وظائف Tabuk Pharmaceuticals

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p><strong><span>Job Responsibilities/Technical and executive:&nbsp;</span></strong></p><br> <ol> <li><strong><span>AutoCAD Drawing Preparation &amp; Updating:</span></strong></li> </ol><ul> <li><span>Prepare, modify, update, and finalize accurate 2D/3D engineering drawings in AutoCAD based on approved layouts, mark-ups, site conditions, and instructions provided by engineers and authorized stakeholders.</span></li> <li><span>Prepare and maintain as-built drawings, architectural and MEP mark-ups, facility layouts, cleanroom drawings, utility drawings, and other engineering documentation required for manufacturing and support facilities.</span></li> </ul> <strong><span>Engineering Drawing &amp; Document Control:</span></strong> <ul> <li><span>Maintain, organize, archive, and update engineering drawings, technical documents, schematics, registers, and related records in accordance with the established Quality Management System (QMS), GMP/GxP requirements, and applicable procedures.</span></li> <li><span>Control drawing numbers, revisions, status, issue dates, approvals, indexing, transmittals, and superseded copies to ensure full traceability and audit readiness.</span></li> </ul> <strong><span>Master Drawings &amp; Facility Documentation:</span></strong> <ul> <li><span>Maintain controlled master drawings for buildings, production areas, warehouses, cleanrooms, utilities, and engineering systems, ensuring that approved changes are accurately incorporated.</span></li> <li><span>Coordinate with Engineering, Projects, Maintenance, QA, EHS, Production, and other concerned departments to collect approved mark-ups and ensure timely updating of affected AutoCAD drawings.</span></li> <li><span>Maintain up-to-date drawing registers, document logs, technical archives, and electronic filing structures, and ensure that the latest approved drawings are readily available to authorized users.</span></li> </ul> <strong><span>Documentation Workflow &amp; Technical Support:</span></strong> <ul> <li><span>Support engineering and project teams by preparing drawing packages, extracting drawing information, converting files to required formats, and following up on drawing/document submissions, reviews, comments, and approvals.</span></li> <li><span>Perform site verification when required to confirm dimensions and existing conditions, and comply with direct manager instructions and department work priorities based on business requirements.</span> <p><strong><span>Mandatory Job Responsibilities (EHS, GMP &amp; QA Compliance):</span></strong></p><br> </li> <li><span>Environment, Health &amp; Safety (EHS):</span></li> <li><span>Change Control &amp; Deviation Management:</span></li> <li><span>Good Manufacturing Practice (GMP):</span></li> </ul> <br><p><strong><span>Required Educational Level and Certificates -&nbsp; </span></strong>Bachelor of Engineering&nbsp;</p><br> <p><strong><span>Required Experience - </span></strong><span><span><span>2- 4 years of experience in a similar position.</span></span></span></p><br> </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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <ul> <li>Oversee end-to-end credit management and ensure full compliance with the company’s credit policy.</li> <li>Conduct credit assessments, assign risk categories, and review customer credit limits periodically.</li> <li>Supervise collections activities and follow up on overdue accounts to minimize DSO and bad debt exposure.</li> <li>Monitor sales orders and release/hold decisions based on credit status and outstanding balances.</li> <li>Prepare periodic A/R, aging, collections, and exposure reports for management review.</li> <li>Coordinate with Commercial teams to align on customer performance, disputes, and collection strategies.</li> <li>Liaise with Treasury to manage credit insurance coverage and adjust limits based on exposure and forecasts.</li> <li>Ensure complete customer documentation and adherence to internal controls and audit requirements.</li> <li>Identify process gaps and implement improvements to enhance efficiency and accuracy.</li> <li>Coach, guide, and evaluate the performance of the credit team.</li> </ul><br><ul> <li>Bachelor’s degree in Accounting, Finance, or Economics.</li> <li>4–6 years of experience in Credit Control, Accounts Receivable, or General Accounting (pharmaceutical/FMCG industry preferred).</li> <li>Strong analytical skills and attention to detail.</li> <li>Proficiency in SAP or other ERP systems.</li> <li>Good communication and stakeholder management skills.</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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> 5+ years </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p><strong><em>Key Responsibilities</em></strong></p><br> <ul> <li>Maintain and update all company insurance policies and related records.</li> <li>Coordinate with the Group regarding insurance policies, coverage, and requirements.</li> <li>Provide accurate information required for insurance renewals and policy arrangements.</li> <li>Coordinate with insurance companies on day-to-day insurance matters.</li> <li>Follow up on policies, certificates, endorsements, and other required documents.</li> <li>Monitor policy expiry dates and ensure continuity of coverage.</li> <li>Coordinate insurance claims from initial notification through settlement.</li> <li>Follow up with insurance companies on outstanding claims.</li> <li>Coordinate with Finance, HR, Operations, Engineering, Supply Chain, and other departments to collect required information.