medical laboratory specialist

CHRISTUS Health

<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

SearchPlus HR

<div>SearchPlus HR is seeking qualified Clinical Pathologist Specialists for positions in the private healthcare sector. These roles offer an excellent opportunity for professionals to apply their expertise in clinical pathology within dynamic private medical institutions.
As a Clinical Pathologist Specialist in the private sector, you will be responsible for performing and interpreting a wide range of laboratory tests and providing accurate diagnostic information to support patient treatment plans. Your role will include collaboration with multidisciplinary teams and contributing to high-quality healthcare services.
Responsibilities:<ul>
<li>Perform and interpret laboratory analyses including hematology, clinical chemistry, microbiology, and immunology tests.</li>
<li>Provide precise and timely diagnostic reports to assist clinical decision-making.</li>
<li>Coordinate with healthcare professionals to optimize patient care and treatment outcomes.</li>
<li>Maintain quality assurance and control standards to ensure the reliability of laboratory results.</li>
<li>Keep abreast of advances in clinical pathology and incorporate new techniques and technologies.</li>
<li>Engage in laboratory management and operational improvement initiatives when applicable.</li> 
</ul> 
 
Requirements 
 
Requirements:<ul>
<li>Medical degree with specialization in Clinical Pathology.</li>
<li>Licensure to practice as a Clinical Pathologist Specialist in the relevant jurisdiction.</li>
<li>Completion of accredited residency in clinical pathology.</li>
<li>Experience working in clinical pathology within private healthcare settings preferred.</li>
<li>Strong knowledge of diagnostic laboratory procedures and pathology principles.</li>
<li>Excellent communication skills for effective collaboration with medical teams.</li>
<li>Proactive approach to quality control and patient-centered care.</li>
<li>Ability to manage multiple cases efficiently while maintaining accuracy.</li> 
</ul> 
 
Benefits 
<ul>
<li>Private Health Insurance</li>
<li>Training &amp; Development</li>
<li>Performance Bonus</li></ul></div>

Clinical Pathologist Specialists - Private Sector

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

Los Alamos National Laboratory

<div>What You Will Do 
 
This position will be filled at either the Computer and Information Security Specialist 1 or 2 level, depending on the skills of the selected candidate. Additional job responsibilities (outlined below) will be assigned if the candidate is hired at the higher level.
 
 
This position is responsible for supporting the Argus Security System at the Los Alamos National Laboratory (LANL) Department of Energy site. The Argus Security System is developed and maintained at Lawrence Livermore National Laboratory (LLNL) and deployed at LANL. The Argus system is a network based distributed computerized control system with significant security and reliability features. This individual will report to the Team Leader and is responsible for a wide range of duties centered around maintenance activities.
 
 
Duties may include: 
 
Computer &amp; Information Security Specialist 1 ($72,800 - $115,400)
 
The selected candidate will ensure maintenance databases in the computerized maintenance management system reflect the current configuration of the Argus perimeter and interior systems. They will generate work orders for Argus corrective and scheduled maintenance activities. They will input scheduling information into the Operations Control schedule utility (Microsoft Outlook). The candidate will be required to create preventive maintenance record worksheets from current system database and distribute to the appropriate team leaders. 
 
Computer &amp; Information Security Specialist 2 ($87,800 - $143,000)
 
 
In addition to what was outlined at the lower level, at this level the selected candidate will retrieve Argus system logs and provide in depth analysis of False and Nuisance Alarm data to create extensive maintenance reports to upper management. Maintain high competency in Microsoft Excel, Splunk, and Tableau software packages. Review utility outage forms and provide clients and security technicians with information on security system impact. 
 
What You Need 
 
Minimum Job Requirements: 
<ul><li>
Demonstrate success in client management and ability to resolve issues successfully.</li><li>
Knowledge of security system functions, technologies, equipment, maintenance, compensatory measures, and operations.</li><li>
Demonstrate knowledge of the Microsoft Office software suite with an emphasis on Excel.</li></ul>
Additional Job Requirements for Computer &amp; Information Security Specialist 2: 
In addition to the requirements outlined above, qualification at the higher level requires: 
<ul><li>
Experience and demonstrated skill in conducting research, investigating alternative solutions, and recommending solutions on problems affecting computer and information security.
</li><li>Understand statistical analysis as related to security sensors and maintenance activities.</li><li>
In-depth knowledge of the Laboratory's computer and information security policies, practices, and procedures.</li></ul>
Computer and Information Security Specialist 1 Education Required: Position requires a minimum of 2 years related experience, or an equivalent combination of education and experience. 
 
