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<h3>Job Description</h3>
Job DescriptionRincon Consultants, Inc. is seeking as-needed Wildlife Biologists and Botanists (Central Valley) to join our team! We are looking for candidates with strong field expertise in botany and wildlife biology, specifically within the Central Valley (Sacramento to Bakersfield). The position will involve conducting habitat assessments, focused and general biological surveys, vegetation surveys and mapping, construction compliance monitoring, report writing, and providing biological construction support for a variety of projects. If you have a passion for fieldwork and a deep knowledge of Central Valley species and habitats, we encourage you to apply! &nbsp; Overview of Key Duties and Responsibilities:&nbsp;
<ul>
<li>Conduct site assessments, surveys, and habitat evaluations for common and special-status plant and wildlife species and map vegetation communities.</li>
<li>Perform biological monitoring and provide compliance support during construction activities, prepare compliance monitoring reports.</li>
<li>Identify plant species using a dichotomous key, focusing on Bay Area and northern Central Valley botany.</li>
<li>Map vegetation communities using standard mapping practices and identify sensitive vegetation communities.</li>
<li>Survey, monitor, and assess habitats for special-status species, including but not limited to the following:
<ul>
<li>California tiger salamander</li>
<li>San Joaquin kit fox</li>
<li>Blunt-nosed leopard lizard</li>
<li>Giant garter snake</li>
<li>Valley elderberry longhorn beetle</li>
<li>Western spadefoot toad</li>
<li>Western pond turtle</li>
<li>Vernal pool invertebrates</li>
<li>Fresno kangaroo rat</li>
<li>Giant kangaroo rat</li>
<li>Nelson’s antelope ground squirrel</li>
<li>Swainson’s hawk</li>
<li>Special-status plants in the Central Valley</li>
</ul>
</li>
<li>Prepare preconstruction survey reports and other technical documentation.</li>
<li>Track compliance with mitigation measures and permit conditions, maintaining accurate field reports and monitoring logs.</li>
<li>Collaborate with multidisciplinary teams and provide additional support to the Natural Resources Team as needed.</li>
<li>Wetland delineation experience is a plus.</li>
</ul>
 This Job Might Be for You If You Have the Following:&nbsp;
<ul>
<li>Bachelor’s or Master’s degree in biology, botany, ecology, environmental science, or a related field, with at least 1-2 years of professional biological fieldwork experience.</li>
<li>Prior approval through the U.S. Fish and Wildlife Service or California Department of Fish and Wildlife as Designated Biologist, Species Specific Monitor or General Biological Monitor for any of the above listed species is preferred.</li>
<li>Expertise in Central Valley ecosystems, including experience with compliance monitoring, habitat assessments, vegetation monitoring, and species-specific surveys.</li>
<li>Familiarity with federal and state environmental laws, including but not limited to federal and state Endangered Species Acts, and the California Environmental Quality Act, as well as incidental take permits, Clean Water Act permits, Lake and Streambed Alteration Agreements, regulatory compliance oversight, and development/implementation of mitigation measures.</li>
<li>Demonstrated experience with the species listed above, including surveying and monitoring in occupied habitats and securing project approvals. </li>
<li>Excellent verbal and written communication skills, including strong technical writing experience preparing field reports, monitoring logs, and preconstruction survey documentation.</li>
<li>Ability to hike 6–8 miles per day in often difficult terrain and variable weather conditions while carrying 25 lbs. </li>
<li>Ability to work 10–12+ hour days, as needed.</li>
</ul>
 *More senior professionals (e.g., 5–10+ years) are also strongly encouraged to apply.&nbsp;Responsibilities and pay will adjust accordingly, with senior-level pay exceeding the posted range. Rincon Consultants, Inc. is an award-winning leader in providing quality environmental consulting services throughout California and is recognized as a ‘Best Environmental Services Firm to Work For’ by the Zweig Group. We partner with clients in sectors such as transportation, energy and infrastructure, sustainability, climate change, oil and gas, water, commercial, private development, and government. Our 400+ associates in 13 offices located in Northern, Central, and Southern California are dedicated professionals who combine their passion with our purpose. The base pay for this on-call position is $27.00–$35.00 per hour. At Rincon, our salary ranges are based on market median of similar jobs, according to third party salary benchmark surveys. The base pay that is actually offered will take into account internal equity and also may vary depending on the candidate’s job-related knowledge, skills, and experience.
Rincon Consultants, Inc does not accept unsolicited applicant/candidate resumes from search firm recruiters and/or temporary agencies that do not have a signed contract and specified work order with Rincon Consultants. Further, such resumes received will be deemed the sole property of Rincon Consultants and no fees will be paid in the event Rincon Consultants subsequently hires such individual. Rincon Consultants is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
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ZAmpNH3ogb

