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<h3>Job Description</h3>
Job Description
MATH COORDINATOR
 
CLOSING DATE: January 15, 2026
PAY RATE: $13.56-$18.99 (Depending on experience and qualifications, with starting wage not typically above the mid-point of the range, $16.27)
SCHEDULE: Monday - Thursday (between the hours of 2:00 pm and 6:00 pm) 
Part-Time position: 20 to 25 hours per week (Specific hours to be determined after hiring.)
DEPARTMENT: Lehi Rippy Literacy Center
 
JOB SUMMARY
 
Employee would be responsible for coordinating the math program and leading a small group of teachers, under the direction of the program director. 
Responsibilities: 
<ul>
<li>Writing lesson plans</li>
<li>Preparing and or creating math materials</li>
<li>Occasionally teaching lessons to small groups of children (K - 4th grade)</li>
<li>Monitoring and supporting other teachers in the math department </li>
</ul>
 
RESPONSIBILITIES AND QUALIFICATIONS
 
<ul>
<li>Ability to interact well with children and redirect, as needed.</li>
<li>Understand young children and how they learn.</li>
<li>Interact professionally and get along well with other staff members.</li>
<li>Provide good customer service and protect confidential information. </li>
<li>Perform a variety of responsibilities with minimum supervision. </li>
<li>Must possess a knowledge of various math strategies and be familiar with the Utah State Core Standards. </li>
<li>Solid background in elementary math concepts.</li>
<li>Knowledge of best practices and various effective math strategies. </li>
<li>Must be 18 years or older.</li>
</ul>
 
Employment in this position is conditional upon passing a pre-employment background and drug test.
 Job Posted by ApplicantPro

Math Program Coordinator

<h3>Job Description</h3>
Job Description
Associate degree preferred with 2+ years chemical manufacturing experience, knowledge of 5S, organic chemical syntheses experience on reactors, Forklift Certified, and trained in EPA, ERCRA HAZWOPER.
 Perform chemical syntheses of active pharmaceutical ingredients (APIs) in strict accordance with written procedures and standard chemical safety practices
 Work on multikilogram scale organic chemical syntheses with reactors larger than 100 gallons
 Record accurate reaction notes, making observations throughout the process
 Maintain a meticulous work environment: return all equipment to the appropriate storage location; clean all tools, equipment, and surroundings after use.
 Conform to applicable safety regulations including proper handling of chemicals and use of all designed safety equipment and PPE
 Maintain meticulous inventory logs of raw materials and finished product.
 Collect and discard chemical waste in accordance with applicable internal, safety, and regulatory requirements.
 Accurately maintain waste and disposal logs.

Chemical Operator

<h3>Job Description</h3>
Job DescriptionJob Title: Scientist (Entry)&amp; Location: Berkeley, CA, 94710&amp; Duration: 9&amp; Months&amp; &amp; Job Type: -Temporary Assignment&amp; Work Type: &amp; Onsite&amp; &amp; &amp; Job Description:&amp; &amp; DEPARTMENT/TEAM DESCRIPTION:
<ul>
<li>CMC and Technology. Performs lab activities and executes studies as part of the CMCT Labs in support of life cycle management activities for launch and commercial products.&amp; </li>
</ul>
POSITION SUMMARY:
<ul>
<li>Performs lab activities and executes studies in CMCT Purification labs&amp; </li>
</ul>
POSITION DUTIES RESPONSIBILITIES:&amp; 
<ul>
<li>Executes purification process development studies following Standard Operation Procedures (SOPs) and laboratory batch records (LBRs)&amp; </li>
<li>Follows laboratory safety protocols&amp; </li>
<li>Documents experimental procedures, observations and outcomes in lab notebooks and digital databases.&amp; </li>
<li>Collaborates with development scientists and cross-functional team members&amp; </li>
<li>Maintains, monitors equipment and may troubleshoot equipment issues.&amp; </li>
<li>Works with minimal supervision after training&amp; </li>
</ul>
Skills Competency Requirements:&amp; 
<ul>
<li>Must be comfortable with routine laboratory operations and documentation systems such as BPRs and SOPs&amp; </li>
<li>Excellent record keeping and communication skills&amp; </li>
<li>Demonstrates general knowledge in laboratory techniques used in protein purification&amp; </li>
<li>Hands-on experience working (1-2 years) with AKTA Explorer/Pure liquid chromatography system&amp; </li>
<li>Able to troubleshoot typical problems encountered during routine lab operation&amp; </li>
</ul>
REQUIREMENTS/PREFERENCES Education Requirement(s):&amp; 
<ul>
<li>BS/BA&amp; </li>
</ul>

