Qureos Mentor

Acino

<div>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. 
As a Validation Lab Specialist, you will be responsible for performing and reviewing all validation laboratory activities. This includes test method validation, process validation analysis, and cleaning validation analysis. Your work will ensure that all validation practices comply with global guidelines and quality standards. The position will be located in our factory in El Obour City and reporting to the QC Lab Manager. 
Your responsibilities:
<ul>
<li>Perform and review all analytical chemical and physical testing related to validation activities. This includes conducting analytical method validation procedures, testing process validation samples, and testing cleaning validation samples. In addition, you will prepare and report all testing results to ensure global guidelines and quality standards.</li>
<li>Perform, generate, and review analytical method and cleaning validation documentation. This includes developing and accessing protocols, preparing and reviewing reports, and ensuring accuracy and compliance in standard operating procedures (SOPs) and working instructions (WIs).</li>
<li>Participate in root cause investigations of finished product failures.</li>
<li>Verify chemical analysis methods received from the R&amp;D department to ensure alignment with global regulatory guidelines. This includes evaluating methods against standards such as the International Council for Harmonization (ICH) guidelines and various pharmacopoeias, ensuring accuracy, reliability, and compliance before implementation in validation activities.</li>
<li>Modify and troubleshoot analytical testing methods during their execution whenever necessary. Adjustments or corrective actions will be implemented only after obtaining approval from the Lab Manager and/or the Lab Section Head.</li>
<li>Follow up on and control all documentation related to validation laboratory instruments. This includes, but is not limited to, maintaining and reviewing logbooks, calibration records, reagents, reference standards, and instrument qualification documents.</li>
<li>Perform and review daily calibration for all lab equipment.</li>
<li>Share in annual preparation for Quality control consumables.</li>
<li>Share in preparation and review working standards used for chemical analysis of finished products.</li>
<li>Record all analysis results.</li></ul> 


Qualification and Experience: 
<ul>
<li>
Bachelor&rsquo;s degree of pharmacy or chemistry.</li>
<li>Work experience: Min. of 2 years of experience with similar industry and experience using HPLC</li>
<li>Analytical skills.</li>
<li>Details oriented. 
</li>
<li>Excellent English language (speaking and writing)</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

Validation Lab. Specialist

<div>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. 
As a Utilities Engineer, you will be responsible for planning and executing utilities, building and HVAC maintenance activities, as well as to provide the required engineering support to technical departments to achieve planned targets within GMP and HSE requirements. The position reports to Utilities &amp; Projects Manager and the location is based in our Cairo site in Al Obour City. 
Your responsibilities:
<ul>
<li>Monitoring utilities, building maintenance, and HVAC processes to prevent breakdowns and production delays.</li>
</ul><ul><li>Coordinating with warehouses to secure spare parts for scheduled and emergency maintenance.</li>
<li>Advising technicians to maximize efficiency and minimize downtime during maintenance activities.</li>
<li>Participating in contractor and supplier selection to ensure quality, timeliness, and cost-effectiveness.</li>
<li>Regularly inspecting firefighting pumps and lines to maintain readiness for emergencies.</li></ul> 


Qualification and Experience:
<ul>
<li>Bachelor of Engineering in Mechanical Power or Electrical.</li>
<li>3&ndash;6 years of experience in a similar industry.</li>
<li>AutoCAD certification is a plus.</li>
<li>Strong problem-solving, planning, and follow-up skills.</li>
<li>High sense of urgency with effective communication and negotiation abilities.</li>
<li>Solid knowledge of health and safety regulations.</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

Utilities Engineer

<div>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. 
As the Senior Water Treatment Engineer, you will oversee the operation and maintenance of the site&rsquo;s water treatment systems, ensuring full compliance with GMP, regulatory standards, and internal quality requirements. You will be responsible for continuously monitoring the performance of purified water, WFI, and related utility systems that support manufacturing and packaging operations. This includes identifying and reporting any deviations, implementing corrective actions, and ensuring system reliability to support uninterrupted production. You will be located in our site in Al Obour City, and reporting to the Utilities and Projects Manager. 
Your responsibilities:
<ul>
<li>Managing purified water treatment stations to meet GMP, pharmacopeia, and EHS standards.</li>
<li>Overseeing clean utilities equipment and networks with preventive maintenance to guarantee continuous supply.</li>
<li>Supporting and troubleshooting small, purified water units for labs and lab equipment.</li>
<li>Preparing annual procurement plans for chemicals, spare parts, and consumables to prevent breakdowns.</li>
<li>Developing preventive maintenance schedules to ensure uninterrupted production and compliance with manufacturing requirements.</li></ul> 


