laboratory specialist

Anotech

<div>
 
 
 Job Purpose:
 
 
 
 
 
 
 
 
 
 Responsible for overseeing and managing all aspects of preparing all necessary laboratory equipment, Manuals and Operating Procedures, and ensuring the laboratory is available and fully operational for plant Start-up: personnel, equipment and adequate supply of chemicals and consumables. Reports directly to the Commissioning &amp; Start-up Methods Lead. The Laboratory Specialist shall develop and implement the permanent Laboratory Information Management System. They shall also ensure mentorship and training of the routine operation laboratory personne
 
 
 
 
 
 
 l
 
 
 
 
 Job Responsibilitie
 
 
 
 
 
 
 s:
 
 
 Commissioning and Start-up preparat
 
 <ul>
 <li>
 ionEnsure design meets all the operational and HSE requireme
 </li>
 <li>
 ntsOrganize laboratory equipment reception and equipment storage. Follow-up on missing and downgraded equipment with Contractor and / or Vendor commissioning procedures, test plans, and system handover documentat
 </li>
 <li>
 ionActively participate in the laboratory pre-commissioning and commissioning. Record punch items and follow-up on punch list clearance with the objective of ensuring the laboratory is available to support plant start
 </li>
 <li>
 -upIdentify potentially required specific analyses which will not be possible on site, and elaborate means and procedures to perform those analyses (sub-contracting to third party laborator
 </li>
 <li>
 iesReview and adjust (with equipment Vendor), calibration of all the laboratory equipm
 </li>
 </ul>
 
 
 
 
 ent
 
 
 Commissioning and Start-up execu
 
 <ul>
 <li>
 tionSupervise Commissioning of all the laboratory equip
 </li>
 <li>
 mentEnsures Laboratory is available and fully operational for plant start-up: personnel, equipment and adequate supplies of chemicals and consuma
 </li>
 <li>
 blesImplement laboratory waste handling in line with site waste management philosophy validated by the HSE depart
 </li>
 <li>
 mentDuring early operation, supervising all laboratory work methods, test analyses, data interpretation, analysis of products quality, refrigerant and effluent w
 </li>
 <li>
 asteDuring early operation, direct and co-ordinate all sampling and testing activities of laboratory, including determining methods of analysis, problem solving and troubleshooting upcoming is
 </li>
 <li>
 suesHandover an established and fully operational laboratory facility to the routing laboratory opera
 </li>
 <li>
 tionAssistance for closed loop start-up and monitoring of the fluid quality in
 </li>
 <li>
 sideParticipate to commissioning activities: Network cleanliness monitoring during flushing operation (closed loops, chemical injection lines); lubricant or hydraulic fluids cleanliness anal
 </li>
 </ul>
 
 
 
 
 
 ysis
 
 
 
 
 Qualifications And Experi
 
 
 
 
 
 <ul>
 <li>
 ence:
 </li>
 <li>
 Master&rsquo;s Degree in Chemical or Petroleum Engin
 </li>
 <li>
 eering15+ years&rsquo; experience in the Oil &amp; Gas industry with a full understanding of laboratory activities and procedures, expertise in laboratory discipline. Experience in projects with large onshore plants and LNG plants is
 </li>
 <li>
 a plus5+ years in an LNG plant laboratory in a supervisory role in a multi-cultural envir
 </li>
 <li>
 onmentTechnical Competencies: Production operations, Laboratory activities, Process operations, Regulations, Certifications, Commissioning and start-up of O&amp;G facilities, Safety of personnel and installations, Maintenance / Inspection, SIMOPS, Operational contract management, Construction, instal
 </li>
 </ul>
 