As-Needed Wildlife Biologists and Botanists (Central Valley)

<h3>Job Description</h3>
Job Description
Validation &amp; Engineering Group, Inc. (V&amp;EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
<ul>
<li>Senior Scientist Lead Investigator</li>
</ul>
Provides operational, scientific expertise and compliance knowledge support to the Manufacturing Sterile Operations. Responsible for executing manufacturing investigations (QE’s), Corrective Action Preventive Action (CAPA’s), NTR’s, NOE’s, procedures development &amp; revision, and process validation documentation. Acts as facilitator for the necessary information related to the support of the existing processes, the fast tracking for documenting, implementing process modifications and technology for products transfers and validation. This incumbent must comply with all Security guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices required by the job functions. Responsibilities:
<ol>
<li>Ensures that all QE’s, NTR’s, NOE’s and CAPA’s are completed / closed within the established timeframe, utilizing the right tools to prevent reoccurrence.</li>
<li>Reviews and provides input to regulatory submissions applicable to area of responsibility.</li>
<li>Leads QE’s and CAPA’s trend evaluation.</li>
<li>Participates in the new product introduction process to determine requirements for documentation, materials, training and equipment modifications.</li>
<li>Supports establishment of process monitoring parameters and control limits.</li>
<li>Supports the assessment of deviations and process monitoring data</li>
<li>Monitors and evaluates parameters in existing (on-going) processes to optimize process times/productivity, equipment performance, yields and quality.</li>
<li>Provides technical assistance to identify, recommend and implement process and equipment modifications to improve process performance; to identify and assist in the implementation of cost reduction projects and assuring the manufacturing area is in cGMP’s compliance.</li>
<li>Write, evaluate and revise the required manufacturing documentation (i.e. SOP’s, MBR’s, etc.) and may assist in providing training on scientific or technical aspects of the processes.</li>
<li>Assists with generation and execution of validation protocols and reports.</li>
<li>Participates in regulatory inspection when necessary.</li>
<li>Assists the area managers and supervisory personnel to solve any production technical problem (i.e. Process / equipment troubleshooting, yield, cycle time, quality and productivity).</li>
<li>Provides alternatives and recommendations to improve and maximize processes and equipment's.</li>
<li>Participates in Environmental Regulatory and Compliance Permits and Process Safety Hazards evaluation.</li>
<li>Promotes and model the BMS Core Behaviors, facilitating teamwork.</li>
<li>Supports all site Initiatives and any other assignments based on business needs</li>
</ol>
 Experience Required:
<ul>
<li>Five (5) years of experience in a Parenteral Manufacturing facility.</li>
<li>Strong technical writing and presentation skills.</li>
<li>Ability to interpret and analyze statistical data.</li>
<li>Knowledge in CGMP’s, OSHA, EPA and other regulatory standards.</li>
<li>Knowledge of computers applications (Microsoft Word, Excel, Power Point).</li>
<li>Excellent interpersonal skills and team work oriented.</li>
<li>Excellent communications skills in Spanish /English.</li>
</ul>
 Education Required:
<ul>
<li>BS Degree in Science, Pharmacy, and/or Engineering</li>
</ul>

