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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><b><br>
Job Summary</b><br>
We are seeking a passionate and talented <b>Quality Assurance 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.<br>
<br>
</p><p><b>Responsibilities:
</b></p><ul><li>Monitor environmental conditions (temperature, humidity, pressure differentials) and ensure they comply with GMP requirements across production and warehouse areas</li>
<li>Participate in raw material dispensing and verify specifications and calculations as per SOPs</li>
</ul><ul><li>Oversee manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirements</li>
<li>Review batch records and logbooks for completeness, accuracy, and compliance with GDP (Good Documentation Practice)</li>
<li>Record and report deviations, non-conformities, and incidents. Participate in root cause investigations and track corrective and preventive actions (CAPA)</li>
</ul><p><b>
Requirements</b></p><ul><li>
Bachelor's degree in Pharmacy.</li><li>
0-2 years of relevant experience in a pharmaceutical QA environment</li><li>
Knowledge of cGMP and GDP principles</li><li>
Understanding of CAPA, change control, and quality documentation systems</li><li>
Familiarity with ISO 9001 and safety programs</li><li>
Awareness of validation principles and basic statistical concepts</li></ul></div>

Quality Assurance 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 an experienced and highly skilled <b>Senior Vaccine Quality Assurance Specialist</b> to join our team.</p><p>
The ideal candidate will provide advanced QA oversight for vaccine manufacturing processes, ensure full compliance with GMP standards, and support continuous improvement initiatives to maintain excellence in product quality and patient safety.</p><p><b><br>
Responsibilities:
</b></p><ul><li>Provide senior-level QA oversight for all vaccine manufacturing, filling, and packaging operations, ensuring strict adherence to GMP, SOPs, and regulatory requirements.
</li><li>Review and approve vaccine batch production records, investigations, protocols, and reports.
</li><li>Lead deviation investigations related to vaccine operations and ensure timely and effective CAPA implementation.
</li><li>Monitor and evaluate environmental conditions in classified areas, ensuring compliance and escalating any concerning trends.
</li><li>Coordinate and support internal audits, regulatory inspections, and external audits related to vaccine processes.
</li><li>Participate in change control assessments and risk assessments for vaccine equipment, materials, and processes.
</li><li>Provide guidance, training, and support to junior QA specialists and production teams on GMP, data integrity, and documentation standards.
</li><li>Identify quality gaps and drive continuous improvement initiatives to enhance vaccine process robustness and compliance.
</li><li>Ensure proper documentation practices (GDP) and data integrity (ALCOA+) throughout all vaccine-related activities.</li>
</ul><p><b>
Requirements</b></p><ul>
<li>
Bachelor&rsquo;s degree in Pharmacy (mandatory).
</li><li>3&ndash;4 years of experience in pharmaceutical Quality Assurance; vaccine manufacturing experience is strongly preferred.
</li><li>Strong knowledge of cGMP, GDP, CAPA systems, change control, and deviation management.
</li><li>Experience supporting audits and inspections (FDA, EMA, WHO, or local authorities is a plus).
</li><li>Solid understanding of cleanroom controls, aseptic practices, and environmental monitoring requirements.
</li><li>Strong analytical, problem-solving, and decision-making skills.
</li><li>Excellent communication skills and ability to collaborate cross-functionally.
</li><li>Proven ability to coach and guide junior team members.</li></ul></div>

Senior Vaccine QA 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>Vaccine Quality Assurance Specialist</b> to join our dynamic team.</p><p>
The ideal candidate will ensure that all vaccine manufacturing and handling processes meet the highest standards of quality and compliance, supporting our mission to enhance human health and well-being.</p><p><b><br>
Responsibilities:
</b></p><ul><li>Monitor environmental conditions (temperature, humidity, pressure differentials) across vaccine production and storage areas, ensuring compliance with GMP requirements.
</li><li>Participate in raw material dispensing for vaccine manufacturing and verify specifications and calculations as per SOPs.
</li><li>Oversee vaccine manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirements.
</li><li>Review batch records and logbooks related to vaccine production for completeness, accuracy, and compliance with GDP.
</li><li>Record and report deviations, non-conformities, and incidents specific to vaccine processes. Participate in root cause investigations and track corrective and preventive actions (CAPA).</li>
</ul><p><b>
Requirements</b></p><ul>
<li>
Bachelor&rsquo;s degree in Pharmacy.
</li><li>0&ndash;2 years of relevant experience in pharmaceutical QA; experience in vaccine manufacturing is a plus.
</li><li>Knowledge of cGMP and GDP principles.
</li><li>Understanding of CAPA, change control, and quality documentation systems.
</li><li>Familiarity with ISO 9001 and safety programs.
</li><li>Awareness of validation principles and basic statistical concepts.</li></ul></div>

Vaccine QA Specialist

Hikma Pharmaceuticals

<p></p><div><div><div><div><div><div><div>Description:
<p><b>Duties &amp; Responsibilities:</b></p>
<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>
<li>Job Location: 6th of October City</li>
</ul>
<p><b>Job Requirements</b></p>
<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></div></div></div><div><div><div><div>Location:
Giza, EG</div></div></div></div></div></div></div><p></p>

