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<h3>Job Description</h3>
Job DescriptionJob Title: QC ChemistJob Description
We are seeking a highly skilled QC Chemist to join our dynamic team. In this role, you will conduct comprehensive testing of raw materials and finished products using a range of advanced analytical techniques. You will ensure the highest quality standards and regulatory compliance in a fast-paced pharmaceutical environment.
Responsibilities
<ul>
<li>Conduct raw material and finished product testing using chromatography (HPLC, UPLC, GC), spectroscopy (UV-Vis, FT-IR), dissolution apparatus, and other analytical techniques.</li>
<li>Independently process and report analytical results, ensuring clear documentation of findings.</li>
<li>Maintain accurate laboratory records and follow methods, specifications, and protocols to ensure reproducibility and compliance with regulatory requirements.</li>
<li>Identify and troubleshoot issues with analytical instruments and techniques.</li>
<li>Ensure products meet regulatory standards, in-house, and regulatory quality specifications.</li>
<li>Collaborate with the quality assurance team to ensure compliance with Good Manufacturing Practices (GMP) or other industry standards.</li>
<li>Operate analytical instruments and equipment, ensuring they are calibrated and functioning properly.</li>
<li>Perform routine maintenance, troubleshooting, and calibration of laboratory instruments.</li>
<li>Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.</li>
<li>Ensure all work is compliant with international regulations, such as FDA and EMA.</li>
<li>Work with R&amp;D and production teams to support product development, scale-up, and product release.</li>
<li>Provide technical support and training to junior team members or other departments when necessary.</li>
</ul>
Essential Skills
<ul>
<li>Proven hands-on experience in a pharmaceutical analytical laboratory.</li>
<li>3-7 years of experience with analytical instruments (HPLC/UPLC, GC, Dissolution apparatus, UV-Vis spectrometer, FT-IR) is highly preferred.</li>
<li>Current Good Manufacturing Practices (cGMP), FDA, and other regulatory requirements knowledge.</li>
<li>Proficiency in dissolution, FT-IR, GC, UV-VIS, KF, TLC, and other analytical techniques.</li>
<li>Basic computer knowledge including MS Word, Excel, and Outlook.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree (minimum) in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.</li>
<li>Ability to document and record analytical experiments and results in detail as per cGMP guidelines.</li>
<li>Excellent attention to detail and problem-solving skills.</li>
<li>Ability to interpret and report complex data clearly.</li>
<li>Knowledge of regulatory guidelines (e.g., GMP, GLP).</li>
</ul>
Work Environment
The role is based in a laboratory setting with exposure to chemicals, reagents, and specialized equipment. The team consists of approximately 10 people. This position may require standing for extended periods and the ability to lift moderate weights (about 25 lbs). Willingness to work overtime may be necessary depending on project deadlines. The workplace fosters growth with new leadership and offers a collaborative atmosphere.
Job Type &amp; Location
This is a Contract to Hire position based out of Cranbury, NJ.
Pay and Benefits
The pay range for this position is $35.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Cranbury,NJ.
Application Deadline
This position is anticipated to close on Jan 16, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