Associate Scientist - Purification

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Bioassays Intern will support discovery research at Arrowhead Pharmaceuticals by contributing to a data-driven project aimed at improving the prediction of optimal cell lines for off-target assessment (OTA) screens. This internship will focus on building a comparative database linking RNA sequencing expression data with qPCR results to evaluate correlation and predictive value. The intern will gain hands-on experience in molecular biology techniques while working closely with scientists to generate data that may significantly accelerate bioassay timelines.
This is an 11-week Summer Internship Program paying $21.00 per hour and requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Perform RNA isolations using good laboratory techniques</li>
<li>Prepare cDNA libraries for downstream analysis.</li>
<li>Perform real-time quantitative PCR (qPCR) assays.</li>
<li>Analyze and organize experimental data using Microsoft Excel.</li>
<li>Support cloning projects under the guidance of a research scientist.</li>
<li>Perform basic laboratory tasks including pipetting, solution preparation, and general bench work.</li>
<li>Present project updates in weekly group meetings.</li>
<li>Prepare final deliverables, including a scientific poster and a ~20-minute presentation summarizing project objectives, results, and learning.</li>
</ul>
Requirements:
<ul>
<li>Currently enrolled in a bachelor's degree program at an accredited university or college and majoring in a scientific discipline such as Biochemistry, Biology, Chemistry, or Engineering.</li>
<li>Previous laboratory experience and familiarity with basic lab techniques.</li>
<li>Excellent verbal and written communication skills, including comfort presenting in group settings.</li>
<li>Strong problem-solving and organizational skills.</li>
<li>Proficiency in Microsoft Office applications.</li>
<li>Ability to lift up to 40 lbs.</li>
<li>Willingness and ability to spend 75% of the workday walking the facility and 25% at a desk.</li>
</ul>
Preferred:
<ul>
<li>Prior laboratory experience, with emphasis on genetics or molecular biology.</li>
<li>Familiarity with qPCR, RNA isolation, or gene expression analysis.</li>
<li>Strong attention to detail and interest in data-driven biological research.</li>
<li>Curiosity, enthusiasm for discovery science, and willingness to learn new approaches and techniques.</li>
</ul>

Wisconsin pay range $9,240—$9,240 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Summer Intern, Bioassays

