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<h3>Job Description</h3>
BS (1-3 years relevant experience) or MS in Biochemistry, Chemistry or Biology
 General Position Summary/Purpose:
 The Quantitative, Translational &amp; ADME Sciences (QTAS) department is seeking a highly motivated fulltime contract Scientist to join the In Vitro ADME Sciences group (IVAS). The successful candidate will work in collaboration with other team members to characterize the CYP Induction properties of candidate drug molecules and may work on other in vitro ADME assays. QTAS works very closely with other disciplines (medicinal chemistry, pharmaceutical sciences, pharmacology, toxicology etc.) to conduct preclinical studies, support clinical evaluation and contribute to IND and NDA filings.
 In this role, you will be a scientist with hands-on experience in conducting in-vitro ADME assays including CYP450 induction assays to characterize candidate drug molecules for potential to induce CYP450 enzymes. Furthermore, you will provide support to project teams to enhance mechanistic understanding of complex drug-drug interactions.
 Core Job Responsibilities:
 • Routinely conduct (hands-on) evaluation of CYP450 induction
 • Conduct qPCR assay
 • Interpretation of in vitro CYP induction data derived from assays in human hepatocytes or reporter gene systems
 • Perform human and rodent hepatocytes cell culture, seeding and maintenance
 • Perform cell viability assessments and use microplate reader to measure endpoints
 • Contribute to the design of invitro ADME assays and data interpretation
 • Analyze data and maintain detailed, accurate and comprehensible study documentations
 • Use BioELN and GraphPad Prism for data analysis
 
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit <a href="http://www.ustechsolutions.com" target="_blank">www.ustechsolutions.com</a>.
 
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
 
Recruiter’s email id: <a href="mailto:satish.prasad@ustechsolutionsinc.com" target="_blank">satish.prasad@ustechsolutionsinc.com</a>
 
Job ID: 25-46866

Scientist

<h3>Job Description</h3>
General Position Summary/Purpose:
The Quantitative, Translational &amp; ADME Sciences (QTAS) department is seeking a highly motivated fulltime contract Scientist to join the In Vitro ADME Sciences group (IVAS). The successful candidate will work in collaboration with other team members to characterize the CYP Induction properties of candidate drug molecules and may work on other in vitro ADME assays. QTAS works very closely with other disciplines (medicinal chemistry, pharmaceutical sciences, pharmacology, toxicology etc.) to conduct preclinical studies, support clinical evaluation and contribute to IND and NDA filings.
In this role, you will be a scientist with hands-on experience in conducting in-vitro ADME assays including CYP450 induction assays to characterize candidate drug molecules for potential to induce CYP450 enzymes. Furthermore, you will provide support to project teams to enhance mechanistic understanding of complex drug-drug interactions.
Core Job Responsibilities:
• Routinely conduct (hands-on) evaluation of CYP450 induction
• Conduct qPCR assay
• Interpretation of in vitro CYP induction data derived from assays in human hepatocytes or reporter gene systems
• Perform human and rodent hepatocytes cell culture, seeding and maintenance
• Perform cell viability assessments and use microplate reader to measure endpoints
• Contribute to the design of invitro ADME assays and data interpretation
• Analyze data and maintain detailed, accurate and comprehensible study documentations
• Use BioELN and GraphPad Prism for data analysis

In Vitro Scientist

<h3>Job Description</h3>
Job Title: Scientist 
 Duration: 06+ months + with possible extension
 Site: South San Francisco, CA
General Position Summary/Purpose:
 The Quantitative, Translational &amp; ADME Sciences (QTAS) department is seeking a highly motivated fulltime contract Scientist to join the In Vitro ADME Sciences group (IVAS). The successful candidate will work in collaboration with other team members to characterize the CYP Induction properties of candidate drug molecules and may work on other in vitro ADME assays. QTAS works very closely with other disciplines (medicinal chemistry, pharmaceutical sciences, pharmacology, toxicology etc.) to conduct preclinical studies, support clinical evaluation and contribute to IND and NDA filings.
 In this role, you will be a scientist with hands-on experience in conducting in-vitro ADME assays including CYP450 induction assays to characterize candidate drug molecules for potential to induce CYP450 enzymes. Furthermore, you will provide support to project teams to enhance mechanistic understanding of complex drug-drug interactions.
 Core Job Responsibilities:
 • Routinely conduct (hands-on) evaluation of CYP450 induction
 • Conduct qPCR assay
 • Interpretation of in vitro CYP induction data derived from assays in human hepatocytes or reporter gene systems
 • Perform human and rodent hepatocytes cell culture, seeding and maintenance
 • Perform cell viability assessments and use microplate reader to measure endpoints
 • Contribute to the design of invitro ADME assays and data interpretation
 • Analyze data and maintain detailed, accurate and comprehensible study documentations
 • Use BioELN and GraphPad Prism for data analysis
 
