laboratory technical specialist

Sidra

<div>JOB SUMMARY 
The Research Specialist I &ndash; Flow Cytometry Core Lab Tech at Sidra Medicine performs all the activities required in the position, and should be eligible or/and hold QCHP license. The incumbent executes under senior supervision laboratory tests necessary for research and clinical activities in the Core. Performs routine and moderately complex scientific laboratory technical work, selecting and applying laboratory procedures and techniques to assignments with clear, specific objectives. Assignments may require investigation of a number of variables and complex features. S/he works with general supervision. The incumbent is required to exercise judgment in making technical decisions related to delegated tasks and escalating complex issues. The incumbent supports the team in Clean Room activities and in Good Manufacturing Practice operations for cell therapy and gene therapy products for clinical and research based on Good Laboratory Practice, in the development and validation of simple and moderately complex laboratory procedures for the manufacturing of cell and gene therapy products. The incumbent observes and maintains a high standard of laboratory health, safety procedures; works based to the institutional, departmental and Flow Cytometry Core&rsquo;s regulations/values/policies/procedures/instructions/protocols/designs and current professional standards and guidelines. Follows MoPH, professional, certification and accreditation bodies requirements. 
KEY ROLE ACCOUNTABILITIES
Clinical activities performed:
<ul><li>Peripheral blood and other tissues processing.
</li><li>Clinical assays.
</li><li>All necessary clinical grade testing for product quality control and quality control equipment used for the purpose.
</li><li>Clinical activity varies based on projects, the time spent in clinical related tasks is 40% or more. 
</li></ul>Research activities performed :
<ul><li>Basic and complex research activities in addition to the above clinical activities.
</li>Other basic and complex research activities related to biomedical science. 
<li>
</li></ul>Note: the incumbent does not interact directly with the patient.
In line with the activities briefly described above, s/he will be also accountable for the following:
<ul><li>Contributes to the delivery of departmental goals, through personal effort in own work area.
</li><li>Actively participates and responsibly performs the technical activities, pre-analytical, and analytical work in the labs: R&amp;D, production and testing. Under senior supervision designs, validates new methods and testing and clinical assays.
</li><li>Defines long term, medium and short term priorities and in daily work plan in accordance with the line manager reporting also outcomes, success and issues.
</li><li>Initiates, performs, reviews and troubleshoots quality control of reagents and test systems.
</li><li>Ensures and validates pre-existing assays for laboratory.
</li><li>Ensures assays comply with current regulations in Qatar or/and with international ones.
</li><li>Liaises with manager and ARC colleagues on production and outcomes, on appropriateness of tests and results.
</li><li>Maintains, monitors, records and reports tests results.
</li><li>Collaboratively maintains laboratory information system (e.g. LIMS/ELN).
</li><li>Maintains laboratory supplies inventory by checking stock to determine inventory level in assigned areas; anticipating needed supplies; and if requested placing and expediting orders for supplies; verifying receipt of supplies.
</li><li>Ensures that any difficulties or problems affecting service provision are reported promptly to colleagues, senior staff and line manager.
</li><li>Understands and adheres to process improvement principles and processes, for example, following standard work and maintaining a robust inventory concept in work area realizing that all processes are driven by the needs of the customer.
