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<h3>Job Description</h3>
Job DescriptionYoh is seeking a Principal Scientist – Biologics Formulation&nbsp;to&nbsp;join our client’s innovative team in El Segundo, CA. This is a unique opportunity to lead protein formulation development efforts for biologic therapeutics in a cutting-edge biopharmaceutical environment. The ideal candidate is a creative and driven Scientist with deep expertise in biologics, drug product formulation, and protein formulation (mAbs).&nbsp; ????&nbsp;El Segundo, CA (Onsite) ????&nbsp;Direct Hire | Biopharmaceuticals ????&nbsp;$150,000 – $160,000/year (based on experience) Key Responsibilities: 
<ul>
<li>Design and develop formulations for biologic drug products.</li>
<li>Expertise in biologics, drug product formulation, and protein formulation (mAbs).</li>
<li>Conduct hands-on laboratory experiments and coordinate with external testing partners.</li>
<li>Collaborate cross-functionally with product development, process engineering, analytical development, and other engineering teams to advance drug development programs.</li>
</ul>
Qualifications: 
<ul>
<li>PhD in Pharmaceutics, Biochemical Engineering, Chemical Engineering, Organic Chemistry, or a related field.</li>
<li>Minimum of 5 years of industry experience in biologics production and protein&nbsp;formulation.</li>
<li>Proven experience with regulatory submissions and addressing regulatory inquiries.</li>
<li>Demonstrated success in biologics and protein formulation and development, supported by peer-reviewed publications and/or scientific presentations.</li>
<li>Strong knowledge of biologic and protein formulation development across various dosage forms, including characterization and scale-up.</li>
<li>Deep understanding of protein stability and product quality attributes.</li>
</ul>
#IND-SPG Estimated Min Rate: $150000.00 Estimated Max Rate: $160000.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: 
<ul>
<li>Medical, Prescription, Dental &amp; Vision Benefits (for employees working 20+ hours per week)</li>
<li>Health Savings Account (HSA) (for employees working 20+ hours per week)</li>
<li>Life &amp; Disability Insurance (for employees working 20+ hours per week)</li>
<li>MetLife Voluntary Benefits</li>
<li>Employee Assistance Program (EAP)</li>
<li>401K Retirement Savings Plan</li>
<li>Direct Deposit &amp; weekly epayroll</li>
<li>Referral Bonus Programs</li>
<li>Certification and training opportunities</li>
</ul>
 Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day &amp; Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit <a href="https://www.yoh.com/applicants-with-disabilities" target="_blank">https://www.yoh.com/applicants-with-disabilities</a> to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.Company DescriptionFounded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day &amp; Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations. Company Website: <a href="https://www.yoh.com/" target="_blank">https://www.yoh.com/</a> 
<h3>Company Description</h3>
Founded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA. Yoh was the nation’s first technology staffing firm. As a business unit of Day &amp; Zimmermann, Yoh has a flourishing global footprint, as our parent company operates from more than 150 worldwide locations.\r\nCompany Website: <a href="https://www.yoh.com/" target="_blank">https://www.yoh.com/</a>

