وظائف هندسة كيميائية (أغسطس 2026) | مطلوب مهندس كيميائي في السعودية

من ٠ إلى ٠ سنة الهدف الأردن

ضابط أعلى للاستدامة

On-site - الأردن ٢ يوليو ٢٠٢٦

مطلوب ضابط أعلى للاستدامة ضمن الشروط التالية: - حاصل على درجة البكالوريوس في الهندسة البيئية أو الهندسة الكيميائية أو أي تخصص ذي صلة. - خبرة عملية لا تقل عن 5 سنوات في مجال إدارة الاستدامة (البيئية والاجتماعية والحوكمة ESG). - معرفة جيدة بمبادئ وممارسات وتقنيات وأهداف الاستدامة والتخطيط والإدارة. - معرفة جيدة بإدارة الاستدامة وإعداد وإدارة الدراسات والتقارير الفنية والتوصيات المتعلقة بها. - معرفة جيدة بأساليب ومصادر جمع البيانات وتحليلها وعرضها بما يخدم إدارة الاستدامة. - معرفة جيدة بأساليب التدريب والتوجيه وتقييم أداء الموظفين. - معرفة جيدة بمبادئ وإجراءات السلامة. - معرفة جيدة بمذكرات التفاهم وآلية تطبيقها، بالإضافة إلى الإلمام بأنظمة وسياسات وإجراءات الموارد البشرية. - حاصل على شهادة مدقق داخلي. - حاصل على شهادة مدقق داخليحاصل على دورات تدريبية في أنظمة ISO 9001 وISO 14001 وISO 50001. - الالتزام بالسرية والمحافظة على خصوصية المعلومات. - إجادة الترجمة من اللغة العربية إلى الإنجليزية وبالعكس. - إجادة استخدام تطبيقات الحاسوب ذات الصلة بمجال العمل. من تنطبق عليهم الشروط اعلاه والمهتمين ارسال السيرة الذاتية على <a href="mailto:jobcvs990@gmail.com">jobcvs990@gmail.com</a> للاستفسار ولمزيد من المعلومات التواصل عبرÂ رقم الهاتف على واتساب 0797403988

دوام كامل من ٤ إلى ٧ سنة تنقيب.كوم

مصفف شعر

On-site - الأردن - عمّان ٢ أغسطس ٢٠٢٦

نظرة عامة عن الشركة والوظيفةيعد مركز مايوركا للتجميل وجهة متكاملة للعناية بالجمال حيث يهدف إلى توفير جميع الخدمات التي تحتاجها المرأة في مكان واحد بما يسهل عليها الاهتمام بنفسها والاستمتاع بيوم عطلتها دون الحاجة إلى التنقل بين عدة مراكز ونحنو نسعى إلى أن تحظى كل عميلة بتجربة متكاملة تجمع بين الراحة والاسترخاء  لذلك نقدم عدة خدمات التي تلبي مختلف احتياجات المرأة وتشمل ( الشعر- الأظافر- مكياج -  البشرة - خدمات الليزر- التاتو التجميلي (Permanent Makeup)- السبا- المساج ) لذلك نحرص على تقديم خدماتنا باستخدام أحدث الأجهزة والتقنيات إلى جانب منتجات عالمية عالية الجودة لضمان تحقيق أفضل النتائج وفق أعلى معايير الجودة والسلامة حيث ان لا تقتصر تجربتنا على تقديم الخدمات التجميلية فحسب بل نحرص على توفير بيئة راقية ومريحة، وخدمة استثنائية، واستشارات احترافية مصممة لتلبية احتياجات كل عميلة بما يتناسب مع شخصيتها وأسلوب حياتها  رسالة مركز مايوركا هي تعزيز ثقة عملائنا بأنفسهم، ومساعدتهم على الظهور بأفضل إطلالة في جميع المناسبات، عبر خدمات متكاملة تُقدَّم بأعلى مستويات الاحتراف والاهتمام.المؤهلات والمتطلبات<ul><li>خبرة عملية من 4 إلى 7 سنوات في صالون تصفيف شعر أو عناية بالشعر فئة عالية الجودة.</li><li>أكاديمية مهنية مثبتة وملموسة في تقنيات القص والتلوين والتصفيف الحديثة.</li><li>إتقان في استخدام أدوات التصفيف والتلوين والمواد الكيميائية مع الالتزام بمعايير السلامة.</li><li>قدرة على التعامل مع العملاء بلباقة وتفاهم عالي وامتلاك حس فني عالي للمظهر والتنسيق.</li><li>المرونة والقدرة على العمل ضمن فريق وفي ساعاتVariable حسب جدول المحل.</li></ul>المهارات المطلوبة<ul><li>إلمام بآخر اتجاهات تصفيف الشعر وتقنيات القص والتلوين والتسريحات العصرية.</li><li>مهارات تواصل قوية وقدرة على فهم احتياجات العملاء وتحويلها إلى نتائج ملموسة.</li><li>القدرة على الإبداع والابتكار في تقديم حلول تصفيف مخصصة.</li><li>مستوى عالٍ من الدقة والانتباه للتفاصيل في العمل وجودة النتائج.</li><li>إدارة الوقت والقدرة على التعامل مع ضغط ساعات العمل خلال فترات الذروة.</li></ul>الفوائد والمزايا<ul><li>راتب تنافسي مع حوافز بناءً على الأداء وإرضاء العملاء.</li><li>بيئة عمل احترافية وفرصة للتطوير المهني والتدريب المستمر في مجموعة منتجات العلامة التجارية.</li><li>إجازات سنويه وتسجيل في مؤسسة الضمان الاجتماعي </li><li>خصومات ومزايا للعناية الشخصية وخدمات الشركة.</li></ul>

من ٠ إلى ٠ سنة بيت.كوم

Senior Process Development Engineer

On-site - الأردن ١٨ يوليو ٢٠٢٦

النفط والغاز والطاقة

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Job Summary Arab Potash Company is seeking a dedicated and experienced Chemical Engineer to supervise and manage process engineering activities throughout the project lifecycle, from conceptual studies and FEED to detailed engineering and project execution. The successful candidate will ensure that process engineering deliverables comply with project specifications, contractual requirements, and engineering standards while coordinating effectively with multidisciplinary teams.  Duties and Responsibilities <ul> <li >Perform  process engineering activities</li> <li >Supervise and manage process engineering activities throughout the project lifecycle (conceptual design, FEED, detailed design, and execution).</li> <li >Coordinate with internal teams, including Process, Production, Mechanical, Electrical, Instrumentation, and Safety, to ensure alignment with project requirements.</li> <li >Review engineering deliverables prepared by contractors and consultants to ensure technical accuracy, completeness, and compliance.</li> <li >Ensure that all process engineering documents comply with project specifications, contractual requirements, and applicable engineering standards.</li> <li >Maintain accurate documentation and implement effective version control for all process engineering deliverables throughout the project phases.</li> <li >Support project execution by providing technical guidance and resolving process engineering issues as required.</li> </ul>     </div><h2 data-automation-id="subHeaderPreferredCandidate" class="h5"> Preferred candidate </h2> <div class="row is-m v-align-top t-small bg-mute"> <div class="col is-3 p5" data-automation-id="label_Years_of_experience"> Years of experience </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> 7+ years </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> Degree </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