 
 
 
 lation
 
</div>

CSU - Laboratory Specialist

Smart Research System

Assistant Laboratory Specialist &ndash; Roads &amp; BridgesAbu DhabiJob Summary:We are seeking a detail-oriented Assistant Laboratory Specialist to support materials testing and quality control activities for Roads &amp; Bridges projects. The role ensures that all construction materials and workmanship comply with project specifications, standards, and regulatory requirements through accurate laboratory testing and reporting.Key Responsibilities:<ul><li>Assist in conducting laboratory and field tests on construction materials such as soil, asphalt, concrete, aggregates, and steel</li><li>Support quality control inspections for Roads &amp; Bridges construction activities</li><li>Ensure all testing is carried out in accordance with approved standards (ASTM, BS, AASHTO, or local authority requirements)</li><li>Record, analyze, and report test results accurately and in a timely manner</li><li>Assist in calibration and maintenance of laboratory equipment</li><li>Ensure proper sample collection, labeling, storage, and tracking procedures</li><li>Support senior laboratory specialists and QA/QC engineers in investigations of non-conformities</li><li>Maintain laboratory documentation, logs, and quality records</li><li>Ensure compliance with health, safety, and environmental procedures in the laboratory</li><li>Coordinate with site teams to ensure material approvals and compliance with specifications</li><li>Assist in preparing laboratory reports for submission to consultants and project management</li></ul>Qualifications &amp; Requirements:<ul><li>Diploma or Bachelor&rsquo;s degree in Civil Engineering, Materials Engineering, or related field</li><li>Minimum 3&ndash;7 years of experience in construction materials testing or laboratory work</li><li>Experience in Roads &amp; Bridges or large infrastructure projects is preferred</li><li>Knowledge of laboratory testing standards (ASTM, BS, AASHTO)</li><li>Familiarity with QA/QC procedures in construction projects</li><li>Strong attention to detail and accuracy in reporting</li><li>Ability to work in a fast-paced site and laboratory environment</li><li>Basic understanding of construction materials and mix designs</li><li>Good communication and coordination skills</li><li>Certification in laboratory testing (preferred but not mandatory)</li></ul>Key Competencies:<ul><li>Materials Testing &amp; Analysis</li><li>Quality Control &amp; Assurance</li><li>Attention to Detail</li><li>Compliance &amp; Standards Adherence</li><li>Reporting &amp; Documentation</li><li>Team Coordination</li></ul>Pay: AED4,000.00 - AED6,000.00 per monthWork Location: In person

