1,518 Diagnostics jobs in the United States

As an Associate Director, Global Procurement, you will be accountable for defining and supporting the implementation of our Companion Diagnostics and Clinical Lab strategies. Your responsibilities will include commercial supplier relationships, supplier selection and managing performance and service delivery.
This position will require you to be on-site 4 days/week at our Warren, NJ, Armonk, NY or Tarrytown, NY locations. We cannot offer a remote or hybrid work option. If eligible, we can offer relocation benefits.
**A typical day may include the following:**
- Works closely with team members across Precision Medicine and align category priorities with Procurement management and other G&A functions.
- Manages negotiations and complex contracts/contracting, supplier management activities, and engagement activities across Companion diagnostic partners.
- Drives value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.
- Represents Global Procurement by participating in scientific forums with critical short and long-term impact on the success, efficiency, growth, and results.
- Manages category activities to ensure compliance with appropriate GxPs and other applicable regulations, as applicable.
- Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron's priorities and business requirements.
- Uses data to drive decision-making for successful category projects.
- Leading and working with others to solve issues of diverse scope and providing analysis considering current business trends.
**This may be for you if you:**
- Enjoy building relationships with collaborators and suppliers to driving results.
- Have knowledge with sourcing contracting tools, ERP's, and eRFx systems preferred. (Icertis, Oracle, Zycus, Ariba, Other)
- Can demonstrate success supporting global supply market evaluation processes using all available market intelligence, risk, compliance, and financial assessment tools.
- Have operated with integrity, focus, and clarity in an environment of ambiguity to inspiring change and continuous improvement.
To be considered you are to have Bachelor's degree in a relevant field of study plus relevant, progressive experience in procurement or a related field, including experience in Clinical Labs within Pharma/BioPharma. Experience successfully managing category processes, including strategy development and execution. Experience successfully establishing and driving Supplier Relationship Management (SRM) programs and governance models. Demonstrated success working with cross-functional teams in clinical diagnostics and clinical labs sourcing, negotiations and contracting. Experience with IVD regulations and requirements. Knowledge regarding rates, unit costs, costing structures, cost models, and TCO.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
**Salary Range (annually)**
$154,800.00 - $252,800.00

Job DescriptionJob Description

Title: Clinical Laboratory & Diagnostics Specialist (2nd Shift)

Payrate: $30-32/hour

Duration: 1-year contract (Excellent potential for permanent)

Hours: Full-time | Monday-Friday | 3pm-11:30pm

Start Date: ASAP

Location: Irvine, CA 92618 (Onsite - Local candidates only)

Summary:

Ready to be part of a global mission to help people live longer, healthier lives? Join a world-class team of innovators, leaders, and problem solvers who develop state-of-the-art instruments and reagents for life science research laboratories and healthcare facilities worldwide. As a Clinical Laboratory & Diagnostics Specialist on our 2nd shift team, you'll play a crucial role in supporting finished product testing and release of company controls. Working in our Quality Control department, you'll combine technical expertise with collaborative teamwork to ensure the highest standards in clinical diagnostic testing. If you're passionate about precision, thrive in a fast-paced lab environment, and want to make a real impact on global healthcare, this is your opportunity to shine.

What You'll Do:

• Operate, maintain, calibrate, and troubleshoot clinical diagnostic laboratory instruments with precision and expertise
• Follow good laboratory practices (GLP) and good documentation practices (GDP) to ensure compliance and quality
• Work collaboratively with team members to achieve daily testing goals and objectives
• Evaluate assay runs for accuracy and acceptability according to Quality Control procedures
• Enter results into appropriate software and database systems with attention to detail
• Order supplies required for testing on assigned instrumentation to maintain seamless operations
• Support finished product testing and release of company controls during 2nd shift operations
• Perform daily maintenance and troubleshooting on clinical diagnostic instrumentation

What You Bring:

• Associate's degree or higher in science field or equivalent clinical lab experience
• 2+ years of experience in clinical laboratory and diagnostics setting
• Experience performing daily maintenance of instrumentation or relevant school experience
• Familiarity with clinical laboratory instruments from manufacturers like Beckman, Roche, Siemens, or Abbott
• Ability to operate, maintain, calibrate, and troubleshoot clinical diagnostic lab instruments
• Excellent multitasking and organizational skills in fast-paced environments
• Basic knowledge of Microsoft Excel, Outlook, and Word
• Strong attention to detail and commitment to quality standards