EEO:
“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

ADME Scientist

<h3>Job Description</h3>
<ul>
<li>Work in an oligonucleotide manufacturing lab to make DNA via solid phase synthesis for R&amp;D use.</li>
<li>Manufactures oligonucleotides on DNA Synthesizers utilizing established and published procedures, and technical and theoretical understanding.</li>
<li>Work may include using gel purification of oligonucleotides.</li>
<li>Assumes responsibility for the accuracy, quality, and timeliness of oligo synthesis results.</li>
<li>Maintains lab supplies and DNA Synthesizers.</li>
<li>Summarizes experimental results, and reviews conclusions with supervisor/project leader.</li>
<li>Works with oligo purification group to ensure smooth handoff of oligos from DNA Synthesis to Oligo Purification.</li>
<li>Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem area.</li>
<li>Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA)</li>
<li>Processes incoming orders and interface with vendors for oligo orders. Processes and delivers outsourced oligo orders.</li>
<li>Works with supervisor to prioritize and triage the orders for in-house manufacturing or for approved external oligo vendor.</li>
<li>Assumes accountability for own lab notebook documentation and documentation of oligo orders made, ensuring synthesis records and results are recorded timely, accurately and consistently, and according to established formats</li>
<li>Participates in routine lab maintenance, lab safety, ISO, and QSR implementation.</li>
<li>Troubleshoots issues related to instrumentation.</li>
<li>Sets up, maintains, and runs oligo synthesis instruments to make oligos according to standard protocols and current priorities.</li>
<li>Synthesize oligos in an efficient, timely, and cost effective manner. Prioritize, schedule, and execute oligo syntheses to accommodate special RUSH or repeat orders.</li>
<li>Batches the orders in the manufacturing process when there are infrequent orders such that there is a balance between manufacturing efficiency and reasonable turnaround times.</li>
<li>Manufacturing Support:Helps maintain the lab/reagent supplies in the lab to ensure that there is no manufacturing downtime.</li>
<li>Helps keep the lab and work areas clean and safe.</li>
<li>Perform routine analyses (HPLC, LCMS, and/or UV spectral) on oligos on an as-needed basis.</li>
<li>Assists others in the manufacturing lab as needed.</li>
<li>Documentation: Responsible for ensuring capture of lab data from instrumentation in SDMS/electronic notebook on time.</li>
<li>Compiles and prepares data for statistical, scientific analyses, reports, or for presentations.</li>
</ul>

Research Associate

<h3>Job Description</h3>
Air Liquide Electronics innovative electronic materials respond to increasingly challenging customer demands for improved mobility, connectivity, computing power and energy consumption. We offer ultra pure carrier gases, a wide range of specialty gases and advanced precursor molecules, enabling equipment for safe distribution, purification and on-line purity control. On site, manufacturers rely on our expertise in providing full management of these gases, advanced molecules and equipment and in helping to continuously improve production processes.
 
Balazs Nanoanalysis is a contract analytical laboratory owned by Air Liquide Electronics is world-wide leader in supplying gases, specialty chemicals and services to a wide variety of industries. Balazs Nanoanalysis operates analytical labs around the world serving both internal and external clients. We support clients in a wide array of industries including semiconductor, biotechnology, aerospace/defense industry, solar, energy storage, automotive and many others. Our highly-skilled chemists assist other scientists and engineers from companies in these fields to support a wide array of activities such as quality assurance, contamination studies, R&amp;D and failure analysis.
 
How will you CONTRIBUTE and GROW?
 
This position is for the Laboratory Supervisor with performance management responsibilities.
 
The Organic Lab in Fremont, CA, located in the San Francisco Bay Area/Silicon Valley, is a specialized facility focused on a wide range of analytical measurements. These include Quality Control/Assurance (QC/QA), Failure Analysis, and Research &amp; Development (R&amp;D) support. The lab utilizes various advanced techniques such as GC-TCD/GC-FID/GC-MS, IC, FTIR, Raman Spectroscopy, UV-Vis, TGA/DSC, ATD-GCMS, HPLC/HPLC-MS, and NMR.
 