Quality Assurance Officer

HUHTAMAKI

<div><div><p><b>Enjoy a career, packaged with care, whilst helping protect food, </b><b>people </b><b>and the planet
</b></p></div><p></p><div><p>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.
</p></div><p></p><div><p>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.
</p></div><p></p><div><p>We offer a place where you can feel safe, be supported, and make an impact so we can all focus on the future together.
</p></div><p></p><p><b>Key Responsibilities
</b></p><ul><li><p>Conduct routine inspections and quality tests for raw materials, in-process, and finished goods.
</p></li><li><p>Ensure compliance with company standards, customer requirements, and BRCGS/ISO/GMP systems.
</p></li><li><p>Record and analyze test data, prepare reports, maintain accurate QC records, test reports and support root cause analysis for quality incidents.
</p></li><li><p>Collaborate with production, maintenance, and QA teams to prevent and resolve quality issues.
</p></li><li><p>Support problem-solving and root cause analysis activities related to product non-conformities.
</p></li><li><p>Work closely with <b>QA, Production, and Maintenance </b>teams to sustain process stability and continuous improvement.
</p></li><li><p>Contribute to Huhtamaki&rsquo;s goal of reducing waste and enhancing customer satisfaction through proactive quality control.
</p></li></ul><p><b>Qualifications
</b></p><ul><li><p>Bachelor&rsquo;s degree in Science, Engineering, or a related field.
</p></li><li><p>1&ndash;3years of experience in Quality Control, preferably in <b>flexible packaging </b>industries.
</p></li><li><p>Familiar with testing methods for films, laminates, inks, and adhesives.
</p></li><li><p>Understanding of quality systems (ISO 9001, BRCGS Packaging, GMP).
</p></li><li><p>Good communication and attention to detail.
</p></li><li><p>Analytical mindset, strong attention to detail, and effective communication skills.
</p></li></ul><p></p><p>Join us. Help protect food, people and the planet .</p></div>

Quality Specialist

<div><div><p><b>Enjoy a career, packaged with care, whilst helping protect food, </b><b>people </b><b>and the planet
</b></p></div><p></p><div><p>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.
</p></div><p></p><div><p>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.
</p></div><p></p><div><p>We offer a place where you can feel safe, be supported, and make an impact so we can all focus on the future together.
</p></div><p></p><p>Assist in standard assignments and tasks. Collect, compile, and analyze relevant data and solve daily issues and challenges related to tasks and development initiatives. Maintain safe working environment and comply with company procedures, rules, and regulations.
</p><p></p><p><b>Key Responsibilities
</b></p><ul><li><p>Conduct routine inspections and quality tests for raw materials, in-process, and finished goods.
</p></li><li><p>Ensure compliance with company standards, customer requirements, and BRCGS/ISO/GMP systems.
</p></li><li><p>Record and analyze test data, prepare reports, maintain accurate QC records, test reports and support root cause analysis for quality incidents.
</p></li><li><p>Collaborate with production, maintenance, and QA teams to prevent and resolve quality issues.
</p></li><li><p>Support problem-solving and root cause analysis activities related to product non-conformities.
</p></li><li><p>Work closely with <b>QA, Production, and Maintenance </b>teams to sustain process stability and continuous improvement.
</p></li><li><p>Contribute to Huhtamaki&rsquo;s goal of reducing waste and enhancing customer satisfaction through proactive quality control.
</p></li></ul><p><b>Qualifications
</b></p><ul><li><p>Bachelor&rsquo;s degree in Science, Engineering, or a related field.
</p></li><li><p>1&ndash;3years of experience in Quality Control, preferably in <b>flexible packaging </b>industries.
</p></li><li><p>Familiar with testing methods for films, laminates, inks, and adhesives.
</p></li><li><p>Understanding of quality systems (ISO 9001, BRCGS Packaging, GMP).
</p></li><li><p>Good communication and attention to detail.
</p></li><li><p>Analytical mindset, strong attention to detail, and effective communication skills.
</p></li></ul><p></p><p>Join us. Help protect food, people and the planet .</p></div>

Quality Control 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></p><p><b>
Job Summary:
</b></p><p>We are seeking a knowledgeable and dedicated <b>Microbiology Specialist</b> to join our team.
</p><p>The ideal candidate will play a crucial role in maintaining the quality and safety of our products through rigorous microbiological analysis and quality assurance.</p><p></p><p><b>
Key Responsibilities:</b></p><ul>
<li>
Conduct microbiological testing on raw materials, in-process samples, and finished products in accordance with relevant regulatory standards</li>
<li>Develop, validate, and implement microbiological testing methods, ensuring compliance with GMP and quality assurance protocols</li>
<li>Monitor environmental conditions within production areas and laboratories, ensuring compliance with microbiological standards</li>
<li>Investigate and resolve microbiological product complaints, deviations, and sterility failures, providing comprehensive reports and recommendations</li>
<li>Support the development and execution of continuous improvement initiatives related to microbiological practices</li>
</ul><p><b>
Requirements</b></p><ul>
<li>
Master's or Bachelor's degree in Science, Pharmacy, or a related field.</li>
<li>0-2 years of experience in microbiology within the pharmaceutical, biotechnology, or related industries</li>
<li>Strong analytical skills with proficiency in laboratory techniques and equipment.</li>
<li>Detail-oriented with a commitment to accuracy and compliance.</li>
<li>Excellent communication and interpersonal skills.</li></ul></div>

Microbiology Specialist

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