Bonus Points If You Have:

• Experience running chemistry/immunoassay/immunology analyzers and/or ELISAs
• Knowledge of LIMS (Laboratory Information Management System)
• Advanced certifications in clinical laboratory technology
• Experience with regulatory compliance in clinical settings
• Background in quality control or quality assurance processes

Make a meaningful impact on global healthcare while advancing your career in a cutting-edge laboratory environment. With competitive hourly pay, weekly pay, and comprehensive benefits, plus excellent potential for permanent placement, you'll have the foundation to excel in this vital role. Apply now to become our next Clinical Laboratory & Diagnostics Specialist and help us continue our mission of improving lives worldwide.

TCWGlobal is an equal opportunity employer. We do not discriminate based on , , , , belief, or .

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

**Discover Your Career at Emory University**
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community.
**Description**
The Marcus Autism Center is seeking an Academic Clinical Psychologist for a leadership position in Clinical Research Operations.
The Marcus Autism Center is one of the largest academic health centers in the US serving children with autism and related neurodevelopmental disabilities and their families, with a strong commitment to health equity. It is also a hub for research with a portfolio ranging from functional genomics to behavioral neuroscience, early brain development, clinical trials and implementation science. We are recruiting for a leadership position for our Clinical Assessment Core, which serves as the clinical nexus for the entire research enterprise.
The Marcus Autism Center is the Division of Autism & Developmental Health at Emory University School of Medicine Department of Pediatrics, which centralizes clinical care and science in autism and developmental social neuroscience at Children's Healthcare
of Atlanta (CHOA). The selected clinician will be a core faculty member in the Department of Pediatrics at a rank commensurate with the candidate's academic achievements.
We are looking for a leading clinician committed to the highest level of excellence in clinical characterization for research, who has expertise in standardized developmental, cognitive and diagnostic procedures. Clinical experience with young children is highly desirable. This clinician will work closely with Dr. Cheryl Klaiman, Director of Clinical Research Operations, and will collaborate closely with Dr. Warren Jones, Director of Research, and Dr. Ami Klin, Director of the Center and Division Chief.
The Marcus Autism Center has wide-ranging research and training collaborations with other divisions and scientific programs at Emory and CHOA, including the Behavioral & Mental Health Center led by Dr. John Constantino and the Center for Neuroscience Research led by Dr. Timothy Gershon, as well as with Emory's Department of Human Genetics led by Dr. Peng Jin and Emory's School of Public Health led by Dr. Daniele Fallin. Collaborations also extend to community-based and state agencies such as EasterSeals, Jewish Federation, Atlanta Public Schools, LaAmistad, and GA Departments of Public Health, Early Care & Learning, and Behavioral Health.
Interested candidates should complete the online application and submit a letter of interest and their cv.
Inquiries may be directed to Ami Klin, PhD ( ) or Cheryl Klaiman, PhD ( ).
**Additional Information:**
Employment will be in the Emory + Children's Pediatric Institute. The Emory + Children's Pediatric Institute is an affiliation between Emory University and Children's Healthcare of Atlanta that is improving the lives of children in Georgia and beyond. The Pediatric Institute combines the unique strengths and resources of each institution in support of our three-part academic missions of providing outstanding clinical care, conducting innovative basic science discovery and clinical research, and coordinating exceptional education of the future healthcare workforce.
NOTE: Position tasks are generally required to be performed in-person at an Emory University location. Remote work from home day options may be granted at department discretion. Emory reserves the right to change remote work status with notice to employee.
**Additional Details**
Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: (V) | (TDD).
Emory University is committed to providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to request a reasonable accommodation, please contact the Department of Accessibility Services at (V) | (TDD). Please note that one week's advance notice is preferred.
**Connect With Us!**
Connect with us for general consideration!
**Job Number** _ _
**Job Type** _Regular Full-Time_
**Division** _Emory+Children's Ped Institute_
**Department** _SOMPI: Marcus Center_
**Campus Location (For Posting) : Location** _US-GA-Atlanta_
**_Location : Name_** _Emory Campus-Clifton Corridor_
**Remote Work Classification** _Primarily On Campus_
**Health and Safety Information** _Position involves clinical patient contact_

Step Into a Role That Blends Innovation with Purpose - Medical Lab Tech Opportunity in Southwestern Ohio

Tucked beside the Great Miami River, there's a town that's undergone a quiet transformation-shifting from its industrial roots into a vibrant hub of art, innovation, and fresh energy. It's the kind of place where brick buildings meet murals, where local makers thrive, and where families and professionals alike feel the pulse of growth alongside a deep appreciation for history. With parks, festivals, galleries, and a true sense of community, this town isn't just a backdrop-it's part of the reason why people stay.