Principal Scientist - Biologics Formulation

<h3>Job Description</h3>
Job Description
Summary: The Clinical Research Compliance Specialist supports clinical research studies by monitoring protocol and regulatory compliance, reviewing research data for accuracy, managing documentation and milestones, auditing essential documents, writing monitoring reports, and developing risk monitoring plans and study-related documents. 
 Essential Duties and Responsibilities: 
<ul>
<li>Conduct SOP/GCP/Compliance Training with coordinators at site.</li>
<li>Ensure sites are adhering to ACN’ s policies and procedures.</li>
<li>Perform on-site and remote audits as a quality assurance tool that is used to evaluate compliance and to ensure human subject protection and data integrity.</li>
<li>Ensure valid findings from the audit/inspection report are managed effectively by the organization, and in accordance with our procedures. Escalate significant findings to CTNx Management.</li>
<li>Coach and Support CRCs and PIs on a continuous basis based upon audit findings.</li>
<li>Monitor the protocol and regulatory compliance of clinical research studies (with low —to high-risk research designs) in multiple treatment areas.</li>
<li>Review research data from source documentation for accuracy, completeness, and timeliness.</li>
<li>Collaborate with the offshore compliance team and the onsite study team to effectively address critical findings.</li>
<li>Strictly adhere to confidentiality and compliance standards.</li>
<li>Collect, review, maintain, and audit essential documents</li>
<li>Assist with developing documents and implementing study-specific risk monitoring plans.</li>
<li>Support ongoing communication with study teams regarding trial qualification, initiation, monitoring, remote monitoring, and close-out activities.</li>
<li>Serves as the main point of contact in compliance audits and interim monitoring visits.</li>
<li>Read and comprehend new research protocols as well as amended protocols.</li>
<li>Meet assigned targets, goals, and completion deadlines.</li>
<li>Utilize analytical, problem-solving, and critical thinking.</li>
<li>Utilize precise attention to detail.</li>
<li>Perform other duties as assigned to meet the goals and objectives of the department and institution</li>
<li>Comply with all company policies, procedures, and conduct.</li>
</ul>
Qualification Requirements: To perform this job successfully, an individual must be able to satisfactorily perform each essential duty. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions. 
 Education and Experience: 
<ul>
<li>An associate degree in healthcare or a related field is preferred.</li>
<li>At least two (2) years of clinical research experience as a Clinical Research Coordinator (CRC) or one (1) year of experience as a Clinical Research Associate (CRA) is required.</li>
<li>Proficient in Microsoft Word, Excel and Adobe Acrobat.</li>
<li>Working knowledge of medical and/or clinical trial terminology.</li>
<li>Working knowledge in relevant scientific fields.</li>
<li>Strong attention to detail.</li>
<li>Must be able to prioritize competing demands.</li>
<li>Must possess excellent verbal and written communication skills.</li>
<li>A proven ability to multi-task in a rapidly changing environment.</li>
</ul>
Special Skills, Knowledge, and Abilities: 
<ul>
<li>Understands the task at hand, seeks out information, and draws conclusions from available data to deliver outcomes.</li>
<li>Adapts quickly to changing priorities to perform as needed in his/her role.</li>
<li>Remains calm when faced with changes to (and in) his/her work.</li>
<li>Effectively relays understanding of diverse perspectives.</li>
<li>Can handle communication upwards and downwards as needed.</li>
<li>Presents information in a clear, well-thought-out way and tailored to the audience.</li>
<li>Shows support for the new direction even when the details have not been finalized.</li>
<li>Spots early indications of underperformance and takes corrective actions. Celebrates successes.</li>
<li>Works with partners inside his/her function to find the best solutions that align with functional priorities. Is easy to work with to find solutions.</li>
<li>Supports the creation/implementation of data management plans by understanding site/study data sourcing techniques and overall compilation.</li>
<li>Independently assists data management tasks/processes in line with study-related data plans.</li>
<li>Identifies and resolves data queries and requirements based on knowledge of the origin, flow, and management of data through a clinical study.</li>
<li>Ensures compliance with SOPs related to data quality within assigned studies.</li>
<li>Contributes to study management and research procedures by consistently executing assigned tasks in compliance with GCP guidelines, with minimal supervision</li>
<li>Applies understanding of clinical study/site operations to address requirements (e.g., study selection and set-up, clinical monitoring, risk mitigation support).</li>
<li>Shows awareness of basic safety, ethical, and HPP considerations, and regulatory requirements in terms of documentation and study conduct.</li>
<li>Assists in the development of relevant technical, study, and/or regulatory materials to ensure compliance with regulatory, safety, &amp; ethical requirements.</li>
</ul>
Certificates, Licenses, Registrations: Maintain GCP certification and other on-the-job certifications as required. 
Travel Required: 5-10% 
Physical Demands and Working Conditions: The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this job. 
<ul>
<li>Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
<li>While performing the duties of this job, the employee is regularly required to stand, walk, sit, kneel, use hands to finger, handle, or feel, and talk or hear.</li>
<li>The employee must occasionally lift and/or move up to 25 pounds.</li>
<li>This job requires Specific vision abilities, including close vision, depth perception, and the ability to adjust focus.</li>
<li>The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.</li>
<li>Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
<li>An essential function of the job is to be able to comply with all applicable federal, state and local safety and health regulations that would apply to this job.</li>
<li>The employee must move about the workspace to access work surface and shelves, cabinets, drawers, and equipment that are at, below or above the work surface.</li>
<li>Nothing in this job description limits management’s right to assign or reassign duties and responsibilities to this job at any time as business needs dictate. This job description reflects management’s assignment of essential functions; it does not proscribe or restrict the tasks that may be assigned. The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor is it intended to be an all-inclusive list of the skills and abilities required to do the job.</li>
</ul>
BENEFITS:
<ul>
<li>401 (k) Retirement Plan</li>
<li>Medical, Dental, and Vision Insurance</li>
<li>Paid Time Off (PTO)</li>
<li>Floating Holidays</li>
<li>And more!</li>
</ul>
While every attempt has been made to outline the basic job responsibilities, adjustments in the process may change and expand the job duties. In addition, employees may be asked to perform duties outside of this description at the discretion of the Executive Management Team.