QC Chemist

<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 Pharmacovigilance Systems Intern will support discovery research at Arrowhead Pharmaceuticals by contributing to laboratory projects that strengthen experimental capabilities and support program progress. This internship offers hands-on experience working with biological assays, data analysis, and scientific collaboration in a research environment. The intern will work alongside experienced scientists and gain exposure to laboratory workflows that help advance understanding of RNA biology.
This is an 11-week Summer Internship Program paying $26.00/hour and requires full-time, on-site work five days per week.
Responsibilities
<ul>
<li>Develop an understanding of the scientific background and workflow for RNA isolation assays and related experimental approaches.</li>
<li>Under supervision, establish and optimize assay parameters and conditions for isolating RNA from specific cellular compartments.</li>
<li>Perform experimental readouts using multiple methods to confirm assay performance and results.</li>
<li>Analyze experimental data and organize results using appropriate analytical tools.</li>
<li>Maintain accurate and well-organized experimental records.</li>
<li>Communicate findings and present results to the project team during meetings.</li>
<li>Collaborate with scientists to support continued assay refinement and project progression.</li>
</ul>
Requirements
<ul>
<li>Currently enrolled student in an accredited university Master's degree program in Biology or a related field.</li>
<li>Familiarity with RNA-related techniques.</li>
<li>Hands-on experience with biological laboratory techniques.</li>
<li>Strong verbal and written communication skills.</li>
<li>Excellent problem-solving and analytical skills.</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>
</ul>
Preferred
<ul>
<li>Previous experience with RNA isolation techniques.</li>
<li>Familiarity with Microsoft Excel and GraphPad Prism.</li>
<li>Strong interest in RNA biology, assay development, or discovery research.</li>
<li>Attention to detail and enthusiasm for learning new experimental approaches.</li>
</ul>
California pay range $11,440—$11,440 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 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 Discovery Chemistry Intern will support discovery research at Arrowhead Pharmaceuticals by contributing to projects focused on identifying and optimizing novel peptide ligands for siRNA delivery to various tissues. This internship offers hands-on experience across the full discovery workflow, including synthesis, screening, analysis, and optimization of peptide candidates. The intern will work closely with experienced scientists and gain exposure to high-throughput screening strategies and medicinal chemistry principles within a collaborative research environment.
This is an 11-week Summer Internship Program paying $26.00 per hour for students pursuing a Masters and $27.00 per hour for students pursuing a PhD. This role requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Synthesize linear and cyclic peptides using solid-phase peptide synthesis (SPPS), both manually and on automated synthesizers.</li>
<li>Support high-throughput screening (HTS) efforts, including synthesis of combinatorial peptide libraries and screening for activity.</li>
<li>Purify and analyze peptides using chromatography (HPLC) and mass spectrometry (LC-MS).</li>
<li>Apply medicinal chemistry principles to support lead optimization, including improving peptide stability and affinity.</li>
<li>Maintain accurate experimental records using an electronic laboratory notebook (ELN).</li>
<li>Follow all EHS and laboratory safety protocols, proactively identifying chemical and physical hazards.</li>
<li>Participate in team meetings, sharing results and contributing to scientific discussions.</li>
<li>Collaborate with team members across the discovery organization.</li>
</ul>
Requirements
<ul>
<li>Currently enrolled student in a Master's or Doctorate degree program in Chemistry or Biochemistry or a related field.</li>
<li>Familiarity with analytical chemistry techniques, including HPLC and LC-MS.</li>
<li>Strong problem-solving skills and ability to quickly learn new procedures and techniques.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Proficiency in Microsoft Office applications.</li>
<li>Willingness and ability to spend 75% of the workday in a laboratory environment and 25% at a desk.</li>
</ul>
Preferred
<ul>
<li>Experience with peptide design, synthesis, or screening.</li>
<li>Interest in drug discovery, delivery technologies, or medicinal chemistry.</li>
<li>Strong curiosity, creativity, and enthusiasm for experimental science.</li>
<li>Prior experience working in a collaborative research environment.</li>
</ul>
California pay range $10,560—$11,440 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, Discovery Chemistry (Peptides)

<h3>Job Description</h3>
Job Description
Job Summary
<ul>
<li>Member of the production team that operates machinery and works within the production process. </li>
<li>Operators typically are involved in cleaning, preparing, and monitoring the heavy machines used to mix and process chemicals. They mix and handle chemicals, record information and observations relating to the mixing process, troubleshoot issues with equipment, and assist in process improvement initiatives and the work plan development process.</li>
</ul>