Qualification and Experience:
<ul>
<li>Bachelor of Engineering in Chemical or Mechanical.</li>
<li>Minimum 6 years&rsquo; experience and in the pharmaceutical industry is preferred.</li>
<li>Strong sense of urgency and accountability.</li>
<li>Advanced communication, problem-solving, and planning skills. 
</li>
<li>Excellent in English language</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

Senior Engineer (Water Treatment)

<div>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. 
Main duties 
<ul>
<li>Completes low and medium complexity regulatory assignments and ensures timely execution of tasks.</li>
<li>Plans, prepares, compiles, and submits high-quality regulatory applications for Egypt in compliance with applicable requirements, and prepares electronic submission files using document management tools such as DocuBridge.</li>
<li>Tracks the status of applications under regulatory review, provides updates to internal and external stakeholders, and maintains regulatory documentation and internal databases such as ARCERA.</li>
<li>Revises and approves artwork for product packaging materials in internal systems according to applicable guidelines and ensures adherence to regulatory compliance and standard operating procedures.</li>
<li>Schedules and organizes meetings with internal and external stakeholders, prepares materials for these meetings, and actively participates in discussions.</li>
<li>Communicates regulatory requirements to other departments, provides regulatory support to project teams and stakeholders, and attends internal trainings in due time.</li>
<li>Forwards all received Product Quality Complaints, Adverse Events, and Medical Information Requests to the relevant teams in Quality Assurance, Pharmacovigilance, and Medical Affairs.</li>
<li>Ensures compliance with applicable legislation, maintains internal regulatory information systems, and supports continuous improvement of regulatory processes.</li>
</ul>
Job Requirements
<ul>
<li>Bachelor&rsquo;s degree in pharmacy, chemistry, biology, or another life science.</li>
<li>Minimum of two years&rsquo; experience in Regulatory Affairs within a relevant discipline; prior experience in a similar role is considered an advantage.</li>
<li>Business English at least at intermediate level</li>
<li>Strong understanding of regulatory requirements, processes, procedures, and submission pathways.</li>
<li>In-depth knowledge of regulatory life cycle management for pharmaceutical products.</li>
<li>Proven ability to collaborate effectively within cross-functional project teams.</li>
<li>Demonstrates alignment with ARCERA principles and organizational values in all actions and decisions.</li>
<li>Exhibits strong verbal and written communication skills, with a high level of accuracy and attention to detail.</li>
<li>Possesses excellent interpersonal skills, with the ability to collaborate effectively across diverse functions, cultures, and organizational levels, including external business partners.</li>
<li>Applies sound project management capabilities to plan, organize, and deliver tasks efficiently.</li>
<li>Shows adaptability and a proactive mindset by embracing challenging assignments and pursuing opportunities that foster professional growth and capability development.</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

Regulatory Affairs Specialist

<div>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. 
As QA Senior Specialist your focus will be on the sterile production area, and you will be responsible for monitoring the manufacturing and packaging process to ensure the agreement with GMP procedures and report any violations during the manufacturing activities. The position reports to QA Senior Section Head of the sterile area and the location are based in our Cairo site in Al Obour City. 
Your responsibilities:
<ul>
<li>Monitor production processes against batch records to ensure GMP compliance and prevent deviations.</li>
<li>Enter manufacturing and expiry dates for the monthly ampoule plan in SAP.</li>
<li>Review and approve monthly ampoule films for printing.</li>
<li>Collect and review batch record documents for market release, record data in annual product review template.</li>
<li>Report violations to the compliance team, ensure root causes are identified, and corrective actions implemented.</li>
<li>Participate in annual quality self-inspection plans to detect and address deviations in manufacturing practices.</li></ul> 


Qualification and Experience:
<ul>
<li>Bachelor&rsquo;s degree of pharmacy or science (Chemistry)</li>
<li>Work experience: 2-5 years</li>
<li>Decision-making and problem-solving skills</li>
<li>Ability to handle stress effectively</li>
<li>Excellent English proficiency and communication skills</li>
<li>Highly detail-oriented</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