<h3>Job Description</h3>
Job DescriptionR&amp;D Sensory Scientist / Sensory Analyst
Industry: Consumer Products Manufacturing Function: Research &amp; Development – Sensory Science Employment Type: Full-Time Location: Hybrid / On-site (role-dependent) Compensation: $90,000 – $100,000 base + full benefits Travel: Occasional Relocation: Possible for ideal candidate
About the Opportunity:
We are seeking a Sensory Scientist / Sensory Analyst to support a core R&amp;D function within a global consumer products organization. This role is responsible for designing, executing, and interpreting robust sensory testing programs that substantiate consumer-relevant product claims and inform formulation and product development decisions.
This position sits at the intersection of science, consumer insight, and innovation, partnering closely with R&amp;D and Marketing teams to deliver high-quality sensory data that supports product performance, differentiation, and commercialization.
What You'll Do:
<ul>
<li>
Design, execute, analyze, and report sensory testing to support consumer-relevant product claims
</li>
<li>
Collaborate with R&amp;D and Marketing partners to define project objectives and appropriate sensory methodologies
</li>
<li>
Administer sensory panel activities, including test material preparation, assessor recruitment, panel execution, and data collation
</li>
<li>
Ensure timely delivery of accurate, well-documented sensory results aligned with project timelines
</li>
<li>
Investigate and apply advanced sensory methods and statistical approaches to uncover insights and trends
</li>
<li>
Interpret sensory, consumer, and technical data to support product recommendations and claims substantiation
</li>
<li>
Participate in cross-functional project meetings to align sensory strategy with business needs
</li>
<li>
Maintain strong organization, documentation, and communication throughout the testing lifecycle
</li>
</ul>
What We're Looking For:
Required Qualifications
<ul>
<li>
Bachelor's degree in Psychology, Food Science, Nutrition, Sensory Science, Chemistry, Market Research, or a related scientific discipline
</li>
<li>
Coursework or training in sensory science, statistics, market research, or business
</li>
<li>
Approximately 5 years of relevant professional experience, ideally with a focus on sensory testing
</li>
<li>
Strong analytical, organizational, and communication skills
</li>
<li>
Ability to partner effectively with cross-functional and external stakeholders
</li>
<li>
Ability to read and interpret technical, sensory, and consumer research data
</li>
</ul>
Preferred Qualifications
<ul>
<li>
Sensory science certification or formal training (e.g., university-based sensory or market research programs)
</li>
<li>
Experience supporting consumer product claims substantiation
</li>
<li>
Background in consumer goods, food, home care, personal care, or related industries
</li>
<li>
Comfort working in fast-paced, collaborative R&amp;D environments
</li>
</ul>
What Success Looks Like:
<ul>
<li>
Sensory studies are executed accurately, efficiently, and on schedule
</li>
<li>
Data and insights are clearly communicated and actionable
</li>
<li>
Cross-functional partners trust and rely on sensory results for decision-making
</li>
<li>
Product claims are supported by defensible, consumer-relevant evidence
</li>
<li>
Sensory methodologies evolve to support innovation and continuous improvement
</li>
</ul>
Why This Role:
<ul>
<li>
High-impact R&amp;D role supporting well-known consumer products (client confidential)
</li>
<li>
Opportunity to influence product development and claims strategy
</li>
<li>
Exposure to advanced sensory methodologies and cross-functional collaboration
</li>
<li>
Strong compensation, benefits, and long-term growth potential
</li>
</ul>
If you are a detail-oriented sensory professional who enjoys blending science, data, and consumer insight to shape products people use every day, we encourage you to apply.
Equal opportunity employer. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected characteristics.

R&D Sensory Scientist/ Sensory Analyst

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
Leads cross-functional collaborations on identifying and developing consumer eyecare products (artificial tears, gels and ointments). Leads the direction, planning, and interpretation of clinical trials or research activities within consumer eye care innovation of one or more programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality data supporting consumer eye care product scientific and business strategy.
Responsibilities:
•Serves as an in-house expert in identification and development of consumer eye care products. As required by program needs, in partnership with Discovery, Translational, and CMC colleagues contribute to design and implement translational strategies. May participate in or lead clinical development contributions to due diligence or other business development activity.
• Serves as a champion for innovation in consumer eye care. Actively solicits opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
•Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff.
•May have responsibility for leading clinical study teams, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for ensuring agreed-upon study enrollment and overall timelines for key deliverables.
•Primary responsibility for and ownership of design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other program documents.
•May oversee the work of Medical and/or Scientific Directors and of Clinical Scientists working on the same or related programs.
•May serve on or co-chair Integrated Evidence Strategy Team(s), with responsibility for development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan with full consideration of contingencies and alternative approaches. In the role of Co- Chair, responsibilities may include supervision of matrix team members; serving as Clinical Research representative to lend clinical development or medical expertise to Asset Development Teams (ADTs).
•Stays abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area. May represent AbbVie at key external meetings.
•Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions.
•Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
Qualifications 
•Bachelors degree in the sciences; advanced degree (e.g., MS, PhD, OD, MD, PharmD) preferred.
•At least 8 years of product development experience with 5 years of experience in consumer eye care in the pharmaceutical industry, academia, or equivalent.
•Direct experience in leading cross-functional and translational development preferred.
•Ability to run a complex clinical research program independently.
•Proven leadership skills and ability to bring out the best in others on a cross-functional global team. Must be able to lead through influence.
•Ability to interact externally and internally to support a global scientific and business strategy.
•Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols.
•Must possess excellent oral and written English communication skills.
•Ability to exercise judgment and address complex problems and create solutions for one or more projects.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientific Director, Clinical Development - Consumer Eye Care Product Development