We're looking for a Medical Laboratory Technician (MLT / CLT) who's ready to grow in a setting where curiosity, collaboration, and compassion are celebrated. Whether you're finishing up your MLT program or just starting out as a new grad, this full-time opportunity offers flexible shifts-including days, nights, and weekends-so you can find a rhythm that works for you. You'll be part of a team that values not just the work you do, but the perspective you bring.

In this role, you'll take on real responsibility from day one. You'll collect, process, and analyze biological specimens like blood, urine, and tissue , using protocols that emphasize both precision and safety. You'll learn to operate modern lab equipment, carry out routine diagnostics, and ensure everything meets high standards of quality control. Just as important, you'll communicate results that help providers make informed decisions-and help patients get the care they need.

We're looking for someone with an associate's degree in Medical Laboratory Technology, Clinical Laboratory Technology, Biology, or a related field . If you're certified (or working toward certification) through ASCP, AMT, or another credentialing organization, that's ideal-but if you're newly qualified or certification-eligible, we're excited to help you grow. You'll succeed here if you're organized, curious, and steady under pressure, with strong communication skills and a willingness to learn.

What makes this role special isn't just the lab-it's the community around it. Here, you'll find a town that's constantly evolving, filled with people who are proud of where they've come from and excited about where they're headed.

You'll have weekends to explore walking trails along the river, pop into a downtown art show, or simply enjoy a coffee in a locally owned café. Whether you're moving here for the first time or returning to your roots, there's room to belong.

At MLR, we believe that strong healthcare starts with strong teams-and that starts with you. We're passionate about supporting new talent, fostering confidence, and creating a workplace where you can thrive not just as a lab tech, but as a person with dreams, ideas, and goals of your own.

If you're ready to take that next step in your lab career and want to do it in a place where innovation, community, and care all come together-we'd love to meet you.

Job Description

Job Description

• The Propulsion Systems OBD team is dedicated to its mission, "Delivering Global Propulsion System OBD Requirements for Client Integration - with flawless Execution!”
• The successful candidate will have the opportunity to work with experts all over the world to interpret OBD regulations and create engineering requirements for Client software, controls, and calibration teams.
• We are looking for talented and self-driven experts that will exceed customers' expectations while inventing, orchestrating, and delivering simpler processes and solutions for the team.

Responsibilities:

• Establishing through and complete methods do deliver OBD technical requirements to all Client internal customers
• Mentoring team members on delivering complete OBD requirements for modules and vehicles including successful delivery of requirements to customers
• Ensure that processes and templates are built, known by the PSO team and applied to produce the Customer approved OBD work-products
• Communicate with teams that support Propulsion Systems OBD (PSO) and Customers
• Verify the good continuity and consistency between the activities of the OBD Tech Fellows, TSRC and the activities within PSO
• Ensure the on-time delivery of the OBD requirements to customers

Requirements:

• Minimum of 8 years' experience in OBD requirements, controls, software, or calibration
• Proficient using INCA, Matlab and Simulink/State flow
• Understanding of the goals of On-Board Diagnostics
• Functional understanding controls, Software and CAN communication
• Basic proficiency with the major purpose & components in an electrified propulsion system
• Excellent written and verbal communication skills and business acumen
• Self-motivated/proactive with strong leadership and interpersonal skills
• Ability to operate both independently and as part of a team
• Basic computer proficiency with Microsoft Excel, Word, PowerPoint, and database applications

Preferred Requirements:

• Master's in Mechanical, Electrical, Software or Controls Engineering
• Experience presenting to, and communicating directly with Government regulatory agencies
• Previous Client Propulsion Systems experience
• Experience designing and implementing new diagnostics
• 12 years' experience in OBD requirements, controls, software, or calibration within the electric, gasoline or diesel industry
• INCA, Matlab, Simulink, State flow, Minitab, C++ and Visual Basic experience

Education:

• Bachelor's in Mechanical, Electrical Engineering, Software or Controls Engineering.

