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<h3>Job Description</h3>
Job DescriptionProject Engineer – Job Description&nbsp;About the Company:Harrington Geotechnical Engineering Inc. (HGEI), a QAI company, has over 50 years of experience in the geotechnical and geological engineering field. With our experts, professional skilled staff, and diverse experience, we offer reliable services in an integrated, efficient, and cost-effective service to clients in the public and private sectors. Our services include Geotechnical Engineering, Geotechnical Engineering Laboratory Materials Testing, Engineering Geology, and Environmental Engineering.&nbsp;We plan to expand geotechnical services and uphold our commitment to quality and client satisfaction. We are growing and looking for an experienced and motivated Project Engineer to join our team.Salary Range: up to $100,000 per year (Depending upon experience)About the Job:As a Project Engineer, you will be involved in the geotechnical and geological aspects of a wide variety of projects. You will play a crucial role which includes daily project management, performing and/or leading field investigations, engineering analysis, calculations, and recommendations, design, and development of plans and specifications, observation and inspection, and the writing/preparation, and review of related reports for the services provided. Review plans and drawings to ensure compliance with the project specifications. Prepare proposals and cost estimates, track and evaluate project progress and budgets, and recommend changes. Research and resolve design and construction problems. Assign, review, and evaluate laboratory or field data for report inclusion. Apply sound engineering principles and be able to communicate complex engineering issues and concepts to technical and non-technical clients and project teams.Primary Job Duties:
<ul>
<li>Conduct geotechnical (preliminary and forensics) and geological investigations&nbsp;</li>
<li>Perform field inspections and testing as required for construction projects&nbsp;</li>
<li>Analyze data and prepare geotechnical reports on soil conditions, stability, foundation design, etc.</li>
<li>Collaborate with architects, engineers, and construction teams to develop effective solutions</li>
<li>Provide technical guidance on geological and geotechnical related issues throughout the project lifecycle</li>
<li>Ensure compliance with industry standards, regulations, and safety protocols</li>
<li>Project management from the planning phase to the completion of the project</li>
<li>Conduct plan reviews</li>
<li>Generate cost proposals&nbsp;</li>
<li>Participate in project meetings and communicate effectively with owners, designers and project authorities</li>
<li>Other job duties as assigned by the Operations Manager or his designee</li>
</ul>
&nbsp;Job Qualifications (Education, Experience, and Skills):
<ul>
<li>Bachelor’s Degree in Civil Engineering with a focus in Geotechnical Engineering</li>
<li>Minimum of 2 years of relevant professional experience (recent graduates are also encouraged to apply).</li>
<li>Professional Engineer or Engineer-in-Training Certification in the state of California. &nbsp;</li>
<li>Strong analytical and critical thinking skills and a sound technical background in soil and rock mechanics</li>
<li>Attention to detail, dedication to quality and accuracy</li>
<li>Experience with various commercial geotechnical software&nbsp;</li>
<li>Strong written and oral communication skills</li>
<li>Ability to work independently or as part of a team</li>
<li>Working knowledge of standard business software including Microsoft Word, Excel, and PowerPoint</li>
</ul>
&nbsp;Key Competencies:
<ul>
<li>Strong knowledge of geotechnical and geological engineering principles and practices</li>
<li>Knowledge with the local and statewide such as the California Building Code, Los Angeles Building, California Residential Code &nbsp;</li>
<li>Proficiency in construction inspection and management</li>
<li>Ability to analyze data and interpret results</li>
<li>Proficient in using software and other engineering tools related to the discipline.</li>
<li>Excellent problem-solving skills and attention to detail</li>
<li>Strong communication skills to collaborate with multidisciplinary teams&nbsp;</li>
<li>Ability to read and interpret schematics and construction drawings</li>
</ul>
Working Conditions and Environment:This position will require general supervision and will have to use independent judgment within established guidelines. Generally, uses advanced knowledge to analyze, interpret, or make deductions from varying facts or circumstances. Will need the ability to establish rapport quickly with others working on the same project and be able to promote a positive team environment. Working knowledge of dealing with a diverse population while using tact, diplomacy, and respect.&nbsp;If you are a motivated Project Engineer looking for an opportunity (or know of someone) to contribute to exciting projects, we encourage you to apply. Join our team and be part of our commitment to excellence in engineering.&nbsp;