<h3>Job Description</h3>
Job Description
At Universal Display Corporation (Nasdaq: OLED) (UDC), we’re changing the way people see the world. If you’re reading this on a smartphone, there’s a good chance UDC’s materials are producing the light and color shining from your screen right now. UDC’s OLED ingredients are key parts of stunning, energy-efficient displays used in everything from smartwatches to phones, tablets, laptops, monitors, TVs and automobiles. Virtually every OLED consumer electronics product around the world uses UDC’s phosphorescent OLED materials and technologies. UDC is a publicly traded company and pioneer in the OLED industry. When you join our global team, you are embarking on a journey at the forefront of display technology and organic electronics that impacts the daily lives of people around the world. From engineers to chemists, Ph.D. scientists, technicians, lawyers and more, our UDC team is continuously advancing our field. With a focus on energy efficiency, UDC’s team is contributing to making a better, more sustainable planet. Please visit us at <a href="http://www.oled.com" target="_blank">www.oled.com</a>. Job Summary: UDC is seeking a highly skilled Analytical Research Scientist to join the Analytical &amp; Thermal Application Team at our Tech and Innovation Center in Ewing, NJ. This role will serve as the primary technical lead for ICP‑MS analysis of OLED emitter, host, and intermediate materials. The scientist will be responsible for method development, trace‑level quantification, contamination studies, instrument performance oversight, and cross‑functional technical guidance.
In addition to ICP‑MS, the position will support the comprehensive analytical characterization of organic electronic materials using advanced chromatographic and mass‑spectrometric techniques. The scientist will collaborate closely with synthetic chemistry, process engineering, and device teams to provide high‑quality analytical data and technical insight.
Key Responsibilities:
<ul>
<li>
Serve as the subject matter expert for ICP‑MS instrumentation, trace‑metal analysis workflows, and contamination‑control strategies.
</li>
<li>
Develop, optimize, and validate ICP‑MS quantitative methods for ultra‑trace elemental analysis of organic and organometallic compounds.
</li>
<li>
Own sample preparation protocols, including acid digestion, microwave digestion, and solvent‑compatibility approaches tailored to small‑molecule OLED materials.
</li>
<li>
Conduct data modeling, spectral interference correction, and isotopic pattern interpretation.
</li>
<li>
Perform root‑cause investigations related to metal impurities, supply‑chain contamination, sample handling, or process deviations.
</li>
<li>
Ensure instrument uptime through preventive maintenance, tuning, calibration, and performance qualification.
</li>
</ul>
<ul>
<li>
Apply advanced chromatographic techniques (HPLC, UHPLC) and mass spectrometry (LC‑MS, GC‑MS, MALDI) to study purity, molecular identity, and impurity profiles of OLED materials.
</li>
<li>
Develop multidimensional analytical approaches by integrating ICP‑MS with chromatographic separations, when needed.
</li>
<li>
Interpret complex spectra and chromatograms to provide mechanistic insight into impurity formation or material degradation pathways.
</li>
<li>
Communicate analytical findings through detailed technical reports and participate in cross‑functional scientific reviews.
</li>
</ul>
Operational &amp; Cross‑Functional Responsibilities
<ul>
<li>
Maintain accurate documentation of methods, sample histories, instrument logs, and analytical results.
</li>
<li>
Guide junior scientists and technicians, in proper analytical techniques and laboratory best practices.
</li>
<li>
Support quality control workflows, sample inventory, and analytical readiness for development milestones.
</li>
<li>
Participate in continuous improvement efforts for analytical capability expansion.
</li>
</ul>
Required Qualifications:
<ul>
<li>
Ph.D. in Chemistry, Analytical Chemistry, Materials Science, or a closely related field
</li>
<li>
Hands‑on expertise with ICP‑MS (≥2 years), including method development, trace‑metal quantification, and spectral analysis
</li>
<li>
Demonstrated experience with sample digestion, interference correction, and elemental speciation
</li>
<li>
Strong technical background in modern chromatographic and mass‑spectrometric techniques
</li>
<li>
Knowledge of organic small‑molecule systems, organometallics, or organic electronic materials (preferred)
</li>
<li>
Experience performing in a high‑precision analytical laboratory environment
</li>
<li>
Proficiency with scientific software for data processing (e.g., Origin, Mnova, MassHunter, Python, or similar)
</li>
<li>
Ability to independently design experiments, troubleshoot complex analytical problems, and document results thoroughly
</li>
<li>
Excellent written and verbal communication skills, with a track record of scientific reporting or publication
</li>
<li>
Ability to work effectively in a multidisciplinary, fast‑paced R&amp;D environment
</li>
</ul>
Current Benefits at UDC:
<ul>
<li>
Competitive base salary and annual bonus program
</li>
<li>
Medical/Prescription Drug coverage, Dental, and Vision for employees and family
</li>
<li>
Option between Flexible Spending account (FSAs) or Health Savings Account (HSA)
</li>
<li>
Group Term Life insurance, short term disability, and long-term disability benefits for employees
</li>
<li>
Employee Stock Purchase Plan (ESPP)
</li>
<li>
401(k) company contribution
</li>
<li>
Ewing Worldwide Headquarters (HQ) cafeteria provides breakfast and lunch to employees at no cost to them
</li>
<li>
Annual charitable matching gift
</li>
<li>
Generous Paid Time Off
</li>
</ul>
Annual compensation range: $105k-120k