</li> <li>Maintain an updated insurance register covering policies, coverage, expiry dates, and other key information.</li> <li>Follow up on insurance premiums and coordinate with Finance/Treasury regarding payments.</li> <li>Prepare regular reports on insurance policies, claims, and outstanding matters.</li> <li>Ensure proper filing and maintenance of insurance-related documentation.</li> <li>Support the Treasury Manager in managing insurance-related risks and costs.</li> <li>Assist with internal and external audits by providing required insurance documentation.</li> <li>Ensure compliance with company policies and Group insurance requirements.</li> </ul><br><p><strong><em>Qualifications &amp; Experience</em></strong></p><br> <ul> <li>Bachelor’s degree in&nbsp;<strong>Finance, Insurance, or a related field</strong>.</li> <li><strong>2–4 years of experience</strong>&nbsp;in insurance or a related role.</li> <li>Experience in a&nbsp;<strong>manufacturing or industrial company</strong>&nbsp;is preferred.</li> <li>Experience dealing with insurance companies, brokers, and claims.</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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <ul> <li><span>Design and develop packaging concepts (structural and graphic) for new and existing products</span></li> <li><span>Create 2D and 3D mockups, prototypes, and keylines using design software</span></li> <li><span>Collaborate with packaging design and production teams to ensure designs meet brand guidelines and functional requirements</span></li> <li><span>Ensure packaging designs comply with legal, safety, and regulatory labeling requirements</span></li> <li><span>Coordinate with vendors and printers to ensure accurate production of packaging materials</span></li> <li><span>Conduct quality checks and testing on packaging prototypes for durability, functionality, and print accuracy</span></li> <li><span>Manage multiple design projects simultaneously while meeting deadlines</span></li> <li><span>Prepare technical specification sheets and artwork files for production</span></li> <li><span>Incorporate sustainability initiatives and eco-friendly packaging solutions where applicable</span></li> <li><span>Maintain design archives and version control of packaging files</span></li> </ul><br><ul> <li><span>Proficiency in design software: Adobe Illustrator, Photoshop, InDesign</span></li> <li><span>Knowledge of 3D design/prototyping tools (e.g., Artios CAD, SolidWorks, Cinema 4D) is a plus</span></li> <li><span>Understanding of keyline creation and print production processes (offset, digital, flexographic printing)</span></li> <li><span>Familiarity with packaging materials and their properties</span></li> <li><span>Knowledge of pre-press and color management</span></li> </ul> <p><strong><span>Education: </span></strong><span>Bachelor’s degree in graphic design, Packaging Design, Industrial Design, Fine Arts, or related field</span></p><br> <p><strong><span>Experience:</span></strong><span>2–5 years of experience in packaging design.</span></p><br> </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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <ul> <li>To follow up on instructions from the Production Officer, Production Supervisor, or Senior Production Supervisor.</li> <li>To check the availability of the required packing POIs and related packaging materials before starting the concerned batch/product.</li> <li>To follow up and arrange QA notification along with the green release label.</li> <li>To arrange the relevant manufacturing POI.</li> <li>To calculate and segregate tablets/capsules according to the POI requirements for different consignees.</li> <li>To follow up on the completion and documentation of the concerned area logbooks, POIs, and WIP logbooks.</li> <li>To follow up on the return of packaging materials after completion of the batch.</li> <li>To inform the Production Officer, Production Supervisor, or Senior Production Supervisor of any breakdown or equipment-related issue.</li> <li>To raise a Job Order in case of any maintenance requirement or breakdown.</li> <li>To ensure that the correct tablet/capsule drums, foil/PVC, and required quantities are brought and verified before starting the batch.</li> <li>To raise a requisition slip for any additional packaging-material requirements.</li> <li>To operate the machine in the absence of the concerned machine operator or in case of operator shortage.</li> <li>To relieve the machine operator during breaks, when required.</li> <li>To assist the machine operator during machine setting and in resolving any operational problems.</li> <li>To check the cleanliness and documentation of the machine in accordance with&nbsp;<strong>SOP-PRD-068</strong>&nbsp;and&nbsp;<strong>SOP-PRD-032</strong>.</li> </ul><br><p>•General Orientation<br>•GMP (Goods Manufacturing Practices)<br>•Leadership &amp; Soft Skills<br>•SOP<br>•Time management skills.</p><br> </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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> 2+ years </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Job Description<br> <p><strong><span>1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Follows approved Departmental SOPs (Standards Operating Procedures).</p><br> <p><strong><span>2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Follows cGMP (Current Good Manufacturing Practice Regulations) and GWP (Good Warehousing Practices).</p><br> <p><strong><span>3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Adheres all safety precaution as per EHS (Environmental Health &amp; Safety) SOPs.