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Job Summary
We are seeking an ambitious Environmental Scientist/Geologist to join an up-and-coming environmental consulting firm in the NYC area. The Environmental Scientist/Geologist will be responsible for extensive outdoor fieldwork, including groundwater sampling and site inspections, along with office-based tasks such as data interpretation and report preparation. Ideal for those passionate about environmental science and geology, this role allows you to work in an environment with skilled senior mentors while contributing to meaningful environmental projects.
Job Duties and Responsibilities
<ul>
<li>Collect groundwater samples and confirm depth to groundwater at designated sites.</li>
<li>Conduct inspections at stormwater outfalls, public works properties, active construction sites, and other environmental sites.</li>
<li>Accurately document field obtained data, including sample collection details, site conditions, and other relevant observations.</li>
<li>Label and organize groundwater or soil sample jars to ensure proper handling and storage for laboratory analysis.</li>
<li>Relay collected data and information back to the main office in a timely and accurate manner. </li>
<li>Assist in preparation of field reports and environmental documentation.</li>
<li>Complete and submit environmental forms, applications and reports to the regulatory agencies associated with the sites.</li>
<li>Utilize ArcGIS for mapping field sites and assisting with environmental data collection.</li>
<li>Perform office-based tasks, including data entry interpretation, report writing, and maintaining field records.</li>
</ul>
Required Qualifications
<ul>
<li>Bachelor's Degree in Environmental Science, Geology, Environmental Engineering, Environmental Policy, or a related field.</li>
<li>At least 6 months of direct experience in environmental fieldwork or a related field.</li>
<li>Proactive attitude with a strong commitment to environmental health and safety.</li>
<li>Ability to lift and carry field equipment, including groundwater sampling gear.</li>
<li>OSHA 40-Hour HAZWOPER Certification.</li>
<li>Reliable transportation with a clean, valid driver's license.</li>
</ul>
Salary: $50,000 - $55,000
**Local candidates will only be considered**
Company Overview
IslandSearch Group, Inc., D/B/A ISG Consultants, is an architecture, engineering, construction and environmental consulting and staff augmentation firm that was established in 2018. As a certified MBE, DBE and SBE firm, we have over 26 years of experience providing professional staff in support of programs and projects within the public and private sectors in the Tri-State area. Please apply directly to <a href="mailto:LL@islandsearchgroup.com" target="_blank">LL@islandsearchgroup.com</a> if you have an interest in exploring this opportunity. IslandSearch Group, Inc. D/B/A ISG Consultants is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, race, color, creed, religion, national origin, ancestry, marital status, sex, affectional or sexual orientation, gender identity or expression, or protected veteran status; and will not be discriminated against based on disability.
#ZR

Environmental Scientist/Geologist

<h3>Job Description</h3>
Job Description
Job Title: Scientist - I
Location: Bothell, WA 98021
Duration: 06 months of Contract (with possible extension)
 
Payrate: $40.00/hr.
Shift timing: Monday–Friday, 8am-4:30pm EST

Job Description
The In Situ Biology team is seeking a motivated associate scientist contractor to assist a team of scientists performing spatial biology experiments aimed at understanding targets for antibody-based therapeutics. The successful candidate will have experience in core histology methodologies, including processing, embedding, and sectioning. The ideal candidate will be energetic and enthusiastic about lab work and flexible in working with different investigators on various projects.
Responsibilities
• Process samples for downstream histological analysis.
• Perform routine histology lab maintenance.
• Perform immunohistochemistry experiments using autostainers.
• Maintain and catalog a biospecimen repository.
• Utilize a LIMS system for documenting experiments.