من ٠ إلى ٠ سنة الهدف الأردن

Senior Sustainability Officer

On-site - الأردن ٢ يوليو ٢٠٢٦

We are looking for a Sustainability Senior Officer with the following qualifications: <ul> <li>Bachelor’s degree in environmental /chemical engineering or any relevant field. </li> <li>A minimum of 5 years of professional sustainability (environment, social &Governance) management experience.</li> <li>A good knowledge of the principles, practices, techniques and purposes of sustainability & planning and management.</li> <li>A good knowledge of sustainability management as applied in administering and directing the preparation of a wide variety of studies, technical reports and recommendations.</li> <li>A good knowledge of the principles, techniques and sources of information applicable to the collection, analysis, and presentation of data pertaining to sustainable management.</li> <li>A good knowledge of the techniques of training, instructing and evaluation of subordinate work performance.</li> <li>A good knowledge of effective safety principles and practices.</li> <li>A working knowledge of memoranda of understanding as they apply to subordinate personnel; a general knowledge of AIG/QAIA personnel rules, policies and procedures. </li> <li>Internal auditor.</li> <li>ISO 9001, 14001 training & 50001. </li> <li>Discretion and confidentiality.</li> <li>Translation from Arabic to English and reverse.</li> <li>Knowledge of computer applications related to the work.</li> </ul> Interested candidates who meet the above requirements are invited to send their CVs to: <a href="mailto:jobcvs990@gmail.com">jobcvs990@gmail.com</a> For inquiries and further information, please contact via WhatsApp at: 0797403988

من ٠ إلى ٠ سنة أخطبوط

Sales Engineer

On-site - الأردن - عمّان ٢٢ يونيو ٢٠٢٦

An engineering and contracting company with head offices in Amman has vacancies for a Sales Engineer.   REQUIREMENTS: - Mechanical, Industrial or Chemical Engineering degree ONLY. Excellent English, Communication, and Computer Skills. Fresh Graduate or relevant experience.   MAIN DUTIES: - Handle and pursue tenders and other business opportunities to submit the best proposals in a timely manner via proposal development strategies. Identify and develop new opportunities within Jordan's Industry Market and regionally. Maintain relationships with existing customers, principals, and suppliers and develop new ones.   KEY COMPETENCIES: - Verbal and written communication skills Attention to details Confidentiality Planning and organizing Time management Interpersonal skills Customer Service orientation Initiative Reliable Stress tolerance

من ٠ إلى ٠ سنة Naukri Gulf

Quality Compliance Senior Officer MS PHARMA

On-site - الأردن - عمّان ٢٤ يونيو ٢٠٢٦

البحث والتطوير

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Establish, maintain and update QMS policies and procedures to ensure that processes meet applicable standards and specifications, provide technical expertise during internal and external audits and manage related corrective and preventive actions.Key Responsibilities:<ul><li>Participate in regulatory authorities and corporate inspections within UPM site, as well participate in providing responses.</li><li>Contact and respond to all regulatory authorities for any requirements.</li><li>Create, Review, and evaluate all documents related to the compliance department (Compliance, Recall, Complaint management, annual product review, self-inspection ).</li><li>Ensuring that work activities are carried out achieving the pre-set performance goals and providing any necessary actions to the direct manager.</li><li>Follow-up on new guidelines and compendial updates, and ensure the update of in-house systems according to new guidelines.</li><li>Perform Quality audits for all quality systems and departments.</li><li>Participate in quality risk management and provide continuous support to all departments.</li><li>Developing, maintaining, and updating the quality system as per GMP.</li><li>Follow-up on the implementation of CAPAs across departments based on timelines and evaluation of the effectiveness of those CAPAs.</li><li>Participate in the investigation of deviations, OOS, and OOT.</li><li>Follow training system and conduct training of employees based on outcomes of trend analysis.</li><li>Participate in process improvement projects.</li></ul>Qualifications & Experience:<ul><li>B.Sc. in Pharmacy, Chemical Engineering, Industrial Engineering , or Science.</li><li>At least two years of experience in a in pharmaceutical industries, Proficiency in written, read and spoken Arabic and English.</li><li>Knowledge in the systems such as ICH, GMP, GLP, WHO</li><li>Knowledge in Quality Requirements (local, regional, EU requirements)</li><li>Troubleshooting & failure investigation.</li><li>Manufacturing processes stages and techniques for pharmaceutical dosage forms (Solids, Semi Solids, and Liquids).</li><li>Able to communicate effectively, build and maintain interpersonal relationships</li><li>Proactively take initiatives and demonstrate a dynamic approach to manage changing business needs and environment</li><li>Ability to manage, develop teams and goals effectively, influence others, and able to reduce conflict in order to preserve a pleasant and productive work environment.</li><li>Statistical Analysis Tracking System</li></ul></div></section><section>Desired Candidate Profile<h2>Qualifications & Experience:</h2><ul><li>B.Sc. in Pharmacy, Chemical Engineering, Industrial Engineering , or Science.</li><li>At least two years of experience in a in pharmaceutical industries, Proficiency in written, read and spoken Arabic and English.</li><li>Knowledge in the systems such as ICH, GMP, GLP, WHO</li><li>Knowledge in Quality Requirements (local, regional, EU requirements)</li><li>Troubleshooting & failure investigation.</li><li>Manufacturing processes stages and techniques for pharmaceutical dosage forms (Solids, Semi Solids, and Liquids).</li><li>Able to communicate effectively, build and maintain interpersonal relationships</li><li>Proactively take initiatives and demonstrate a dynamic approach to manage changing business needs and environment</li><li>Ability to manage, develop teams and goals effectively, influence others, and able to reduce conflict in order to preserve a pleasant and productive work environment.</li><li>Statistical Analysis Tracking System</li></ul></section>

من ٠ إلى ٠ سنة Naukri Gulf

Supply Chain Officer

On-site - الأردن - عمّان ٢٢ يونيو ٢٠٢٦

اللوجستيات وسلاسل الإمداد والمشتريات

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">We are looking for a talented Officer, Supply Chain API (chemicals ) plant to join us. At Hikma you ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.If you want to be part of a team that cares about impact, this is the place for you.Key Responsibilities:<ul><li>Perform planning of production lines in alignment with customer orders and material ordering and delivery.</li><li>Creating Purchase Requisitions for the required components in the production plan.</li><li>Sourcing, contacting, and following up with suppliers on components needed in the production plan.</li><li>Following up on Purchase Orders with the centralized Procurement Team.</li><li>Performing qualifications for Key Starting Materials vendors.</li><li>Performing claim reports related to QCIRs.</li><li>Monitoring stock levels and reorder points of components in warehouse.</li><li>Updating Master Data of components when required.</li><li>Follows up on client requests concerning shipments, in order to arrange for shipping requests as per agreed shipping standards,</li><li>Prepares and maintains an up to date and organised filing of shipping process, to send all shipping related documents for clients such as clearance, invoices, and packing lists.</li><li>Monitors vendor s conformance with contracts to develop the capability of vendors and ensure that the quality is maintained.</li><li>Forecasts the needed inventory for the departments to ensure that the materials are readily available.</li><li>Resolve basic or minor problems escalated from buyers to ensure the cost-effectiveness of solutions.</li><li>Develops and maintains relationships with customers to ensure continuity of work.</li><li>Follows up with Operations and Quality, to ensure the execution of the shipment in a quick and effective manner.</li></ul></div></section><section>Desired Candidate ProfileWe are looking for candidates whose experience and skills align closely with the qualifications outlined below:Minimum Qualifications<ul><li>Bachelor s degree in Chemical Engineering, Supply Chain, Industrial Engineering, or a related field.</li></ul>Minimum Experience<ul><li>1 3 years of experience in supply chain (preferably in chemical or pharmaceutical industry).</li></ul>Core Competencies<ul><li>Chemical knowledge.</li><li>Experience in a cGMP/Manufacturing facility.</li><li>Understanding of supply chain principles</li><li>Familiarity with ERP/IBP systems and data analysis tools</li><li>Strong analytical and problem-solving skills</li><li>Attention to detail and data accuracy</li><li>Effective communication and teamwork skills</li><li>Ability to manage priorities and meet deadlines</li></ul></section>