Assistant Laboratory Specialist – Roads & Bridges

CHRISTUS Health

<div>Description 
Summary:
Performs clinical testing in assigned section/s such as general laboratory, Blood Bank and Microbiology sections, with all duties necessary for accurate and timely results including quality control, performance improvement, proficiency testing, and preventative maintenance of equipment. Recognizes abnormal critical values and follows proper guidelines for notifying medical team members of results. Performs clerical, general, and phlebotomy duties related to daily operations in the laboratory. Provides/dispenses blood products as requested by medical staff.
Responsibilities: 
<ul><li>Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders.
</li><li>Ensures that the company philosophy and core values are evident in the service delivered to customers.
</li><li>Specimen Collection/Handling/Processing&ndash; obtains blood specimens via venipuncture and/or fingerstick, accurately identifies and labels appropriately; answers pneumatic tube system; follows procedures for processing and testing specimens, including operating various centrifuges; obtains other designated patient specimens as listed in procedure manuals.
</li><li>Result Reporting &ndash; recognizes errors or improbable results and takes appropriate action; reports critical values per Policy and Procedure; performs tests within established timeframe; performs laboratory testing, if designated, in the following sections: Hematology, Urinalysis, Coagulation, Chemistry, Special Chemistry, ER Stat Lab, and Microbiology; performs blood bank procedures, including crossmatching, ab id&rsquo;s, and dispensing of blood products; operates laboratory automated analyzers according to established procedures.
</li><li>Performs, analyzes, and records QC according to Policy &amp; Procedure following CLIA, CAP, AABB, and JCAHO guidelines; performs and records Performance Improvement indicators and reports results.
</li><li>Performs established daily and periodic preventative maintenance with documentation; troubleshoots minor problems and initiates service calls as needed; orders (or notifies assigned associate) and restocks supplies/reagents; reviews policy &amp; procedure manual; dates reagents and discards expired reagents.
</li><li>Takes responsibility for seeking and achieving professional growth and continued education.
</li><li>Assists in training new associates and students in Laboratory practices.
</li><li>Follows CAP, AABB, Compliance, CLIA, JCAHO, and OSHA standards.
</li><li>Follows established protocols for safety, infection control, security, compliance, and the use of hazardous materials.
</li><li>Utilizes LIS and HIS computer systems appropriately to perform, charge, and report laboratory results.
</li><li>Completes annual competency assessment successfully and by assigned date.</li></ul>
Job Requirements: 
Education/Skills
<ul><li>Associates Degree or higher in clinical laboratory science or medical laboratory technology from an accredited institution or equivalent laboratory training and experience meeting the requirements defined in the CLIA regulation 42CFR493.1489:
<ul><li>Successfully completed an official U.S. military medical laboratory procedures training course of at least 50 weeks duration and currently hold the military enlisted occupational specialty of medical laboratory specialist (laboratory technician);
OR
</li><li>60 semester hours or equivalent from an accredited institution that, at a minimum, includes either 24 semester hours of medical laboratory technology courses, OR 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology, and 12 semester hours of chemistry, biology or medical laboratory technology in any combination;
AND
</li><li>Laboratory training including either completion of a clinical laboratory training program approved or accredited by the ABHES, NAACLS, or other organization approved by HHS (note that this training may be included in the 60 semester hours listed above), or at least three months documented laboratory training in each specialty in which the individual performs high complexity testing.
</li></ul></li></ul>Experience
<ul><li>No experience required for graduates of a clinical laboratory training program approved or accredited by NAACLS, or other organizations approved by HHS.
OR
</li><li>Six Months of approved clinical laboratory experience, which must include a clinical rotation through the following sections of the laboratory: Blood Banking, Microbiology, Chemistry, and Hematology, Immunology, and Urinalysis/Body Fluids in the U.S. or with an accredited laboratory within the last 5 years. (This meets the AMT MLT eligibility requirement).</li>
</ul>Licenses, Registrations, or Certifications
<ul><li>Louisiana requires State Licensure.</li>
<li>New Graduate that is Board Certified or eligible (must complete Board Certification in 1 year of hire, Louisiana excluded).</li></ul> 
Work Schedule: 
PRN
Work Type: 
Per Diem As Needed</div>