</li><li>Participates actively in Core meetings and if required in Quality Systems development/ improvement.
</li><li>Proposes changes to SOPs, relating to duties/ accountabilities, and under the instruction from the line manager drafts new versions or produces new operating procedures as addressed.
</li><li>Responsible for maintaining competencies required in Flow Cytometry Core and performs in accordance with laboratory and Sidra policy to provide accurate lab activities.
</li><li>Operates and maintains complex and basic instruments and equipment used in the laboratory, and properly sets up, calibrates, maintains, operates and shuts down such instruments (as needed);
</li><li>Maintains competence in Laboratory Information System that is crucial to the quality operations of the laboratory and patient care.
</li><li>Operates and performs daily preventive maintenance of equipment according to written procedures and documents; reports equipment malfunctions and requests service as necessary.
</li><li>Participates in research and development as directed.
</li><li>Maintains competence in Laboratory Information System and in Laboratory Management System that is crucial to the quality operations of the laboratory and patient care.
</li><li>Actively participates in Quality Improvement Programs essential to ensure that laboratory testing is accurate, timely and meets customer needs.
</li><li>Maintains policies and procedures for adherence to the current professional standards.
</li><li>Works with quality representative to develop systems to deliver quality services which satisfy Quality standards requirements.
</li><li>Accomplishes all the organizational mandatory requirements (i.e. Learning and Development requirements, use of PPE, etc.)
</li><li>Adheres to Sidra&rsquo;s standards as they appear in the Code of Conduct and Conflict of Interest policies.
</li><li>Adheres to and promotes Sidra&rsquo;s Values.
</li></ul>In view of the evolving needs and opportunities within Sidra, this position may be required to perform other duties as assigned and reporting relationships may vary. 
QUALIFICATIONS, EXPERIENCE AND SKILLS &ndash; SELECTION CRITERIA 
Education
Bachelor&rsquo;s Degree in Biomedical Sciences/ Clinical Laboratories or other relevant program.
Experience
3+ years&rsquo; experience in a research laboratory environment including:
<ul><li>Experience in cell cultures
</li><li>Experience in flow cytometry procedures
</li><li>Experience in molecular biology procedures
</li>Experience in proteins detection. 
<li>
</li></ul>Certification and Licensure
Essential
Eligibility for Licensure in the State of Qatar.
Preferred
License recognized in Qatar, EU, US or Canada. 
Job Specific Skills and Abilities.
Essential
<ul><li>Cell culture of primary blood cells, as lymphocytes
</li><li>Molecular biology procedures, as nucleic acids extraction, PCR, RT-PCR
</li><li>Flow cytometry stainings and basic data analysis
</li><li>Protein detection / functional assays
</li><li>Demonstrated excellent communication and interpersonal skills.
</li><li>Openness to teach and interact with other staff members.
</li><li>Proficiency with Microsoft Office suite.
</li><li>Fluency in written and spoken English
</li></ul>Preferred
<ul><li>Experience in bacterial cloning.
</li><li>Flow cytometry acquisition of samples.</li></ul></div>
 <div><div>About US</div>
<div><div>Sidra Medicine a healthy population is essential to a strong, prosperous society, and throughout 2020, Sidra continued to provide uninterrupted comprehensive specialist healthcare services for children and young people; and exceptional maternity, gynecology, and reproductive medical services for women, previously unavailable in Qatar and the region.&rdquo; &ndash; H.H Sheikha Moza bint Nasser, Chairperson of Qatar Foundation
</div><div>Sidra Medicine represents the vision of Her Highness Sheikha Moza bint Nasser who serves as its Chairperson. This high-tech facility is home to world-class patient care, scientific expertise, and educational resources.</div></div></div><div></div>