</p><br> <p><strong><span>4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Reports to Officer Senior / Supervisor.&nbsp;</p><br> <p><strong><span>5.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Loading&nbsp;/ Unloading / Transfer of Raw, Packaging, Consumables, Assets and Finished Goods in the warehouse.</p><br> <p><strong><span>6.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Cleaning of the received materials.</p><br> <p><strong><span>7.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Segregation of the received material.</p><br> <p><strong><span>8.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Operating forklift to move, transfer and place the materials on locations</p><br> <p><strong><span>9.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Transfer / Handling of materials.&nbsp;</p><br> <p><strong><span>10.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Cleaning of floor, racks, pallets etc., in the warehouse.&nbsp;</p><br> <p><strong><span>11.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Co-worker with Dispensing Staff.</p><br> <p><strong><span>12.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Helps Dispensing Staff in verification.</p><br> <p><strong><span>13.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Places the dispensed material on the pallets.</p><br> <p><strong><span>14.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Packs dispensed material in shrink wrap before sending to Production.</p><br> <p><strong><span>15.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Returns the remaining quantity of the material to their respective location after dispensing the required quantity.</p><br> <p><strong><span>16.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Performs balance verification and updates logbook.</p><br> <p><strong><span>17.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Performs double check of all the material dispensed to Production.</p><br> <p><strong><span>18.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Makes entry on POI in Production after physical check.</p><br> <p><strong><span>19.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Checks all Balance Verification Logbooks.</p><br> <p><strong><span>20.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Takes part in the annual stock count.</p><br> <p><strong><span>21.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></strong>Performs other applicable tasks and duties assigned by the supervisor.</p><br> <br><br><p>&nbsp;&nbsp;&nbsp; -Secondary School Certificate (Preferable).</p><br> </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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <span><strong>1. Laboratory Oversight &amp; Operations</strong></span> <ul> <li>Supervise and coordinate daily QC testing activities within the Raw Materials section.</li> <li>Plan, schedule, and allocate routine and non-routine testing to meet material release timelines.</li> <li>Ensure timely analysis and approval of raw materials to support uninterrupted manufacturing operations.</li> <li>Monitor laboratory housekeeping, safety practices, and compliance with EHS requirements.</li> <li>Ensure the availability, calibration, qualification, and proper maintenance of analytical instruments used for raw material testing (e.g., FTIR, Raman, UV-Vis, HPLC, GC, and wet chemistry).</li> </ul> <span><strong>2. Review, Approval &amp; Data Integrity</strong></span> <ul> <li>Review and approve raw data, analytical results, specifications, Certificates of Analysis (COAs), and test reports.</li> <li>Ensure compliance with ALCOA+ data integrity principles across all laboratory records and electronic systems.</li> <li>Review and approve transactions and analytical results in SAP/LIMS, ensuring accurate maintenance of vendor-related data.</li> <li>Perform trend analysis of raw material and water testing results to identify recurring issues and opportunities for improvement.</li> <li>Maintain and periodically review the approved raw material vendor list.</li> </ul> <span><strong>3. Quality &amp; Compliance</strong></span> <ul> <li>Ensure compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), ICH guidelines, pharmacopeial requirements (USP/EP), and internal SOPs.</li> <li>Maintain inspection readiness and participate in internal and external regulatory audits (e.g., FDA, EMA, SFDA, WHO).</li> <li>Investigate and document Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and non-conformances, ensuring timely closure with effective CAPAs.</li> <li>Support the implementation, maintenance, and continuous improvement of the Quality Management System (QMS).</li> <li>Participate in supplier qualification and requalification activities, including vendor audits, COA verification, and supplier performance monitoring.</li> </ul> <span><strong>4. Documentation &amp; SOP Management</strong></span> <ul> <li>Oversee the preparation, review, approval, issuance, and periodic revision of SOPs, analytical methods, logbooks, forms, and templates.</li> <li>Ensure all QC documentation is accurate, complete, controlled, and fully traceable.</li> <li>Prepare and review analytical reports and provide QC documentation to support Regulatory Affairs submissions.</li> <li>Ensure documentation practices comply with data integrity requirements and support audit readiness.</li> </ul> <span><strong>5. People Management &amp; Training</strong></span> <ul> <li>Lead, mentor, supervise, and evaluate QC analysts within the Raw Materials section.