من ٠ إلى ٠ سنة بيت.كوم

Engineer, Technical Support

On-site - الأردن ٨ يوليو ٢٠٢٦

النفط والغاز والطاقة

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Location: Amman, Jordan Job Type: Full-time Hashtag: #LI-OS1 About Us For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,400+ empowered colleagues are central to this mission. As a trusted and reliable partner of over 825 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 3 R&D hubs across MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.  Description: We are looking for a talented Engineer, Technical Support to join us. At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We’re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together. If you want to be part of a team that cares about impact, this is the place for you. Job Purpose: Closely monitoring and analyzing manufacturing process flows to improve product quality, cost utilization, and manufacturing throughput. Preparing, filing, and maintaining departmental SOPs, reports, protocols, batch records, and related documentation. Additionally, identifying potential hazards and safety issues, conducting the necessary engineering analysis, and applying preventive measures accordingly. Responsibilities also include following up on validation matters, as well as handling procurement, warehouse management, logistics, CAPEX and OPEX activities, spare parts management, equipment qualification and calibration, and training follow-ups. Key Responsibilities: <ul> <li>Ensuring adherence to cGMPs, safety, quality, health, and environmental procedures </li> <li>throughout all manufacturing activities. </li> <li>Creation, modification, reviewing and approving of Standard Operating Procedures </li> <li>(SOPs). </li> <li>Follow up on biennial SOP review and update. </li> <li> Creating, reviewing, and approving protocols/reports/risk assessments/comparison. </li> <li>Participating in Scale-ups designing process with R&D function. </li> <li>Participates in execution of day-to-day manufacturing activities (Production, Packaging </li> <li>& labeling). </li> <li>Initiating and updating master batch records (MBRs), Packaging batch records (MPRs) and Block Flow Diagram (BFDs) as it comes necessary through all the product life cycle in complete coordination with R&D and quality teams. </li> <li>Preparing the assigned process relevant investigation reports, justification, incidents, and variances, while following up on CAPAs implementation and closure. </li> <li> Initiating production APRs while ensuring that all commitments are properly made and fulfilled. </li> <li>Issuing of P.O for the production batches, applying confirmation and MIGO SAP transactions. </li> <li>Suggest modifications & development for manufacturing equipment. </li> <li> Capability of troubleshooting and properly solving the operational problems inside the production area and the related utilities </li> <li>Monitor consumables stocks and prepare a periodic list with the department needs. </li> <li>Follow up on implementation of equipment Calibration, qualification/re-qualification, and Preventive Maintenance programs. </li> <li>Follow up on six system quality internal audits observations and response while coordinating CAPAs with the people concerned. </li> <li>Ensure that all valves, pipes, lines & systems inside the plant are properly tagged & identified along with the layouts. </li> <li>Inspecting and reporting manufacturing area /equipment/process status on daily basis. </li> <li>Communicate departmental operation needs with supervisor including OPEX and CAPEX items as to ensure manufacturing progression without delays or consequences. </li> <li>Training of plants team on new policies, procedural and manufacturing updates to ensure compliance prior commencing the operations. </li> <li> Follow up on plants employees training files and training schedule.</li> </ul> Qualifications: We are looking for candidates whose experience and skills align closely with the qualifications outlined below: <ul> <li>Bachelor’s degree in chemical engineering or a related field.</li> <li>1 - 3 years of related quality experience.</li> </ul> Technical Skills: Applying Good Manufacturing Practices (GMP) Applying Standard Operating Procedures (SOPs) Data Analysis Data Integrity Documentation Equipment Knowledge Process Improvement Safety Awareness Troubleshooting Visual Examination Communication & Influence Collaboration & Teamwork Planning & organizing Initiative & Drive for Results Resilience & Adaptability Change & Innovation Problem Solving & Decision Making Learn more about Hikma in Jordan https://www.hikma.com/media/jukhqqdl/hikma-jordan-factsheet_-en-nov-2025.pdf </div>

من ٠ إلى ٠ سنة Naukri Gulf

Technical Support Engineer

On-site - الأردن - عمّان ٢ يوليو ٢٠٢٦

الهندسة

<section>Job DescriptionRoles & Responsibilities<div class="paragraph"> Location: Amman, Jordan Job Type: Full-time Hashtag: #LI-OS1 About Us For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,400+ empowered colleagues are central to this mission. As a trusted and reliable partner of over 825 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 3 R&D hubs across MENA, North America and Europe, our footprint allows us to play a critical role in serving patients. Description: We are looking for a talented Engineer, Technical Support to join us. At Hikma you ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together. If you want to be part of a team that cares about impact, this is the place for you. Job Purpose: Closely monitoring and analyzing manufacturing process flows to improve product quality, cost utilization, and manufacturing throughput. Preparing, filing, and maintaining departmental SOPs, reports, protocols, batch records, and related documentation. Additionally, identifying potential hazards and safety issues, conducting the necessary engineering analysis, and applying preventive measures accordingly. Responsibilities also include following up on validation matters, as well as handling procurement, warehouse management, logistics, CAPEX and OPEX activities, spare parts management, equipment qualification and calibration, and training follow-ups. Key Responsibilities: <ul> <li>Ensuring adherence to cGMPs, safety, quality, health, and environmental procedures </li> <li>throughout all manufacturing activities. </li> <li>Creation, modification, reviewing and approving of Standard Operating Procedures </li> <li>(SOPs). </li> <li>Follow up on biennial SOP review and update. </li> <li> Creating, reviewing, and approving protocols/reports/risk assessments/comparison. </li> <li>Participating in Scale-ups designing process with R&D function. </li> <li>Participates in execution of day-to-day manufacturing activities (Production, Packaging </li> <li>& labeling). </li> <li>Initiating and updating master batch records (MBRs), Packaging batch records (MPRs) and Block Flow Diagram (BFDs) as it comes necessary through all the product life cycle in complete coordination with R&D and quality teams. </li> <li>Preparing the assigned process relevant investigation reports, justification, incidents, and variances, while following up on CAPAs implementation and closure. </li> <li> Initiating production APRs while ensuring that all commitments are properly made and fulfilled. </li> <li>Issuing of P.O for the production batches, applying confirmation and MIGO SAP transactions. </li> <li>Suggest modifications & development for manufacturing equipment. </li> <li> Capability of troubleshooting and properly solving the operational problems inside the production area and the related utilities </li> <li>Monitor consumables stocks and prepare a periodic list with the department needs. </li> <li>Follow up on implementation of equipment Calibration, qualification/re-qualification, and Preventive Maintenance programs. </li> <li>Follow up on six system quality internal audits observations and response while coordinating CAPAs with the people concerned. </li> <li>Ensure that all valves, pipes, lines & systems inside the plant are properly tagged & identified along with the layouts. </li> <li>Inspecting and reporting manufacturing area /equipment/process status on daily basis. </li> <li>Communicate departmental operation needs with supervisor including OPEX and CAPEX items as to ensure manufacturing progression without delays or consequences. </li> <li>Training of plants team on new policies, procedural and manufacturing updates to ensure compliance prior commencing the operations. </li> <li> Follow up on plants employees training files and training schedule.</li> </ul> Qualifications: We are looking for candidates whose experience and skills align closely with the qualifications outlined below: <ul> <li>Bachelor s degree in chemical engineering or a related field.</li> <li>1 - 3 years of related quality experience.</li> </ul> Technical Skills: Applying Good Manufacturing Practices (GMP) Applying Standard Operating Procedures (SOPs) Data Analysis Data Integrity Documentation Equipment Knowledge Process Improvement Safety Awareness Troubleshooting Visual Examination Communication & Influence Collaboration & Teamwork Planning & organizing Initiative & Drive for Results Resilience & Adaptability Change & Innovation Problem Solving & Decision Making Learn more about Hikma in Jordan https://www.hikma.com/media/jukhqqdl/hikma-jordan-factsheet_-en-nov-2025.pdf </div></section>