Research Specialist I - Research Specialist I – Flow Cytometry Core Lab Tech.

Smith+Nephew

<div>Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.
Laboratory Validation Specialist
The Laboratory Validation Specialist is responsible for validations supporting the Quality Control laboratories. Primarily the role is responsible for the validation, verification, and/or qualification of test methods used in the laboratories, analytical instruments, and computerized systems used in a GMP-regulated pharmaceutical environment. This role ensures that test methods, equipment, and processes are compliant with regulatory requirements, including method validation standards, data integrity standards and computer system validation (CSV), while supporting reliable and accurate laboratory operations. This role also serves as a Quality Control representative for other site validations that requiring Quality Control support.
U.S. Sponsorship or H1B transfer is not available for this role
What will you be doing?
Validation
<ul><li>Lead and execute qualification activities for laboratory instruments (e.g., dissolution, spectroscopy systems).
</li><li>Develop and execute validation protocols for methods.
</li><li>Manage execution of IQ/OQ/PQ protocols for new and existing equipment.
</li>Represent QC in the development, review, and execution of validation supporting other site projects and processes. 
<li>
 
</li></ul>Data Integrity &amp; Compliance
<ul><li>Ensure compliance with ALCOA+ data integrity principles.
</li><li>Review audit trails, electronic records, and system access controls.
</li><li>Support and lead data integrity assessments and gap remediation plans.
</li>Participate in regulatory inspections and audits. 
<li>
 
</li></ul>Documentation &amp; Quality Systems
<ul><li>Author, review, and approve validation protocols, reports, SOPs, and work instructions.
</li><li>Support deviations, investigations, CAPAs, and change control related to validation activities.
</li>Maintain validation lifecycle documentation in accordance with GMP requirements. 
<li>
 
</li></ul>Risk Management &amp; Lifecycle Approach
<ul><li>Apply risk-based validation approaches per GAMP 5 guidelines.
</li><li>Perform impact and risk assessments for changes to validated systems.
</li>Ensure continued process verification and system performance monitoring. 
<li>
 
</li></ul>Cross-Functional Collaboration
<ul><li>Work closely with R&amp;D, QA, QC, Manufacturing, IT, Metrology, and Engineering teams.
</li><li>Interface with vendors for system implementation, validation support, and troubleshooting.
</li>Provide technical guidance on validation requirements and best practices. 
<li>
 
</li></ul>Training &amp; Continuous Improvement
<ul><li>Train laboratory personnel on validated systems and compliance expectations.
</li><li>Identify opportunities for process improvements and efficiency in validation practices.
</li><li>Support digitalization and automation initiatives in the lab.
</li></ul>What will you need to be successful?
Education:
Bachelor&rsquo;s degree in Chemistry, Biology, Engineering, Computer Science, or related scientific field. 
<ul><li>
 
</li></ul>Experience:
<ul><li>2&ndash;6+ years in pharmaceutical, biotech, or regulated laboratory environments.
</li><li>Experience with laboratory test method validation, equipment qualification and/or CSV.
</li><li>Familiarity with LIMS, CDS (e.g., Empower, OpenLab), or other lab systems.
</li><li>Experience supporting regulatory inspections is preferred.
</li>Experience with automation or system integration (LIMS/ERP) is a plus. 
<li>
 
</li></ul>Knowledge:
<ul><li>GMP (Good Manufacturing Practices)
</li><li>Test Method Validation
</li><li>Computer System Validation (CSV)
</li><li>21 CFR Part 11 / EU Annex 11
</li><li>GAMP 5 guidelines
</li><li>Data Integrity (ALCOA+)
</li><li>Experience with validation lifecycle documentation (URS, IQ/OQ/PQ)
</li><li>Understanding of audit trails, electronic signatures, and system security
</li><li>Knowledge of risk management tools (e.g., FMEA) is a plus.
</li></ul>Competences:
<ul><li>Strong analytical and problem-solving skills
</li><li>Attention to detail and documentation accuracy
</li>Effective communication and teamwork across departments 
<li>
 
</li></ul>You Unlimited.
We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
<ul><li>Inclusion and Belonging - Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website (https://www.smith-nephew.com/).
</li><li>Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement
</li><li>Work/Life Balance: Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day
</li><li>Your Wellbeing: Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program
</li><li>Flexibility: Hybrid Work Model (For most professional roles)
</li><li>Training: Hands-On, Team-Customized, Mentorship
</li><li>Extra Perks: Discounts on fitness clubs, travel and more!
</li></ul>Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
<div>Stay connected by joining our Talent Community .
We're more than just a company - we're a community! Follow us on L inkedIn to see how we support and empower our employees and patients every day.
</div><div><div>Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You . Unlimited . , life, culture, and benefits at S+N.
</div><div>Explore our website and learn more about our mission, our team, and the opportunities we offer.</div></div></div>

Laboratory Validation Specialist (Fort Worth, TX)