</li> <li>Ensure effective onboarding, technical training, competency assessments, and continuous professional development of laboratory personnel.</li> <li>Conduct performance evaluations, support succession planning, and address employee performance and conflict resolution as required.</li> <li>Foster a culture of quality, accountability, teamwork, and continuous improvement.</li> <li>Maintain audit readiness by ensuring ongoing staff training in data integrity, GMP, and regulatory compliance.</li> </ul> <span><strong>6. Continuous Improvement &amp; Performance Management</strong></span> <ul> <li>Drive laboratory efficiency through continuous improvement initiatives, including Lean, Six Sigma, automation, and digitalization projects.</li> <li>Establish, monitor, analyze, and report Quality Control Key Performance Indicators (KPIs).</li> <li>Promote cost awareness and optimize laboratory resources to improve productivity and operational efficiency.</li> <li>Identify opportunities to streamline laboratory processes while maintaining compliance, quality, and data integrity.</li> </ul><br><span><strong>Qualifications &amp; Experience</strong></span> <ul> <li>Bachelor's degree in Pharmacy, Chemistry, or a related scientific discipline (Master's degree preferred).</li> <li>13–15 years of Quality Control experience in the pharmaceutical industry, including a minimum of 5 years in a supervisory or leadership role.</li> <li>Extensive knowledge of pharmacopeial requirements (USP, EP, BP, and JP) related to raw material testing.</li> <li>Hands-on experience with analytical techniques used for raw material testing, including FTIR, Raman spectroscopy, UV/Vis spectrophotometry, HPLC, GC, wet chemistry, and pharmacopeial identification and assay methods.</li> <li>Thorough understanding of current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), ICH guidelines, and regulatory inspection requirements.</li> <li>Proficiency in SAP, LIMS, and electronic laboratory documentation and data management systems.</li> <li>Demonstrated experience in regulatory inspections, audit preparation, supplier qualification, and quality risk management.</li> <li>Strong analytical, problem-solving, and decision-making skills with the ability to manage multiple priorities in a GMP-regulated environment.</li> <li>Excellent leadership, communication, coaching, and cross-functional collaboration skills.</li> <li>Proven ability to drive continuous improvement initiatives and effectively manage laboratory performance through quality metrics and KPIs.</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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Build data base about tenders’ time tables, potential and decision makers establish new business opportunities and channels.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Capture ad-hoc (direct purchases) business opportunities through regular KA (Key Accounts) visits and lobby of concerned persons (Purchasers, Pharmacists).</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Initiate, negotiate and receive RFQ along with quotation preparation, delivery &amp; approval.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Receive purchasing order &amp; submit back to the concerned department.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Get profit from synergies with other territory teams and other field players.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Introduce and promote existing products and new launches through promotion to doctors, clinical pharmacists, Product technical committees and pharmacists. In addition to managing evaluation studies when required</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Manage promotional budget to balance between customers’ scientific support and return on related investment.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Participate in trade shows, conferences, standalone meetings, Group Meetings and conventions.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Plan for target achievement and split between accounts.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Report plan progress on weekly basis, identify gaps and plan of action to close it.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Prepare &amp; update reports about customers’ profile, needs, problems, interests, competitive activities, and potential for new products and services.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Perform market research for under registration products.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Report product applications, technical services, market conditions, competitive activities, advertising and promotional trends through different channels.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Update the company database frequently</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Ensure confidentiality of all documents and information related to work.</span></p><br> <p><span>·&nbsp; &nbsp; &nbsp; &nbsp;Perform any other duties related to the job according to the business needs.</span></p><br><br><p><span>- Bachelor Degree in Pharmacy.</span></p><br> <p><span>-&nbsp;</span><span>1 - 3 years of experience in a similar position.</span></p><br> <p><span>- Saudi .</span></p><br> </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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Prepare professional presentations to introduce the company products to doctors &amp; other healthcare providers.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Pay frequent visits to doctors based on cold calling or already arranged appointments.