Analytical Research Scientist

<h3>Job Description</h3>
Job Description
BASIS Baton Rouge Primary Mid City Campus is seeking a Math Specialist to start ASAP!
Visit <a href="https://enrollbasis.com/baton-rouge-mid-city/" target="_blank">https://enrollbasis.com/baton-rouge-mid-city/</a> to learn more about us!
BASIS Charter Schools offers an incredible opportunity to be deeply involved in an academic community that is dynamic, exciting and unpredictable. You’ll join others in a highly social, supportive and collaborative environment!
Job responsibilities include but are not limited to:
The Math Specialist supports, supplements, and extends classroom teaching, and works collaboratively to implement a quality math program that is research-based and meets the needs of students
<ul>
<li>Support teachers in analyzing and understanding the results of various assessment tools</li>
<li>Plan and collaborate with K-4 teachers to design and implement engaging instruction that leads to fluency and comprehension all content areas.</li>
<li>Attend weekly planning sessions with classroom teachers to identify students in need of differentiated instruction. Suggest accommodations and appropriate lesson structures to support identified students needing intensive intervention</li>
<li>Provides intervention support to ensure comprehension and fluency in K-5 classrooms</li>
<li>Conduct, organize, and analyze on-going assessments of student performance using multiple assessment tools</li>
<li>Model best teaching practices for teachers with the goal of developing their capacity to support, differentiation, and classroom accommodations</li>
<li>Meet regularly with administration and other professionals to discuss student progress</li>
<li>Attend parent-teacher conferences as needed</li>
</ul>
Minimum Qualifications:
<ul>
<li>A Bachelor's degree with a major (or 24+ credit hours) in the teaching subject, Advanced degree preferred.</li>
<li>A valid fingerprint clearance and/or satisfactory applicable state background check.</li>
<li>Must possess the required credentials to teach in your home country or state which may include a Bachelor's degree and documentation of passage of a state authorized subject test in the teaching.</li>
<li>Must have a minimum of 2 years of teaching experience.</li>
</ul>