Qualifications
• 1-2+ years’ experience working in a laboratory.
• BS or BA in in a biological science.
• Experience with histopathology techniques.
• Experience with sectioning a plus, preference given to Histology Technicians (HTs).
• Ability to work collaboratively in a cross-functional research environment.
• Highly organized with the ability to multitask.
• Quick learner with willingness to learn new skills and technologies.
• Excellent teamworking and communication skills and a proactive attitude.
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Biological Scientist

<h3>Job Description</h3>
Job DescriptionOur Story
Build your future at SUPERIOR, a stable, employee-owned leader in chemical products and services for nearly 100 years. Here, you can count on long-term job security with a company that’s proven resilient and continues to grow.
As an employee-owner, you’ll help shape Superior’s success while building your own retirement wealth through our Employee Stock Ownership Program (ESOP) and 401(k) plan. We offer top-tier health, dental, vision, life, and disability coverage — with medical premiums either paid by Superior or highly subsidized — so you and your family can access great benefits with minimal cost.
You’ll also join a supportive team, where paid training and experienced coworkers help you learn, grow, and succeed from day one. 
At SUPERIOR, you get more than a job — you gain ownership in your future, outstanding benefits, and the backing of a dedicated team committed to success.
What We’re Looking For
We are currently seeking a Chemical Handler to work at our Louisville, KY location.
This role is responsible for:
<ul>
<li>Daily production</li>
<li>Unloading raw materials</li>
<li>Completing paperwork</li>
<li>Maintaining a safe operation</li>
</ul>
Schedule:
<ul>
<li>Full-time, 1st shift</li>
<li>Monday–Friday, 8:00 a.m. – 4:30 p.m.</li>
<li>Additional hours may be required</li>
</ul>
What You’ll Do
You will:
<ul>
<li>Transfer products into and out of pails, drums, and totes using transfer pumps and hoses</li>
<li>Read paperwork with chemical amounts and blending instructions</li>
<li>Pull product samples and submit them to the Lab for quality control</li>
<li>Label containers and secure closures</li>
<li>Inspect, label, store, and prepare products for shipment</li>
<li>Stage, load, and unload pails, drums, and totes</li>
<li>Operate a forklift</li>
<li>Wear required PPE for safety</li>
<li>Keep your work area safe, clean, and orderly</li>
<li>Lift and/or move 55 lbs</li>
<li>Cross-train in areas such as shipping/receiving, bulk handling, inventory control, chemical packaging, fiberglass handling, tote cleaning, preventive maintenance, and yard truck spotting</li>
</ul>
Candidates Should Possess
<ul>
<li>High School Diploma or equivalent</li>
<li>Strong safety mindset</li>
<li>Forklift certification (training is provided)</li>
<li>Effective verbal and written communication skills to work with co-workers, chemists, administrative staff, delivery personnel, and management</li>
</ul>
What We Offer
At Superior, we take care of our people. Our comprehensive benefits package includes:
<ul>
<li>Medical Insurance – 100% company-paid HDHP or a low-cost PPO option</li>
<li>Employee Stock Ownership Plan (ESOP)</li>
<li>401(k) Retirement Plan</li>
<li>Flexible Spending Accounts (FSA)</li>
<li>Paid Time Off &amp; Paid Holidays</li>
<li>Dental, Vision &amp; Life Insurance</li>
<li>Short-Term &amp; Long-Term Disability (STD &amp; LTD)</li>
<li>Paid Training from day one</li>
</ul>
Join a company that invests in you — personally, professionally, and financially.
EOE including disability/veteran/drug free