Essential Functions / General Accountabilities
<ul>
<li>Package and transfer chemicals safely. </li>
<li>Perform packaging operations into various sized containers.</li>
<li>Load and unload bulk tank trailers.</li>
<li>Operate forklifts and material moving equipment.</li>
<li>Process chemicals by following guidelines and instructions on equipment such as reactors, distillation systems, etc. </li>
<li>Follow a strict blend sheet and mix chemicals for drumming.</li>
<li>Complete all necessary paperwork, including packing sheets, checklists.</li>
<li>Conduct all tasks in a safe manner and utilize appropriate personal protective equipment per site policies.</li>
<li>Complete janitorial duties and general laborer work as directed, including housekeeping activities.</li>
<li>*The company reserves the right to add or change duties at any time.</li>
</ul>
Job Qualifications
<ul>
<li>Education: High school diploma or equivalent</li>
<li>Experience: 1-2 years of related experience in manufacturing (preferred)</li>
<li>Forklift Certified (preferred)</li>
</ul>
Skills
<ul>
<li>Understanding of chemical process.</li>
<li>Basic computer skills.</li>
<li>Verbal and written communication skills.</li>
<li>A desire to work with team members to improve processes and product quality in a fast-paced, physically demanding environment.</li>
<li>Willingness to comply with safety and quality regulations, including wearing protective gear when necessary.</li>
</ul>
 
Work Environment
<ul>
<li>Outdoors</li>
<li>Warehouse</li>
</ul>
Physical Demands
 
<ul>
<li>Physical requirements of the position, including walking, standing, or sitting for extended periods, lifting heavy objects, climbing, crouching, operating tools, and wearing safety gear.</li>
<li>Ability to lift 50lbs or more.</li>
</ul>
 
*This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.
 Monday - Friday, 8 AM to 4 PM.

Drumming and Blending Chemical Operator

<h3>Job Description</h3>
Job Description
Flexcompute is architecting the next generation of multi-physics simulation. We are moving beyond legacy solvers to build a platform defined by speed and physical fidelity. We are seeking a Computational Scientist to lead the development of our new structural mechanics solver.
We prioritize fundamental understanding over tool proficiency. We are looking for an architect who can derive the governing equations from first principles and implement them into a robust numerical framework.
About Flexcompute
We are a “Physics Intelligence” company making hardware innovation as easy as software. Our solvers (Flow360, Tidy3D) are not just faster; they are effectively instant, reducing simulation times from days to minutes using massive GPU parallelism and proprietary algorithms.
<ul>
<li>Intellectual Density: We maintain an exceptionally high talent bar. Our team of ~90 includes over 50 PhDs from MIT, Stanford, and top research labs. You will work alongside peers who will challenge your thinking and elevate your work daily.</li>
<li>Impact: Our technology is currently used to design optical interconnects, 3D chiplets, quantum computing chips, eVTOL aircraft, and next-gen wind turbines. You are building the “math engine” that drives real-world engineering breakthroughs.</li>
<li>Stability &amp; Growth: We are a Series C stage company with significant funding, revenue-generating products, and a clear path to disrupting the $20B+ simulation market.</li>
</ul>
Requirements
<ul>
<li>Education: Ph.D. in Applied Mechanics, Physics, Applied Mathematics, or a related field.</li>
<li>Deep Physics Intuition: You possess an intuitive grasp of continuum mechanics—elasticity, plasticity, contact mechanics, and wave propagation. You can predict how a structure should behave before the simulation runs.</li>
<li>Advanced Numerical Analysis: You have a theoretical mastery of numerical PDEs. You can mathematically prove the consistency, stability, and convergence of a scheme. You understand the trade-offs between implicit/explicit integration and various spatial discretizations.</li>
<li>Strong General Programming: Proficiency in at least one high-level language (C++, Python, Julia, Rust, or Fortran) with a focus on algorithmic efficiency. You understand data structures, computational complexity (Big O), and how to write maintainable research code.</li>
<li>First-Principles Thinking: Demonstrated ability to solve novel problems where no textbook solution exists.</li>
</ul>
Preferred (But Not Required)
<ul>
<li>Interest in learning High-Performance Computing (HPC) and GPU architecture.</li>
<li>Experience with C++ for scientific computing.</li>
<li>Exposure to multi-physics coupling (fluid-structure interaction, thermal-stress).</li>
</ul>

