biomedical supervisor

Shifamed LLC

<div><div>Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana&trade; Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing NavIQ&trade;, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&amp;D and manufacturing center in Doha, Qatar. To learn more about Akura Medical, please visit www.akuramed.com. 
 
ABOUT SHIFAMED 
Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology. 
 
Description:</div>
<div> 
This position represents an exciting opportunity to join the Akura team at an early stage where you will creatively design and develop components, both consumable and capital equipment, of a blood clot removal system. The role focuses on mechanical design of various components and assemblies for catheter systems, a console, and cross-functional leadership from concept through high volume manufacturing. You will be responsible for the design, vendor relationships and testing per applicable standards. This is a full-time, on-site position at our Doha, Qatar office. 
 
Responsibilities, Skills &amp; Hands-On Experience:</div>
<ul><li>Lead design and development of plastic/composite and metallic parts from concept to high volume manufacturing; drive DFM/DFS, manufacturing and tooling decisions with suppliers.</li>
<li>Drive the full mechanical lifecycle: requirements, concepts, prototyping, detailed design, V&amp;V, and transition to production.</li>
<li>Integrate mechanical designs with electronics, firmware, fluid, and user-interface elements in collaboration with cross-functional teams.</li>
<li>Guide analysis (tolerance stacks, FEA, material selection, root-cause) on critical subsystems.</li>
<li>Creative solutions and product designs to satisfy unmet clinical needs in thrombectomy.</li>
<li>Be a primary contributor to the intellectual property position of the company via invention disclosures and prototypes to demonstrate reduction to practice.</li>
<li>Interact with physicians to assist with product demonstrations and product testing.</li>
<li>Effectively document work throughout the development process though design reviews, manufacturing instructions, test methods, and test reports.</li>
<li>Expertise in design and development of medical devices.</li>
<li>Expertise in electromechanical and mechanism design of durable medical devices.</li>
<li>Substantial experience in design of higher volume disposable components.</li>
<li>Substantial experience in design for molding and machining.</li>
<li>Substantial experience in design for manufacturing. Pilot production experience.</li>
<li>Expertise in product, tool and fixture design using SolidWorks.</li>
<li>Performance test apparatus and test method development.</li>
<li>Process development on both a prototype and manufacturing level.</li>
<li>Mentoring and assisting team members with less experience.</li>
<li>Participating in lab and cleanroom environment builds.</li>
<li>Process optimization and design of experiment based on statistical methodology.</li>
<li>Selecting and managing suppliers, including understanding of capabilities, materials, and fabrication processes</li>
<li>Working independently and in a project team setting.</li>
<li>Supporting regulatory filings including writing technical sections and providing general technical input.</li>
</ul>
<div> 
Education &amp; Work Experience:</div>
<ul><li>Bachelor's Degree or higher in Mechanical/Biomedical Engineering.</li>
<li>At least 15 years of experience in complex product development, including regulated products.</li>
<li>Advanced SolidWorks proficiency.</li>
<li>Demonstrated track record as a lead/principal engineer or product design of medical devices from concept through launch.</li>
<li>Strong expertise in injection molding and RIM molding (part design, materials, DFM, cosmetic and structural considerations).</li>
<li>Strong experience with medical devices under FDA/ISO 13485 or equivalent regulatory frameworks.</li>
<li>Previous experience working with clinical testing, trials, data collection, and statistical analysis.</li>
</ul><div><div>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.</div>
<div></div><div>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.</div></div></div>

Principal Mechanical Design Engineer

Airswift

<div>
 Vacancy Overview
 
 
 
 Construction Supervisor (Piping)
 
 
 
 Airswift is an international workforce solutions provider within the energy, process, and infrastructure industries. Airswift serves as a strategic partner to our clients, offering a turnkey workforce solution to capture and deliver the top talent needed to complete successful projects by aligning with the unique needs of our clients. With over 1,000 employees and 9,000 contractors operating in over 70 countries, our geographical reach and pool of talent available is unmatched in the industry.
 