Chemical Handler

<h3>Job Description</h3>
Job Description
Location: Anaheim, CA (Company plans to relocate to Georgia in mid-next year)
Employment Type: Full-Time / Part-Time / Temporary (This position is available on a part-time or temporary basis through the relocation period)
A leading company in the cosmetics and chemical industry is seeking an experienced R&amp;D Research Scientist to support its product development team during its current operations in California. This role will focus on product formulation, ingredient research, and regulatory compliance to support the development and enhancement of cosmetic and chemical products until the company’s planned relocation to Georgia in mid-next year.
This position is well-suited for candidates seeking part-time or temporary opportunities, as well as those open to full-time engagement during this transition period.
Key Responsibilities:
<ul>
<li>
Develop and improve formulations for cosmetics and chemical-based products.
</li>
<li>
Conduct research on raw materials, active ingredients, and product stability.
</li>
<li>
Ensure compliance with cosmetic regulations and safety assessments.
</li>
<li>
Collaborate with internal teams to enhance product performance and innovation.
</li>
<li>
Optimize product textures, stability, and functionality through ingredient research and testing.
</li>
</ul>
Qualifications:
<ul>
<li>
Degree in Chemistry, Chemical Engineering, or a related field.
</li>
<li>
Experience in cosmetics or chemical product development.
</li>
<li>
Strong understanding of formulation design and ingredient interactions.
</li>
<li>
Knowledge of cosmetic industry regulations and safety assessments.
</li>
<li>
Ability to conduct raw material analysis and apply innovative research to product development.
</li>
</ul>
Benefits (availability may vary based on employment type):
<ul>
<li>
Health Insurance (for eligible full-time employees)
</li>
<li>
Paid Time Off (PTO)
</li>
<li>
401(k) Retirement Plan
</li>
<li>
Performance-Based Employee Awards
</li>
<li>
Reimbursement for Business-Related Expenses
</li>
<li>
Complimentary Lunch Provided
</li>
</ul>

R&D Chemist - Cosmetics Products (Part-Time / Temporary)

<h3>Job Description</h3>
Job Description
Schutz Container System a Global Packaging Container Company located in Kenosha, Wisconsin looking for a Chemical Engineer -Waste Water Manager
Job Duties,
<ol>
<li>Strong knowledge and understanding of SDS sheets to make risk assessments, chemical classifications and waste determinations</li>
<li>Knowledge and understanding of RCRA and EPA regulations and rules</li>
<li>Experience and strong knowledge in chemical neutralization and understanding the difference between an Acid and a base.</li>
<li>Classify all incoming fill goods as needed.</li>
<li>Neutralize corrosive residues in Elementary Neutralization Units</li>
<li>Manage all waste streams produced at the facility for proper disposal</li>
<li>Hands on environment with 50% of time split between office work and monitoring the reconditioning process and waste streams.</li>
</ol>
Job Requirements
<ol>
<li>4 year Chemical Degree</li>
<li>3-5 year Manufacturing Experience</li>
<li>Strong verbal and written communication skills</li>
<li>Computer knowledge of MS Windows and SAP</li>
</ol>
Company DescriptionSchuetz Container Systems is a world-class leader in the manufacturing of industrial containers across multiple business lines. In addition, our sister company, Cardinal Container Systems, reconditions industrial packaging for use in a wide range of commercial applications. A vital part of this process involves the collection and return of used containers that can be reconditioned in our state of the art factories and reused by our diverse customer base. 
<h3>Company Description</h3>
Schuetz Container Systems is a world-class leader in the manufacturing of industrial containers across multiple business lines. In addition, our sister company, Cardinal Container Systems, reconditions industrial packaging for use in a wide range of commercial applications. A vital part of this process involves the collection and return of used containers that can be reconditioned in our state of the art factories and reused by our diverse customer base.