The selected candidate will join a dynamic and fast-paced team of highly skilled chemists and scientists. Key responsibilities include:
 
Team Leadership and Management:
<ul>
<li>Manage a team of chemists, scientists, and/or lab technicians.</li>
<li>Oversee performance management, employee coaching and development, and goal setting.</li>
<li>Manage and approve timesheets and Paid Time Off (PTO) requests.</li>
<li>Prioritize daily production activities and ensure adequate resources to meet customer requirements.</li>
<li>Provide daily updates to the Laboratory Manager/Sr. Lab Manager.</li>
</ul>
 
Operational Excellence and Quality Assurance:
<ul>
<li>Ensure staff adherence to Standard Operating Procedures (SOPs) and manage change requests to keep SOPs current and accurate.</li>
<li>Participate in the Quality/Intelex program, ensuring accurate evaluation, interpretation, and verification of data (samples, calibration, quality control) for analyses performed by the team.</li>
<li>Ensure proper maintenance of the team's instrument fleet.</li>
<li>Troubleshoot and apply analytical thinking to chemical analyses and processes.</li>
<li>Support the Laboratory Manager/Sr. Lab Manager with the procurement of consumables and spare parts.</li>
<li>Sustain the 6S program.</li>
<li>Identify and implement continuous improvements, demonstrating a continuous improvement mindset.</li>
</ul>
 
Training and Development:
<ul>
<li>Ensure the team is adequately trained, including preparing a cross-training plan based on a training gap analysis.</li>
<li>Production and Support:</li>
<li>Participate in production activities during team absences and periods of high capacity demand.</li>
<li>Support various activities such as quality assurance, contamination studies, R&amp;D, and failure analysis.</li>
</ul>
 
Work Schedule: Monday - Friday, 9:00 am to 6:00 pm. Some holiday and weekend coverage may be required.
 
_____________________
 
Are you a MATCH? 
 
Education Requirements:
<ul>
<li>B.S. in Chemistry or a related field with 2-4 years of experience, or an equivalent combination of education and experience. </li>
<li>1-2 years of supervisory experience in a laboratory environment is preferred.</li>
</ul>
 
General Requirements:
<ul>
<li>Safety: Adhere to and promote all safety protocols, ensure a safe working environment, and maintain up-to-date safety training for the team.</li>
<li>Flexibility: Adapt to changing customer needs and priorities, and provide support to other laboratory areas as needed.</li>
<li>Technical Skills: Demonstrated understanding of a wide variety of analytical techniques and experimental design, particularly GC (coupled with TCD, FID, MSD) and LC-MS analyses.</li>
<li>Computer Skills: Excellent proficiency in analytical instrumentation software, Microsoft Office Suite/Google Suite, and LIMS.</li>
<li>Teamwork and Communication: Ability to work effectively in a team, with strong written and spoken communication skills.</li>
<li>Personal Attributes: Self-motivated, proactive, organized, detail-oriented with good record-keeping skills, resourceful, and possesses strong problem-solving abilities.</li>
<li>Physical Demands: Ability to lift loads up to 35 lbs. and wear all required personal protective equipment.</li>
</ul>
 
 
The Salary rate range for this position in California is $110,000.00 to $115,000.00
Benefits offered: Medical, Dental, Vision, Life Insurance, Short-Term Disability, Long-Term Disability, 401(k) match, Flexible Spending Accounts, EAP, Education Assistance, Parental Leave, Paid time off, and Holidays. 
For more information you can go to Air Liquide Benefit Offerings
 
The candidate must have valid unrestricted employment authorization in the U.S. and must not require visa sponsorship now or in the future.