 
 
 Airswift is seeking for Construction Supervisor (Piping) to work in Qatar with a major Oil &amp; Gas Company.
 
 
 
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree or Diploma in Mechanical Engineering from an internationally recognized University.
 </li>
 <li>
 Preferably having formal training in QA/QC functional aspects
 
 
 </li>
 </ul>
 
 EXPERIENCE
 
 
 
 <li>
 Candidate shall be a safety leader.
 </li>
 <li>
 Candidate should have a minimum of 10 years overall experience in piping erection (UG &amp; AG), pressure testing, mechanical completion and construction of oil and gas facilities.
 </li>
 <li>
 Experience as an EPIC Contractor supervisor is essential. Experience as a Client or PMC supervisor is preferred.
 </li>
 <li>
 Current experience in State of Qatar industrial cities and/or other GCC countries is required.
 </li>
 <li>
 Piping inspection and rotating equipment experience is an advantage, and inspection coordination experience in the.
 </li>
 <li>
 Extensive knowledge of international and industry specific piping codes and standards, including ASME, ANSI B31.3 &amp; B31.1, SHELL DEP&rsquo;s, etc. Piping, Welding / NDT inspector certificates (AWS / ASNT / CSWIP / API) would be an advantage.
 </li>
 <li>
 Extensiveexperience in pipe coating systems and procedures, including painting, galvanizing, wrapping, insulation, etc. BGAS certification would be an advantage.
 </li>
 <li>
 Extensive experience in fabrication pipe spooling, pipe supports and erection of carbon steel, stainless/alloy steel, uPVC and GRE/GRV piping systems, including pressure testing, pre-commissioning and mechanical completion inspection.
 </li>
 <li>
 Excellent written and oral English skills. Able to read piping drawings, P&amp;ID&rsquo;s and manufacturer&rsquo;s instructions, etc.
 </li>
 <li>
 The candidate shall have specific stated experiences in;
 </li>
 <ul>
 <li>
 Greenfield/new build construction sites, o Brownfield/live process plants,
 </li>
 <li>
 Permits to work, incl Isolation &amp; Lock Out/Tag Out of live services,
 </li>
 <li>
 Tie-in to live facilities, including testing and integration to existing systems, Extensive knowledge in Lifting Plan and Crane Studies.
 </li>
 <li>
 If candidate have Approved Lifting Supervisor Certificate it would be advantage.
 </li>
 <li>
 Stage Inspection and Testing of Construction activities as per approved ITPs
 </li>
 <li>
 Strong technical, prioritization and management skills.
 </li>
 <li>
 Good communication, influencing and interface skills.
 </li>
 <li>
 Proficient knowledge of computer programs (MSOffice, Outlook, Excel, Words, PDF, Power Point, etc) and engineering software applications relevant to the discipline.
 
 
 </li>
 </ul>
 
 Primary Duties And Responsibilities
 
 
 