MV01-050925 Sr. Scientist Lead Investigator

<h3>Job Description</h3>
Job Descriptionjob summary: 
Are you an experienced analytical chemist with a passion for solving complex analytical challenges? Join a cutting-edge team at a global healthcare leader, where you'll drive impactful work in impurity and nitrosamine testing using advanced LC-MS/MS techniques. You'll work side-by-side with subject matter experts, directly supporting essential research in drug safety and quality.
This position will contribute analytical and technical support for nitrosamines and impurities analysis. Specifically, this candidate will collaborate with Company subject matter experts (SMEs) by leading and executing laboratory experiments. This position requires daily in-person and on-site laboratory work at Company's Round Lake site.
 location: Round Lake, Illinois job type: Contract salary: $38.00 - 42.58 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Conduct nitrosamines and impurities evaluations (routine and non-routine) by performing chemical analysis utilizing LC / MS / MS and associated wet chemistry and sample preparation techniques.</li>
<li>Conduct chemical analyses and preparation, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies.</li>
<li>Perform experiments specifically for nitrosamines and E&amp;L analysis, within specified timelines.</li>
<li>Operate, maintain, and troubleshoot MS instrumentation.</li>
<li>Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results.</li>
<li>Independently plan and execute method development activities utilizing LC/MS/MS.</li>
<li>Generate scientific sound experimental data following written procedures including protocols and standard operating procedures (SOPs).</li>
<li>Independently author and contribute to experimental protocols, summaries, and technical reports.</li>
<li>Document and review laboratory work using an electronic laboratory notebook per Company's good documentation practices (GDP) and general good laboratory practices (GLP).</li>
<li>Follow Company's Quality Manual, SOPs, and Environmental Health, Safety &amp; Sustainability (EHS&amp;S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement.</li>
<li>Provide support to maintain a compliant, safe, and clean working environment/laboratory.</li>
<li>Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions, and/or project goals.</li>
<li>Competent in interpreting analytical data and presenting in a form that is suitable for a diverse audience.</li>
<li>Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>PhD in Chemistry (0-3 yrs), MS (3-5 yrs), or BS (5-7 yrs) in Chemistry or related field</li>
<li>Hands-on experience with LC-MS/MS (preferably Agilent MassHunter), HPLC / UHPLC, and sample preparation</li>
<li>Strong analytical chemistry knowledge, lab skills (wet chemistry, instrumental).</li>
</ul>
Preferred:
<ul>
<li>Background in analytical or organic chemistry</li>
<li>Prior experience with impurity profiling or nitrosamines analysis in a regulated environment</li>
</ul>
#LI-DB1
 skills: HPLC, Analytical Chemistry, Chemistry, GLP (Good Laboratory Practice) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.

