microbiologist

Arab Center for Engineering Studies

<div>
 
 
 
 About the Arab Center of Engineering Studies (ACES):
 
 
 
 
 ACES is a Leading Specialized Engineering Company in the Middle East. At ACES we offer a wide range of specialized engineering services including site and geotechnical investigation, materials technology and testing, quality control of projects, special studies, land and marine surveying, and chemical and environment testing.
 
 
 With our wealth of experience, strong relationships, technical knowledge, and focus, we help our clients with fast, reliable, cost-effective, and quality engineering solutions that meet their expectations.
 
 
 
 
 
 
 
 What ACES is Looking For?
 
 
 
 
 ACES is looking for a
 
 Microbiologist
 
 to join our team in Doha, Qatar.
 
 
 
 
 
 
 
 Job Summary:
 
 
 
 
 Performs microbiological sampling and laboratory analysis on variety of samples (environmental, food, etc.) as per established standard test methods/standard operation procedures.
 
 
 
 
 
 .
 
 
 Duties and Responsibilities:
 
 
 
 <ul>
 <li>
 Conduct various microbiological testing assigned to him/her including sampling, sample and media preparation.
 </li>
 <li>
 Ensure the microbiological sampling and tests are carried out according to required standard test methods/SOPs and per customers&rsquo; requirements.
 </li>
 <li>
 Record test data accurately in accordance with related test methods and SOPs. Check laboratory worksheets for accuracy of data entry and calculations before their submission to concerned supervisor for review and reporting.
 </li>
 <li>
 In accordance with the applicable SOPs, conduct and record data for reagents and media preparation, for sterility checks of pre-sterilized consumables and laboratory supplies, and for verification of reagents, media, microbiological cultures.
 </li>
 <li>
 Conducting method validation experiments under the direction of the Senior Microbiologist.
 </li>
 <li>
 Analysis of PT samples assigned to him/her.
 </li>
 <li>
 Participate in training sessions and seminars, provide on the job training to other fellow chemists.
 </li>
 <li>
 Monitor and record environmental conditions in the microbiological lab including ambient temperature, humidity, air quality and the indications of temperature and humidity conditioning devices.
 </li>
 <li>
 Applies the requirements for good housekeeping, including sterile/aseptic techniques, cleaning and sterilization of consumables, glassware, equipment, laboratory, etc.
 </li>
 <li>
 Maintain laboratory equipment and apparatus in good working order, following appropriate procedures for usage, clean-up/sterilization, calibration and maintenance. Inform Senior Microbiologist for equipment defects/breakdowns when required.
 </li>
 <li>
 Implement ACES Quality Management System requirements.
 </li>
 <li>
 Implements the requirements of ACES HSE Management system including using of appropriate protective tools and safe work with and disposal of hazardous materials.
 </li>
 <li>
 Any duties or responsibilities assigned by the management.
 </li>
 </ul>
 
 
 
 
 
 
 Reporting To:
 
 
 
 
 This position will directly report to the Civil Lab Supervisor.
 
 
 
 
 
 
 
 Education &amp; Experience:
 
 
 
 <ul>
 <li>
 Bachelor's degree in biology or microbiology.
 </li>
 <li>
 0-2 years of experience in testing laboratory specialized in microbiological testing of food, and environmental samples.
 </li>
 </ul>
 
 
 
 
 
 
 Knowledge, skills, and abilities:
 
 
 