 <ul>
 <li>
 Acts as a safety leader, ensuring EPIC Contractor&rsquo;s work in compliance to Company Life Saving Rules and all safety and environmental regulations of Company and the State of Qatar.
 </li>
 <li>
 Reporting to the Discipline Construction Lead/Senior Construction Supervisor on main issues, events at site, progress reporting, trends and recommendation for improvement.
 </li>
 <li>
 Assist functional supervisor in review and / or approval of Construction documentation, including Method Statements, JHAs, MARs etc., and attend HSE Walkthroughs.
 </li>
 <li>
 Supervise all EPIC contractors piping (Process and Utility piping system with various material pipe classes for above ground &amp; underground piped services) installation activities are based on approved the engineering documentation and project schedule during the execution of construction activities
 </li>
 <li>
 Attend Requests For Inspections (RFIs) as per approved ITPs, including Material Receiving Inspections in coordination with Reconstruction Supervisor, and sign off relevant inspection and test reports / RFIs.
 </li>
 <li>
 Ensuring the quality of manufacturing and erection works, dimensional accuracy and orientation, accessory and inline items installed in the correct orientation and material design specification.
 </li>
 <li>
 Lead the EPIC construction contractor(s) on all mechanical aspects of the piping works.
 </li>
 <li>
 Supervise with EPIC contractor during execution of the piping installation, line check, punch clearing, hydrotest and re-instatement at site.
 </li>
 <li>
 Manage and lead final mechanical completion inspections and punch closing.
 </li>
 <li>
 Supervise the Pre-Com activities to ensure safety and the quality of the completed work.
 </li>
 <li>
 Undertake technical integrity and HSE reviews/audits
 </li>
 <li>
 Participate in process safety management
 </li>
 <li>
 Participate in PSSR and provide support to Operations pre &amp; start up activity where instructed.
 </li>
 <li>
 Co-ordinate mobilization of contractors on site.
 </li>
 <li>
 Carryout daily checks on contractor&rsquo;s staff and work carried out during the previous day in order to ensure compliance with prescribed contractual specifications.
 </li>
 <li>
 Good knowledge in reading and understanding P&amp;ID, GA, ISOs, piping standard drawings (incl support drawings) and Equipment Layout drawings.
 </li>
 <li>
 Maintain a daily record of progress (daily diary) noting special comments. Reports to Snr Supervisor work anomalies or contractual deviations committed by contractor personnel and recommend corrective actions.
 </li>
 <li>
 Sign work permits on behalf of Company and to ensure that contractor&rsquo;s compliance with work permits.
 </li>
 <li>
 Participate in development of as-built drawings/documentation.
 </li>
 <li>
 Accountable for supervising contractor&rsquo;s work that is in progress, inspecting work, reporting problems and preventing accidents occurring because of negligence, by enforcing Company safety standards on the work site.
 </li>
 <li>
 Liaise and report with the QA/QC Inspector on quality related matters
 </li>
 </ul>
</div>

Construction Supervisor (Piping)

<div><div><div>Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana&trade; Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing NavIQ&trade;, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&amp;D and manufacturing center in Doha, Qatar.</div>
<div></div><div>ABOUT SHIFAMED</div>
<div>Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.</div>
</div><div></div>Description:
This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&amp;D, and Executive Leadership to support U.S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands-on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.
Responsibilities, Skills &amp; Hands-On Experience:
 
Regulatory Strategy &amp; Product Development:
<ul><li>Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies.</li>
<li>Serve as regulatory lead on cross-functional product development teams from concept through commercialization.</li>
<li>Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes.</li>
<li>Partner with Quality and R&amp;D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements.</li>
</ul>FDA Regulatory Affairs
<ul><li>Lead preparation, review, and submission of U.S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable.</li>
<li>Monitor evolving FDA requirements and assess impact on development and commercialization plans.</li>
</ul>International Regulatory Expansion
<ul><li>Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets.</li>
<li>Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants.</li>
<li>Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries.</li>
<li>Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners.</li>
</ul>Clinical &amp; Regulatory Operations
<ul><li>Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies.</li>
<li>Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways.</li>
<li>Support regulatory submissions associated with clinical trial approvals across multiple countries and regions.</li>
<li>Participate in investigator meetings, regulatory inspections, audits, and agency interactions.</li>
</ul>Agency Interactions &amp; Compliance
<ul><li>Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities.</li>
<li>Support preparation for regulatory inspections and audits.</li>
<li>Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership.</li>
<li>Contribute to regulatory intelligence activities and long-term market expansion planning.</li>
</ul>Cross-Functional Leadership
<ul><li>Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&amp;D teams to ensure regulatory requirements are incorporated throughout the product lifecycle.</li>
<li>Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities.</li>
<li>Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.</li>
</ul>Qualifications &amp; Experience:
<ul><li>Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.</li>
<li>10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred.</li>
<li>Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements.</li>
<li>Experience supporting clinical-stage medical device programs and global clinical studies.</li>
<li>Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks.</li>
<li>Experience interacting directly with regulatory agencies, notified bodies, and international health authorities.</li>
<li>Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable.</li>
<li>Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development.</li>
<li>Excellent written, verbal, and presentation skills.</li>
<li>Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams.</li>
</ul>Preferred Qualifications:
<ul><li>Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies.</li>
<li>Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets.</li>
<li>Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.</li>
</ul>
<div></div><div><div>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.</div>
<div></div><div>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.</div></div></div>