Medical Laboratory Technician I - Lab AdminGeneral

<div>Description 
Summary:
The Medical Laboratory Technician II performs complex clinical testing in assigned section/s such as general laboratory, Blood Bank, and Microbiology sections, with all duties necessary for accurate and timely results including quality control, performance improvement, proficiency testing, and preventative maintenance of equipment. Associates in this job recognize abnormal critical values and follow proper guidelines for notifying medical team members of results. Performs clerical, general, and phlebotomy duties related to daily operations in the laboratory. Provides/dispenses blood products as requested by medical staff.
Responsibilities: 
<ul><li>Meets expectations of the applicable OneCHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders.</li></ul>
<ul><li>Specimen Collection/Handling/Processing&ndash; obtains blood specimens via venipuncture and/or fingerstick, accurately identifies and labels appropriately; answers pneumatic tube system; follows procedures for processing and testing specimens, including operating various centrifuges; obtains other designated patient specimens as listed in procedure manuals.</li><li>
Result Reporting &ndash; recognizes errors or improbable results and takes appropriate action; reports critical values per Policy and Procedure; performs tests within established timeframe; performs laboratory testing, if designated, in the following sections: Hematology, Urinalysis, Coagulation, Chemistry, Special Chemistry, ER Stat Lab, and Microbiology; performs blood bank procedures, including crossmatching, ab id&rsquo;s, and dispensing of blood products; operates laboratory automated analyzers according to established procedures.</li><li>
Performs, analyzes, and records QC according to Policy &amp; Procedure following CLIA, CAP, AABB, and JCAHO guidelines; performs and records Performance Improvement indicators and reports results.</li><li>
Performs established daily and periodic preventative maintenance with documentation; troubleshoots minor problems and initiates service calls as needed; orders (or notifies assigned associate) and restocks supplies/reagents; reviews policy &amp; procedure manual; dates reagents and discards expired reagents.</li></ul>
<ul><li>Takes responsibility for seeking and achieving professional growth and continued education.</li><li>
Assists in training new associates and students in Laboratory practices.</li></ul>
<ul><li>Follows CAP, AABB, Compliance, CLIA, JCAHO, and OSHA standards.</li><li>
Follows established protocols for safety, infection control, security, compliance, and the use of hazardous materials.</li><li>
Utilizes LIS and HIS computer systems appropriately to perform, charge, and report laboratory results.</li><li>
Completes annual competency assessment successfully and by assigned date.</li></ul>
Job Requirements: 
Education/Skills
<ul><li>Associate degree or higher in clinical laboratory science or medical laboratory technology from an accredited institution or equivalent laboratory training and experience meeting the requirements defined in the CLIA regulation 42CFR493.1489:
<ul><li>Successfully completed an official U.S. military medical laboratory procedures training course of at least 50 weeks duration and currently hold the military enlisted occupational specialty of medical laboratory specialist (laboratory technician);
OR
</li><li>60 semester hours or equivalent from an accredited institution that, at a minimum, includes either 24 semester hours of medical laboratory technology courses, OR 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology, and 12 semester hours of chemistry, biology or medical laboratory technology in any combination;
AND
</li><li>Laboratory training including either completion of a clinical laboratory training program approved or accredited by the ABHES, NAACLS, or other organization approved by HHS (note that this training may be included in the 60 semester hours listed above), or at least three months documented laboratory training in each specialty in which the individual performs high complexity testing.
</li></ul></li></ul>Experience
<ul><li>No experience required for graduates of a clinical laboratory training program approved or accredited by NAACLS, or other organizations approved by HHS.
OR
</li><li>Six Months of approved clinical laboratory experience, which must include a clinical rotation through the following sections of the laboratory: Blood Banking, Microbiology, Chemistry, and Hematology, Immunology, and Urinalysis/Body Fluids in the U.S. or with an accredited laboratory within the last 5 years. (This meets the AMT MLT eligibility requirement)
AND
</li><li>less than 5 years of experience as a Medical Laboratory Technician (MLT).
</li></ul>Licenses, Registrations, or Certifications
<ul><li>MLT from ASCP, AMT, AAB, or HEW/HHS required.
</li><li>If certification with an expiration date is held, the certification must be maintained and kept current.
</li><li>Louisiana requires State Licensure.
</li><li>New Graduate that is Board Certified or eligible (must complete Board Certification within 1 year of hire, Louisiana excluded).</li></ul> 
Work Schedule: 
5 Days - 8 Hours
Work Type: 
Full Time</div>

Medical Laboratory Technician II - Lab AdminGeneral

Nawah Scientific

<div>
 
 Job Brief
 
 
 
 We're seeking for
 
 R&amp;D Methodology Specialist
 
 who will be responsible for sample testing, data recording and performing routine checks to ensure the quality and integrity of data.
 
 
 
 Job Description
 
 
 
 
 Laboratory Performance
 
 
 
 <ul>
 <li>
 Participate in all lab performance activities and, whenever applicable, compliance of lab activities with ISO/IEC 17025/GLP requirements.
 </li>
 <li>
 Implementing laboratory procedures effectively to control lab activities.
 </li>
 <li>
 Execute the approved internal quality control program to ensure proper control of technical processes.
 </li>
 <li>
 Execute equipment operation protocols, intermediate check procedures, and maintenance plan.Record results daily and report immediately any malfunction or abnormal results.
 </li>
 <li>
 Implement environmental monitoring program to affirm compliance with laboratory safety protocols and international regulations and maintain clean laboratory conditions.
 