QA Senior Specialist

<div>We are hiring for the positions of Medical Representatives and Product Specialists to join the different relevant therapy areas, business units as mentioned hereunder, the position is based in Egypt and will report directly to First Line Manager. The roles will be responsible to achieve agreed sales, MS, productivity and performance targets within a given territory. Build productive scientific-based HCP relationships taking responsibility for satisfaction and loyalty by meeting their healthcare needs. 
Your Responsibilities will be:
<ul>
<li>To meet or exceed sales targets (Sales Growth/Market Share Growth) within agreed budgets and timescales.</li>
<li>To achieve agreed contact, coverage and frequency targets (Quantity &amp; Quality) through face-to-face meetings and detailing the assigned Doctors and Pharmacists and deliver agreed customer centric activities within operating budget.</li>
<li>To promote defined Acino products according to campaign briefs and policies and appropriate use of Brand visuals (Detail aid, Brand Reminder, Medical Reference), in face-to-face meeting and detailing the assigned doctors and pharmacists and in line with campaign brief and policies approved by FLM and Marketing team.</li>
<li>Periodical visits to HCPs in hospitals, Polyclinics, and pharmacies to establish a strong scientific-based relationship and position Acino as the Company of choice for the HCPs.</li>
<li>To ensure all doctors/HCP/KOL receive the right message, information, and clinical studies.</li>
<li>To ensure outstanding personal and team knowledge, and understanding of Acino priority products, technical information, product knowledge, strategy, positioning, key messages and marketing program.</li>
<li>Identity business opportunities within the respective area and evaluate learning's to develop business initiatives and tactics to realize the real potential.</li>
<li>Understand and respond to competitive activities and initiate and recommend actions to counter-act these in order to help protect our market position.</li>
<li>Participate in daily and/or weekly meetings to discuss the market situation, problems that were faced, and to appraise the activities versus the monthly KPIs.</li>
<li>Monitor all competitor activities, medical conferences, and round tables and report it to management.</li>
<li>Build strong relationships to targeted HCPs and mapping the Decision-Making networks.</li>
<li>Strict professional handling of samples and maintaining the appropriate storage condition from receiving till handling to customer.</li>
<li>Effective execution of AVA Local/International conferences and meetings with Health Care professionals in line with campaign brief and policies in line with the AVA plan.</li>
</ul>
Your Profile:
<ul>
<li>Bachelor's degree in pharmacy or a relevant field.</li>
<li>1-3 years of experience in sales as medical Rep/ Product specialist.</li>
<li>Experience in consumer health, Cardiovascular and specialty portfolios are preferred</li>
<li>Outstanding sales acumen and business aptitude.</li>
<li>Excellent communication skills and influencing ability.</li>
<li>High degree of customer focus.</li>
<li>Excellent command of English (spoken and written).</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

Medical Representative - Alex Center

<div>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. 
Main duties:
<ul>
<li>Participate in the deployment, enhancement, and effective operation of the Integrity &amp; Compliance (I&amp;C) Program in Egypt, ensuring alignment with global frameworks, regional priorities, and local regulatory requirements.</li>
<li>Lead and coordinate compliance reviews and risk assessments, ensuring internal controls are properly designed, implemented, and consistently followed. Provide clear recommendations to management where improvements are needed.</li>
<li>Provide guidance to business units and functional teams on compliance matters, including oversight of third‑party due diligence, review of HCP/HCO engagements, and support for data privacy requirements.</li>
<li>Oversee the localization, communication, and implementation of compliance policies and procedures, ensuring they reflect current legal and regulatory standards. Serve as a reliable point of contact for compliant business practices.</li>
<li>Manage periodic compliance monitoring and reporting activities, helping identify risks, trends, and improvement opportunities, and contribute to reports prepared for the Compliance Committee.</li>
<li>Oversee the speak‑up process, including intake, preliminary assessment, and follow‑up of reported concerns to ensure proper documentation and action.</li>
<li>Plan and deliver compliance training programs tailored to business needs, promoting awareness of ethical standards and strengthening the organization&rsquo;s compliance culture.</li>
<li>Work closely with regional and global compliance teams to support ongoing program improvements and share best practices.</li></ul> 


Your Profile: 
<ul>
<li>Bachelor&rsquo;s degree in law (preferred), Business, Life Sciences, or a related discipline.</li>
<li>Advanced degree or recognized compliance certification (e.g., CCEP, ETHICS, IFCA) strongly preferred.</li>
<li>Minimum of 7 years of experience in Compliance and/or Legal, including at least 4&ndash;5 years in the pharmaceutical or healthcare industry, with demonstrable experience in managing compliance programs.</li>
<li>Proven track record in leading compliance monitoring, conducting investigations, and driving remediation activities. Strong analytical, problem‑solving, and risk‑assessment capabilities.</li>
<li>Proficiency in Microsoft Office applications and other relevant digital tools. Fluency in English with strong communication and influencing skills. Ability to travel regionally and internationally for meetings, audits, and trainings.</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

Integrity and Compliance Manager

Join Acino and explore 20   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.