 <ul>
 <li>
 Fundamentals of Biology and Microbiology.
 </li>
 <li>
 General knowledge of general science and mathematics including algebra, statistics and data analysis.
 </li>
 <li>
 A good knowledge of the microbiological principles, techniques, terminology and procedures applicable to the separation, preservation and identification of microorganisms.
 </li>
 <li>
 Proper sample collection procedures and techniques.
 </li>
 <li>
 Mathematical calculations used in microbiology analyses.
 </li>
 <li>
 Standard reference methods and standard operation procedures.
 </li>
 <li>
 International and local technical specifications related to the scope of tested materials (GSO, QCC, WHO, etc. as applicable)
 </li>
 <li>
 Proper use, calibration and maintenance of laboratory equipment, including the sterilization of equipment, supplies, and hazardous biological materials
 </li>
 <li>
 Awareness of requirements of ISO 17025 and ACES Quality Management System
 </li>
 <li>
 Awareness of requirements of ACES HSE Management System and especially, working with hazardous chemicals and hazardous waste disposal.
 </li>
 <li>
 Good technical reading and writing skills in English language
 </li>
 <li>
 LIMS, Ms. Word, MS Excel, Ms. Outlook.
 </li>
 <li>
 Safety and Environmental Issues
 </li>
 </ul>
 
 
 
 
 
 
 Why work for ACES?
 
 
 
 
 At ACES, we believe in potential. We strive to create a work environment that is professionally stimulating, intellectually challenging, and personally rewarding.
 
 
 ACES is committed to recruiting and retaining qualified, motivated staff who can support our clients effectively on projects throughout the Middle East. We are involved in a wide array of projects, large and small, in various markets. Our extensive portfolio provides numerous opportunities for our staff to improve their skills and to meet new challenges.
 
 
 ACES has a diverse employee base, made up of individuals with widely varying backgrounds who are at different stages of their professional careers. They share a common goal: serving our clients according to the highest standards of excellence.
 
 
 
 
 
 
 
 Our Commitment to Sustainability
 
 
 
 
 At ACES, sustainability is integrated into our daily operations and strategic direction, guided by the ISO 14001 Environmental Management Standard. We maintain a fully digitized, paperless environment to reduce our ecological footprint, while our Board and executive management have embedded environmental sustainability into our governance framework. We actively seek environmentally conscious talent and provide ongoing training and awareness programs to empower employees, along with opportunities to contribute to sustainability initiatives and projects.
 
</div>

Microbiologist

Mars

<div>
 
 Job Description
 
 
 
 
 Supervise micro sampling and samples handling in OCT to ensure samples are taken at the right quantity, at the time and frequency; and dispatched to the External Micro Lab in good conditions with the right labels.
 
 
 
 
 Ensure implementation of Inbound testing plan, make sure of sampling &amp; testing of RM is compliant with sampling plan. Follow up with external chemical labs the analysis &amp; results communication.
 
 
 
 
 Verify the External Micro Lab equipment, resources, analysis procedures and working environment are consistently compliant to the required standards.
 
 
 
 
 Verify the micro lab results, monitor the trend, analyze and report any micro deviation and non-compliance with product specifications.
 
 
 
 
 Timely release of all micro &amp; chemical tested products and materials through Hold &amp; Release module in ATLAS Q&amp;FS.
 
 
 
 
 Participateto the External Micro Lab with Regional Microbiologist/Food Safety Manager, identify the gap and opportunities to improve and follow up with the external lab to close the audit finding actions. Support the External Micro Lab to maintain Good Laboratory practices.
 
 
 
 
 Manage the budget of R&amp;D testing as per the operating plan and work on continuous improvement plan to reduce R&amp;D testing cost through optimization in the testing plan and efficient execution.
 
 
 
 
 Support the site in the investigation and trouble-shooting of micro-related incidents and non-conformances; and verify the effectiveness of corrective and preventive actions for the micro issues.
 
 
 
 
 Support the site in creating awareness of micro hazards and to improve GMP/GHP.
 
 
 
 
 Contribute to the risk assessment &amp; investigation activities related to micro issues, e.g. in Material Risk Assessment, Packaging Risk Assessment, Change Management, Exceptional Release, Derogation/Waiver, &amp; consumer complaints.
 
 
 
 
 compliance to Micro Verification and IVT standards as owner for the site.
 
 
 
 
 Participate actively as HACCP team member for all value streams.
 