Key Responsibilities
<ul>
<li>Solver Formulation: Derive and implement governing equations for structural mechanics, ensuring thermodynamic consistency and physical accuracy across linear and non-linear regimes.</li>
<li>Numerical Architecture: Design the core numerical framework. You will determine the optimal discretization strategies (FEM, DG, IGA, etc.) to balance stability, accuracy, and computational cost.</li>
<li>Algorithmic Development: Specific language is secondary to code quality. You will write clean, modular, and efficient algorithms to solve large-scale systems of equations.</li>
<li>Physics-Driven Validation: Diagnose solver behavior not just as code execution, but as physical modeling. You must distinguish between numerical instability and physical phenomena.</li>
</ul>
Benefits
<ul>
<li>Collaborative Autonomy: We operate with high trust. You own your module, but you have immediate access to world-class experts in electromagnetics and fluid dynamics for cross-domain problems.</li>
<li>Continuous Learning: We host regular internal seminars where team members teach each other—from “Advanced Linear Algebra” to “GPU Memory Hierarchies.”</li>
<li>Compensation: Competitive salary + meaningful equity in a fast-growing startup.</li>
<li>Well-being: Comprehensive Medical, Dental, and Vision insurance; 401(k); and a gym/fitness allowance.</li>
<li>Environment: A flat hierarchy where the “best idea wins,” regardless of job title.</li>
</ul>

Computational Mechanics Scientist (Structural Solver)

<h3>Job Description</h3>
Job DescriptionJob Title: Microbiology Laboratory Analyst II/III or Senior AnalystJob Description
The Microbiology Laboratory Analyst II/III or Senior Analyst will play a crucial role in our team, contributing to both routine and complex laboratory testing, sample management, and laboratory maintenance. Reporting to the Manager of Microbiology, this position involves working collaboratively to achieve departmental goals, ensuring compliance with various regulatory standards and maintaining a high-quality laboratory environment.
Responsibilities
<ul>
<li>Perform microbiological tests following SOPs, cGMP, cGLP, USP, EP, ISO/IEC, and other regulatory requirements to support the release of intermediates and finished products.</li>
<li>Conduct cleaning and disinfection validations, both manual and automated.</li>
<li>Execute Container Closure Integrity Test (CCIT) and Package Integrity Evaluation.</li>
<li>Engage in custom studies and additional testing as per client requests.</li>
<li>Develop, modify, verify, and assist with method validation testing.</li>
<li>Participate in method transfer activities and suitability studies under leadership guidance.</li>
<li>Support Quality Management System investigations for non-conformance or out-of-specification results.</li>
<li>Complete assigned CAPA tasks and manage change controls.</li>
<li>Ensure laboratories are clean, safe, and compliant with cGMP standards.</li>
<li>Perform regular inventory checks of reagents, consumables, and materials.</li>
<li>Prepare in-house reagents, stock solutions, media, and microbial suspensions.</li>
<li>Carry out biowaste autoclave sterilization cycles and other laboratory housekeeping tasks.</li>
<li>Maintain accurate and complete test records, always being audit-ready.</li>
<li>Deliver results within pre-determined turnaround times, ensuring accuracy from the first attempt.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in aseptic techniques and cleaning/disinfection validation.</li>
<li>Experience with GMP and GLP standards.</li>
<li>A background in Biology, Pharmaceutical Sciences, Biotechnology, or a related field, with relevant experience in microbiology.</li>
<li>2+ years of GMP/GLP laboratory/FDA experience.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>BS/BA in Biology, Pharmaceutical Sciences, Biotechnology, or equivalent, with a preference for a Microbiology degree.</li>
<li>2+ years of relevant microbiology experience or an Associate degree with 5+ years of experience in a related field, or a High school diploma with 7+ years of experience.</li>
<li>Related training certifications and self-learning are advantageous.</li>
</ul>
Work Environment
The work environment requires physical capabilities such as lifting up to 30 pounds and standing for long periods (up to 6 hours). The role involves repetitive motion tasks and working at a lab bench for most of the day (up to 8 hours). Safety is paramount, with the need to tolerate the smell of Gram-negative organisms and disinfectants, and the ability to work safely with BSL II microorganisms and bloodborne pathogens. The position may require working off-shift hours and weekends when necessary.
Job Type &amp; Location
This is a Contract to Hire position based out of Hercules, CA.
Pay and Benefits
The pay range for this position is $28.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hercules,CA.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Microbiology Analyst