 
 </li>
 </ul>
 
 External Customers
 
 
 
 <ul>
 <li>
 Provides, when required, clarifications and answers to customer inquiries to attain customer satisfaction.
 
 
 </li>
 </ul>
 
 External Suppliers and Services
 
 
 
 <ul>
 <li>
 Report on the unavailability of any lab supplies and write purchasing requests for missed products including supplies specifications.
 </li>
 <li>
 Analyze Proficiency Test (PT) samples according to provider instructions and document sample results.
 
 
 </li>
 </ul>
 
 Improvement
 
 
 
 <ul>
 <li>
 Provide suggestions for laboratory operation improvement.
 </li>
 <li>
 Stay up to date with Scientific updates/ regulatory requirements.
 
 
 </li>
 </ul>
 
 Sample Testing Activities
 
 
 
 <ul>
 <li>
 Analyze laboratory samples according to laboratory procedures, customer test request, and Lab head instructions to produce reliable results.
 </li>
 <li>
 Read and record samples results in appropriate technical forms.
 </li>
 <li>
 Execute method verification/validation protocols.
 
 
 </li>
 </ul>
 
 Must-have
 
 
 
 
 Job requirements:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in any of the following: Biotechnology, Science, Pharmacy or relevant scientific speciality.
 </li>
 <li>
 At least 4 years of Methodology experience in Pharmaceutical company or QC laboratories.
 </li>
 <li>
 Good command of both written and spoken in English.
 </li>
 <li>
 Strong attention to detail and accuracy in analytical work.
 </li>
 <li>
 Adhere to ICH, WHO, USP, and cGMP requirements in daily work.
 </li>
 <li>
 Effective communication and teamwork skills.
 </li>
 <li>
 Good problem-solving and troubleshooting skills.
 </li>
 <li>
 Ability to handle multiple projects and meet deadlines.
 </li>
 <li>
 Detail-oriented with strong documentation practices.
 
 
 </li>
 </ul>
 
 Nice To Have
 
 
 
 <ul>
 <li>
 Experience in HPLC/GC operations.
 </li>
 <li>
 Familiarity with chromatographic and spectroscopic techniques.
 
 
 </li>
 </ul>
 
 What We Offer
 
 
 
 <ul>
 <li>
 Work with a supportive and energetic team in a dynamic research environment that fosters collaboration and innovation.
 </li>
 <li>
 Enjoy annual salary increases and additional benefits based on your performance and contribution.
 </li>
 <li>
 Receive an annual family bonus as a token of appreciation for your loyalty and commitment to the company.
 </li>
 <li>
 Earn a great quarterly incentive for achieving your goals and exceeding expectations.
 </li>
 <li>
 Benefit from comprehensive social and medical insurance coverage for you.
 </li>
 <li>
 Participate in an annual cycle meeting to review your progress and plan your future development.
 </li>
 </ul>
</div>

Research Specialist - R&D Methodology Lab

Aspetar سبيتار

<div>
 
 
 
 Role Purpose:
 
 
 
 
 To provide support to the Orthobiologics Laboratory in the day to day running and regulatory compliance of the cellular therapies facility and associated clinical activities; to perform technical laboratory functions in specialty areas specific to his/her competency and as determined by the Management of the Laboratory Department.
 