Preferred Qualifications: The Math Specialist has specialized knowledge of assessment and diagnosis that is vital for developing, implementing, and evaluating the math program in general, and in designing instruction for individual students. Subject matter postgraduate work (Master's or Ph.D.) is preferred or a combination of subject matter undergraduate degree with a Master’s in Education. Together with a high level of educational attainment, a successful applicant will demonstrate strong communication skills in teaching ideas, texts, and concepts with precision and confidence. Critically, an applicant must possess a high GPA in his/her major, excellent recommendations, experience working with children, not necessarily in the classroom, and be open to new ideas in teaching.
About BASIS Ed: The BASIS academic program is consistently ranked among the top 10 programs nationally and is competitive on an international scale. The mission of BASIS Schools is to provide an academically excellent and rigorous liberal arts college preparatory education to all Lower and Upper School students.
Benefits and Salary:
<ul>
<li>Salary for this position is competitive and dependent on education and experience</li>
<li>BASIS Ed offers a comprehensive benefits package, including but not limited to:
<ul>
<li>Employer paid medical and dental insurance</li>
<li>Vision insurance</li>
<li>PTO</li>
<li>Ability to add dependents</li>
<li>401k with partial match that grows over time</li>
<li>Employee Assistance Program</li>
<li>Childcare Savings Opportunity (KinderCare tuition discount)</li>
</ul>
</li>
</ul>
Reasonable Accommodations Statement To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
Notice of Non-Discrimination: In accordance with Title VI of the Civil Rights Act of 1964, Title IX of the Education Amendments of 1972, Section 504 of the Rehabilitation Act of 1973, the Age Discrimination Act of 1975, Title II of the Americans with Disabilities Act of 1990, the Boy Scouts of America Equal Access Act and applicable state law, BASIS* does not discriminate on the basis of actual or perceived race, color, religion, national origin, sex, age, disability, gender identity or expression, or any other classification protected by law in any of its business activities, including its educational programs and activities which comply fully with the requirements of state and federal law and Title IX. The following person has been designated to handle inquiries regarding BASIS’ non-discrimination policies: Beverly Traver, Compliance and Equity Investigator, BASIS Educational Group, LLC., 7975 N. Hayden Rd, Scottsdale, AZ 85258, (480) 289-2088. *As used in this policy, the term "BASIS" refers to: BASIS Educational Group, LLC, BASIS Charter Schools, Inc., BTX Schools, Inc., BDC, A Public School, Inc., BBR Schools, Inc., and all affiliated entities.

Math Specialist - Immediate start!

<h3>Job Description</h3>
Job Description
At WestLand Engineering and Environmental Services, a Trinity Consultants team, we are driven by purpose, innovation, and a shared commitment to the work that we do. As part of Trinity Consultants' Water and Ecology division, we tackle complex environmental challenges, blending expertise in environmental consulting, wetlands, cultural resources, GIS, landscape architecture, and engineering.
WestLand empowers our teams to develop their unique skills while fostering career growth within a company that is large enough to offer diverse opportunities yet agile enough to value individual contributions. Collaboration is at the heart of what we do-our professionals work together on meaningful and impactful projects, delivering solutions that help clients navigate regulatory complexities and see positive project outcomes. Make a difference with us at WestLand!
WestLand is actively seeking Field Biologists to support our environmental consulting practice across the Southwest on an on-call basis. WestLand specializes in the technical and procedural requirements necessary for compliance with the National Environmental Policy Act (NEPA), the Clean Water Act, the Endangered Species Act, and more. Our botanical resources practice includes: development of natural resources management plans; conducting ecological investigations and base-line studies; and mitigation planning, design and implementation. This position may be based out of our Phoenix or Tucson office.
What will I be doing?
<ul>
<li>Conducting field surveys and investigations.</li>
<li>Management and training junior field crewmembers.</li>
<li>Developing permitting/compliance documents.</li>
<li>Managing some project-related tasks.</li>
<li>Supporting other projects within the department.</li>
</ul>
What qualifications are required for this role?
<ul>
<li>Bachelor's degree in a related field. Advanced degree strongly preferred.</li>
<li>Demonstrated experience with field-oriented investigations and managing field crews.</li>
<li>Ability to identify on sight Great Basin flora.</li>
<li>Excellent communication skills.</li>
<li>Ability to navigate physically in various environments including those with exposure to extreme temperatures and rough terrain.</li>
<li>Experience in the Western United States strongly preferred.</li>
<li>Working knowledge of relevant biological/botanical permitting processes also preferred</li>
</ul>
The salary range for this position is $26.00 - $34.00 per hour.
What does WestLand offer you?
<ul>
<li>Comprehensive benefits package: 9 paid holidays, healthcare benefits, PTO, and 401k matching for full-time employees. Flexible work schedules and remote/hybrid possibilities for most roles.</li>
<li>Multidisciplinary environment: Unique, creative, and challenging projects where you can develop your vision of clientele and work with industry leaders daily.</li>
<li>Success-oriented environment: Two-way mentorship, financial incentives to publish work, tuition reimbursement, and a career path structure to help you reach the next steps in your career.</li>
<li>Collaborative work environment: Clear and frequent communication, shared information and ideas across teams, and a welcoming atmosphere for everyone</li>
</ul>
WestLand is committed to creating a diverse environment and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability, or veteran status. We maintain a safe and drug-free workplace and perform pre-employment substance abuse and background testing.
To apply, visit Westland Resources Job Listings
Resumes submitted by a recruiting/staffing agency without current/valid vendor agreement will become property of WestLand. Any recruiting/staffing agency wishing to do business with WestLand must contact the Human Resources Department through our website. Recruiting/staffing agents may NOT contact hiring managers directly. Firms that do not honor this request will be removed from consideration.
 Job Posted by ApplicantPro