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Follow up with doctors &amp; other healthcare providers about stock supply &amp; consumptions of the company product along with feedback.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Plan forecasting of sales target for each successive month and acts accordingly.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Liaise with and persuade targeted doctors to prescribe our products utilizing effective selling skills.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Make telephone calls and pay in-person visits to provide details to existing and prospective customers to cover all assigned medical centers according to their potentiality.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Cooperate and coordinate with sales &amp; collection teams frequently.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Research sources for developing prospective customers and for information to determine their potential.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Develop clear and effective written proposals/quotations for current and prospective customers.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Create and manage a customer value plan for existing customers highlighting profile, share and value opportunities to achieve the assigned target on monthly, quarterly and annually basis.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Pursue continuous learning and professional development and stay up-to-date with latest medical data</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Plan and organize personal sales strategy by maximizing the Return on Time Investment for the territory/segment.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>Stay up to date with new developments in the field in order to provide competitive information to customers.</span></p><br> <p><span>·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span><span>&nbsp;Provide the management with oral and written reports on customer needs, problems, interests, competitive activities, and potential for new products and services.</span></p><br><br><p><span>-&nbsp;</span><span>Bachelor Degree in Pharmacy.</span></p><br> <p><span>-&nbsp;</span><span>Saudi .&nbsp;</span></p><br> <p><span>-</span><span>&nbsp;1 - 3 years of experience in a similar position</span></p><br> </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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p> Review and check the raw data generated under his supervision.<br> Plan and distribute the daily routine work.<br> To assist analyst for trouble shooting of instrumental problems.<br> To ensure availability of reference and working standards.<br> To ensure that all instruments are calibrated as per schedule.<br> To maintain instrument parts, columns, etc.<br> Review and maintain the logbooks, COAs, specifications and test procedures related to his section responsibility.<br> Analysis and approval of cleaning validation / verification samples.<br> Release/Rejection of products and materials and issue of release or rejection labels.<br> Approving of receiving logbook.<br> Report to QC Manager about the out of specification results obtained in routine analysis and retesting in order to perform proper investigation to verify the deviation.<br> To ensure the approved procedures and specifications are followed.<br> To check the artwork forwarded by R&amp;D.<br> Perform proper training for employees.<br> Perform trend analysis.<br> Signing off on COA etc.<br> To ensure availability of adequate media, reagents, glassware and solutions.<br> To ensure preparation and sterilization of media and documentation for preparation of media as per designed procedure.<br> To ensure proper maintenance of media stock.<br> To ensure disposition of samples and used media.<br> To perform developmental activities.<br> Maintain proper control for raw material supplier’s qualification program.<br> Performing required risk approach for all critical tests (Heavy metals, Residual Solvents ,…etc.).<br> To be aware about pharmacopeia analytical requirements.<br> Has long experience for different analytical techniques.</p><br> </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"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> No experience required </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<p>We are seeking an experienced Corporate Senior Quality Risk Management Supervisor to lead risk-based quality oversight across pharmaceutical manufacturing sites, projects, and facility upgrades.</p><p>The successful candidate will have proven experience in a multinational, EU GMP, or US FDA-regulated pharmaceutical manufacturing organization, with strong expertise in Quality Risk Management, Compliance, qualification, validation, and project execution.</p><p><br></p><p><strong>Key Responsibilities: </strong></p><ul><li>Design, maintain and ensure implementation of harmonized corporate policies and tools related to Quality risk management</li><li>Ensure alignment with ICH Q9/Q9(R1), ISPE, EU GMP, US FDA expectations, Annex 1, contamination control, data integrity, and GxP computerized-system requirements. </li><li>Design and implement a certification process for QRM champions across corporate functions and sites</li><li>Assess all Quality management systems and ensure that Risk management is embedded with the process and systems such as non-conformance, change management, internal audits, investigations, supplier qualification etc.</li><li>Ensure that all major systems are assessed for any potential risk of failures and the appropriate risk mitigation actions are identified, implemented and effective.