 
 
 
 
 
 
 Key Accountabilities &amp; Activities:
 
 
 
 <ul>
 <li>
 Adherence and compliance with cleanroom regulations that focus on aseptic techniques in cleanroom facilities.
 </li>
 <li>
 Perform GMP Manipulation in Clean Rooms following accreditation standards and perform aseptic tissue processing and production of cellular therapies for clinical use, ensuring that harvested tissue is safely retrieved, processed, and destroyed according to the documented procedures.
 </li>
 <li>
 Comply with protocols for the culture and transplantation of different cell sources for use in the orthopaedic setting.
 </li>
 <li>
 Be skilled and certified in cleanroom cell therapy Lab, able to aseptically prepare tissue culture media, supplements, and reagents.
 </li>
 <li>
 Acquiring and analyzing specimen data by flow cytometer.
 </li>
 <li>
 Perform quality control procedures, verify, document, and validate the accuracy of the laboratory data to assess the reproducibility and validity of current laboratory methods.
 </li>
 <li>
 Monitor Key Performance Indicators for cleanroom facility.
 </li>
 <li>
 Participate in the routine maintenance of the clean room environment and ancillary facilities, including equipment checks and calibration, environmental monitoring and cleaning as directed in SOPs.
 </li>
 <li>
 To have, to acquire and to develop specialist skills to recognize anomalies and ensure these are communicated / documented properly and be able to undertake investigation and remedial action, if directed to do so.
 </li>
 <li>
 Maintain strict confidentiality and proper storage and back-up of patient records and test results.
 </li>
 <li>
 Assist in the development of research protocols and procedures.
 </li>
 <li>
 Assists with evaluation and implementation of relevant new laboratory services.
 </li>
 <li>
 Participate in quality improvement and quality surveillance activities within Aspetar, including audits and inspections.
 </li>
 <li>
 Interact with other staff to solve problems and interpret patients&rsquo; laboratory results within the framework of the Orthobiological Laboratory.
 </li>
 <li>
 Review and maintain internal and external laboratory safety programmes, including safe handling and proper disposal of specimens and other laboratory materials, and implementing of corrective actions, when necessary, in compliance with statutory requirements.
 </li>
 <li>
 Assist in environmental monitoring procedures (measure, monitor and accurately record), using agreed quality control procedures, other duties related to QA.
 </li>
 <li>
 Monthly review of building management system documents for Liquid Nitrogen levels and temperatures in cryogenic tanks.
 </li>
 <li>
 Ensure the health, safety and welfare of fellow employees, visitors and contractors, so far as is reasonably practicable.
 </li>
 <li>
 Participate in Laboratory as well as Hospital Training and Education Programs.
 </li>
 <li>
 Provide appropriate training to other employees, as required.
 </li>
 <li>
 Process human samples using validated protocols and techniques with a high degree of competency.
 </li>
 <li>
 Record and maintain complete documentation throughout all phases of laboratory testing according to Laboratory and/or Hospital requirements.
 </li>
 <li>
 Record and maintain effective inventory control to ensure uninterrupted workflow.
 </li>
 <li>
 Record applicable patient data/results in Laboratory Information System.
 </li>
 <li>
 Inform the Laboratory Director in case of any procedural discrepancies for appropriate action.
 </li>
 <li>
 Participate in preparing the laboratory for accreditation by national and international bodies.
 </li>
 <li>
 Comply with national and international accreditation requirements.
 </li>
 <li>
 Comply with policies set down by the Qatar Ministry of Public Health and the Aspetar Hospital.
 </li>
 <li>
 Ensure compliance with relevant accreditation standards, laboratory safety regulations and quality control / quality assurance programs.
 </li>
 <li>
 Demonstrate a commitment to providing a quality service.
 </li>
 <li>
 Comply with employee obligations regarding Occupational Health and Safety, Infection Prevention and Control and Quality Improvement as set down in Aspetar Hospital&rsquo;s Policy and Procedure Manual.
 </li>
 <li>
 Maintain confidentiality in relation to discussions, disclosure of records, and information concerning the Aspetar.
 </li>
 <li>
 Maintain a discrimination and harassment free workplace.
 </li>
 <li>
 Comply with responsibilities listed under the Aspetar&rsquo;s Code of Conduct.
 </li>
 <li>
 Assume any other responsibilities as directed by the direct supervisor.
 </li>
 </ul>
 
 
 
 
 
 
 Necessary knowledge and Experience to be able to do the job:
 
 
 