<h3>Job Description</h3>
Job DescriptionPrincipal Geotechnical Engineer (GE) Principal Geotechnical Engineer (GE) Position Overview We are seeking a highly skilled Principal Geotechnical Engineer to lead our geotechnical engineering projects. The successful candidate will be responsible for overseeing foundation design, engineering geology, and environmental engineering aspects of projects while ensuring compliance with industry standards and regulations. This role requires a deep understanding of geotechnical principles and the ability to manage complex projects and teams. Key Responsibilities
<ul>
<li>Lead and manage geotechnical engineering projects from inception to completion.</li>
<li>Conduct site investigations and analyze soil and rock samples for geotechnical properties.</li>
<li>Design foundations and earthworks in accordance with project requirements and standards.</li>
<li>Perform slope stability analyses and groundwater assessments to inform design decisions.</li>
<li>Prepare technical reports and documentation to communicate findings and recommendations.</li>
<li>Collaborate with project managers, architects, and other engineers to integrate geotechnical solutions into overall project plans.</li>
<li>Conduct risk assessments related to geotechnical issues and propose mitigation strategies.</li>
<li>Mentor and train junior engineers in geotechnical practices and principles.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's degree in Civil Engineering or related field; Master's degree preferred.</li>
<li>Professional Engineering (PE) license is required.</li>
<li>Minimum of 10 years of experience in geotechnical engineering, with a focus on foundation design and environmental engineering.</li>
<li>Strong knowledge of soil mechanics, geotechnical analysis, and site investigation techniques.</li>
<li>Experience with AutoCAD and Microsoft Project for project design and management.</li>
<li>Familiarity with risk assessment processes and technical reporting standards.</li>
<li>Excellent communication and interpersonal skills, with the ability to lead teams and manage client relationships.</li>
</ul>
Benefits
&nbsp;
401(k) 401(k) matching Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Parental leave Professional development assistance Retirement plan Tuition reimbursement Vision insurance
 - For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. CyberCoders will consider for Employment in the City of Los Angeles qualified Applicants with Criminal Histories in a manner consistent with the requirements of the Los Angeles Fair Chance Initiative for Hiring (Ban the Box) Ordinance.This job was first posted by CyberCoders on 12/18/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. &nbsp;CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at <a href="mailto:Benefits@CyberCoders.com" target="_blank">Benefits@CyberCoders.com</a> to make arrangements.

Principal Geotechnical Engineer (GE)

<h3>Job Description</h3>
Job Description
Position Title: Research Project Coordinator 
Department: Administration
 Reports To: Clinical Director
POSITION SUMMARY 
The Research Project Coordinator is responsible for the oversight of protocol operation, supervising research assistants, and assisting the Clinical Director in implementing research activities at Tarzana Treatment Centers, Inc. (TTC). 
CATEGORIES OF DUTIES 
1. Monitor recruitment and tracking of research study participants, as well as study records, participant tracking logs, and study regulatory binders.
 2. Assure that interviews with study participants are conducted by research assistants in a timely and ethical manner. 
3. Maintain good working relationships and contact with protocol team members. 
4. Assist research assistants in adhering to study protocols, including the reporting Serious Adverse Events to the appropriate parties as they occur for research study participants. 
5. Prepare for regular visits from Quality Assurance monitors and other regulatory monitors. 
6. Attend protocol trainings, specific measurement trainings, research-oriented trainings, and protocol-related meetings, as necessary.
7. Conduct research assistant duties (data collection, reporting, and participant interviews) as needed, in the event of an absence of research assistant(s). 
8. Provide administrative oversight to RAs, including the completion of e-time, work schedules, time off, and progressive discipline, as needed. 
9. Complete annual Performance Evaluations for research assistants. 
10. Supervise the work activities and quality of work of research assistants. 
11. Attend research meetings, as required. 
12. Participate in TTC committees as needed and required. 
13. Represent TTC at research and community meetings, as required. 
14. Conduct data analyses to assist in internal program evaluation, performance improvement, and research activities.
15. Write reports and discuss or interpret data, as required, to other staff within the organization. 
16. Additional functions as requested by the Clinical Director. 
EDUCATION/TRAINING/EXPERIENCE 
Bachelors Degree or Master’s in a social science, with a solid knowledge of research methods. Prior research experience as a research assistant (or a similar position) in behavioral health research studies, essential. Knowledge of computers and statistical software programs such as SPSS. Prior data entry and word processing experience. 
LICENSES/CERTIFICATES
 None 
SETTING 
Tarzana Treatment Centers, Inc. is a non-profit corporation which provides behavioral healthcare services including chemical dependency. 
EQUAL OPPORTUNITY EMPLOYER 
Tarzana Treatment Centers, Inc. does not discriminate as to race, nationality, religion, gender, sexual orientation and disability in its hiring practices. 
ADA REQUIREMENT
 Tarzana Treatment Centers, Inc. supports the Americans with Disabilities Act. Discrimination is prohibited in all aspects of employment against disabled persons, who, with reasonable accommodations, can perform the essential functions of a job. 
#SJ2021