Laboratory Supervisor

<h3>Job Description</h3>
Job Description 
Company Overview
Pulmuone’s mission is a company that creates a healthy future for people and the earth with wholesome foods. Pulmuone Foods USA brands include Nasoya, Wildwood, Emerald Valley Kitchen, Monterey Gourmet Foods, and Cibo Naturals. Pulmuone’s family of brands provide our consumers a wide variety of delicious products that are inspired by contemporary flavor palates and encourage a healthy and sustainable lifestyle. Visit <a href="http://www.pulmuonefoodsusa.com" target="_blank">www.pulmuonefoodsusa.com</a> to learn more about the company and brands.
 This position centers on conducting sensory evaluations of food products to uphold quality standards within the New Product Development (NPD) process. The primary focus is to ensure that sensory insights contribute to innovation and product excellence management. Alongside these responsibilities, the position involves assisting in the control of R&amp;D budgets and managing administrative tasks. In addition, there is an active involvement in seizing opportunities to support new product development within the designated area.
Job Responsibilities:
<ul>
<li>Conduct sensory evaluations of food products to assess various attributes for NPD and product excellence management.</li>
<li>Organize, train, and maintain sensory panels, ensuring consistent and reliable data collection.</li>
<li>Interpret sensory data, providing actionable insights to guide product development and enhance product excellence management.</li>
<li>Collaborate with cross-functional teams, primarily Marketing, to align sensory goals with product strategies.</li>
<li>Identify opportunities to optimize sensory evaluation processes for efficiency and accuracy.</li>
<li>Stay updated on sensory analysis techniques and industry trends to enhance evaluation processes.</li>
<li>Communicate sensory findings to food scientists and stakeholders, facilitating well-informed decision-making.</li>
<li>Balance sensory evaluation duties with project management and administration responsibilities.</li>
<li>Monitor R&amp;D budgets and expenses to ensure adherence to financial constraints.</li>
<li>Participate and assist in the new product development limited to the possibly contributable area as assigned.</li>
<li>Evaluate and improve R&amp;D administrative processes for greater efficiency.</li>
<li>Responsible for monitoring industry trends and competitors.</li>
</ul>
Skills/Qualifications
<ul>
<li>Bachelor’s degree required in Food Science or related field.</li>
<li>3+ year’s experience in CPG food sensory evaluation.</li>
<li>Experience in food product development and new product development is a plus.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Intermediate proficiency in MS Office, Outlook, Excel, Word, and PowerPoint.</li>
<li>Strong interpersonal, organizational, and time management skills.</li>
<li>Ability to organize tasks independently with minimal supervision.</li>
<li>Outstanding ability to maintain and deal with confidential information and documentation.</li>
<li>Demonstrated professional work characteristics, high initiative, dependability, and credibility.</li>
<li>Strong administrative skills and be able to interface with all management levels.</li>
<li>Bilingual in Korean.</li>
<li>This position is fully onsite at our Fullerton location. Remote or hybrid work is not available for this position.</li>
</ul>
We offer competitive pay and benefits package, including health (~80-90% company paid) for employee and dependents, dental, vision, life insurance, long-term disability, company match 401K plan, vacation, floating holidays, and company holidays.
Pulmuone is a global, distributed workforce in four countries. We are an Equal Opportunity Employer and embrace people with different experiences, strengths, and backgrounds, who share a passion for making a healthier tomorrow for people and the planet with wholesome foods.

Product Excellence & Sensory Scientist (Bilingual in Korean)