 <ul>
 <li>
 Minimum experience of 5-7 years in which 2-3 years should be in a similar position / responsibility, preferably in a similar Industry.
 </li>
 <li>
 Must be well experienced and have sufficient knowledge of Orthobiological laboratory methods and techniques relevant to his/her specific job description.
 </li>
 <li>
 Must have specialised knowledge and experience related to handling / processing aseptic tissues, i.e. Stem cell culture, sub culturing, cell count, cell viability assay, cell maintenance &amp; cell freezing.
 </li>
 </ul>
 
 
 
 
 
 
 
 Skills and Abilities:
 
 
 
 
 <ul>
 <li>
 Excellent hand and eye co-ordination required, i.e. able to manipulate aseptic materials within isolators / laminar flow cabinets;
 </li>
 <li>
 Able to work in a restricted position for a substantial proportion of the working time.
 </li>
 <li>
 Meticulous and pays attention to detail.
 </li>
 <li>
 Ability to work shifts and demonstrable willingness to be placed on a 24-hour on-call roster, if required.
 </li>
 <li>
 Good interpersonal and communication skills.
 </li>
 <li>
 Good understanding of sciences and fundamental scientific principles related to orthobiological processes and analysis.
 </li>
 <li>
 Ability to work well as part of a multi-disciplinary team.
 </li>
 <li>
 Ability to work independently with initiative and to be adaptive to changes.
 </li>
 <li>
 Ability to multi-task and to work with frequent interruptions.
 </li>
 <li>
 Ability to work well under pressure.
 </li>
 <li>
 Previous experience working in the Middle East or within another culture or remote settings is preferable.
 </li>
 </ul>
 
 
 
 
 
 
 Education and Certification requirements:
 
 
 
 <ul>
 <li>
 Bachelor of Medical Laboratory Science/Technology or any other related filed.
 </li>
 <li>
 Fulfil all licensing requirements if required. Relevant Medical Licensure.
 </li>
 </ul>
 
 
 