Research Project Coordinator

<h3>Job Description</h3>
Job Description&nbsp;Aerospace Non-Destructive Testing Company located in North Hollywood is currently seeking a Chemical Processing Operator. Position Description:&nbsp; This is an Entry Level position, no experience necessary, we will train.&nbsp; The ideal candidate will train on our material finishing process.&nbsp; Requirements are as follows:&nbsp; 
<ul>
<li>Eager to listen, take instructions and learn the task at hand.</li>
<li>Punctual</li>
<li>Good organizational skills and work habits.</li>
<li>Ability to multitask.</li>
<li>Team Player.</li>
<li>Good Verbal Communication Skills</li>
</ul>
 Due to the ITAR requirements, if hired all applicants must be able to provide legal proof of U.S. citizenship or permanent residency. Benefits and Salary: Salary commensurate with abilities, Medical, Dental and Personal Time off (P.T.O.) &nbsp; Consideration will be first to Local Applicants. &nbsp; If you feel you are the right candidate for this position call David Beltran @ (818) 432-8764 &nbsp;

Chemical Processing Operator

<h3>Job Description</h3>
Job Description
HELP WANTED – HORTICULTURAL TECHNICIAN 
Apply online with ZipRecruiter or Call 817-589-2040 Ask for Gary
&nbsp;
Full-Time Position
Do you enjoy working with plants and being out and about instead of stuck behind a desk? We’re looking for a reliable, friendly Horticultural Technician to help care for beautiful tropical plants inside commercial buildings throughout the area.
&nbsp;
What you’ll do:
<ul>
<li>Maintain tropical plants in lobbies, offices, hotels, banks, malls, restaurants and more</li>
<li>Water, prune, clean, and keep plants looking their best</li>
<li>Work independently while visiting a variety of professional locations</li>
<li>Represent our company with a positive, professional attitude</li>
</ul>
&nbsp;
What we’re looking for:
<ul>
<li>Experience with plants is very helpful (but we’re willing to train the right person)</li>
<li>Dependable, detail-oriented, and self-motivated</li>
<li>Comfortable working indoors at different commercial sites</li>
<li>A valid driver’s license (company vehicle provided)</li>
</ul>
&nbsp;
What we offer:
<ul>
<li>Company vehicle provided for technicians</li>
<li>Steady, full-time work</li>
<li>Regular weekday schedule (no late nights)</li>
<li>Work with living plants in clean, professional environments</li>
<li>If you enjoy plants, take pride in your work, and like variety in your day, this could be a great fit.</li>
</ul>
&nbsp;
Apply today and grow with us!
&nbsp;
Company DescriptionFull time Horticultural Technician. Job duties – maintaining tropical plants inside commercial buildings, such as plants in lobbies of buildings, malls, banks, restaurants, hotels, offices etc. Experience would be very helpful. Company vehicles are provided for technicians. 
<h3>Company Description</h3>
Full time Horticultural Technician. Job duties – maintaining tropical plants inside commercial buildings, such as plants in lobbies of buildings, malls, banks, restaurants, hotels, offices etc. Experience would be very helpful. Company vehicles are provided for technicians.

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