6 - 13 Years Naukri Gulf

Analytical Research Supervisor

On-site - الأردن - عمّان ٥ أغسطس ٢٠٢٦

البحث والتطوير

Supervise and provide guidance and support to junior staff in areas such as training and development. Ensure adherence to SOPs and GLP requirements in analytical research development, validation and all stability related activities. Finally review and approve all reports generated by subordinates to be submitted to the documentation team. Plan, organize, and supervise weekly and monthly Analytical Research/Stability activities to ensure timely execution and achievement of departmental objectives. Review, approve, and maintain departmental documentation, including SOPs, analytical method development, validation/verification reports, stability protocols and reports, and laboratory records. Prepare and review drug substance and drug product specifications, justification reports, and regulatory submission documents in accordance with applicable guidelines. Manage analytical and stability programs, including supplier qualification (DMF evaluation), pharmacopeia updates, stability studies, stability chamber monitoring, and maintenance coordination. Lead investigations of OOS results and technical issues by conducting troubleshooting and root cause analysis and implementing appropriate corrective actions. Supervise, train, and coach team members, providing technical guidance and supporting analytical activities and experiments as required. Review and verify stability batches, labeling, documentation, quantities, and logbook entries to ensure accuracy and regulatory compliance. Ensure compliance with GLP, GMP, SOPs, Health & Safety requirements, and participate in internal and external regulatory inspections. Coordinate effectively with internal departments and external stakeholders to ensure timely communication, issue resolution, and successful project execution. Drive continuous improvement by supporting quality initiatives, making sound technical decisions, adapting to business needs, and performing other duties assigned by the Department Head or Line Manager.Desired Candidate Profile<ul><li>B.Sc. degree in Chemistry or Chemical Engineering</li><li>6 – 8 years of relevant experience in analytical work</li><li>Good written and spoken Arabic and English Languages</li></ul>

0 - 4 Years Naukri Gulf

Validation Engineer

On-site - الأردن - عمّان ٣١ يوليو ٢٠٢٦

الهندسة

Carry out the required validation tests and perform installation and operational protocol duties, analyze the results of testing and determine the acceptability of results against predetermined criteria in a timely manner and in compliance with cGMP and SOPs and manufacturing instructions.Prepare the Validation Master Plan (VMP).Prepare and execute qualification (IQ, OQ, PQ) and requalification protocols for production machines and analytical instruments in coordination with Production, Quality Control, and R&D.Conduct validation studies following related SOPs, protocols, and policies.Prepare SOPs related to validation activities.Follow up on the execution of validation plans and make the required arrangements for that.Conduct temperature and relative humidity mapping studies for warehouses and stability chambers and prepare protocols for validating the method of storage in warehouses and stability chambers.Prepare and execute utilities qualification protocols, manufacturing process validation protocols, cleaning validation protocols, and software and computerized systems validation protocols.Check and follow up on air and water quality validation.Ensure that all validation tools and instruments are kept clean and in good condition.Follow up on the calibration of validation instruments in order to execute all validation tasks using properly calibrated equipment.Report to the Manager of Validation any deviations from SOPs, protocols, or policies.Coordinate with other departments or outside contractors/vendors to complete validation tasks.Coordinate with external entities responsible for analytical devices marketing to conduct qualification studies for new devices.Adhere to the current good manufacturing practices in all activities.At MS Pharma, we are guided by our Triple T values: Take Charge Lead with accountability and courage Together for Better Collaborate with trust and respect Thrive Drive innovation, growth, and continuous improvementDesired Candidate ProfileBSc in Chemical engineering, Mechatronics engineering or any related field as per the country regulations0-2 years experience in a related field.Good written, read and spoken Arabic and English.Knowledge in (ISO 14001) systemMinistry of Health RegulationsMinistry of Environment s RegulationsKnowledge in ISO 14001, I14644-1, -2, -3, & -4FDA RegulationsKnowledge in the systems such as ICH, GMP, GLP, WHOProcess, design, installation, operation, manufacturing machines, utilities

0 - 3 Years Naukri Gulf

Operator

On-site - الأردن - عمّان ٢٢ يوليو ٢٠٢٦

اللوجستيات وسلاسل الإمداد والمشتريات

We are looking for a talented Operator, Manufacturing , to join us. At Hikma, you'll be supported by a culture of progress and belonging where people are encouraged to develop, well-being is prioritized, and our inclusive approach values contributions from all. We're seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.If you want to be part of a team that cares about impact, this is the place for you.Key Responsibilities:Ensuring adherence to cGMPs, safety, quality, health, and environmental procedures throughout all manufacturing activities to ensure a healthy and safe work environment.Cleaning of manufacturing Equipment & utensils according to the relevant standard operating procedures and protocols.Operation of equipment & machines according to relevant standard operating procedures.Proper implementation of steps mentioned in the manufacturing batch and packaging batch records (MPRs).Proper documentation for all manufacturing & cleaning activities on related logbooks, batch records, and packaging records on a daily basis.Provides input and suggestions for troubleshooting operational problems, process improvements, as well as for procedure writing and revision.Preparing daily reports and shift handling communications on a shift basis.All other duties as assigned.Desired Candidate ProfileWe are looking for candidates whose experience and skills align closely with the qualifications outlined below:Experience:0 3 years of relevant experience as an operator.Education:Diploma in chemical engineering, pharmacy, chemistry, or any related field.Additional Requirements:Ability to perform tasks requiring physical effort.Required Skills:Ability to use computers to perform a variety of data-entry transactions and to retrieve information (procedures; safety, employment, and other information).Preferred to have the ability to perform data entry/maintenance in SAP or equivalent systems.Good English language skills (especially in reading and writing) is required.Pharmaceutical or other regulatory (GMP) experience is preferred.Employee may be required to stand continually throughout the shift.Employee may be required to attend on morning or night shift with long shift is required.Employee may be required to attend weekend.Job involves frequent bending, twisting, pushing, pulling and lifting.