</div>

Medical Technologist – Orthobiologic

سبيتار

<div>Role Purpose:
To provide support to the Orthobiologics Laboratory in the day to day running and regulatory compliance of the cellular therapies facility and associated clinical activities; to perform technical laboratory functions in specialty areas specific to his/her competency and as determined by the Management of the Laboratory Department.
Key Accountabilities &amp; Activities:
<ul><li>Adherence and compliance with cleanroom regulations that focus on aseptic techniques in cleanroom facilities.
</li><li>Perform GMP Manipulation in Clean Rooms following accreditation standards and perform aseptic tissue processing and production of cellular therapies for clinical use, ensuring that harvested tissue is safely retrieved, processed, and destroyed according to the documented procedures.
</li><li>Comply with protocols for the culture and transplantation of different cell sources for use in the orthopaedic setting.
</li><li>Be skilled and certified in cleanroom cell therapy Lab, able to aseptically prepare tissue culture media, supplements, and reagents.
</li><li>Acquiring and analyzing specimen data by flow cytometer.
</li><li>Perform quality control procedures, verify, document, and validate the accuracy of the laboratory data to assess the reproducibility and validity of current laboratory methods.
</li><li>Monitor Key Performance Indicators for cleanroom facility.
</li><li>Participate in the routine maintenance of the clean room environment and ancillary facilities, including equipment checks and calibration, environmental monitoring and cleaning as directed in SOPs.
</li><li>To have, to acquire and to develop specialist skills to recognize anomalies and ensure these are communicated / documented properly and be able to undertake investigation and remedial action, if directed to do so.
</li><li>Maintain strict confidentiality and proper storage and back-up of patient records and test results.
</li><li>Assist in the development of research protocols and procedures.
</li><li>Assists with evaluation and implementation of relevant new laboratory services.
</li><li>Participate in quality improvement and quality surveillance activities within Aspetar, including audits and inspections.
</li><li>Interact with other staff to solve problems and interpret patients&rsquo; laboratory results within the framework of the Orthobiological Laboratory.
</li><li>Review and maintain internal and external laboratory safety programmes, including safe handling and proper disposal of specimens and other laboratory materials, and implementing of corrective actions, when necessary, in compliance with statutory requirements.
</li><li>Assist in environmental monitoring procedures (measure, monitor and accurately record), using agreed quality control procedures, other duties related to QA.
</li><li>Monthly review of building management system documents for Liquid Nitrogen levels and temperatures in cryogenic tanks.
</li><li>Ensure the health, safety and welfare of fellow employees, visitors and contractors, so far as is reasonably practicable.
</li><li>Participate in Laboratory as well as Hospital Training and Education Programs.
</li><li>Provide appropriate training to other employees, as required.
</li><li>Process human samples using validated protocols and techniques with a high degree of competency.
</li><li>Record and maintain complete documentation throughout all phases of laboratory testing according to Laboratory and/or Hospital requirements.
</li><li>Record and maintain effective inventory control to ensure uninterrupted workflow.
</li><li>Record applicable patient data/results in Laboratory Information System.
</li><li>Inform the Laboratory Director in case of any procedural discrepancies for appropriate action.
</li><li>Participate in preparing the laboratory for accreditation by national and international bodies.
</li><li>Comply with national and international accreditation requirements.
</li><li>Comply with policies set down by the Qatar Ministry of Public Health and the Aspetar Hospital.
</li><li>Ensure compliance with relevant accreditation standards, laboratory safety regulations and quality control / quality assurance programs.
</li><li>Demonstrate a commitment to providing a quality service.
</li><li>Comply with employee obligations regarding Occupational Health and Safety, Infection Prevention and Control and Quality Improvement as set down in Aspetar Hospital&rsquo;s Policy and Procedure Manual.
</li><li>Maintain confidentiality in relation to discussions, disclosure of records, and information concerning the Aspetar.
</li><li>Maintain a discrimination and harassment free workplace.
</li><li>Comply with responsibilities listed under the Aspetar&rsquo;s Code of Conduct.
</li><li>Assume any other responsibilities as directed by the direct supervisor.
</li></ul>Necessary knowledge and Experience to be able to do the job:
<ul><li>Minimum experience of 5-7 years in which 2-3 years should be in a similar position / responsibility, preferably in a similar Industry.
</li><li>Must be well experienced and have sufficient knowledge of Orthobiological laboratory methods and techniques relevant to his/her specific job description.
</li><li>Must have specialized knowledge and experience related to handling / processing aseptic tissues, i.e. Stem cell culture, sub culturing, cell count, cell viability assay, cell maintenance &amp; cell freezing.
</li></ul>Skills and Abilities:
<ul><li>Excellent hand and eye co-ordination required, i.e. able to manipulate aseptic materials within isolators / laminar flow cabinets;
</li><li>Able to work in a restricted position for a substantial proportion of the working time.
</li><li>Meticulous and pays attention to detail.
</li><li>Ability to work shifts and demonstrable willingness to be placed on a 24-hour on-call roster, if required.
</li><li>Good interpersonal and communication skills.
</li><li>Good understanding of sciences and fundamental scientific principles related to orthobiological processes and analysis.
</li><li>Ability to work well as part of a multi-disciplinary team.
</li><li>Ability to work independently with initiative and to be adaptive to changes.
</li><li>Ability to multi-task and to work with frequent interruptions.
</li><li>Ability to work well under pressure.
</li><li>Previous experience working in the Middle East or within another culture or remote settings is preferable .
</li></ul>Education and Certification requirements:
<ul><li>Bachelor of Medical Laboratory Science/Technology or any other related filed.
</li><li>Fulfil all licensing requirements if required. Relevant Medical Licensure.</li></ul></div>

Medical Technologist - Orthobiologic Lab

Search 6221+ Laboratory specialist jobs near you this May. New roles added regularly across leading industries. Apply today.