 
 
 
 Owner of the Environmental &amp; Hygiene module in ATLAS Q&amp;FS module, ensure proper utilization of the system and manage the database and reporting through the system.
 
 
 
 
 Own the Micro Score Card for OCT and report periodically with the right level of details.
 
</div>

Site Microbiologist

Medical Specialists Centre

We are looking for a Microbiologist Technician to join our laboratory team in Dubai. Candidates must have a valid DHA license or DHA eligibility (mandatory).Interested candidates can apply through Indeed or send their CV.Job Type: Full-timeWork Location: In person

Microbiology Technician

Mirus Consulting Group

<div>m&icirc;rus Consulting Group is a Puerto Rico based technical services firm headquartered in Humacao. The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States. Its services include the assessment and validation of automation systems, network infrastructures, and business processes, as well as comprehensive project management support to ensure compliance, efficiency, and operational excellence. 
 
Job Summary 
The Specialist Quality Control functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. The Specialist Quality Control is responsible for supporting quality control laboratory operations within a regulated pharmaceutical environment. This role ensures compliance with quality standards, regulatory requirements, and internal procedures through scientific data analysis, method validation and transfer, sample management, and quality process management. 
 
Key Responsibilities
<ul><li>Perform and support scientific data analysis for Quality Control activities.</li>
<li>Strong Technical Writing (English and Spanish) mainly focuses.</li>
<li>Utilize Microsoft Excel as a primary tool for data analysis and trending.</li>
<li>Support sample management activities including receipt, tracking, testing, and disposition.</li>
<li>Participate in project management activities related to method validation, method transfer, and quality improvements.</li>
<li>Support and maintain quality process management, ensuring compliance with GMP and internal procedures.</li>
<li>Assist with computer system validation and analytical method validation (preferable experience).</li>
<li>Support equipment preventive maintenance, basic troubleshooting, and documentation.</li>
<li>Develop inspection, qualification, or validation protocols under short timelines.</li>
<li>Prioritize critical tasks efficiently in a fast-paced and regulated environment.</li>
<li>Collaborate cross-functionally and communicate effectively with internal stakeholders.</li>
<li>Demonstrate strong negotiation and problem-solving skills when dealing with quality issues.</li>
</ul>Minimum Requirements 
One of the following combinations is required:
<ul><li>Doctorate degree in a scientific field or</li>
<li>Master&rsquo;s degree with a minimum of 2 years of directly related experience or</li>
<li>Bachelor&rsquo;s degree with a minimum of 4 years of directly related experience
</li><li>Field of Study
<ul><li>Scientific background in Science or Engineering</li>
</ul></li><li>Experience in the Pharmaceutical Industry, preferably within Quality Control laboratories</li>
<li>Background or experience as Microbiologist, Chemist, Biochemist, Molecular Scientist, or Chemical Engineer</li>
<li>Experience with laboratory testing, method validation, method transfer, and quality processes</li>
</ul>Required Skills and Competencies
<ul><li>Strong technical writing skills (English/Spanish)</li>
<li>Excellent communication and interpersonal skills</li>
<li>Strong organizational and time management skills</li>
<li>Ability to manage multiple priorities and meet deadlines</li>
<li>High attention to detail and commitment to quality and compliance</li>
<li>Ability to work independently and as part of a multidisciplinary team</li>
</ul>This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.</div>

Specialist Quality Control - 35191

Sutter Health

<div>We are so glad you are interested in joining Sutter Health!
Organization:
SRMC-Sutter Roseville Med Center
Position Overview:
Executes procedures in assigned areas of the Laboratory to deliver accurate results in a timely manner. Maintains competence to perform pre-analytic, analytic and post-analytic procedures on biological specimens to aid health care providers in the diagnosis, treatment, monitoring and prevention of disease. Performs a variety of basic and complex Laboratory procedures, including phlebotomy, specimen processing, quality control, quality assurance, and waived, moderate or high complexity testing (as classified by the Clinical Laboratory Improvement Amendments - CLIA). If assigned to the Transfusion Service, performs moderate or high complexity testing and other duties such as blood inventory management, blood product preparation, and issuing blood products for transfusion. Adheres to all local/state/federal regulations, codes, policies and procedures to ensure patient privacy and maintain the highest level of safety and reliability in testing. Note: Assignments and scope of duties are consistent with type of limited CLS license (e.g. Clinical Chemist Scientist, Clinical Microbiologist Scientist, and Clinical Immunohematologist Scientist)
Job Description: 
EDUCATION: 
 