Manager / Sr. Manager, Regulatory Affairs

Shifamed

<div>
 Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana&trade; Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing NavIQ&trade;, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&amp;D and manufacturing center in Doha, Qatar.
 
 
 
 About Shifamed
 
 
 
 Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.
 
 
 Description:
 
 
 This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&amp;D, and Executive Leadership to support U.S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands-on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.
 
 
 Responsibilities, Skills &amp; Hands-On Experience:
 
 
 Regulatory Strategy &amp; Product Development:
 
 
 <ul>
 <li>
 Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies.
 </li>
 <li>
 Serve as regulatory lead on cross-functional product development teams from concept through commercialization.
 </li>
 <li>
 Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes.
 </li>
 <li>
 Partner with Quality and R&amp;D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements.
 
 
 
 </li>
 </ul>
 FDA Regulatory Affairs
 
 
 <ul>
 <li>
 Lead preparation, review, and submission of U.S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable.
 </li>
 <li>
 Monitor evolving FDA requirements and assess impact on development and commercialization plans.
 
 
 
 </li>
 </ul>
 International Regulatory Expansion
 
 
 <ul>
 <li>
 Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets.
 </li>
 <li>
 Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants.
 </li>
 <li>
 Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries.
 </li>
 <li>
 Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners.
 
 
 
 </li>
 </ul>
 Clinical &amp; Regulatory Operations
 
 
 <ul>
 <li>
 Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies.
 </li>
 <li>
 Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways.
 </li>
 <li>
 Support regulatory submissions associated with clinical trial approvals across multiple countries and regions.
 </li>
 <li>
 Participate in investigator meetings, regulatory inspections, audits, and agency interactions.
 
 
 
 </li>
 </ul>
 Agency Interactions &amp; Compliance
 
 
 <ul>
 <li>
 Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities.
 </li>
 <li>
 Support preparation for regulatory inspections and audits.
 </li>
 <li>
 Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership.
 </li>
 <li>
 Contribute to regulatory intelligence activities and long-term market expansion planning.
 
 
 
 </li>
 </ul>
 Cross-Functional Leadership
 
 
 <ul>
 <li>
 Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&amp;D teams to ensure regulatory requirements are incorporated throughout the product lifecycle.
 </li>
 <li>
 Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities.
 </li>
 <li>
 Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.
 
 
 
 </li>
 </ul>
 Qualifications &amp; Experience:
 
 
 <ul>
 <li>
 Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.
 </li>
 <li>
 10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred.
 </li>
 <li>
 Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements.
 </li>
 <li>
 Experience supporting clinical-stage medical device programs and global clinical studies.
 </li>
 <li>
 Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks.
 </li>
 <li>
 Experience interacting directly with regulatory agencies, notified bodies, and international health authorities.
 </li>
 <li>
 Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable.
 </li>
 <li>
 Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development.
 </li>
 <li>
 Excellent written, verbal, and presentation skills.
 </li>
 <li>
 Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams.
 
 
 
 </li>
 </ul>
 Preferred Qualifications:
 
 
 <ul>
 <li>
 Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies.
 </li>
 <li>
 Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets.
 </li>
 <li>
 Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.
 