من ٠ إلى ٠ سنة Naukri Gulf

Associate Manager, Quality Compliance

On-site - الأردن - عمّان ٩ يوليو ٢٠٢٦

البحث والتطوير

<section>Job DescriptionRoles & Responsibilities<div class="paragraph"> Description: We are looking for a talented Associate Manager, Quality Compliance to join us. At Hikma you ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together. If you want to be part of a team that cares about impact, this is the place for you. Key Responsibilities: Strategic <ul> <li>Providing support and guidance to the Hikma injectable sites including compounding by:</li> <li>Lead auditing coordination, approach, and execution for injectables/Oral/ laboratory/Data Integrity manufacturing/contract manufacturing CMOs</li> <li>Ensuring internal injectable/Oral Hikma site compliance with Hikma s rules and policies through internal audits</li> <li>Following up on all observations by Hikma and third parties which includes CAPA plan implementation and ensuring timely completion.</li> </ul> Technical capabilities <ul> <li>Providing concerned Hikma employees with the required guidance related to the injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes to ensure that the related international standards and specifications are applied on all Hikma concerned processes</li> <li>Investigating and studying different problems related to injectables/Oral/ laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes that might occur in all Hikma concerned functions and recommending the corrective actions accordingly</li> <li>Ensuring that health and safety regulations are followed in the concerned processes to avoid accidents in the workplace during executed audits protecting the auditors</li> <li>Ensuring that the entire injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes are in compliance with the set standard operating procedures (SOPs</li> <li>Ensuring that all injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes, activities, procedures comply with related internal/external regulations</li> <li>Conducting periodic checks to ensure that all injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes are performed correctly and conforming the international standards and specifications</li> <li>Assessing different Hikma functions compliance with the set standards and specifications in order to detect the deviations and recommending the necessary corrective actions accordingly</li> <li>Providing the Corporate Compliance Director with periodic reports illustrating the work flow of the injectables/Oral/microbiology, laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes through Hikma corporate functions</li> <li>Documenting different related transactions in all Hikma corporate functions to be used as a reference in the future when needed</li> <li>Performing other duties related to the job as assigned by the direct supervisor</li> </ul> Administrative <ul> <li>Preparing periodic reports with respect to the Compliance (Injectables/Orals) function's activities and achievements to be submitted to the direct supervisor</li> <li>Ensuring that instructions, circulars and organizational and technical decisions are followed and applied</li> <li>Implementing Internal quality auditing and Hikma subsidiaries audit program, ensuring that Hikma Internal sites maintain a state of cGMP compliance where all activities within the Hikma Pharmaceutical function comply with the adopted standards, policies, and procedures.</li> <li>implementing follow up auditing program for Hikma internal sites, ensuring that response is covered and communicated properly with Hikma quality management.</li> <li>Providing Technical Support to Injectable/Oral strategic Under license projects, by qualifying suppliers, upgrading systems of our partners, conducting gap analysis and providing the needed support before/ during and after authorities audits to sites, up to end of registration of the product. </li> <li> </li> </ul> Qualifications: We are looking for candidates whose experience and skills align closely with the qualifications outlined below: <ul> <li>B.Sc. degree in Chemistry, Biological, Microbiology, Chemical Engineering or equivalent</li> <li>M.Sc. degree in TQM or equivalent </li> <li>(10) years of experience in a related position, of which at least (5) in a supervisory position</li> <li>Experience in a pharmaceutical industry, Oral and Injectables manufacturing.</li> <li>Quality certification on auditing e.g. ASQ/ISO9001 . etc </li> </ul> Skills: <ul> <li>Computer Skills</li> </ul> Performs moderately difficult tasks using job related applications, Office applications, and other relevant programs, as well as uses the functions of the internet effectively <ul> <li>Data Analysis</li> </ul> Performs complex data analysis utilizing multi-sourced set of data, prepares reports illustrating the results through professional graphs, charts, and other visual aids <ul> <li>Documentation / Recording Information</li> </ul> Applying and using various techniques in documenting and recording information in written or electronic/magnetic formats <ul> <li>English Language</li> </ul> Demonstrates mastery of the language; near native; ability to read, understand and write extremely difficult or abstract prose, a wide variety of vocabulary, idioms, colloquialisms, and slang <ul> <li>Government Relations</li> </ul> Represents the company externally within the government sector and develops and maintains good rapport with its employees <ul> <li> Laws & Legislations</li> </ul> Possesses knowledge in laws and legislations of several countries that Hikma operates in, including MENA region, USA and Europe <ul> <li>Project Management</li> </ul> </div></section>

بيت.كوم

Operator

On-site - الأردن ٢٢ يوليو ٢٠٢٦

الإنشاءات والعقارات

من ٠ إلى ٠ سنة Naukri Gulf

Associate Director, API R&D

On-site - الأردن - عمّان ٢٢ يونيو ٢٠٢٦

الطب والرعاية الصحية

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">We are looking for a talented Associate Director, API R&D to join us. At Hikma you ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.If you want to be part of a team that cares about impact, this is the place for you.Job PurposeTo lead the strategic direction, governance, and execution of research and development activities across the function, ensuring the successful design, development, scale-up, regulatory readiness, and commercialization of pharmaceutical products in alignment with business objectives, quality standards, and global regulatory expectations.Key Responsibilities:Strategy & LeadershipDefine and drive the overall R&D vision, strategy, and innovation roadmap aligned with organizational growth priorities and portfolio needs.Ensure vertical alignment with corporate strategy and horizontal integration with Quality, Regulatory Affairs, Manufacturing, Supply Chain, and Commercial functions.Lead portfolio prioritization, technology selection, and resource allocation to maximize development success and return on investment.Governance, Policies & ComplianceEstablish, approve, and continuously enhance R&D policies, processes, and operating models to ensure compliance with global regulatory and quality standards.Ensure adherence to all relevant legislative, safety, environmental, and quality requirements across R&D operations.Scientific & Technical OversightProvide executive scientific leadership across synthesis, formulation, analytical development, validation, technology transfer, and scale up activities for standard and complex pharmaceutical products.Oversee experimental design, data interpretation, stability strategies, and technical risk mitigation to ensure robust, commercially viable products.Guide regulatory enabling development activities and ensure readiness for submissions and inspections in relevant markets.Maintain awareness of emerging technologies, intellectual property landscapes, and industry trends to sustain competitive advantage and innovation.Project & Portfolio ManagementGovern end to end development programs from concept through commercialization, ensuring delivery within agreed timelines, scope, quality, and budget.Lead cross functional decision making, issue resolution, and risk management for complex development projects.Oversee external partnerships, CRO/CDMO collaborations, and technical alliances to ensure quality, efficiency, and knowledge transfer.Financial StewardshipDirect the preparation, optimization, and control of the R&D budget, ensuring effective utilization of resources and identification of cost efficiency opportunities.Monitor financial performance and implement corrective actions to maintain alignment with strategic and operational objectives.People & CultureBuild, lead, and develop high performing multidisciplinary R&D teams through clear objectives, capability development, succession planning, and performance management.Foster a culture of scientific excellence, innovation, collaboration, accountability, and continuous improvement.Continuous Improvement & InnovationChampion operational excellence, digital enablement, and process optimization across R&D to enhance productivity, quality, and speed to market.Promote knowledge sharing, research visibility, and adoption of international best practices.Reporting & Stakeholder ManagementProvide executive level reporting on R&D performance, portfolio progress, risks, and strategic opportunities.Represent R&D in senior governance forums and with external stakeholders, partners, and regulatory bodies as required.Safety, Quality & EnvironmentEnsure a safe, compliant, and environmentally responsible R&D workplace aligned with corporate standards and regulatory expectations.Related AssignmentsPerform additional leadership or strategic duties as required by the organization.</div></section><section>Desired Candidate ProfileWe are looking for candidates whose experience and skills align closely with the qualifications outlined below:Minimum QualificationsPhD degree in Pharmacy, Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline.Minimum ExperienceSignificant progressive experience in pharmaceutical Research & Development, including senior leadership responsibility across multidisciplinary teams and complex product development portfolios.Core CompetenciesStrategic leadership and innovation managementDeep scientific and technical expertise in pharmaceutical developmentRegulatory and quality compliance knowledgePortfolio and project governanceFinancial and operational managementStakeholder engagement and executive communicationTalent development and organizational leadershipContinuous improvement and change leadership</section>