A Bachelor's degree in Biology or related-field. 
 
CERTIFICATION &amp; LICENSURE:<ul><li>
CA Licensed Clinical Laboratory Scientist (CLS) or Clinical Immunohematologist Scientist</li></ul>
TYPICAL EXPERIENCE: 
 
2 years recent relevant experience. 
 
SKILLS AND KNOWLEDGE: 
 
Demonstrated knowledge and technical competence in routine specimen collection, preparation, testing applications, laboratory operations, and quality assurance in assigned clinical specialty areas appropriate for licensure; examples Transfusion Service or Microbiology. 
 
Ability to organize and prioritize job duties and assigned tasks for completion within expected timeframes 
 
Ability to accurately, precisely, and reliably perform job duties and assigned tasks. Demonstrates sound judgment and problem solving relevant to assigned duties. 
 
Culturally Competent Communication: Ability to compassionately and effectively interact with patients of diverse ages, backgrounds, values, beliefs and behaviors 
 
Workflow Management Ability to appropriately respond to: 1) fluctuations in volume; 2) unexpected situations or problems such as equipment or IS failure; 3) shift to-shift hand-offs; 4) STAT test orders; 5) specimen integrity issues 6) regular review of pending logs, priority assignments, etc. 
 
Adherence to Practices &amp; Procedures: Ability to follow standard practices, processes, and procedures in sequence. Knowledge of applicable local/state/federal regulations, codes, policies, and procedures aimed at ensuring the privacy and safety of patients. 
Job Shift:
Nights
Schedule:
Part Time
Shift Hours:
8
Days of the Week:
Variable
Weekend Requirements:
Every other Weekend
Benefits:
Yes
Unions:
No
Position Status:
Non-Exempt
Weekly Hours:
28
Employee Status:
Regular
Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans.
Pay Range is $64.85 to $81.06 / hour
The compensation range may vary based on the geographic location where the position is filled. Total compensation considers multiple factors, including, but not limited to a candidate&rsquo;s experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs. Base pay is only one component of Sutter Health&rsquo;s comprehensive total rewards program. Eligible positions also include a comprehensive benefits package.</div>

Clinical Laboratory Scientist - Transfusion Services

<div>We are so glad you are interested in joining Sutter Health!
Organization:
PAMF-Palo Alto Medical Foundation CAD
Position Overview:
Executes procedures in assigned areas of the Laboratory to deliver accurate results in a timely manner. Maintains competence to perform pre-analytic, analytic and post-analytic procedures on biological specimens to aid health care providers in the diagnosis, treatment, monitoring and prevention of disease. Performs a variety of basic and complex Laboratory procedures, including phlebotomy, specimen processing, quality control, quality assurance, and waived, moderate or high complexity testing (as classified by the Clinical Laboratory Improvement Amendments - CLIA). If assigned to the Transfusion Service, performs moderate or high complexity testing and other duties such as blood inventory management, blood product preparation, and issuing blood products for transfusion. Adheres to all local/state/federal regulations, codes, policies and procedures to ensure patient privacy and maintain the highest level of safety and reliability in testing. Note: Assignments and scope of duties are consistent with type of license - either a CLS - Generalist or one of the limited CLS license (e.g. Clinical Chemist Scientist, Clinical Microbiologist Scientist, and Clinical Immunohematologist Scientist)
Job Description:
These Principal Accountabilities, Requirements and Qualifications are not exhaustive but are merely the most descriptive of the current job. Management reserves the right to revise the job description or require that other tasks be performed when the circumstances of the job change (for example, emergencies, staff changes, workload, or technical development). 
 