Computer and Information Security Specialist 2 Education Required: Position requires a bachelor's degree and 5 years related experience; or, an equivalent combination of education and experience directly related to the occupation. 
 
Desired Qualifications: 
<ul><li>
Proven success in working with multiple, diverse teams both internal and external (including the Protective Force) to collaboratively achieve task goals utilizing interpersonal, oral, and written communication skills.</li><li>
Knowledge and experience with DOE &amp; NNSA policies and orders. Specifically, DOE O 473.1A Physical Protection Programs.</li><li>
Knowledge of the Argus Security System, Protective Force operations and responses, especially alarm console operations.</li><li>
Knowledge of computer system data logs and programming data retrieval software for analysis.</li><li>
Knowledge of network server administration including updating software and resolving vulnerability reports.</li></ul> 

Work Environment: 
 
Work Location: The work location for this position is onsite and located in Los Alamos, NM. All work locations are at the discretion of management. 
 
Work Environment: Work Environment: Indoors, working alone, working overtime or irregular schedules. 
 
Position Commitment: Regular appointment employees are required to serve a period of continuous service in their current position in order to be eligible to apply for posted jobs throughout the Laboratory. If an employee has not served the time required, they may only apply for Laboratory jobs with the documented approval of their Division Leader. The position commitment for this position is 1 year. 

 
Note to Applicants: For full consideration, applicants must submit a comprehensive cover letter that addresses the key requirements of the position.
 
<ul><li>Minimal travel is anticipated but may be required for training purposes.</li><li>
References will be required.</li><li>
Must maintain a valid New Mexico driver's license.</li></ul>
Due to federal restrictions contained in the current National Defense Authorization Act, citizens of the People's Republic of China - including the special administrative regions of Hong Kong and Macau - as well as citizens of the Islamic Republic of Iran, the Democratic People's Republic of Korea (North Korea), and the Russian Federation, who are not Lawful Permanent Residents (&quot;green card&quot; holders) are prohibited from accessing facilities that support the mission, functions, and operations of national security laboratories and nuclear weapons production facilities, which includes Los Alamos National Laboratory. 
 
Where You Will Work 
 
Located in beautiful northern New Mexico, Los Alamos National Laboratory (LANL) is a multidisciplinary research institution engaged in strategic science on behalf of national security. Our generous benefits package includes:<ul><li>
PPO or High Deductible medical insurance with the same large nationwide network</li><li>
Dental and vision insurance</li><li>
Free basic life and disability insurance</li><li>
Paid childbirth and parental leave</li><li>
Award-winning 401(k) (6% matching plus 3.5% annually)</li><li>
Learning opportunities and tuition assistance</li><li>
Flexible schedules and time off (PTO and holidays)</li><li>
Onsite gyms and wellness programs</li><li>
Extensive relocation packages (outside a 50 mile radius)</li></ul> 

Additional Details 
 
Directive 206.2: Employment with Triad requires a favorable decision by NNSA indicating employee is suitable under NNSA Supplemental Directive 206.2. Please note that this requirement applies only to citizens of the United States. Foreign nationals are subject to a similar requirement under DOE Order 142.3A. 
 
Clearance: Q (Position will be cleared to this level). Selected applicants will be subject to a background investigation conducted by or on behalf of the Federal Government, and must meet eligibility requirements* for access to classified matter. This position requires a Q clearance. and obtaining such clearance requires US Citizenship except in extremely rare circumstances. Dependent upon the position, additional authorization to access classified information may be required, which may or may not be available to dual citizens. Receipt of a Q clearance and additional access authorization ultimately is a decision of the Federal Government and not of Triad. 
 
<ul><li>Eligibility requirements: To obtain a clearance, an individual must be at least 18 years of age; U.S. citizenship is required except in very limited circumstances. See DOE Order 472.2 for additional information.</li></ul>
 
New-Employment Drug Test: The Laboratory requires successful applicants to complete a new-employment drug test and maintains a substance abuse policy that includes random drug testing. Although New Mexico and other states have legalized the use of marijuana, use and possession of marijuana remain illegal under federal law. A positive drug test for marijuana will result in termination of employment, even if the use was pre-offer. 
 
Regular Position: Term status Laboratory employees applying for regular-status positions are converted to regular status. 
 
Internal Applicants: Regular appointment employees who have served the required period of continuous service in their current position are eligible to apply for posted jobs throughout the Laboratory. If an employee has not served the required period of continuous service, they may only apply for Laboratory jobs with the documented approval of their Division Leader. Please refer to Policy P701 for applicant eligibility requirements. 
 