من ٠ إلى ٠ سنة بيت.كوم

Associate Manager, Quality Compliance

On-site - الأردن ٩ يوليو ٢٠٢٦

المحاسبة والمالية والبنوك

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Location: Amman, Jordan Job Type: Full-time Hashtag: #LI-AA2 About Us: For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission. As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 3 R&D hubs across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.  Description: We are looking for a talented Associate Manager, Quality Complianceto join us. At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We’re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together. If you want to be part of a team that cares about impact, this is the place for you. Key Responsibilities: Strategic <ul> <li>Providing support and guidance to the Hikma injectable sites including compounding by:</li> <li>Lead auditing coordination, approach, and execution for injectables/Oral/ laboratory/Data Integrity manufacturing/contract manufacturing CMOs</li> <li>Ensuring internal injectable/Oral Hikma site compliance with Hikma’s rules and policies through internal audits</li> <li>Following up on all observations by Hikma and third parties which includes CAPA plan implementation and ensuring timely completion.</li> </ul> Technical capabilities <ul> <li>Providing concerned Hikma employees with the required guidance related to the injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes to ensure that the related international standards and specifications are applied on all Hikma concerned processes</li> <li>Investigating and studying different problems related to injectables/Oral/ laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes that might occur in all Hikma concerned functions and recommending the corrective actions accordingly</li> <li>Ensuring that health and safety regulations are followed in the concerned processes to avoid accidents in the workplace during executed audits protecting the auditors</li> <li>Ensuring that the entire injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes are in compliance with the set standard operating procedures (SOPs</li> <li>Ensuring that all injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes, activities, procedures comply with related internal/external regulations</li> <li>Conducting periodic checks to ensure that all injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes are performed correctly and conforming the international standards and specifications</li> <li>Assessing different Hikma functions compliance with the set standards and specifications in order to detect the deviations and recommending the necessary corrective actions accordingly</li> <li>Providing the Corporate Compliance Director with periodic reports illustrating the work flow of the injectables/Oral/microbiology, laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes through Hikma corporate functions</li> <li>Documenting different related transactions in all Hikma corporate functions to be used as a reference in the future when needed</li> <li>Performing other duties related to the job as assigned by the direct supervisor</li> </ul> Administrative <ul> <li>Preparing periodic reports with respect to the Compliance (Injectables/Orals) function's activities and achievements to be submitted to the direct supervisor</li> <li>Ensuring that instructions, circulars and organizational and technical decisions are followed and applied</li> <li>Implementing Internal quality auditing and Hikma subsidiaries audit program, ensuring that Hikma Internal sites maintain a state of cGMP compliance where all activities within the Hikma Pharmaceutical function comply with the adopted standards, policies, and procedures.</li> <li>implementing follow up auditing program for Hikma internal sites, ensuring that response is covered and communicated properly with Hikma quality management.</li> <li>Providing Technical Support to Injectable/Oral strategic Under license projects, by qualifying suppliers, upgrading systems of our partners, conducting gap analysis and providing the needed support before/ during and after authorities audits to sites,  up to end of registration of the product.  </li> <li>Assisting in process standardization through Hikma based on international best practices, in addition to supporting the functions’ managers in taking the required corrective and preventive actions.</li> <li>Supporting Hikma new projects by providing the needed technical and administrative support for Hikma new projects with new partners (Toll manufacturers, Finished product formulators).</li> <li>Participating in audits whenever Hikma audited by third party or authority. By presenting Corporate Compliance role, auditing system.</li> </ul> Qualifications: We are looking for candidates whose experience and skills align closely with the qualifications outlined below: <ul> <li>B.Sc. degree in Chemistry, Biological, Microbiology, Chemical Engineering or equivalent</li> <li>M.Sc. degree in TQM or equivalent</li> <li>(10) years of experience in a related position, of which at least (5) in a supervisory position</li> <li>Experience in a pharmaceutical industry, Oral and Injectables manufacturing.</li> <li>Quality certification on auditing e.g. ASQ/ISO9001…. etc </li> </ul> Skills: <ul> <li>Computer Skills</li> </ul> Performs moderately difficult tasks using job related applications, Office applications, and other relevant programs, as well as uses the functions of the internet effectively <ul> <li>Data Analysis</li> </ul> Performs complex data analysis utilizing multi-sourced set of data, prepares reports illustrating the results through professional graphs, charts, and other visual aids <ul> <li>Documentation / Recording Information</li> </ul> Applying and using various techniques in documenting and recording information in written or electronic/magnetic formats <ul> <li>English Language</li> </ul> Demonstrates mastery of the language; near native; ability to read, understand and write extremely difficult or abstract prose, a wide variety of vocabulary, idioms, colloquialisms, and slang <ul> <li>Government Relations</li> </ul> Represents the company externally within the government sector and develops and maintains good rapport with its employees <ul> <li>Laws & Legislations</li> </ul> Possesses knowledge in laws and legislations of several countries that Hikma operates in, including MENA region, USA and Europe <ul> <li>Project Management</li> </ul> Ability to manage projects through effective planning, implementation, monitoring and completion of projects, while ensuring best utilization of resources; time, human resources, budget Learn more about Hikma in Jordan hikma-jordan-factsheet-aug-2025-en.pdf </div>