 
 
 </li>
 </ul>
 Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.
 
 
 NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
</div>

Aamal Services

Required Position: Facilities Management (FM) Civil SupervisorCompany: Maintenance and Management Solutions(MMS)A Civil Supervisor focusing on finishing works oversees the final, detailed stages of construction to ensure high-quality aesthetics and functionality before project handover. They bridge the gap between structural completion and occupancy, managing tasks like painting, tiling, plastering, and carpentry. [1, 2, 3, 4, 5]Key Responsibilities &amp; Duties<ul><li>Finishing Supervision: Monitor and direct daily activities for finishing trades (blockwork, plastering, tiling, painting, gypsum, and carpentry).</li><li>Quality Control: Inspect completed works to ensure compliance with drawings, specifications, and client standards.</li><li>Punch List Management: Identify, track, and close out snagging/punch list items prior to final handover.</li><li>Resource Coordination: Manage site manpower, materials, and equipment to meet tight finishing deadlines.</li><li>Safety Compliance: Ensure all finishing activities strictly adhere to Occupational Health and Safety (HSE) standards.</li><li>Documentation: Prepare daily/weekly progress reports, maintain as-built records, and support engineer documentation. [1, 2, 3, 4, 5]</li></ul>Required Qualifications &amp; Skills<ul><li>Experience: 3&ndash;10+ years of experience in civil supervision, specifically in interior fit-out, residential villas, or commercial finishing.</li><li>Technical Knowledge: Proficiency in reading construction blueprints, interior design drawings, and elevation drawings.</li><li>Education: Diploma in Civil Engineering or equivalent technical certification.</li><li>Leadership: Strong leadership skills to direct, train, and manage subcontractors and trade foremen.</li><li>Communication: Proficiency in English (Hindi/Arabic is a plus) for coordinating with multicultural teams. [1, 2, 3, 4, 5, 6, 7]</li></ul>Common Job Requirements in Qatar (May 2026)<ul><li>Location: Doha, Qatar (Multiple opportunities for [Fit-out] and [Maintenance] supervisors).</li><li>Industry: Facilities Management, Construction, and Interior Fit-Out companies.</li><li>Special Requirements: Often requires PTW (Permit to Work) authorization and knowledge of high-end finishes (glass, stone).</li><li>Salary Range: Frequently listed between QAR 3,500 &ndash; QAR 6,000, depending on experience and role scope. [1, 2, 3, 4, 5]</li></ul>Typical Job Titles<ul><li>Interior Fit-Out &amp; Finishing Supervisor</li><li>Facilities Management (FM) Civil Supervisor</li></ul>Job Type: PermanentPay: QAR1.00 per monthWork Location: In person

Civil Supervisor

<div>
 Airswift are a Global Manpower Provider specialising in the Energy, Infrastructure &amp; IT sectors. Present in more than 70 countries around the world, our reach, and capabilities in the markets we service is unparalleled in the industry.
 
 
 We are working with a national operator to source a
 
 Construction Supervisor (Building)
 
 . This is a long-term contract role working on a residential basis. Please see details below.
 
 
 Title:
 
 Construction Supervisor (Building)
 
 
 
 Start Date: ASAP (typically within 1 month notice)
 
 
 Location: Qatar Site - Mesaieed
 
 
 Working Schedule: 6 days per week / 8-10 hours per day or as per project requirements.
 