Field Biologist

<h3>Job Description</h3>
Job Description
As a Senior Staff Bioinformatics Scientist at AccuScan Science, you will lead the development and improvement of statistical and algorithmic methods for NGS-based variant detection and minimal residual disease (MRD) calling. This role focuses on tumor/normal variant calling in tissue samples as well as ultra–low-frequency mutation detection in cfDNA.
You will work closely with assay development, bioinformatics engineering, and R&amp;D teams to translate new technologies into robust, production-ready analytical pipelines. The ideal candidate brings deep statistical modeling expertise, strong hands-on implementation skills, and experience working with WGS or large-scale sequencing data. Prior exposure to regulated (FDA/IVD) environments and machine learning is a strong plus.

Key Responsibilities
<ul>
<li>Improve and extend somatic variant-calling algorithms for tumor tissue and cfDNA-based mutation detection</li>
<li>Develop, validate, and refine MRD-calling algorithms with an emphasis on sensitivity, specificity, and robustness</li>
<li>Design and implement benchmarking, evaluation, and quality control (QC) methodologies</li>
<li>Lead troubleshooting efforts, including root-cause analysis of analytical or pipeline failures, and drive corrective actions</li>
<li>Implement algorithms in production-quality code and collaborate with engineering teams to integrate methods into scalable pipelines and workflows</li>
<li>Partner with assay development teams on new technologies and assay iterations requiring customized analysis strategies and algorithm development</li>
<li>Document analytical methods, validation results, and design decisions; clearly communicate findings, limitations, and trade-offs to technical and cross-functional stakeholders</li>
</ul>
Requirements
<ul>
<li>Ph.D. in Statistics, Biostatistics, Computer Science, Bioinformatics, Computational Biology, Applied Mathematics, or a related field, with relevant postdoctoral or industry experience</li>
<li>Strong foundation in statistical inference and modeling, including uncertainty quantification and decision thresholding</li>
<li>Prior experience working with genomics data, including WGS or large-scale NGS datasets, and a solid understanding of technical and biological noise sources</li>
<li>Demonstrated software implementation skills in Python and/or a performance-oriented language (e.g., C++, Rust, Java), with experience writing maintainable, testable, production-quality code</li>
<li>Familiarity with standard genomics data formats and tooling (e.g., FASTQ, BAM/CRAM, VCF) and common processing workflows</li>
<li>Experience working in regulated product development environments (e.g., FDA, IVD), including documentation practices, analytical validation, and design controls</li>
<li>Excellent communication and collaboration skills, with the ability to work effectively across research, engineering, and assay development teams</li>
</ul>

Preferred Qualifications
<ul>
<li>Hands-on experience with cfDNA analysis and/or MRD detection, including ultra–low-frequency variant calling and/or epigenetics-based analyses</li>
<li>Machine learning experience, particularly in settings involving class imbalance, model evaluation, calibration, and decision optimization</li>
<li>Experience collaborating closely with assay development teams on experimental design, data analysis planning, and iterative assay optimization</li>
</ul>
Benefits
<ul>
<li>Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401k, IRA)</li>
<li>Paid Time Off (Vacation, Sick &amp; Public Holidays)</li>
</ul>

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