بيت.كوم

Manager, Formulation Development

On-site - الأردن الجمعة

الطب والرعاية الصحية

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Location: Amman, Jordan Job Type: Full-time Hashtag: #LI-OS1 About Us For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,400+ empowered colleagues are central to this mission. As a trusted and reliable partner of over 825 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 3 R&D hubs across MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.  Description: We are looking for a talented Manager, Formulation Development to join us. At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We’re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together. If you want to be part of a team that cares about impact, this is the place for you. Job Purpose: The Manager, Formulation Development will lead formulation development activities for oral solid dosage forms and other suitable dosage forms from concept to commercialization. The role requires strong technical expertise in QbD-based product development, execution of registration/submission batches, technology transfer, regulatory support, troubleshooting, and leadership of a high-performing team. The incumbent will collaborate closely with Analytical Development, Regulatory Affairs, Quality, Manufacturing, Supply Chain, and Project Management teams to ensure timely and successful product development and regulatory submissions. The candidate should Secures and manages resources to meet project objectives within defined time, cost, and quality parameters. Introduces innovative methods and solutions to address challenges and improve performance. Ensures that standards and processes—including SOPs, cGMP, and H&S—are developed, maintained, and effectively implemented. Oversee departmental performance, aligning scientific initiatives with organizational goals. Develops staff capabilities and ensures resource optimization. Operates independently within global networks and leads cross-functional teams to align efforts with strategic goals. Key Responsibilities: Formulation Development & Product Lifecycle Management <ul> <li>Lead formulation development activities for generic (Regulated markets such as USA, Europe, Canada, MENA etc) and brand products from feasibility through dossier filing and commercialization.</li> <li>Design and develop robust, scalable, and commercially viable formulations using scientific and risk-based approaches.</li> <li>Apply Quality by Design (QbD) principles throughout product development.</li> <li>Establish Quality Target Product Profile (QTPP), Critical Quality Attributes (CQAs), Critical Material Attributes (CMAs), and Critical Process Parameters (CPPs).</li> <li>Utilize Design of Experiments (DOE) and statistical tools to optimize formulations and processes.</li> <li>Support development of differentiated and value-added product opportunities.</li> </ul> Regulatory Submission Support <ul> <li>Drive preparation and review of formulation-related sections for ANDA and global generic submissions.</li> <li>Ensure adequacy and compliance of development reports, product development documents, and regulatory filing documentation.</li> <li>Provide scientific justification and responses to regulatory deficiencies, agency questions, and information requests.</li> <li>Represent Formulation Development during regulatory inspections, audits, and agency interactions as required.</li> </ul> Submission Batches & Technology Transfer <ul> <li>Lead execution and monitoring of exhibit, registration, scale-up, validation, and submission batches.</li> <li>Ensure effective transfer of technologies from R&D to manufacturing sites.</li> <li>Collaborate with Manufacturing, Engineering, Quality Assurance, and Validation teams to ensure successful commercialization.</li> <li>Resolve scale-up and manufacturing challenges through scientific evaluation and risk mitigation.</li> </ul> Technical Leadership & Troubleshooting <ul> <li>Provide technical leadership in resolving formulation, process, scale-up, and commercial manufacturing challenges.</li> <li>Investigate product performance issues and implement scientifically sound corrective actions.</li> <li>Lead root cause investigations and troubleshooting activities related to formulation and process performance.</li> <li>Evaluate and implement innovative formulation technologies for pipeline enhancement.</li> </ul> Innovation & Technology Advancement <ul> <li>Continuously assess emerging technologies and novel drug delivery/formulation platforms.</li> <li>Recommend innovative approaches to improve product performance, development timelines, and commercial success.</li> <li>Drive knowledge sharing and adoption of current industry best practices.</li> </ul> Cross-Functional Collaboration <ul> <li>Lead multi-disciplinary project teams and ensure alignment across functions.</li> <li>Collaborate effectively with Analytical Development, Regulatory Affairs, Quality, Manufacturing, Procurement, Project Management, and Commercial teams.</li> <li>Drive project execution through proactive communication, risk assessment, and stakeholder management.</li> <li>Foster a culture of partnership and accountability across departments.</li> </ul> People Leadership <ul> <li>Lead, mentor, and develop formulation scientists and junior team members.</li> <li>Create a learning-oriented environment that supports technical growth and succession planning.</li> <li>Encourage innovation, scientific rigor, accountability, and continuous improvement.</li> <li>Build team capability through coaching, performance management, and development planning.</li> <li>Promote employee engagement and a culture of care, respect, and collaboration.</li> </ul> Qualifications: We are looking for candidates with relevant pharmaceutical formulation development experience with significant exposure to Generic/Brand product development and submissions whose experience and skills align closely with the qualifications outlined below: Minimum Qualifications <ul> <li>Advanced degree in Pharmacy, Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline (PhD/Masters or equivalent preferred).</li> </ul> Minimum Experience • PhD degree with 8 - 10 years of work experience in Formulation Development • Master’s degree with 10 - 12 years of work experience in Formulation Development • Bachelor’s degree with 12 - 15 years of work experience in Formulation Development Minimum Achievements: <ul> <li>Substantial submissions for highly regulated markets such as USA, Europe, Canada</li> <li>Number of MENA submission: ≥ 25</li> </ul> Core Competencies <ul> <li>Problem Solving & Decision Making </li> <li></li></ul> </div>

8 - 15 Years Naukri Gulf

Manager, Formulation Development

On-site - الأردن - عمّان الجمعة

البحث والتطوير

We are looking for a talented Manager, Formulation Development to join us. At Hikma you ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.If you want to be part of a team that cares about impact, this is the place for you.Job Purpose:The Manager, Formulation Development will lead formulation development activities for oral solid dosage forms and other suitable dosage forms from concept to commercialization. The role requires strong technical expertise in QbD-based product development, execution of registration/submission batches, technology transfer, regulatory support, troubleshooting, and leadership of a high-performing team. The incumbent will collaborate closely with Analytical Development, Regulatory Affairs, Quality, Manufacturing, Supply Chain, and Project Management teams to ensure timely and successful product development and regulatory submissions.The candidate should Secures and manages resources to meet project objectives within defined time, cost, and quality parameters. Introduces innovative methods and solutions to address challenges and improve performance. Ensures that standards and processes including SOPs, cGMP, and H&S are developed, maintained, and effectively implemented. Oversee departmental performance, aligning scientific initiatives with organizational goals. Develops staff capabilities and ensures resource optimization. Operates independently within global networks and leads cross-functional teams to align efforts with strategic goals.Key Responsibilities:Formulation Development & Product Lifecycle ManagementLead formulation development activities for generic (Regulated markets such as USA, Europe, Canada, MENA etc) and brand products from feasibility through dossier filing and commercialization.Design and develop robust, scalable, and commercially viable formulations using scientific and risk-based approaches.Apply Quality by Design (QbD) principles throughout product development.Establish Quality Target Product Profile (QTPP), Critical Quality Attributes (CQAs), Critical Material Attributes (CMAs), and Critical Process Parameters (CPPs).Utilize Design of Experiments (DOE) and statistical tools to optimize formulations and processes.Support development of differentiated and value-added product opportunities.Regulatory Submission SupportDrive preparation and review of formulation-related sections for ANDA and global generic submissions .Ensure adequacy and compliance of development reports, product development documents, and regulatory filing documentation.Provide scientific justification and responses to regulatory deficiencies, agency questions, and information requests.Represent Formulation Development during regulatory inspections, audits, and agency interactions as required.Submission Batches & Technology TransferLead execution and monitoring of exhibit, registration, scale-up, validation, and submission batches.Ensure effective transfer of technologies from R&D to manufacturing sites.Collaborate with Manufacturing, Engineering, Quality Assurance, and Validation teams to ensure successful commercialization.Resolve scale-up and manufacturing challenges through scientific evaluation and risk mitigation.Technical Leadership & TroubleshootingProvide technical leadership in resolving formulation, process, scale-up, and commercial manufacturing challenges.Investigate product performance issues and implement scientifically sound corrective actions.Lead root cause investigations and troubleshooting activities related to formulation and process performance.Evaluate and implement innovative formulation technologies for pipeline enhancement.Innovation & Technology AdvancementContinuously assess emerging technologies and novel drug delivery/formulation platforms.Recommend innovative approaches to improve product performance, development timelines, and commercial success.Drive knowledge sharing and adoption of current industry best practices.Cross-Functional CollaborationLead multi-disciplinary project teams and ensure alignment across functions.Collaborate effectively with Analytical Development, Regulatory Affairs, Quality, Manufacturing, Procurement, Project Management, and Commercial teams.Drive project execution through proactive communication, risk assessment, and stakeholder management.Foster a culture of partnership and accountability across departments.People LeadershipLead, mentor, and develop formulation scientists and junior team members.Create a learning-oriented environment that supports technical growth and succession planning.Encourage innovation, scientific rigor, accountability, and continuous improvement.Build team capability through coaching, performance management, and development planning.Promote employee engagement and a culture of care, respect, and collaboration.Desired Candidate ProfileWe are looking for candidates with relevant pharmaceutical formulation development experience with significant exposure to Generic/Brand product development and submissions whose experience and skills align closely with the qualifications outlined below:Minimum QualificationsAdvanced degree in Pharmacy, Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline (PhD/Masters or equivalent preferred).Minimum ExperiencePhD degree with 8 - 10 years of work experience in Formulation DevelopmentMaster s degree with 10 - 12 years of work experience in Formulation DevelopmentBachelor s degree with 12 - 15 years of work experience in Formulation DevelopmentMinimum Achievements:Substantial submissions for highly regulated markets such as USA, Europe, CanadaNumber of MENA submission: 25Core CompetenciesProblem Solving & Decision MakingApplying Good Manufacturing Practices (GMP)Applying Standard Operating Procedures (SOPs)Corrective and Preventive Action- (CAPA)Good Laboratory Practices (GLP)Strategic leadership and innovation managementDeep scientific and technical expertise in pharmaceutical developmentRegulatory and quality compliance knowledgePortfolio and project governanceFinancial and operational managementStakeholder engagement and executive communicationTalent development and organizational leadershipContinuous improvement and change leadershipTechnical CompetenciesExtensive experience in ANDA/Generic product development and regulatory submissions.Strong exposure to execution of registration/submission batches and commercial scale-up.Proven experience in Technology Transfer to manufacturing sites.Demonstrated experience in handling and responding to regulatory agency queries and deficiencies.Strong knowledge and practical application of QbD principles.Hands-on expertise in Design of Experiments (DOE) and statistical data analysis.Knowledge of pharmaceutical development regulations and cGMP requirements.Experience with risk assessment tools and product lifecycle management.Exposure to novel formulation technologies, platform approaches, and differentiated dosage forms.Strong troubleshooting and problem-solving capabilities.Leadership CompetenciesProven experience managing and developing teams.Strong mentoring and people nurturing mindset.Ability to influence and lead without authority across matrix organizations.Excellent stakeholder management and communication skills.Strong project management and prioritization capability.Demonstrated ability to lead cross-functional teams collaboratively.