 
 
 Experience Required
 
 
 
 Key Job Accountabilities
 
 
 <ul>
 <li>
 To supervise the EPIC Contractors during the execution of construction activities at construction site.
 </li>
 <li>
 Participate in reviewing detailed design drawings, method statements, material requisitions, and etc.
 </li>
 <li>
 Co-ordinate mobilization of contractors on site.
 </li>
 <li>
 Supervise and approve construction activities and co-ordinate various aspects of project construction including inspections, material submissions and working drawings from contractors, and processing documentation as required.
 </li>
 <li>
 Carryout daily checks on contractor&rsquo;s staff and work carried out during the previous day in order to ensure compliance with prescribed contractual specifications.
 </li>
 <li>
 Handle all aspects of Mechanical Construction activities including site investigations, site surveys and etc.
 </li>
 <li>
 Supervise installation of Fire Electric/Diesel Pumps and Jockey pumps.
 </li>
 <li>
 Supervise installation of deluge system piping works and underground firefighting piping works.
 </li>
 <li>
 Supervise installation of Fire water tanks.
 </li>
 <li>
 Good knowledge in Deluge and Sprinkler System.
 </li>
 <li>
 Maintain a daily record of progress (daily diary) noting special comments. Reports to supervisor work anomalies or contractual deviations committed by contractor personnel and recommend corrective actions.
 </li>
 <li>
 Sign work permits on behalf of CLIENT and to ensure that contractors compliance with conditions fixed on consolidated work permits
 </li>
 <li>
 Participate in development of as-built drawings/documentation.
 </li>
 <li>
 Prepare Punch list for finished work prior to hand over to CLIENT by contractor by paying special attention to all equipment including Quality checks.
 </li>
 <li>
 Works closely with other CLIENT Construction Supervisors (Elect/ Arch / Instrument).
 </li>
 <li>
 Report to CLIENT Senior Construction Supervisor on main issues, events at site, progress reporting, trends and recommendation for improvement.
 </li>
 <li>
 Accountable for supervising contractor&rsquo;s work that is in progress, inspecting work, reporting problems and preventing accidents occurring as a result of negligence, by enforcing CLIENT safety standards on the work site.
 </li>
 <li>
 Liaise and report with the QC Inspector on quality related matters.
 </li>
 <li>
 Liaise with the HSE Supervisor on safety related matters.
 </li>
 <li>
 To prepare daily report of activities and inform CLIENT/asset holders (as per approved distribution matrix) of the progress/constraints and look ahead.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 --Minimum Requirements--
 
 
 <ul>
 <li>
 Candidate must possess a Degree or Diploma in Mechanical Engineering from an internationally recognized University.
 
 
 </li>
 </ul>
 Knowledge and Key Skills
 
 
 <ul>
 <li>
 Candidate should have a minimum of 10 to 15 years overall experience in Construction of EHV Substations up to 132kV and above with exposure to mechanical works connected with substation Electrical equipment, HVAC equipment, Fire alarm &amp; Loss prevention and Building Services.
 </li>
 <li>
 Must have good verbal and written communication skills to interface and communicate with internal and external departments, agencies, contractors and vendors.
 
 
 </li>
 </ul>
 If you would like to be considered for the position, please apply direct to this advertisement with your CV with contact details.
</div>

Construction Supervisor (Building)

Swan Global WLL

HIRING &ndash; MECHANICAL SUPERVISOR (Rigging) Location - RLICDuration : 1 yearWorking hours : 5 days and 8 hours per dayMax Salary: QAR 4,000/monthFood + Transport + Accommodation: By ClientRequirements:<ul><li>Supervise all rigging, lifting &amp; field maintenance activities</li><li>Plan and execute lifts in compliance with QHSSE requirements</li><li>Coordinate with engineering, HSE and operations teams</li><li>Minimum 5+ years as Mechanical/Rigging Supervisor in O&amp;G or LNG</li><li>Strong knowledge of lifting equipment, PTW, and LOTO</li><li>QatarEnergy, RLIC or LNG plant experience preferred</li><li>English language proficiency required</li></ul>Pay: QAR4,000.00 per monthApplication Question(s):<ul><li>Freelance or company visa?</li></ul>Work Location: In person

Mechanical Supervisor

Explore 35+ Biomedical supervisor in Doha this July. Find roles across top companies and apply now to boost your career.

35 biomedical supervisor jobs In Doha

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