Clinical Research Compliance Specialist

<h3>Job Description</h3>
Donald L. Mooney Enterprises, LLC dba NURSES Etc STAFFING is sourcing&nbsp;Board Certified Chief Therapeutic Medical Physicist, PhD&nbsp;for the Tibor Rubin VAMC (Long Beach, CA) location. Schedule:
<ul>
<li>0800- 1630 daily Monday to Friday, with an option of compressed schedule of 10-hour shifts/4 days a week, 0700-1730.</li>
</ul>
Estimated Contract Start Date:&nbsp;May 18, 2025
Contract Length:&nbsp;Up to 5 years Qualifications:&nbsp; Chief Therapeutic Medical Physicists must be Board Certified in Medical Physics or Therapeutic Medical Physics by the ABR and maintain licensure with the Board of Licensure for Professional Medical Physicists, if applicable. Certification must be maintained throughout the contract POP. If contractor’s medical physicist(s) is/are not directly employed by the treating facility, documentation must be provided to ensure adequate certification.
Requirements: Board Certified Chief Therapeutic Medical Physicist–Ph. D Level: Must have at least five (5) years of documented post-board experience after board certification and at least three (3) years of continuous work experience within the last five (5) years to ensure the TMP’s experience is current and relevant. Senior TMP must also have the following minimum years of experience, expertise, and knowledge on the following procedures, equipment, and software: Five (5) years of experience – Documentation detailing experience in performing QA procedures. Three (3) years of experience – Documentation detailing Therapeutic Medical Physics in a healthcare system that is ACR or APEx certified. Three (3) years of experience - Varian Linear Accelerators: TrueBeam with Brain Lab Accessories following standards of TG-142 Three (3) years of experience -Image Guided Radiation Therapy (IGRT) including Cone Beam CT (following standards of TG-142). Three (3) year of experience - Eclipse treatment planning system; and ARIA record &amp; verify system, including the following treatment modalities: 2D/3D Conformal, SRS, SRT, SBRT, and IMRT/VMAT (following standards of TG-53) Three (3) years of experience - IMRT QA: MapCheck (or equivalent). Three (3) years of experience –GE Discovery CT Simulator (or equivalent) and following standards of TG-66 Three (3) year of experience - Using Superficial X-ray Machine. Successfully perform one (1) acceptance testing (i.e., work with vendor to ensure proper working condition during installation) on a linear accelerator. Successfully perform one (1) commission of (i.e., gathered necessary measurements or data) a linear accelerator for a treatment planning system
If you are interested in this position,&nbsp;please email me at <a href="mailto:Vvazquez@nursesetc.net" target="_blank">Vvazquez@nursesetc.net</a> About Nurses Etc Staffing At NURSES Etc STAFFING, we are committed to our mission of providing healthcare facilities with top-quality nursing and allied health professionals, excellent customer service, and professional staffing solutions. Founded in 2000, we have always placed a strong emphasis on building relationships with healthcare providers based on open communication, respect, and recognition for the important work they do. Equal Employment Opportunity Statement:&nbsp;Donald L. Mooney Enterprises provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. All employment is decided on the basis of qualifications, merit, and business need.