Diageo

<div>Job Description :
Job Description :<div><div><div>
About us
With over 200 brands sold in nearly 180 countries, we&rsquo;re the world&rsquo;s leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you&rsquo;ll test new ideas, learn and grow, and unlock a brighter, more exciting future.
Join us to create a career worth celebrating.
About the Function
Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo&rsquo;s 30,000+ people work in Supply Chain and Manufacturing. It&rsquo;s an intricate and sophisticated operation that&rsquo;s the product of logistical, manufacturing, and technical collaborations.
Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We&rsquo;re committed to realising our &lsquo;Society 2030: Spirit of Progress&rsquo; goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we&rsquo;ll help you to thrive in our inclusive culture.
About the role
We are looking for Laboratory Specialist to join our team at our Alasehir Factory. The ideal candidate will ensure the creation of warehouses for quality control, reporting, and records of raw materials, packaging materials, auxiliary features, semi-finished products, and finished products in accordance with company rules, legal requirements, local and global standards and quality plans. Maintaining the control and continuity of the Quality Food Safety management system in the factory where the company works.
Role Responsibilities<ul><li>
Perform analyses of all types of materials and substances, such as raw materials, semi-finished products, finished products, etc., according to experimental instructions and technical specifications.</li><li>
Inform the supervisor and initiate corrective actions when nonconformities are detected in the analysis results of samples analyzed in the laboratory, and follow up on the process.</li><li>
Check the compliance of all parameters affecting product quality.</li><li>
Handle customer complaints, analyze and control non-compliant products, participate in root cause analysis studies, and conduct product, defect, and statistical studies.</li><li>
Perform statistical analysis and error analysis related to the analyses and controls conducted.</li><li>
Participate in necessary activities for establishing the HACCP Food Safety System in the factory and perform required checks to ensure the continuity of the system.</li><li>
Conduct periodic GMP field inspections (e.g., GMP audits, FSSC 22000 field audits), initiate corrective actions for identified nonconformities, and follow up on the process.</li><li>
Participate in projects related to quality, food safety, and other topics.</li></ul>
Experience / skills required<ul><li>
Associate degree (2-year) in Chemistry, Food Technology, Laboratory, or a related field</li><li>
Preferably 0&ndash;3 years of experience in laboratory analysis or quality control</li><li>
Basic knowledge of laboratory equipment and analytical methods</li><li>
Familiarity with quality and food safety systems such as HACCP and GMP is an asset</li><li>
Experience in handling non-conforming products and supporting corrective actions is a plus</li><li>
Basic understanding of data recording, reporting, and simple statistical analysis</li><li>
Attention to detail and strong sense of responsibility in following procedures and instructions</li><li>
Ability to work in a structured environment in compliance with technical specifications</li><li>
Good communication skills and ability to work collaboratively with cross-functional teams</li><li>
Open to learning, proactive, and disciplined working approach</li><li>
Basic level of English is preferred</li></ul> 
Diversity statement
Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.
We embrace diversity in the broadest possible sense. This means that you&rsquo;ll be welcomed and celebrated for who you are just by being you. You&rsquo;ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.
Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.
Feel inspired? Then this may be the opportunity for you.</div></div></div>
Worker Type :
Regular
Primary Location:
Alasehir Plant
Additional Locations :
Job Posting Start Date :
2026-04-10</div>