Wastewater Manager Chemical Engineer

<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 
<ul>
<li>Contribute to design, analysis and reporting of clinical trials or other scientific research studies. Assist with development of protocols and/or statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation. Work under supervision to implement sound statistical methodology in scientific investigations.</li>
<li>Assist in identifying scientifically appropriate data collection instruments. Identify and report data issues or violations of study assumptions. Provide programming specifications for derived variables and analysis datasets. Collaborate with Data Science in preparing for database lock.</li>
<li>With supervision perform statistical analyses as per the analysis plan. Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines. Evaluate appropriateness of available software for planned analyses and assess needs for potential development of novel statistical methodology.</li>
<li>With supervision, develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures. Ensure the accuracy of the statistical component of scientific reports and/or publications with high quality.</li>
<li>Work collaboratively with cross-functional teams. Clearly explain statistical concepts to non-statisticians. Provide responses to questions and pursue analyses suggested by data under supervision. Support communications between assigned product team(s) and functional management. Build/drive cross-functional relationships and collaboration.</li>
<li>(SSG) Contribute to benefit-risk planning and assessment. Contribute to cross-functional development of output specifications to address both pre-planned safety analyses and ad hoc requests.</li>
<li>(SSG) Collaborate within the Safety Statistics Group to implement strategic initiatives that address processes related to interpreting, monitoring, assessing, and reporting safety data to better characterize the safety profile of AbbVie products, improve efficiencies, and provide greater consistency across therapeutic areas.</li>
<li>(GMA Stat) In collaboration with GMA, Clinical Statistics, Data Sciences, Statistical Programming and other stakeholders to evaluate existing databases, both clinical studies and real-world databases, assist with feasibility assessment to identify fit-for-purpose data sources to address research questions, and develop detailed and actionable analysis plans for evidence generation to deliver high quality, patient-centric evidence and insights to drive decisions.</li>
</ul>
Qualifications 
<ul>
<li>MS (with 4+ years of experience) or PhD in Statistics, Biostatistics, or a highly related field.</li>
<li>High degree of technical competence and effective communication skills, both oral and written</li>
<li>Able to perform statistical computations and simulations</li>
<li>Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others</li>
<li>Able to build strong relationship with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo</li>
</ul>
 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;ofthis 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&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​
</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&nbsp;participate&nbsp;in our short-term incentive&nbsp;programs.&nbsp;​
</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 anybonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's soleand&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;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 Statistician, Research

<h3>Job Description</h3>
Job Description
Why Join Us?
Parabilis Medicines, Inc is a biopharmaceutical company pioneering the discovery and development of Helicon™ peptide therapeutics; these ultra diverse alpha-helical peptides are capable of efficient cell entry and modulation of both protein-protein and protein-DNA interactions. Through Helicon therapeutics, Parabilis is poised to revolutionize the medical possibilities for patients by precisely drugging intracellular targets long understood to be significant drivers of disease but never before drugged due to the limitations of existing drug modalities to act within the cell. FOG-001, the company's first-in-class TCF-blocking β-catenin inhibitor, is being evaluated in a Phase 1/2 study for patients with advanced solid tumors, including desmoid tumors and colorectal cancer. Parabilis is fully leveraging the unprecedented potential Helicons present by deploying proprietary, custom-built machine learning and computational methods as part of its discovery and development process. Parabilis Medicines has raised more than $500 million to date from leading life sciences investors. Parabilis is headquartered in Cambridge, Mass.