Physician Other - Competitive Salary

<h3>Job Description</h3>
Job Description
Job Description:&nbsp;Ninyo &amp; Moore Geotechnical &amp; Environmental Sciences Consultants has an immediate opening for a Project or Senior Project Geotechnical Engineer in our Irvine, California office. The successful candidate will manage geotechnical, forensic, and construction projects, including meeting and interacting with the client, and managing budgets. The Project Engineer will also coordinate and participate in field activities, including logging of borings, test pits, trenches and cores; evaluation of geologic and seismic hazards; forensic evaluation of distressed structures and failed slopes; perform liquefaction, slope stability, and settlement analyses; and prepare geotechnical engineering proposals and reports. Experience with construction and grading activities is strongly desired. Duties of the Project Engineer will also include providing technical support to staff-level engineers, geologists and field technicians.
Education:&nbsp;B.S./B.A. required (Civil Engineering, Geotechnical Engineering, Construction Engineering), M.S. preferred.
Required Skills:&nbsp;The successful candidate should be a licensed professional engineer with 45years experience in geotechnical consulting. The ideal candidate will bring local experience and familiarity with the local engineering practice. Candidate should be a team player, be detail oriented and have excellent verbal and written communication skills.&nbsp;
Status:&nbsp;Full time
Location:&nbsp;Irvine, CA
Reference ID:&nbsp;PGE-IRV
 