Laboratory Specialist

<div>Job Description :<div><div><div>
About us
With over 200 brands sold in nearly 180 countries, we&rsquo;re the world&rsquo;s leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you&rsquo;ll test new ideas, learn and grow, and unlock a brighter, more exciting future.
Join us to create a career worth celebrating.
About the Function
Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo&rsquo;s 30,000+ people work in Supply Chain and Manufacturing. It&rsquo;s an intricate and sophisticated operation that&rsquo;s the product of logistical, manufacturing, and technical collaborations.
Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We&rsquo;re committed to realising our &lsquo;Society 2030: Spirit of Progress&rsquo; goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we&rsquo;ll help you to thrive in our inclusive culture.
About the role
We are looking for Laboratory Specialist to join our team at our Nevsehir Factory. The ideal candidate will ensure the creation of warehouses for quality control, reporting, and records of raw materials, packaging materials, auxiliary features, semi-finished products, and finished products in accordance with company rules, legal requirements, local and global standards and quality plans. Maintaining the control and continuity of the Quality Food Safety management system in the factory where the company works.
Role Responsibilities<ul><li>
Perform analyses of all types of materials and substances, such as raw materials, semi-finished products, finished products, etc., according to experimental instructions and technical specifications.</li><li>
Inform the supervisor and initiate corrective actions when nonconformities are detected in the analysis results of samples analyzed in the laboratory, and follow up on the process.</li><li>
Check the compliance of all parameters affecting product quality.</li><li>
Handle customer complaints, analyze and control non-compliant products, participate in root cause analysis studies, and conduct product, defect, and statistical studies.</li><li>
Perform statistical analysis and error analysis related to the analyses and controls conducted.</li><li>
Participate in necessary activities for establishing the HACCP Food Safety System in the factory and perform required checks to ensure the continuity of the system.</li><li>
Conduct periodic GMP field inspections (e.g., GMP audits, FSSC 22000 field audits), initiate corrective actions for identified nonconformities, and follow up on the process.</li><li>
Participate in projects related to quality, food safety, and other topics.</li></ul>
Experience / skills required<ul><li>
Associate degree (2-year) in Chemistry, Food Technology, Laboratory, or a related field</li><li>
Preferably 0&ndash;3 years of experience in laboratory analysis or quality control</li><li>
Basic knowledge of laboratory equipment and analytical methods</li><li>
Familiarity with quality and food safety systems such as HACCP and GMP is an asset</li><li>
Experience in handling non-conforming products and supporting corrective actions is a plus</li><li>
Basic understanding of data recording, reporting, and simple statistical analysis</li><li>
Attention to detail and strong sense of responsibility in following procedures and instructions</li><li>
Ability to work in a structured environment in compliance with technical specifications</li><li>
Good communication skills and ability to work collaboratively with cross-functional teams</li><li>
Open to learning, proactive, and disciplined working approach</li><li>
Basic level of English is preferred</li></ul> 
Diversity statement
Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.
We embrace diversity in the broadest possible sense. This means that you&rsquo;ll be welcomed and celebrated for who you are just by being you. You&rsquo;ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.
Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.
Feel inspired? Then this may be the opportunity for you.</div></div></div>
Worker Type :
Regular
Primary Location:
Nevsehir Plant
Additional Locations :
Job Posting Start Date :
2026-03-26</div>

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

Chenega Corporation

<div>Overview:
<div>
Come join a company that strives for Extraordinary People and Exceptional Performance! Chenega Professional &amp; Technical Services, LLC, a Chenega Professional Services&rsquo; company, is looking for a Laboratory Technician 4 &ndash; Senior Biomarker Technical Support. The Laboratory Technician 4 &ndash; Senior Biomarker Technical Support contractor will lead and execute biomarker verification protocols in high-containment laboratory environments (BSL-2 to BSL-4). This role supports approximately 3&ndash;6 research projects annually, involving advanced molecular diagnostics, sequencing technologies, and sample processing. The contractor will also serve as a lab supervisor, contribute to scientific reporting, and support both domestic and international diagnostic missions.</div><div></div><div> 
Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee&rsquo;s knowledge, critical thinking, innovative solutions for our clients.</div>
Responsibilities:
<ul><li>Independently develop and execute biomarker verification protocols in collaboration with project leads or principal investigators.</li><li>
Conduct experiments in BSL-2, BSL-3, and BSL-4 environments as required by project design.</li><li>
Support planning and execution of laboratory research for ~5 projects per year.</li><li>
Perform advanced molecular diagnostics including:</li><li>
Next-generation sequencing</li><li>
Nanostring immunological and inflammatory panels</li><li>
Luminex-based platforms</li><li>
miRNA quantification</li><li>
Detect etiologic agents in animal, clinical, or environmental samples.</li><li>
Supervise assigned laboratory spaces to ensure safety, functionality, and inventory compliance.</li><li>
Assist in preparing SOPs, technical reports, and manuscripts for publication.</li><li>
Execute novel sample collection and processing techniques including Nanotrap Concentration and DNA/mRNA purification from NHP and human clinical matrices.</li><li>
Present protocols and data at weekly meetings.</li><li>
Contribute to quarterly and annual reports for associated projects.</li><li>
Submit data and SOPs to the TPOC by the last workday of each month.</li><li>
Participate in CONUS/OCONUS travel as needed for diagnostic missions.</li><li>
Maintain enrollment in the Biological Personnel Reliability Program (BPRP) per contract and regulatory requirements.</li><li>
Other duties as assigned.</li></ul>
Qualifications:
<ul><li>Experience working in BSL-2, BSL-3, and BSL-4 laboratory environments.</li><li>
Eligibility and commitment to maintain BPRP enrollment.</li><li>
Must maintain an active Secret clearance.</li><li>
Proficiency in molecular diagnostic platforms and sequencing technologies.</li><li>
Demonstrated ability to supervise laboratory operations and maintain compliance.</li><li>
Strong technical writing skills for SOPs and scientific publications.</li><li>
Willingness and ability to travel domestically and internationally.</li></ul><div>
Preferred Qualifications:</div><ul><li>
Prior experience with Nanotrap Concentration and purification techniques for NHP and human samples.</li><li>
Familiarity with government or military research protocols.</li><li>
Experience contributing to multi-project research environments and reporting cycles.</li></ul>
Teleworking Permitted?: false Estimated Salary/Wage: USD $70,000.00/Yr. Up to USD $80,000.00/Yr.</div>