Analytical Chemist - R&D

<h3>Job Description</h3>
Job DescriptionRincon Consultants, Inc. is seeking as-needed Wildlife Biologists and Botanists (Mojave and Colorado Deserts) to join our team! We are looking for candidates with strong field expertise in botany and wildlife biology, specifically within the Mojave and Colorado Desert regions. The position will involve conducting habitat assessments, focused and general biological surveys, vegetation surveys and mapping, construction compliance monitoring, report writing, and providing biological construction support for a variety of projects. If you have a passion for fieldwork and a deep knowledge of California desert species and habitats, we encourage you to apply! &nbsp; Overview of Key Duties and Responsibilities:&nbsp;
<ul>
<li>Conduct site assessments, surveys, and habitat evaluations for common and special-status plant and wildlife species and map vegetation communities.</li>
<li>Perform biological monitoring and provide compliance support during construction activities, prepare compliance monitoring reports.</li>
<li>Identify plant species using a dichotomous key, focusing on Bay Area and northern Central Valley botany.</li>
<li>Map vegetation communities using standard mapping practices and identify sensitive vegetation communities.</li>
<li>Survey, monitor, and assess habitats for special-status species, including but not limited to the following:
<ul>
<li>Desert tortoise</li>
<li>Flat-tailed horned lizard</li>
<li>Burrowing owl</li>
<li>Golden eagle</li>
<li>Mohave ground squirrel</li>
<li>Desert kit fox</li>
<li>Bighorn sheep</li>
<li>Mountain lion</li>
<li>Special-status plants in the Mojave and Colorado Desert regions</li>
</ul>
</li>
<li>Prepare preconstruction survey reports and other technical documentation.</li>
<li>Track compliance with mitigation measures and permit conditions, maintaining accurate field reports and monitoring logs.</li>
<li>Collaborate with multidisciplinary teams and provide additional support to the Natural Resources Team as needed.</li>
<li>Wetland delineation experience is a plus.</li>
</ul>
 This Job Might Be for You If You Have the Following:&nbsp;
<ul>
<li>Bachelor’s or Master’s degree in biology, botany, ecology, environmental science, or a related field, with at least 1-2 years of professional biological fieldwork experience.</li>
<li>Prior approval through the U.S. Fish and Wildlife Service or California Department of Fish and Wildlife as Designated Biologist, Species Specific Monitor or General Biological Monitor for any of the above listed species is preferred.</li>
<li>Expertise in Mojave and Colorado Desert ecosystems, including experience with compliance monitoring, habitat assessments, vegetation monitoring, and species-specific surveys.</li>
<li>Familiarity with federal and state environmental laws, including but not limited to federal and state Endangered Species Acts, and the California Environmental Quality Act, as well as incidental take permits, Clean Water Act permits, Lake and Streambed Alteration Agreements, regulatory compliance oversight, and development/implementation of mitigation measures.</li>
<li>Demonstrated experience with the species listed above, including surveying and monitoring in occupied habitats and securing project approvals. </li>
<li>Excellent verbal and written communication skills, including strong technical writing experience preparing field reports, monitoring logs, and preconstruction survey documentation.</li>
<li>Ability to hike 6–8 miles per day in often difficult terrain and variable weather conditions while carrying 25 lbs. </li>
<li>Ability to work 10–12+ hour days, as needed.</li>
</ul>
 *More senior professionals (e.g., 5–10+ years) are also strongly encouraged to apply.&nbsp;Responsibilities and pay will adjust accordingly, with senior-level pay exceeding the posted range. Rincon Consultants, Inc. is an award-winning leader in providing quality environmental consulting services throughout California and is recognized as a ‘Best Environmental Services Firm to Work For’ by the Zweig Group. We partner with clients in sectors such as transportation, energy and infrastructure, sustainability, climate change, oil and gas, water, commercial, private development, and government. Our 400+ associates in 13 offices located in Northern, Central, and Southern California are dedicated professionals who combine their passion with our purpose. The base pay for this on-call position is $27.00–$35.00 per hour. At Rincon, our salary ranges are based on market median of similar jobs, according to third party salary benchmark surveys. The base pay that is actually offered will take into account internal equity and also may vary depending on the candidate’s job-related knowledge, skills, and experience. &nbsp;
Rincon Consultants, Inc does not accept unsolicited applicant/candidate resumes from search firm recruiters and/or temporary agencies that do not have a signed contract and specified work order with Rincon Consultants. Further, such resumes received will be deemed the sole property of Rincon Consultants and no fees will be paid in the event Rincon Consultants subsequently hires such individual. Rincon Consultants is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
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As-Needed Wildlife Biologists and Botanists (Mojave, Colorado Deserts)

<h3>Job Description</h3>
Job DescriptionSalary: $100,000 - $125,000 
About Sonoma Biotherapeutics: 
 
Sonoma Biotherapeutics is a South San Francisco and Seattle-based clinical-stage biotechnology company developing engineered regulatory T cell (Treg) therapies to treat serious autoimmune and inflammatory diseases by restoring balance to the immune system. Founded by pioneers in Treg biology and cell therapy, the company brings together leading expertise and proprietary methodologies for the discovery and development of disease modifying and curative therapies. Sonoma Bio has initiated two Phase 1 studies to evaluate the safety and proof-of-mechanism of the companys lead Tregcell therapy candidate, SBT-77-7101, in patients with rheumatoid arthritis and hidradenitis suppurativa. The company has a partnership with Regeneron to discover, develop and commercialize novel regulatory T cell therapies. More information at <a href="http://www.sonomabio.com" target="_blank">www.sonomabio.com</a>.
 