What's the opportunity?
As a senior scientist at Parabilis and a biology lead for a preclinical oncology program, you'll help drive the biological strategy through candidate selection and IND-enabling studies, integrating mechanistic insight and in vitro/in vivo pharmacology for our one of our novel HeliconTM peptide programs. We're looking for a highly motivated Senior Scientist with significant experience in cell and molecular biology to report to the Sr. Director, Biology. 
Key Responsibilities: 
<ul>
<li>Independently design, execute, and interpret in vitro assays (e.g., viability, degradation, CRISPR/RNAi perturbation).</li>
<li>Work closely with pharmacology and chemistry colleagues to support in vivo validation studies and SAR decision making.</li>
<li>Oversee external work with CROs: write SOWs, ensure scientific rigor, timelines, and budget adherence. Work onsite with limited travel to oversee CROs.</li>
<li>Sit on a core team as the Biology Lead to help drive go/ no-go recommendations. In partnership with the Program Lead, drive the biology strategy for a preclinical oncology program; define key hypotheses, decision points, and a data driven plan from hit to lead through IND enabling.</li>
<li>Mentor junior scientists and foster high standards for experimental design, documentation (ELN), and reproducibility.</li>
<li>Communicate clearly across levels: crisp slides, data packages, experimental plans, and narrative that link results to program decisions.</li>
</ul>
What you'll need to be successful:
<ul>
<li>Ph.D. and 5+ years of industry experience in cancer biology as a biology lead.</li>
<li>Experience in drug discovery, hit-to-lead process, degrader programs, and matrixed teams</li>
<li>Innovative, creative, inquisitive, motivated researcher with strong problem-solving skills.</li>
<li>Proficiency in a broad range of molecular and cellular techniques including: NanoBRET and HiBiT assays, western blotting, qPCR. transfection, immunofluorescence, flow cytometry, cell-based functional assays.</li>
<li>Experience in managing relationships with collaborators and/or CROs.</li>
<li>Excellent written and oral communication skills, and a track record of cross-functional collaboration</li>
<li>Proficiency in data analysis and statistics (e.g., GraphPad Prism, FlowJo; familiarity with R/Python or Spotfire is a plus).</li>
</ul>
Preferred but not required:
<ul>
<li>Biotech experience with ADC programs. </li>
<li>People management experience.</li>
<li>Publication/patent record that demonstrates depth in oncology or molecular/cell biology.</li>
<li>Familiarity with functional genomics (CRISP screens), multi-omics (RNAseq/singlecell/spatial), and imaging based pharmacodynamic readouts.</li>
<li>Prior contribution to IND submissions or regulatory interactions for nonclinical pharmacology.</li>
</ul>
Core Values
Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit.
<ul>
<li>Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.</li>
<li>In(ter)dependent. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.</li>
<li>Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.</li>
<li>All-In. We're All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.</li>
</ul>
The base salary range for this position is $135,000-$165,000, depending on experience, qualifications, and internal practices. Parabilis's total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitivebenefits designed to support our employees' overall well-being.
As an equal opportunity employer, Parabilis Medicines values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.
30 Acorn Park Drive | Cambridge, MA 02140 | <a href="http://www.parabilismed.com" target="_blank">www.parabilismed.com</a>