Laboratory Technician 4 – Senior Biomarker Technical Support

Nahdi

<div>Perform routine clinical laboratory tests done in hematology, chemistry, immunohematology, microbiology, immunology and coagulation. He/she will have gained basic laboratory skills required for entry-level positions in these and other emerging laboratory fields, such as molecular diagnostics. Also, perform some responsibilities related to information processing, training and quality control within the laboratory.
Accountabilities
<ul><li>Receives blood and body fluid samples at the lab reception and starts the pre-analytical processing of the samples.
</li><li>Performs daily checks on equipment to ensure its safety and correct operability.
</li><li>Performs all analytical processes on the hematology, biochemistry, serology and hormone lab machines.
</li><li>Performs daily quality control tests on regents
</li><li>Analyzes blood cells by counting and identifying cells, using microscopic techniques and procedures.
</li><li>Performs microscopic preparation and examination of urine and stools.
</li><li>Maintains laboratory supplies inventory by checking stock to determine inventory level; anticipating needed supplies; placing and expediting orders for supplies; verifying receipt of supplies.
</li><li>Conserves laboratory resources by using equipment and supplies as needed to accomplish job results.
</li><li>Informs medical staff of critical test results.
</li><li>Prepares reports of technological findings by collecting, analyzing, and summarizing information.
</li><li>Maintains professional and technical knowledge by attending educational workshops and reviewing professional publications.
</li><li>Maintains safe and clean working environment by complying with procedures, rules, and regulations.
</li><li>Protects patients and employees by adhering to infection-control and hazardous waste policies and procedures.
</li><li>Maintains patient confidence and protects the hospital by keeping information confidential.
</li></ul>The employee&rsquo;s duties are not limited to the above-mentioned accountabilities. The manager can assign other duties based on the business need.
Work Environment
<ul><li>Indoors : 100%
</li><li>Outdoors : 0%
</li><li>Working Days : 6 Working Days
</li><li>Days off : 1 Days Off
</li><li>Working Hours : 8 net working hours according to shift schedule approved by head of department.
</li></ul>Job Requirement
<div><div><div><div><div>Education 
</div><div><ul><li>Bachelor&rsquo;s degree in Applied medical science (laboratory section) 
</li></ul></div></div> 
<div><div>Experience 
</div><div><ul><li>2 years of practical experience following graduation. 
</li></ul></div></div> 
<div><div>Computer Skills 
</div><div><ul><li>Office &amp; Health Information System 
</li></ul></div></div> 
<div><div>Languages 
</div><div><ul><li>English and Arabic (fluent speaking and writing)</li></ul></div></div></div></div></div></div>

Laboratory Technique Specialist -Dammam

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Laboratory Technique Specialist -Dammam