Company Description

Zobility (RGBSI), is dedicated to providing the highest quality of services to our clients and employees. We are proud to be the primary partner to top companies in the automotive, aerospace & defense, IT, media & entertainment, sports, energy, and finance industries. As a result of our clients' continued growth, we are looking for energetic, personable professionals to partner with these leading US companies

Company Description

Zobility (RGBSI), is dedicated to providing the highest quality of services to our clients and employees. We are proud to be the primary partner to top companies in the automotive, aerospace & defense, IT, media & entertainment, sports, energy, and finance industries. As a result of our clients' continued growth, we are looking for energetic, personable professionals to partner with these leading US companies

Responsibilities

In this position, the qualified individual will design new enclosure systems, and design repairs for existing enclosure systems. They will perform review of enclosure systems for new construction, renovation, and restoration projects. The qualified individual will investigate and determine the service life of building enclosure assemblies. They will perform enclosure review to assess air infiltration, rain water control, heat transfer, and vapor transmission. They will perform building performance analysis including evaluate day-lighting, solar heat gain, thermal energy transfer, and holistic integration of the enclosure with building mechanical, lighting, and plumbing systems.

A sound technical background and excellent oral and written communication skills are required. A technical background in CADD and building performance modeling software is required.

Specific job responsibilities will include:

• Lead projects with team of internal consultants
• Assist Senior Project Managers with project tasks
• Perform project management duties
• Facilitate client meetings
• Prepare technical presentations for client meetings
• Prepare proposals for new project pursuits
• Review enclosure details and specifications prepared by other consultants
• Work closely with architects and contractors to develop high performance details
• Research building codes and industry standards
• Write assessment reports
• Perform field investigations, including water leakage, non-destructive testing, travel required
• Perform modeling of enclosure assemblies using different software
• Analyze proposed repair/design options
• Design and draft repair drawings and details
• Prepare construction documents such as repair drawings and specifications
• Observe construction and installation of repairs/designs in the field, including quality assurance testing
• Prepare site visit reports and meeting minutes
• Interact with project clients, sub-consultants, and repair contractors

Qualifications

• 3-10+ years' experience in building enclosure design, review, and assessments
• Professional Engineer (PE) or Registered Architect (RA)
• M.S. in Civil Engineering, M.S. in Architectural Engineering, or Master of Architecture in Building Science/Building Enclosures/Historic Preservation
• Having an RRO/RRC/RWC is a plus
• Experience in building enclosure design, repair, and retrofit and the integrated design and delivery of high performance buildings
• Experience with exterior wall, below-grade waterproofing, and roofing assemblies
• Understanding of building science and thermal analysis concepts as well as a knowledge of modeling building performance and sustainability
• Demonstrated strength in providing excellent customer service
• Excellent communication skills, both written and verbal

Skills should include:

• Microsoft Office (WORD, EXCEL, POWERPOINT)
• Computer Aided Drafting/Design (AUTOCAD, REVIT, Rhino, Grasshopper)
• Strong technical, written and verbal communication
• Ability to multi-task and meet tight deadlines
• Experience with building performance modeling, software preferred, including some or all of the following: ECOTECT, VASARI, ENERGYPLUS, EQUEST, DESIGNBUILDER, DIVA, IES-VE, THERM, SKETCHUP, WUFI
• Expertise with exterior wall systems
• Expertise with roofing assemblies
• Familiarity with building structural systems
• Experience with working on suspended scaffolding and vertical heights

Walter P Moore is an equal opportunity employer and provides all of its employees with a competitive compensation and benefits package.

This position has an annual salary range as stated below and is, in good faith, an estimate. The actual offered salary will be dependent on the candidate's knowledge, skills abilities, geographic location, industry experience and internal equity. Walter P Moore reserves the right to offer more or less than the posted range based on the criteria previously stated and will do so in a manner that does not discriminate against a candidates protected status per local, state and federal law.