Senior Scientist, Biology

<h3>Job Description</h3>
Job DescriptionOur mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine’s greatest challenges. GRAIL is headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit grail.com. The focus of the clinical laboratory associate will be on the receipt, triage, and accessioning of patient samples submitted to the CLIA laboratory for testing. This position works on-site full-time at our office located in Durham, NC.Responsibilities:
<ul>
<li>Responsible for unpacking samples from shipping containers and accessioning samples into LIMS including troubleshooting sample issue and LIMS errors.</li>
<li>Be able to prioritize workload to meet production goals in throughput and quality.</li>
<li>Responsible for equipment maintenance according to the laboratory’s standard operating procedures.</li>
<li>Responsible for maintaining sufficient inventory of materials, supplies, and equipment in the laboratory for performance of duties.</li>
<li>Check, monitor, and record temperature and perform root cause analysis of deviations and implement a resolution or initiate a service request as necessary.</li>
<li>Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications.</li>
<li>Assist in performing annual review of standard operating procedures.</li>
<li>Manage organizing and maintaining laboratory, equipment, personnel, and training documents.</li>
<li>Report all concerns of test quality and/or safety to the Supervisor or Safety Officer.</li>
<li>Identify process improvement opportunities and report to laboratory management.</li>
<li>Write and revise standard operating procedures, as needed.</li>
<li>Perform other duties as assigned.</li>
<li>These responsibilities summarize the role’s primary responsibilities and are not an exhaustive list. They may change at the company’s discretion.</li>
</ul>
Required Qualifications:
<ul>
<li>Requires AA or high school diploma with lab experience.</li>
<li>Requires 3 + years of related experiences in a high complexity laboratory.</li>
<li>Flexibility of work schedule to meet the needs of GRAIL’s Clinical Laboratory is required.</li>
</ul>
 Preferred Qualifications:
<ul>
<li>Demonstrate a high level of competency when following processing steps in protocol and in all other supporting functions.</li>
<li>Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed.</li>
<li>Strong organizational skills and meticulous attention to detail.</li>
<li>Able to integrate and apply feedback in a professional manner.</li>
<li>Able to prioritize and drive to results with a high emphasis on quality.</li>
<li>Ability to work as part of a team within a highly collaborative environment.</li>
<li>Strong computer skills.</li>
<li>Ability to proactively communicate consistently, clearly and honestly.</li>
<li>Ability to prioritize tasks with a high emphasis on quality.</li>
<li>Ability to participate in projects and complete assignments as expected.</li>
<li>Ability to analyze and solve basic issues.</li>
<li>High volume laboratory experience is preferred.</li>
</ul>
Physical Demands and Working Environment
<ul>
<li>Hours and days may vary depending on operational needs</li>
<li>Works on-site full-time at Durham, NC.</li>
<li>Working with dry ice may be necessary</li>
<li>Standing or sitting for long periods of time may be necessary.</li>
<li>May be exposed to hazardous materials, blood specimens and instruments with moving parts, heating or freezing elements, and high speed centrifugation (Generally laboratory and customer service employees only)</li>
<li>Repetitive manual pipetting may be necessary</li>
<li>Some lifting (up to 25 pounds) may be necessary</li>
</ul>
The expected, full-time, annual base pay scale for this position is $27.88/hour - $32.69/hour. Actual base pay will consider skills, experience, and location.&nbsp; Based on the role, colleagues may be eligible to participate in an annual bonus plan tied to company and individual performance, or an incentive plan. We also offer a long-term incentive plan to align company and colleague success over time. In addition, GRAIL offers a competitive benefit package, including flexible time-off, a 401(k) with a company % match, medical, dental, and vision insurance plans, and carefully selected mindfulness offerings, in accordance with our applicable plans and policies.&nbsp; GRAIL is an equal employment opportunity employer, and we are committed to building a workplace where every individual can thrive, contribute, and grow. It is GRAIL policy to provide equal employment opportunities without regard to race, color, religion, national origin, sex, gender, gender identity, sexual orientation, age, marital status, protected veteran status, disability status, medical condition, or any other class or characteristic protected by applicable federal, state, and local laws. This policy applies to all phases of employment, including, but not limited to: recruiting, hiring, training, promotion, and termination at all levels of employment. GRAIL maintains a drug-free workplace. Additionally, GRAIL will consider all qualified job-seekers with criminal histories in a manner consistent with applicable law and provide reasonable accommodations to qualified individuals with disabilities so that they can participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us at <a href="mailto:rc@grailbio.com" target="_blank">rc@grailbio.com</a> if you require an accommodation to apply for an open position. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. We welcome job-seekers from all backgrounds to join us!