Compensation details: 92000-120000 Yearly Salary
 
PI31ff6c083d05-25405-38425166

Project or Sr. Project Geotechnical Engineer

<h3>Job Description</h3>
Description
Are you a motivated Principal Resilient Systems Scientist with a technical vision and hands-on knowledge of mission-focused systems? The Leidos Innovations Center’s newly established Information and Data Science Division is seeking a Senior Resilient Systems Scientist to help lead strategic solution developments and projects. This role will drive capture of strategic customer-funded software R&amp;D. The ideal candidate will have a proven track record in developing technology-based approaches that yield novel, innovative capabilities while advancing the state of the art. We are looking for a proven researcher who can develop and lead a groundbreaking research portfolio using both internal and customer funding.&nbsp;
The ideal candidate will be able to work out of our San Diego, CA; Arlington, VA or Dayton, OH offices.&nbsp;&nbsp;
Primary Responsibilities&nbsp;
<ul>
<li>Develop innovative solutions to challenging problems of interest to the Defense Applied Research Projects Agency (DARPA) and U.S. Department of Defense (DoD). &nbsp;</li>
</ul>
<ul>
<li>Engaging R&amp;D customers and transition partners to understand technical gaps and needs for resilient systems solutions in mission critical systems.&nbsp;</li>
</ul>
<ul>
<li>Leading teams of researchers and engineers in the development, adaptation, and extension of innovative approaches to resilient systems solutions across a range of technical areas and application domains to advance the state of the art while addressing long-term problems of importance to national security such as embedded systems.&nbsp;</li>
</ul>
<ul>
<li>Develop novel approaches for the generation of assurance evidence for critical software, at scale&nbsp;</li>
</ul>
<ul>
<li>Collaborate in cross-discipline teams to deliver innovations that provide measurable resilient mission impact.&nbsp;</li>
</ul>
<ul>
<li>To ensure technical relevancy, they will track software technology trends in the customer community and broader R&amp;D communities as well as identify future software R&amp;D funding opportunities.&nbsp;</li>
</ul>
Basic Qualifications&nbsp;
<ul>
<li>Proven track record in proposing, winning, and executing work with customers such as DARPA, IARPA or similar agencies within the last 5 years&nbsp;</li>
</ul>
<ul>
<li>Bachelor’s degree in Computer Science, Mathematics, or a related field and 12+ years prior relevant experience, M.S degree with 10+ years of prior relevant experience, or Ph.D. with 8+ years of experience (Ph.D. preferred)&nbsp;</li>
</ul>
<ul>
<li>Industrial and/or academic experience advancing the state of the art in FPGA development, embedded systems, formal verification, developing technologies such as program analysis, constraint-solving, symbolic execution, or theorem proving&nbsp;</li>
</ul>
<ul>
<li>Proven track record in proposing, winning, and executing Contract R&amp;D&nbsp;</li>
</ul>
<ul>
<li>At least 4 years of experience with programming languages such as Java, Scala, C/C++, Ruby, Rust, or Python&nbsp;</li>
</ul>
<ul>
<li>Experience with test and evaluation, software analysis and software specification&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Strong verbal and written communication skills, with experience engaging with senior leadership and technical teams as well as ability to present complex software solutions in a clear, understandable manner&nbsp;</li>
</ul>
<ul>
<li>Qualified candidates must possess a Secret clearance as well as the ability to obtain a Top Secret&nbsp;</li>
</ul>
Preferred Qualifications&nbsp;
<ul>
<li>Ph.D. in Computer Science, Mathematics, or related degree&nbsp;</li>
</ul>
<ul>
<li>FPGA development and testing, embedded systems design and innovation, applying formal methods, using technologies such as theorem provers for first-order logic and higher-order logic, proof assistants, solvers, or other automated reasoning tools&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Experience conducting applied research areas of CPS such as autonomous vehicles, smart sensors, or Internet of Things, fusing data collected from cyber and physical systems to develop novel approaches to address emerging technical challenges in domains relevant to U.S. national security&nbsp;</li>
</ul>
<ul>
<li>Experience in semantic analysis of software&nbsp;</li>
</ul>
<ul>
<li>Strong and proven customer relationship skills including the ability to discover the true technical challenges and requirements associated with opportunities, recommending alternative technical approaches, and shaping future opportunities&nbsp;</li>
</ul>
<ul>
<li>Experience applying and leading the application of formal methods in fundamental research contexts, to problems in complex domains, under conditions of uncertainty, and dynamic and evolving technical challenges&nbsp;</li>
</ul>
<ul>
<li>Ability to work in a fast-paced environment&nbsp;</li>
</ul>
<ul>
<li>Excellent written and oral skills in communicating technical information with an ability to present complex technical information clearly and coherently&nbsp;</li>
</ul>
<ul>
<li>Proven experience forming strong teams composed of members from academia and industry for competitive research and development opportunities&nbsp;</li>
</ul>
<ul>
<li>Experience developing software for critical applications that require software certification&nbsp;</li>
</ul>
At Leidos, we don’t want someone who "fits the mold"—we want someone who melts it down and builds something better. This is a role for the restless, the over-caffeinated, the ones who ask, “what’s next?” before the dust settles on “what’s now.”
If you’re already scheming step 20 while everyone else is still debating step 2… good. You’ll fit right in.
Original Posting:September 2, 2025
For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.
Pay Range:Pay Range $126,100.00 - $227,950.00
The Leidos pay range for this job level is a general guideline only&nbsp;and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

Principal Resilient Systems Scientist

<h3>Job Description</h3>
We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.
Benefits:
<ul>
<li>This is a full-time or part-time REMOTE position</li>
<li>You’ll be able to choose which projects you want to work on</li>
<li>You can work on your own schedule</li>
<li>Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work</li>
</ul>
Responsibilities:
<ul>
<li>Give AI chatbots diverse and complex chemistry problems and evaluate their outputs</li>
<li>Evaluate the quality produced by AI models for correctness and performance</li>
</ul>
Qualifications:
<ul>
<li>A current, in progress, or completed Masters and/or PhD is preferred but not required</li>
<li>Fluency in English (native or bilingual level)</li>
<li>Detail-oriented</li>
<li>Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning</li>
</ul>
Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.

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