, water heating heat pumps, hybrids, domestic ventilation, air handling and solar thermal systems. The group also stands out for its continuous investment in technological innovation, digitalization, and advanced connectivity solutions. The group operates under global strategic brands Ariston, Elco and Wolf, and brands such as Calorex, NTI, HTP, Atag, Brink, Chromagen, Racold, as well as Thermowatt and Ecoflam in the components and burners business.</div><div><br>
   Location: Giza, Egypt<br>
   Full-time</div><br>
<div></div>
<div>
We&rsquo;re looking for a recent graduate with a passion for purchasing to join our local team at our Giza Plant as Procurement Specialist. In this role you will have the opportunity to grow into a key player in our sourcing strategy. This is your chance to work closely with experts, contribute to exciting R&amp;D projects, and shape the future of procurement.</div><br>
<div></div>
<div><b>
What You&rsquo;ll Do</b></div>
<div>
As our Procurement Specialist, you&rsquo;ll report to the Procurement Manager and be involved in:</div>
<ul>
<li>Supporting internal teams to define needs and assess market conditions</li>
<li>Helping shape sourcing strategies aligned with our tech roadmap</li>
<li>Managing the full order process: from technical requirements to negotiation and coordination</li>
<li>Ensuring data accuracy and sharing insights across departments</li>
<li>Analyzing supplier KPIs and performance (cost, quality, delivery)</li>
<li>Participating in cost reduction initiatives and long-term contract negotiations</li>
<li>Collaborating with Product Management and Supplier Quality Assurance</li>
<li>Engaging suppliers early in R&amp;D projects to drive innovation</li></ul><br>
<div></div>
<div><b>
What We&rsquo;re Looking For</b></div>
<ul>
<li>Recent graduate with a degree in business, engineering, or related fields</li>
<li>Strong English proficiency (written and spoken)</li>
<li>Solid Excel and Office skills</li>
<li>A data-driven mindset, with strong analytical and organizational skills</li>
<li>Excellent negotiation abilities and a proactive attitude</li>
<li>Willingness to travel and work in a fast-paced, international environment</li></ul><br>
<div></div>
<div><b>
Why Join Us?</b></div>
<ul>
<li>Be part of a forward-thinking team that values innovation and collaboration</li>
<li>Gain hands-on experience in strategic procurement and supplier management</li>
<li>Work on real projects that impact product development and business success</li>
<li>Enjoy a supportive environment with mentorship and growth opportunities</li></ul><br>
<div></div>
<div>
We are committed to the principle of equal employment opportunity for all people, by offering a work environment accessible, welcoming and inclusive in compliance with legal obligations.</div></div>

PROCUREMENT SPECIALIST

Ariston Group

<div>
 Job description:
 <br/>
 <br/>
 <p>
  📍 Location: Giza, Egypt
  <br/>
  🕒 Full-time
 </p>
 <p>
  <br/>
  Are you passionate about quality and building strong supplier partnerships? Join our team as a Supplier Quality Assurance Engineer, where you&rsquo;ll play a key role in ensuring our suppliers deliver top-quality components that meet our standards for performance, cost, and reliability.
 </p>
 <p>
  &nbsp;
 </p>
 <p>
  <strong>
   What You&rsquo;ll Do
  </strong>
 </p>
 <ul>
  <li>
   Work closely with R&amp;D and Procurement to select and qualify top-performing suppliers.
  </li>
  <li>
   Evaluate supplier capabilities and ensure compliance with ISO 9001, ISO 14001, and other standards.
  </li>
  <li>
   Lead supplier development projects to improve quality, reduce costs, and support new product launches.
  </li>
  <li>
   Manage supplier changes, capacity studies, and engineering updates.
  </li>
  <li>
   Drive the Production Part Approval Process (PPAP) and ensure smooth integration of new components.
  </li>
  <li>
   Solve quality issues and lead improvement initiatives with suppliers.
  </li>
  <li>
   Build strong relationships with internal teams and supplier partners.
  </li>
 </ul>
 <p>
  &nbsp;
 </p>
 <p>
  <strong>
   What We&rsquo;re Looking For
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Mechanical, Industrial, Electrical Engineering, or a related technical field.
  </li>
  <li>
   Certifications Six Sigma or Lean Manufacturing are highly valued.
  </li>
  <li>
   5-8 years of experience in quality assurance or supplier quality roles, preferably in automotive industry.
  </li>
  <li>
   Experience conducting supplier audits (process, product, and system audits).
  </li>
  <li>
   Proficiency in tools like FMEA, PPAP, APQP, 8D, 5 Why, and Root Cause Analysis.
  </li>
  <li>
   Understanding of metrology, calibration, and statistical process control (SPC).
  </li>
  <li>
   Ability to read and interpret technical drawings and understand manufacturing processes.
  </li>
  <li>
   Strong analytical and problem-solving abilities, excellent communication, attention to detail and organizational skills, Ability to work independently and manage multiple priorities, Team-oriented with a proactive mindset.
  </li>
  <li>
   Strong teamwork, customer focus, and communication skills.
  </li>
  <li>
   Proficient in Excel and SAP ERP.
  </li>
  <li>
   Fluent in Arabic and English (written and spoken).
  </li>
 </ul>
</div>


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