Clinical Laboratory Associate IV, Accessioning #4391

<h3>Job Description</h3>
Job Description Location(s): Santa Barbara County, San Luis Obispo County, Monterey County (Central Coast of California) Practice/Department: Cultural Internal Title: As-Needed Field Technician Work Environment: Field Work Compensation: $18-31/hourly * Dudek’s journey began in 1980 with a vision to serve Southern California’s water and wastewater agencies. Today, we are a 100% employee-owned firm supporting clients nationwide and delivering projects that improve and protect the built and natural environments of communities throughout the United States. Our work has been recognized by leading industry organizations, and we’ve been honored with multiple national Top Workplace Awards. Our employee-owners are unified by a singular commitment to supporting projects that address key societal issues, such as the transition to renewable energy, infrastructure hardening and repair, environmental protection, and community resilience. Learn more about our award-winning culture, the benefits and perks of being a Dudekian, and the projects you will have the opportunity to shape. Who You Are As an employee-owner, you embrace accountability, working safely, and collaboration while thinking resourcefully and independently. Like all Dudekians, you are curious and solution-oriented, with the ability to adapt quickly to changes and approach challenges with a spirit of innovation. How You’ll Make an Impact We are seeking qualified, experienced Archaeological Field Technicians for various archaeological projects on the Central Coast of California (Santa Barbara, San Luis Obispo, and Monterey Counties). An archaeological field technician must possess basic archaeological field and laboratory skills for various survey, excavation, laboratory, and construction monitoring work. Additional assignments may be available for qualified individuals who work well with our team. Competitive wages are based on level of education and experience. Duties and Responsibilities 
<ul>
<li>Archaeological survey, excavation, and monitoring</li>
<li>During archaeological monitoring the applicant would be responsible for on-site communication with construction and Native American personnel, and for maintaining daily logs that include detailed descriptions of construction activities, communication, and future plans</li>
<li>During survey work the applicant will be expected to communicate effectively with crew leader to verify understanding of instructions or site-specific information. Scientific photography, measurement, artifact identification, and recordation of resources will be required</li>
<li>During excavation, the applicant will be expected to work well with a team to ensure clear communication. Ability to identify buried resources and document them effectively while working in a team will be necessary</li>
</ul>
 Minimum Qualifications
<ul>
<li>Bachelor’s degree in Archaeology or Anthropology</li>
<li>The ability to safely operate a 4wd vehicle</li>
<li>Physical ability to carry equipment and supplies (up to 40 lbs.) and walk or hike for long hours during fieldwork</li>
<li>Willingness to travel to a project location for several consecutive days</li>
<li>Must possess a valid driver’s license and have active personal automobile liability insurance by first day of employment</li>
<li>Must possess a valid driver’s license and have active personal automobile liability insurance by the first day of employment</li>
</ul>
 Preferred Qualifications
<ul>
<li>Completed an accredited field school certification</li>
<li>Previous archaeological survey experience in California, the Desert West, the Pacific Northwest and/or the Mid-Atlantic, and experience recording a variety of site and isolate types in the respective region(s)</li>
<li>Experience with a wide range of archaeological field methods including pedestrian survey, testing/evaluation, and monitoring</li>
<li>Understanding and willingness to safely accommodate difficult weather and other environmental conditions and challenges</li>
<li>Ability to operate field equipment, including GPS equipment, cameras, and tablets</li>
<li>Knowledge of and experience using ESRI Collector and/or Field Maps</li>
</ul>
 Compensation: $18-31/hourly* *Final agreed-upon compensation will be based on a variety of factors including, but not limited to, an individual’s related experience, education, certifications, skills, and work location. Successful candidates must pass a pre-employment drug test and background check prior to beginning employment. Working Conditions: Environment
<ul>
<li>This job operates in a remote or office-based environment and this role routinely uses standard office equipment such as computers, phones, printers, etc.</li>
<li>This job may also require occasional project site visits, based outdoors which can include excessive noise, uneven walking surfaces, extreme weather, and moving vehicles and equipment.</li>
</ul>
Physical Requirements The physical demands described here are representative of those that must be met to successfully perform the essential functions of the job. This job requires the following:
<ul>
<li>Working on a computer, sitting, or standing for long periods of time in an office or remote office setting.</li>
<li>Employees must be capable of bending, squatting, climbing ladders, and lifting up to 35 lbs. unassisted; 50lbs in a team lift (two or more employees).</li>
<li>Attending meetings, both in person and virtually, and speaking on the phone with peers, clients, etc.</li>
<li>Specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.</li>
</ul>
 Dudek is committed to creating a workplace where all employees, regardless of their background, feel valued, respected, and have equal opportunities to succeed. We believe that a diverse and inclusive workforce is essential to our business success, and we are dedicated to fostering a culture where everyone can thrive. We are committed to fair and equitable processes, based on merit, free from any discrimination. Dudek is genuinely committed to equal employment opportunities within our company and on our project teams. Dudek is also committed to compliance with all applicable laws providing equal employment opportunities. This commitment applies to all persons involved in Dudek’s operations and prohibits unlawful discrimination by any employee of Dudek, including supervisors and coworkers. Equal employment opportunities will be extended to all persons (including those with disability and veteran status) in all aspects of the employment relationship, including recruitment, hiring, training, promotion, transfer, compensation, benefits, discipline, layoff, recall, and termination. Any employee who violates this policy and Dudek’s commitment to equal employment opportunities will be subject to disciplinary action. Dudek is a U.S.-based employer. All positions are based in the United States and require U.S. work authorization. &nbsp;
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