Summary
 
The Associate Scientist opportunity is a lab-based individual contributor role responsible for process development of autologous Treg Cell Therapies. This role reports to the Director of Process Development and will work in close collaboration with scientists across the organization to execute process development, IND-enabling studies, and support tech transfer to CMOs. Proficiency in this role requires a track record of demonstrated success as well as personal attributes including initiative, independent thinking, a solution-focused mindset, and collaborative skills. This position requires knowledge of aseptic cell culture technique, clinical-stage manufacturing, process characterization, IND- and BLA- enabling study design, and other activities as deemed necessary by program leadership.
 
Responsibilities:
<ul>
<li>Planning, analysis, and execution of studies designed to drive successful process development and process characterization of cell therapies</li>
<li>Assist in technical transfer from process development to clinical MFG</li>
<li>Culture human regulatory T-cells (Tregs) in various conditions</li>
<li>Assist with media preparation and kitting</li>
<li>Support bulk material generation of cellular products to support internal development organizations</li>
</ul>
In this role, you will:
<ul>
<li>Assist in manufacturing engineered Treg cell products and intermediates in support of process development, analytical development, and process characterization efforts</li>
<li>Execute experiments with appropriate documentation, data analysis, and drafting of technical reports</li>
<li>Assist in MSAT activities such as tech transfer to CMO</li>
<li>Prepare batches of media for cell culture and prepare cytokines for cell culture</li>
<li>Buffer, cell culture media, and cytokine preparation</li>
<li>Kitting for manufacturing</li>
<li>Assist in the development of cell isolation, purification, expansion and formulation protocols and technologies in support of product development from clinical to commercial scale</li>
<li>Participate in cross-functional collaborations to meet project timelines and material supply requirements</li>
<li>Assist in the development of standard operating procedures (SOPs), Batch Records and product specifications</li>
<li>Critically assess experimental data, provide interpretation of results, and ensure data quality and integrity</li>
<li>Authoring of technical documents critical to process development, process characterization, and tech transfer of cell therapy programs</li>
</ul>
Qualifications:
<ul>
<li>A minimum BS in Biology, Chemical Engineering, Bioengineering or relevant scientific discipline with 5-8 years of industry experience</li>
<li>Desire and drive to learn about cell therapy process and analytical development </li>
</ul>
Position Requirements:
<ul>
<li>Knowledge and experience in designing process development and process characterization studies of cell therapy or biologics manufacturing processes. Understanding of Design of Experiments (DOE) and Quality by Design (QBD)</li>
<li>Highly organized, detail-oriented individuals with strong problem-solving skills</li>
<li>Flexibility in working schedule to accommodate weekend work if necessary</li>
<li>Travel to support tech transfer activities</li>
<li>Must be able to communicate through excellent verbal and writing skills and multi-task within a fast-paced, highly collaborative team environment with a high degree of self-motivation and organization</li>
<li>Embodies the company culture of empowerment, diversity, and inclusion</li>
<li>Ideal candidates will possess experience in:
<ul>
<li>Flow cytometry</li>
<li>GMP manufacturing of cell therapy or biological products</li>
<li>Process Characterization of cell therapy clinical programs</li>
</ul>
</li>
</ul>
Physical Considerations:
 
This position requires the ability to occasionally lift and/or move up to 30 pounds and stand for multiple hours at one time. Specific vision abilities for this job include close vision, depth perception, and ability to adjust focus. Must be able and willing to gown in an aseptic environment on a regular basis. The common requirements of an office environment (computers, computer screens, workstations, etc.) apply when not working in or around the laboratory environment.