Equal Opportunity: Los Alamos National Laboratory is an equal opportunity employer and supports a diverse and inclusive workforce. All employment practices are based on qualification and merit, without regard to race, color, national origin, ancestry, religion, age, sex, gender identity, sexual orientation, marital status or spousal affiliation, physical or mental disability, medical conditions, pregnancy, status as a protected veteran, genetic information, or citizenship within the limits imposed by federal laws and regulations. The Laboratory is also committed to making our workplace accessible to individuals with disabilities and will provide reasonable accommodations, upon request, for individuals to participate in the application and hiring process. To request such an accommodation, please send an email to applyhelp@lanl.gov or call 1-505-664-6947 option 2.</div>

Argus Computer and Information Security Specialist 1 OR 2

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

North Oaks Health System

<div>Status: Full Time
Shift: Rotating 7on/7off nights - Thurs to Wed. Shift hours: 2030-0700 weekdays, 1830-0700 weekend and holidays.
Exempt: No
Summary: 
 
Performs clinical laboratory testing on patient specimens in any Laboratory discipline including Blood Bank and/or Microbiology in accordance with established policies and procedures. Correlates and interprets the data obtained based on knowledge of techniques, principles and instruments. Investigates and seeks to resolve testing problems. Performs corrective and preventive maintenance on equipment. Ensures accuracy of results by monitoring test quality. May consult with other members of the healthcare team. 
Other information: 
 
1. Previous Experience Required: one (1) year experience as a generalist preferred
2. Specialized or Technical Education Required:
&sect; Bachelor&rsquo;s degree in a chemical, physical or biological science required with a degree in clinical laboratory science/medical technology preferred
&sect; Completion of an accredited clinical laboratory training program required
&sect; Current license by Louisiana State Board of Medical Examiners as a Clinical Laboratory Scientist &ndash; Generalist or Clinical Laboratory Scientist &ndash; Specialist
&sect; To be eligible to assume Section Supervisor duties: meets current minimum Technical Supervisor personnel requirements for high-complexity testing in compliance with CLIA federal regulations Section 493-Subpart M
3. Manual or Physical Skill Required:
Distinguishes and identifies color.
Requires manual and finger dexterity, eye-hand coordination, and corrected vision and hearing to normal range.
4. Physical Effort Required/Physical Demands:
Strength: Moderate
Push: Occasionally
Pull: Occasionally
Carry: Occasionally
Lift: Occasionally
Sit: Frequently
Stand: Frequently
Walk: Frequently
Responsibilities: 
 
DESCRIPTION OF DUTIES:
1. Proficiently performs a variety of laboratory tests and procedures following established policies, procedures and requirements of accrediting and regulating agencies in assigned work section(s) which may include any or all of the following Laboratory disciplines: Blood Bank, Chemistry, Coagulation, Hematology, Full Microbiology, Microbiology specimen preparation, Serology, and Urinalysis.
2. Plans, organizes, and prioritizes work to accomplish maximum quantity and quality of work assignments
<div><ul><li>Monitors testing analyzers for optimum performance. Performs preventive maintenance and troubleshoots problems as needed.
</li></ul></div>4. Performs and evaluates quality control and record results. Troubleshoots quality control problems as needed.
5. Records and reports test results. Maintains all required records, reports and statistical logs and files. Identify, verify and report &ldquo;critical results&rdquo; per established Laboratory/hospital policy.
6. Reports any unusual laboratory findings or problems using established departmental and organizational quality and safety avenues, and escalates appropriately to Supervisor, Clinical Manager, Laboratory Director or Pathologist.
7. Monitors and maintains adequate supplies and reagents associated with assigned duties.
8. Maintains appropriate working knowledge of hospital/department computer software and other digital systems, including computer downtime operations.
9. Attends and participates in meetings (administrative, departmental, section, in-service, etc.) as necessary. Represents the department at conferences and working committees, as directed. Provides input to Section Supervisor for staff meeting agenda items.
10. Ensures own professional growth and development through literature review, seminars, conferences and professional affiliations.
11. Assists in all aspects of emergency response. May be required to work other shifts, weekends and holidays as assigned.
12. Follows North Oaks Health System&rsquo;s Compliance Programs and Federal and State Regulatory guidelines.
13. Performs all duties in a safe manner, follow North Oaks Health System&rsquo;s safety policies and procedures, follow the North Oak&rsquo;s Health System Compliance Program, and Federal/ State Regulatory guidelines.
14. Performs other duties as required or requested by the Director or designee. This may include assuming the responsibilities of a Lead Scientist or Section Supervisor</div>