Overview

Walter P Moore is an international company of engineers, architects, innovators, and creative people who solve some of the worlds most complex structural and infrastructure challenges. Providing structural, diagnostics, civil, traffic, parking, transportation, enclosure, WPM technology and construction engineering services, we design solutions that are cost- and resource-efficient, forward-thinking, and help support and shape communities worldwide. Founded in 1931 and headquartered in Houston, Texas, our 1000+ professionals work across 24 U.S. offices and 7 international locations.

Building Enclosure Consultant

Walter P Moore is an international company of engineers, innovators, and creative people who solve some of the world's most complex structural and infrastructural challenges. Providing structural, diagnostics, civil, water resources, traffic, transportation engineering, and parking consulting services, we engineer solutions that are cost- and resource-efficient, forward-thinking, and help support and shape our communities. Founded in 1931, we are headquartered in Houston, Texas and have more than 800 professionals working across 24 U.S. offices and 7 international locations.

We have immediate openings for a Building Enclosure Consultant with professional experience in building enclosure design, modeling, assessment, testing, and repair to join our growing Building Enclosure Practice in our Diagnostics Group, based in our Atlanta office.

Responsibilities:

In this position, the qualified individual will design new enclosure systems, and design repairs for existing enclosure systems. They will perform review of enclosure systems for new construction, renovation, and restoration projects. The qualified individual will investigate and determine the service life of building enclosure assemblies. They will perform enclosure review to assess air infiltration, rain water control, heat transfer, and vapor transmission. They will perform building performance analysis including evaluate day-lighting, solar heat gain, thermal energy transfer, and holistic integration of the enclosure with building mechanical, lighting, and plumbing systems.

Qualifications

• 3-7 years' experience in building enclosure design, review, and assessments
• Professional Engineer (PE) or Registered Architect (RA) is required
• S. in Civil Engineering, M.S. in Architectural Engineering, or Master of Architecture in Building Science/Building Enclosures/Historic Preservation.
• Having an RRO/RRC/RWC is a plus.
• Experience in building enclosure design, repair, and retrofit and the integrated design and delivery of high performance buildings.
• Experience with exterior wall, below-grade waterproofing, and roofing assemblies.
• Understanding of building science and thermal analysis concepts as well as a knowledge of modeling building performance and sustainability.
• Demonstrated strength in providing excellent customer service.
• Excellent communication skills, both written and verbal.

As a Hybrid Firm, Walter P Moore combines the best of both worlds blending work options to include in-office and home office environments. This allows us to offer more flexibility and work-life integration to our employees. Candidates applying for this position should have the ability to commute to or periodically travel to the affiliated office.

Walter P Moore is an equal employment opportunity employer, and provides equal employment opportunities (including offering competitive compensation and benefit packages) to all employees and applicants for employment. We prohibit discrimination and harassment of any type without regard to any characteristic protected by federal, state or local laws and encourage all to apply including veterans and individuals with disabilities.

Overview

Walter P Moore is an international company of engineers, architects, innovators, and creative people who solve some of the world's most complex structural and infrastructure challenges. Providing structural, diagnostics, civil, traffic, parking, transportation, enclosure, WPM technology and construction engineering services, we design solutions that are cost- and resource-efficient, forward-thinking, and help support and shape communities worldwide. Founded in 1931 and headquartered in Houston, Texas, our 1000+ professionals work across 24 U.S. offices and 7 international locations.

Job Responsibilities

In this position the qualified individual will investigate and determine the service life of building enclosure assemblies. The qualified individual will assess enclosure systems, and design repairs for existing enclosure systems. They will perform enclosure review to assess air infiltration, rain water control, heat transfer, and vapor transmission. They will perform building performance analysis including evaluate daylighting, solar heat gain, thermal energy transfer, and holistic integration of the enclosure with building mechanical, lighting, and plumbing systems. A sound technical background and excellent oral and written communication skills are required. A technical background in CADD and building performance modeling software is preferred. You'll develop a strong background in building faade and roofing assemblies, understanding of building science and thermal analysis concepts as well as a knowledge of modeling building performance and sustainability. Job Responsibilities will include:

• Assist Project Manager with project tasks
• Review and organize project-related documents
• Research building codes and industry standards
• Write assessment reports
• Perform field investigations, including non-destructive testing, travel required
• Performance modeling of enclosure assemblies using different software
• Analyze proposed repair/design options.
• Design and draft repair drawings and details
• Prepare construction documents such as repair drawings and specifications
• Observe construction and installation of repairs/designs in the field, including quality assurance testing
• Prepare site visit reports and meeting minutes
• Interact with project clients, sub-consultants, and repair contractors

Qualifications

• B.S. in Architectural Engineering or Architecture in Building Science/Building Enclosures/Historic Preservation; Masters degree preferred.
• Registered Architect or P.E. license required
• Experience in building enclosure design, repair, retrofit and the integrated design and delivery of high performance buildings.