</li><li> Leading QRM activities for major projects such as new facilities, and new lines</li><li>Develop and execute remediation plans with clear milestones, accountable owners, risk controls, effectiveness checks, and sustainable closure.</li><li>Support quality transformation programs focused on:</li><li>Simplification and harmonization of global quality processes.</li><li>Strengthening quality culture and management ownership.</li><li>Digital QMS, risk-based workflows, data analytics, and performance dashboards.</li><li>Improved right-first-time performance, inspection readiness, and operational resilience</li><li>Facilitate and review risk-based assessments.</li><li>Support risk assessments for deviations, CAPA, change controls, OOS/OOT investigations, complaints, recurring events, and inspection readiness.</li><li>Promote responsible adoption of digital QRM/eQMS tools, analytics and dashboards, AI-assisted risk identification, digital validation, automation, smart manufacturing, and sustainable facility design, with appropriate governance, validation, human oversight, and data-integrity controls.</li></ul><p><br></p><p><strong>Required Experience and Qualifications: </strong></p><ul><li>Bachelor’s degree in Pharmaceutical Sciences, Engineering, Chemistry, Microbiology, or a related discipline.</li><li>Typically, +12 years of relevant pharmaceutical experience in Quality, Validation, Engineering, Technical Operations, or GMP projects.</li><li>Proven experience leading and governance of QRM activities within a reputable pharmaceutical manufacturing organization, preferably a multinational, EU GMP, or US FDA-regulated company.</li><li>Demonstrated experience with new facilities, major facility upgrades, new production or packaging lines, critical utilities, and technology transfer projects.</li><li>Strong working knowledge of GMP, pharmaceutical quality systems, validation, contamination control, data integrity, and risk-based decision-making.</li><li>Experience in sterile, aseptic, biologics, non-sterile, high potent &amp; other highly regulated manufacturing is highly desirable.</li><li>Excellent facilitation, technical writing, stakeholder-management, influencing, and cross-site leadership skills.</li></ul>

We are seeking an experienced and results-driven Pharmaceutical Marketing professional to drive effective marketing initiatives aligned with company objectives. The successful candidate will leverage market and industry insights to develop and execute impactful marketing strategies, optimize promotional activities, enhance brand visibility, and ensure compliance with applicable regulatory requirements.<br>Key Responsibilities Develop, manage, and execute comprehensive marketing plans, strategies, tactics, campaigns, and initiatives aligned with company objectives and industry trends. Prepare and recommend the assigned marketing portfolio budget based on relevant analysis, business requirements, and available data. Monitor the financial performance of the assigned marketing portfolio against approved budgets, identify variances, and recommend timely corrective actions and performance improvement opportunities. Manage the day-to-day operations of the assigned marketing portfolio, ensuring effective implementation of work processes in accordance with established policies, procedures, and controls. Analyze market trends, industry insights, and market data to identify opportunities and contribute to forecasting marketing requirements. Establish and maintain marketing metrics and analytics to track key performance indicators, including ROI, market share, customer engagement, and campaign performance. Track and analyze marketing performance data to identify trends, patterns, gaps, and opportunities for improvement. Monitor market data and analytics systems to ensure data accuracy, reliability, and effective utilization. Create, update, review, and validate promotional materials for the assigned marketing portfolio while ensuring compliance with company standards and applicable regulatory requirements. Prepare timely and periodic reports, dashboards, and presentations in line with company and departmental requirements, policies, and standards. Guide and support Sales teams in responding to market dynamics and achieving sales objectives through effective marketing tools, materials, and insights. Provide support and guidance to marketing team members on marketing-related matters and assist in addressing challenges through analysis, problem-solving, and solution implementation. Collaborate with cross-functional teams and other departments to ensure alignment and synergy in achieving organizational objectives. Recommend enhancements and improvements to departmental policies, processes, and procedures. Ensure compliance with all applicable policies, processes, procedures, controls, and relevant regulatory and legislative requirements across the assigned marketing portfolio. Ensure adherence to relevant safety, quality, and environmental management policies, procedures, and controls while delivering quality and cost-effective services. Demonstrate excellent interpersonal, communication, leadership, analytical, collaboration, and problem-solving skills.<br>Qualifications Bachelor's degree in Pharmacy. MBA or equivalent postgraduate qualification from a recognized business school is preferred. Minimum 7 years of experience in the pharmaceutical industry, including at least 2 years of experience in Marketing. Proven experience in the pharmaceutical industry is required. Experience in Primary Care is preferred. Saudi National is preferred.