EDUCATION:<ul><li>
[Equivalent experience will be accepted in lieu of the required degree or diploma]</li><li>
Bachelor's degree</li></ul> 
CERTIFICATION &amp; LICENSURE:<ul><li>
CLSL-CA Licensed Clinical Lab Scientist.</li></ul> 
TYPICAL EXPERIENCE:<ul><li>
2 years recent relevant experience.</li></ul> 
SKILLS AND KNOWLEDGE:<ul><li>
Demonstrated knowledge and technical competence in routine specimen collection, preparation, testing applications, laboratory operations, and quality assurance in one or more assigned clinical specialty areas; examples: Chemistry, Special Chemistry, Hematology/Coagulation, Urinalysis and Transfusion Service.</li><li>
Ability to accurately, precisely, and reliably perform job duties and assigned tasks. Demonstrates sound judgment and problem solving relevant to assigned duties.</li><li>
Ability to compassionately and effectively interact with patients of diverse ages, backgrounds, values, beliefs and behaviors</li></ul>
Workflow Management Ability to appropriately respond to:<ul><li>
1) Fluctuations in volume.</li><li>
2) Unexpected situations or problems such as equipment or information systems failure.</li><li>
3) Shift-to-Shift hand-offs.</li><li>
4) STAT test orders.</li><li>
5) Specimen integrity issues.</li><li>
6) Regular review of pending logs, priority assignments, etc.</li><li>
Ability to follow standard practices, processes, and procedures in sequence. Knowledge of applicable local/state/federal regulations, codes, policies, and procedures aimed at ensuring the privacy and safety of patients.</li><li>
Knowledge of applicable local/state/federal regulations, codes, policies, and procedures aimed at ensuring the privacy and safety of patients.</li><li>
Ability to organize and prioritize job duties and assigned tasks for completion within expected timeframes.</li></ul> 
Job Shift:
Days
Schedule:
Part Time
Shift Hours:
8
Days of the Week:
Variable
Weekend Requirements:
As Needed, Saturday, Sunday
Benefits:
Yes
Unions:
No
Position Status:
Non-Exempt
Weekly Hours:
20
Employee Status:
Regular
Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans.
Pay Range is $68.50 to $85.62 / hour
The compensation range may vary based on the geographic location where the position is filled. Total compensation considers multiple factors, including, but not limited to a candidate&rsquo;s experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs. Base pay is only one component of Sutter Health&rsquo;s comprehensive total rewards program. Eligible positions also include a comprehensive benefits package.</div>

Clinical Laboratory Scientist Generalist

Sharp HealthCare

<div>[California Clinical Laboratory Scientist (CLS) Generalist license - CA Department of Public Health
Hours:
Shift Start Time:
10 AM
Shift End Time:
6:30 PM
AWS Hours Requirement:
8/40 - 8 Hour Shift
Additional Shift Information:
Weekend Requirements:
Every Other
On-Call Required:
No
Hourly Pay Range (Minimum - Midpoint - Maximum):
$49.700 - $64.130 - $71.820 
The stated pay scale reflects the range that Sharp reasonably expects to pay for this position. The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant&rsquo;s years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices. 
What You Will Do 
Provides the technical knowledge, expertise and judgment required to support the Sharp HealthCare (SHC) mission and scope of laboratory services. 
 