Skills should include:

• Microsoft Office (WORD, EXCEL, POWERPOINT)
• Computer Aided Drafting/Design (AUTOCAD, REVIT, Rhino, Grasshopper)
• Experience with building performance modeling, software preferred (ECOTECT, VASARI, ENERGYPLUS, EQUEST, DESIGNBUILDER, DIVA, IES-VE, THERM, WUFI)
• Familiarity with exterior wall systems
• Familiarity with roofing assemblies
• Familiarity with building structural systems
• Experience with working on suspended scaffolding and vertical heights

Walter P Moore is an equal employment opportunity employer, and provides equal employment opportunities (including offering competitive compensation and benefit packages) to all employees and applicants for employment. We prohibit discrimination and harassment of any type without regard to any characteristic protected by federal, state or local laws and encourage all to apply including veterans and individuals with disabilities.

Overview

Walter P Moore is an international company of engineers, architects, innovators, and creative people who solve some of the world's most complex structural and infrastructure challenges. Providing structural, diagnostics, civil, traffic, parking, transportation, enclosure, WPM technology and construction engineering services, we design solutions that are cost- and resource-efficient, forward-thinking, and help support and shape communities worldwide. Founded in 1931 and headquartered in Houston, Texas, our 1000+ professionals work across 24 U.S. offices and 7 international locations.

JOB SUMMARY:

The Molecular Diagnostics Technologist II position is designed for a knowledgeable and experienced laboratory professional with a minimum of three years of experience as a certified Medical Technologist (MT), Clinical Laboratory Scientist (CLS), or Specialist in Molecular Technology (MB), or an individual with appropriate training and experience qualified to perform high complexity testing under CLIA 42CFR . This individual is responsible for day to day specimen processing, analysis, and results reporting. The person in this position is expected to possess the skills necessary to perform the essential functions of a laboratory technologist independently and with minimal supervision.

JOB RESPONSIBILITIES

ESSENTIAL FUNCTIONS:

• Receives and process specimens according to department protocols.
• Assists the Supervisor, Manager and Director with administrative functions such as ordering supplies and maintaining inventory.
• Produces, interprets and reports accurate and precise test results.
• Identifies and correct problems that may adversely affect test performance or result reporting of patient samples.
• Communicates pertinent section information/issues to supervisor, manager or other appropriate individuals.
• Performs instrument maintenance and method troubleshooting.
• Validates new methods.
• Completes CAP surveys.
• Assists in documentation and maintaining effective department QA/QC programs and monitors.
• Performs within the productivity expectations as set forth by current departmental guidelines.
• Exercises all laboratory safety precautions and adhere to lab procedures as stated in procedure manuals.
• Performs all job responsibilities in alignment with the industry's best security practices and regulatory guidelines to protect the confidentiality, integrity, and availability of protected health information and other sensitive company data.
• Must be familiar with and abide by the Corporate Compliance Program and all Corporate Policies, including the Privacy and Security policies.
• Addresses Client Concerns.

NON-ESSENTIAL FUNCTIONS:

• Work with other departments within PathGroup and subsidiaries.
• Other duties as assigned.
• Nothing in the job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.

EDUCATION & LICENSURE:

• Bachelor's degree in Medical Technology or Molecular Technology, or equivalent education and training in clinical, chemical, physical, or biological science.
• National certification by the American Society of Clinical Pathology (ASCP) as a Medical Technologist (MT), Clinical Laboratory Specialist (CLS) or Specialist in Molecular Technology (MB) is preferred.
• Tennessee State Laboratory License is preferred.
• Must maintain appropriate continuing education for certification and licensure as applicable.

EXPERIENCE

• Three or more years of job-related experience preferred.
• Computer proficiency preferred.