<h3>Job Description</h3>
Job Description
POSITION SUMMARY:
Responsible for daily supervision of lab staff performing duties such as laboratory testing and data review. Duties include but are not limited to coaching, motivating, staffing, evaluating, and training staff. Works closely with Manager to ensure company, department, and team goals are met.
PRIMARY RESPONSIBILITIES:
<ul>
<li>
Responsible for day-to-day staffing/scheduling/setting up sample run schedules.
</li>
<li>
Ensures production work is consistently completed according to department goals.
</li>
<li>
Ensures all case samples are processed and accounted for.
</li>
<li>
Monitors team members to ensure adherence to SOPs and safety procedures
</li>
<li>
Oversees training for new hires: works in conjunction with lead to train new hires.
</li>
<li>
Document nonconformance reports and all corrective actions taken when test systems deviate from the established performance specifications as needed. Escalates protocol deviation to lead/supervisor.
</li>
<li>
Assists manager in initiating and completing CAPAs.
</li>
<li>
Handles employee issues. Collaborates with Manager to resolve issues.
</li>
<li>
Ensures alignment with team for reasoning behind instructions/processes, changes that are made, why certain ideas cannot be implemented effectively.
</li>
<li>
Meets regularly with individual team members to discuss goals and progress.
</li>
<li>
Responsible for staff performance reviews.
</li>
<li>
Plans and leads shift meetings
</li>
<li>
Keeps team morale up and maintains professionalism of team members, including by acting as role model.
</li>
<li>
Adheres to Departmental Expectations
</li>
<li>
Ensures compliance with all regulatory agency requirements through documentation, audits, and corrective action.
</li>
<li>
Go-to person when manager is not present.
</li>
<li>
Assists the team in day to day lab work.
</li>
<li>
Approves timecards and PTO requests
</li>
<li>
Escalates lab issues and team concerns to manager. Communicates the problem and suggests possible solutions.
</li>
<li>
Understands the entire lab process and can identify and troubleshoot issues when they arise.
</li>
<li>
Understands when and how to escalate issues appropriately.
</li>
<li>
Makes sure the goals set by manager for the team are being met in the lab.
</li>
<li>
Performs and completes side projects assigned by the manager.
</li>
<li>
Actively interacts with interdepartmental teams such as OPS, Accessioning, Extractions, Engineering, Stats, R&amp;D, and Support.
</li>
<li>
Provides direction to employees according to established policies and management guidance.
</li>
<li>
Administers company policies that directly affect subordinate employees.
</li>
<li>
Recommends changes to unit or sub-unit policies.
</li>
<li>
Provides direct supervision to professional individual contributors and/or skilled, support individual contributors
</li>
<li>
Acts as advisor to unit or sub-units and may become actively involved, as required, to meet schedules and resolve problems.
</li>
<li>
This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job
</li>
<li>
Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.
</li>
<li>
Must maintain a current status on Natera training requirements.
</li>
<li>
Performs other duties as assigned.
</li>
</ul>
QUALIFICATIONS:
<ul>
<li>
2+ years of experience as a Medical Technologist or equivalent in a clinical laboratory environment.
</li>
<li>
BS/BA degree (or equivalent) in Medical Technology, Biological Sciences, or a related field
</li>
<li>
Current MT/MLS/CLS certification preferable from ASCP, AMT, or AAB.
</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>
Proven leadership experience
</li>
<li>
Able to take on projects with little supervision.
</li>
<li>
Excellent interpersonal, communication, computer, troubleshooting, and pipetting skills.
</li>
<li>
Experience in Molecular Biology, GMP, and QSR.
</li>
<li>
Excellent oral and written communication skills.
</li>
<li>
Word processing and data management skills.
</li>
</ul>
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.San Carlos, CA $98,500—$147,900 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit <a href="http://www.natera.com" target="_blank">www.natera.com</a>.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents. 
Link: <a href="https://www.natera.com/notice-of-data-collection-california-residents/" target="_blank">https://www.natera.com/notice-of-data-collection-california-residents/</a>
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information: - BBB announcement on job scams - FBI Cyber Crime resource page

Supervisor CLS

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>401(k)</li>
<li>Competitive salary</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Paid time off</li>
<li>Vision insurance</li>
</ul>
 Rare opportunity to learn and grow with our company! Liberty EnviroLab is currently seeking Full Time Experienced Laboratory Analysts specializing in wildfire, structure fire, asbestos, and mold analysis. Liberty EnviroLab is located in San Marcos in the northern San Diego County. Liberty offers a variety of analytical testing services to support environmental investigations focused on wildfire, structure fire, asbestos, mold (microbiology). Our management team has over 71 years of combined experience in particulate analysis and trace evidence examination. We believe in empowering our customers with accurate and defensible analytical results. Some Responsibilities Include: Safely perform analyses on samples according to Libertys Standard Operating Procedures (SOPs) using advanced instruments. Follow all laboratory QA/QC requirements Record data using computer software and programs. Maintain equipment according to manufacturer guidelines and company procedures. Perform other assigned duties, as requested by supervisor. Requirements: Associates or Bachelors Degree in a life science (biology, chemistry, environmental science, etc.) preferred. 1-2 years of Polarized light microscopy (PLM) experience required. 1 year of Phase contrast microscopy (PCM) experience required. Self-motivated, independent, and team oriented. Must be able to work in a fast-paced setting, multi-task, and prioritize assignments. Good communication, computer, typing, and organizational skills.. Visit our website for more information about our company. <a href="http://www.libertyenvirolab.com" target="_blank">www.libertyenvirolab.com</a> Please submit your resume, or call us at 760-539-7024 for assistance! About UsOur experience and cutting-edge, high-performance instruments combined with our solutions-focused customer service empower our clients with accurate and defensible analytical results. We Dont Settle For Anything But The Best Our investment employing the most advanced, state-of-the-art instruments and uniquely experienced scientists and analysts, provides an unparalleled opportunity and experience for our customers. Our court approved experts have decades of experience in particulate analysis and trace evidence examination using various techniques of light microscopy, electron microscopy, infrared microspectroscopy and Raman spectroscopy. Our highly experienced staff have instructed forensic microscopy courses in university science graduate programs and have distinguished careers in developing and implementing quality assurance/quality control programs for laboratories across the nation.

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