Required Qualifications<ul><li>
Other Education required for CA State CLS or CLS specialty.</li><li>
California Clinical Laboratory Scientist (CLS) Generalist license - CA Department of Public Health OR California Clinical Chemist Scientist License - CA Department of Public Health OR California Clinical Microbiologist Scientist License - CA Department of Public Health OR California Clinical Toxicologist Scientist License - CA Department of Public Health OR California Clinical Genetic Molecular Biologist Scientist License - CA Department of Public Health OR California Clinical Cytogeneticist Scientist License - CA Department of Public Health OR California Clinical Histocompatability Scientist License - CA Department of Public Health -REQUIRED</li></ul> 
Preferred Qualifications<ul><li>
Experience in a clinical laboratory as a CLS.</li></ul> 
Other Qualification Requirements<ul><li>
The CLS license must be respective to the department&rsquo;s assigned area. 
 
ASCP preferred.</li></ul> 
Essential Functions<ul><li>
Analytical Testing Procedures 
Completes testing procedures using written policies, procedures and other appropriate resources; identifies issues in and submits necessary revisions to policies and procedures. 
Performs new procedures and policies within acceptable training time intervals; meets/exceeds department turnaround time goals. 
Documents activities and results consistently, thoroughly and legibly; proof reads and double checks own work to achieve zero defects and zero harm. 
Reviews operational reports for possible clerical and analytical errors and make correction as necessary. 
Evaluates data for accuracy and verifies any questionable finding with thorough investigation and appropriate follow-through. 
Performs pre-analytical (patient reception, sample collection, processing) and analytical procedures and demonstrates assessment of testing factors with regard to patient age and population specific groups. 
Demonstrates emotional intelligence, critical thinking and logical decision making, especially under critical and stressful situations to reach acceptable resolutions. 
Acts as a key resource for employee/student training, development and competency assessment. 
Act as a key operator for testing, validation, analyzers and technology. 
Performs additional duties to meet operational needs. 
Participates in writing and revision of policies and procedures.</li><li>
Equipment Management 
Utilizes equipment (including phone, copier, fax, printer, etc.,) analyzers, products, and other tools per manufacturer's and training instructions and according to established procedures; facilitates issue resolution. 
Reports, documents and resolves or facilitates resolution of equipment/analyzers/tool/reagent issues and failures in a timely and efficient manner. 
Removes defective equipment/analyzers from use, documents problem, and notifies appropriate personnel for repair; verifies equipment/analyzers inspections are up-to-date. Follows through on problem resolution and validates equipment/analyzers performance post repair. 
Participates in analyzer and test methodology, evaluation and selection and provides input in decision making processes. 
Demonstrates competency and efficient use of tool applications (IS, PC, other system/software) and equipment to produce the end product. 
Performs and validates required preventive and corrective maintenance on equipment/analyzers/tools. 
Actively manages inventory and demonstrates ability to evaluate consumables (reagent/supply) inventory to prevent shortages; alerts ordering personnel.</li><li>
Quality Assurance 
Coordinates and completes processes to meet standards established to maintain quality testing, including collaboration and engagement in continuous improvement of processes. 
Represent laboratory department in entity or system committees, taskforces, or workgroups as necessary. 
Communicates clearly using tools Closed Loop and SBAR. 
Supervises work activities performed by Medical Lab Technicians, Certified Phlebotomy Technicians and Laboratory Assistants, and promotes accountability, mutual respect and teamwork. 
Completes and assesses QC performance, proficiency testing, test validation/calibration/linearity with indicated corrective action and resolution as needed. 
Has knowledge of and reviews quality assurance indicators and monitors and works with the laboratory team to meet/exceed the established thresholds. 
Completes and validates daily position tasks within expected timeframes to meet QA indicator goal expectations. 
Identifies errors and follows-through with investigation, correction, documentation, and notification to appropriate caregiver and lab leadership. 
Demonstrates process of self-discovery, including knowledge of strengths and weaknesses and views deficiencies as opportunities for growth; sets goals for self-improvement. 
Performs shift lead duties as necessary. 
Receives feedback well and provides thoughtful feedback to others. 
Participates in regulatory and safety compliance activities as assigned.</li></ul>
Sharp HealthCare is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability or any other protected class</div>

Clinical Laboratory Scientist - Copley Lab - Day Shift - Full Time

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