من ٠ إلى ٠ سنة بيت.كوم

Laundry Attendant

On-site - الأردن ١٤ يوليو ٢٠٢٦

الضيافة والسياحة

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Job Description Key Deliverables and Responsibilities Planning & Organizing: <ol><li>Plan cleaning schedule according to the Room Status Sheet allocation.</li><li>Ensure Housekeeping trolley is stocked daily in a neat and organised manner.</li><li>Maintain strong knowledge of the local area to ensure you are equipped to answer guest enquiries and provide accurate directions</li></ol>Operations: Washing and Cleaning: <ul><li>Laundry Processing:<ul><li>Sort soiled linens, towels, uniforms, and other items based on fabric type, color, and cleaning requirements.</li><li>Operate industrial washing machines and dryers to wash and dry laundry in an efficient and timely manner.</li><li>Pre-treat stains and heavily soiled items using appropriate chemicals and techniques.</li></ul></li><li>Handling Delicate Fabrics:<ul><li>Follow specific washing instructions for delicate or special items such as uniforms, guest laundry, and high-quality linens.</li><li>Use the correct washing cycles, water temperatures, and cleaning solutions to ensure fabric preservation.</li></ul></li><li>Chemicals and Detergents:<ul><li>Use the correct amount of detergents, softeners, and chemicals for each load of laundry.</li><li>Ensure proper handling and storage of cleaning chemicals in compliance with safety protocols.</li></ul></li></ul>Quality Control: <ul><li>Inspection and Folding:<ul><li>Inspect all washed items for stains, damage, or incomplete cleaning and rewash items if necessary.</li><li>Fold, iron, and neatly organize clean laundry, ensuring it meets the resort’s quality standards.</li></ul></li><li>Equipment Maintenance:<ul><li>Maintain and clean washing machines, dryers, and other laundry equipment to ensure they operate smoothly.</li><li>Report any equipment malfunctions or breakdowns to the Laundry Supervisor immediately.</li></ul></li></ul>Guest Laundry Service: <ul><li>Personalized Laundry Service:<ul><li>Handle guest laundry requests by washing, drying, and folding guest clothes according to their specific instructions.</li><li>Ensure timely delivery of clean laundry back to guests, providing an exceptional level of service.</li></ul></li></ul>Health, Safety, and Hygiene: <ul><li>Health & Safety Compliance:<ul><li>Adhere to all health and safety guidelines, including the safe handling of chemicals and following proper laundry procedures.</li><li>Wear protective gear and follow safety protocols to prevent injuries or accidents in the laundry area.</li></ul></li><li>Cleanliness:<ul><li>Ensure that the laundry room and all equipment are kept clean, sanitized, and organized at all times.</li><li>Dispose of waste and lint from dryers according to proper procedures.</li></ul></li></ul>Coordination and Teamwork: <ul><li>Team Support:<ul><li>Work closely with other members of the laundry and housekeeping teams to meet daily laundry quotas and schedules.</li><li>Assist other laundry staff with sorting, folding, and ironing when required.</li></ul></li><li>Communication:</li></ul><ul><li><ul><li>Communicate any laundry-related issues or special requests to the Laundry Supervisor.</li><li>Report any damaged items or concerns about quality to the supervisor promptly.</li></ul></li></ul>Administration: Use the duty shift checklists to ensure tasks are completed. </div>

من ٠ إلى ٠ سنة Naukri Gulf

Laundry Attendant

On-site - الأردن - العقبة ١٤ يوليو ٢٠٢٦

المبيعات

<section>Job DescriptionRoles & Responsibilities<div class="paragraph">Plan cleaning schedule according to the Room Status Sheet allocation. Ensure Housekeeping trolley is stocked daily in a neat and organised manner. Maintain strong knowledge of the local area to ensure you are equipped to answer guest enquiries and provide accurate directions Operations: Washing and Cleaning: Laundry Processing: Sort soiled linens, towels, uniforms, and other items based on fabric type, color, and cleaning requirements. Operate industrial washing machines and dryers to wash and dry laundry in an efficient and timely manner. Pre-treat stains and heavily soiled items using appropriate chemicals and techniques. Handling Delicate Fabrics: Follow specific washing instructions for delicate or special items such as uniforms, guest laundry, and high-quality linens. Use the correct washing cycles, water temperatures, and cleaning solutions to ensure fabric preservation. Chemicals and Detergents: Use the correct amount of detergents, softeners, and chemicals for each load of laundry. Ensure proper handling and storage of cleaning chemicals in compliance with safety protocols. Quality Control: Inspection and Folding: Inspect all washed items for stains, damage, or incomplete cleaning and rewash items if necessary. Fold, iron, and neatly organize clean laundry, ensuring it meets the resort s quality standards. Equipment Maintenance: Maintain and clean washing machines, dryers, and other laundry equipment to ensure they operate smoothly. Report any equipment malfunctions or breakdowns to the Laundry Supervisor immediately. Guest Laundry Service: Personalized Laundry Service: Handle guest laundry requests by washing, drying, and folding guest clothes according to their specific instructions. Ensure timely delivery of clean laundry back to guests, providing an exceptional level of service. Health, Safety, and Hygiene: Health & Safety Compliance: Adhere to all health and safety guidelines, including the safe handling of chemicals and following proper laundry procedures. Wear protective gear and follow safety protocols to prevent injuries or accidents in the laundry area. Cleanliness: Ensure that the laundry room and all equipment are kept clean, sanitized, and organized at all times. Dispose of waste and lint from dryers according to proper procedures. Coordination and Teamwork: Team Support: Work closely with other members of the laundry and housekeeping teams to meet daily laundry quotas and schedules. Assist other laundry staff with sorting, folding, and ironing when required. Communication: Communicate any laundry-related issues or special requests to the Laundry Supervisor. Report any damaged items or concerns about quality to the supervisor promptly. Administration: Use the duty shift checklists to ensure tasks are completed.</div></section><section>Desired Candidate Profile </section>

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