CLINICAL LABORATORY SCIENTIST/MED TECH II - LAB

VITROLIFE

<div>At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. 
Make Quality Matter &mdash; Where It Impacts Lives.
We are looking for a Quality Assurance Specialist to strengthen and advance our local quality operations in Riyadh. This role sits at the intersection of regulatory excellence, operational quality, and continuous improvement, ensuring that our laboratory services meet the highest international and local standards.
You will play a key role in driving compliance, enabling safe and effective services, and embedding a proactive quality culture &mdash; working closely with both local teams and regional quality leadership.<h4 class="jobSectionHeader"> 
Your Impact</h4>
As a Quality Assurance Specialist, you will:<h6 class="jobSectionHeader">
Drive Quality Operations &amp; Compliance</h6><ul><li>
Oversee day-to-day quality activities and ensure adherence to local and regional requirements</li><li>
Maintain accurate quality records and actively participate in quality management forums</li><li>
Ensure compliance with MOH, SFDA, CBAHI, and other applicable regulations</li></ul><h6 class="jobSectionHeader">
Strengthen the Quality Management System (QMS)</h6><ul><li>
Manage document control processes to ensure procedures are current, compliant, and accessible</li><li>
Support implementation and updates of local and global procedures</li><li>
Contribute to continuous improvement of QMS processes</li></ul><h6 class="jobSectionHeader">
Lead Audits, Risk &amp; Continuous Improvement</h6><ul><li>
Plan and conduct internal audits; manage findings and CAPA implementation</li><li>
Support external audits and regulatory inspections</li><li>
Lead local risk assessments and foster a proactive risk management culture</li></ul><h6 class="jobSectionHeader">
Manage Deviations, CAPA &amp; Performance</h6><ul><li>
Investigate deviations and ensure effective CAPA closure</li><li>
Monitor KPIs, incidents, and nonconformities</li><li>
Identify trends and escalate critical insights to Regional Quality Management</li></ul><h6 class="jobSectionHeader">
Enable Regulatory &amp; Operational Excellence</h6><ul><li>
Monitor regulatory changes and ensure timely implementation</li><li>
Support licensing, certifications, and renewals</li><li>
Ensure quality alignment in new or modified services</li></ul><h6 class="jobSectionHeader">
Collaborate &amp; Build Capability</h6><ul><li>
Train and support staff on quality and regulatory requirements</li><li>
Evaluate the external critical suppliers/service provider and referral laboratories to ensure compliance</li><li>
Contribute to regional and global quality initiatives and harmonization efforts</li></ul><h4 class="jobSectionHeader">
Who You Are</h4>
You are a structured, analytical, and proactive quality professional who thrives in regulated environments and enjoys collaborating across teams.<h4 class="jobSectionHeader">
Qualifications</h4><ul><li>
Bachelor&rsquo;s degree in Laboratory Sciences, Biomedical Sciences, or related field</li><li>
SCFHS license (preferred)</li><li>
Certification in Quality Assurance or Regulatory Affairs is a plus</li></ul><h4 class="jobSectionHeader">
Experience</h4><ul><li>
3&ndash;4 years in a similar QA/regulatory role</li><li>
Experience within laboratory or medical environment</li><li>
Strong knowledge of:<ul><li>
MOH and SFDA regulations (required)</li><li>
CBAHI standards (required)</li><li>
ISO 15189 and CAP accreditation (preferred)</li></ul></li></ul><h4 class="jobSectionHeader">
Skills</h4><ul><li>
Strong understanding of QMS, audits, and documentation</li><li>
Experience with QMS/LIS systems</li><li>
Excellent problem-solving and organizational skills</li><li>
Strong communication and collaboration abilities</li><li>
Fluent in Arabic and English (written and spoken)</li></ul><h4 class="jobSectionHeader">
What You Bring Beyond the Basics</h4><ul><li>
A proactive mindset &mdash; you don&rsquo;t wait for issues, you prevent them</li><li>
The ability to translate regulations into practical, working processes</li><li>
Confidence to challenge, improve, and influence</li><li>
A strong sense of ownership and accountability</li></ul><h4 class="jobSectionHeader">
Why Join Us</h4><ul><li>
Be part of an organization where quality is central to patient impact</li><li>
Work in a collaborative regional and global environment</li><li>
Contribute to high-standard laboratory services and continuous improvement</li><li>
Grow within a culture that values expertise, structure, and innovation</li></ul><h6 class="jobSectionHeader">
Additional Information</h6><ul><li>
Preference will be given to Saudi Nationals</li></ul>
Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.
We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.</div>

Quality Assurance Specialist

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