Equal Employment Opportunity
 
At Sonoma Biotherapeutics, we believe that the highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse, and inclusive culture for all employees.
Sonoma Biotherapeutics is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws.
Weve learned from experience that some of the best people dont always match our requirements perfectly - if youre interested and think you could fit, please dont hesitate to apply. Please submit your resume along with a cover letter to <a href="mailto:careers@sonomabio.com" target="_blank">careers@sonomabio.com</a> - resumes may also be submitted without applying for a specific job.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited or unable to access or use this online application process and need an alternative method for applying, please contact us at <a href="mailto:careers@sonomabio.com" target="_blank">careers@sonomabio.com</a>

Associate Scientist, Cell Therapy Process Development

<h3>Job Description</h3>
Job Description
Toeroek Associates is seeking qualified candidates for the Chemical Weapons Convention (CWC) National Security Analyst position to assist the Naval Treaty Implementation Program (NTIP) with the preparation of multi-phased instructional products, training plans, and exercises ranging from classroom tutorials to small team-size field training to full-scale multi-day exercises. This position is in Alexandria, VA.
 
In-office support is expected (mix between Alexandria, VA and the Navy Yard, Washington DC), must be willing to support 5 days a week as needed. Travel is 10% or less per year to prepare for and support exercises as needed. International travel may be required. 
Applicants must have an active DoD SECRET clearance, Chemical Weapons Convention (CWC) experience desired, and 3+ years Arms Control, DoD, and/or national security experience to be eligible for this role. 
This opportunity and description are subject to change pending the release of the final solicitation by the Navy. Start of work is tentatively late September / early October 2025.
Duties
<ul>
<li>Ability to prioritize work and complete multiple tasks under deadlines.</li>
<li>Must be able to effectively communicate in writing and verbally on both technical and non-technical subjects to senior leaders.</li>
<li>Assist in management of storage, monthly testing (according to the manufacturer's recommendations), and maintenance of Challenge Inspection support equipment (Government Furnished Property).</li>
<li>Support preparation of multi-phased instructional products, training plans and exercises ranging from classroom tutorials to small team-size field training, to full scale multi-day exercises.</li>
<li>Support the planning, facilitation, execution, and assessment of Challenge Inspections and Challenge Inspection training events and exercises. Exercise support includes but not limited to training event facilitation, assisting in exercise design and development, and After-Action Review support.</li>
<li>Provide analyses and reports in the form of standard correspondence (Executive Summaries, Information Papers, Memoranda, briefings, etc.), to assess the impacts of USG policy guidance, OSD and Joint Staff implementation guidance, and current DoD planning and provide assistance to the Treaty Manager and other USG staff.</li>
<li>Monitor and assess the status of arms control treaties and other nonproliferation agreements.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's degree (B.A. or B.S.) or equivalent.</li>
<li>ACTIVE DOD SECRET CLEARANCE REQUIRED.</li>
<li>3+ years in arms control, chemical, and/or DoD consultant support required.</li>
<li>Working knowledge of other arms control treaties and agreements desired.</li>
<li>Ability to comprehend complex issues, organize and prioritize work schedule.</li>
<li>Ability to communicate and work with people at all levels of the organization.</li>
<li>Must be able and willing to travel domestically and / or internationally to support various levels of exercises (less than 10% of time).</li>
<li>Career background in WMD, CBRN, and/or Arms Control with an understanding of CWC Challenge Inspection desired.</li>
</ul>
The target salary hiring range is $80,000 - $120,000 annually, DOQ. This is a good faith and reasonable estimate of the base compensation at the time of posting. Toeroek offers a competitive benefits package including medical, dental, vision, Life, LTD, STD, and 401K. Qualified applicants should include their resume, and completed application for further consideration. 
Toeroek Associates is a dynamic small business provider of specialty consulting and analysis services to the U.S. Government. Our National Security experts include technical and policy specialists in biological threat reduction, nuclear non-proliferation, arms control and treaty compliance, nuclear stockpile management, and CBRN support to the warfighter. We currently support DTRA, Air Force, Army, Navy, OSD, and EPA as both prime contractors and subcontractor team members.
Toeroek Associates, Inc. is an Equal Employment Opportunity employer.
Toeroek Associates, Inc. maintains the policy of equal employment opportunity (EEO) shall apply to all terms, conditions, and privileges of employment, including hiring, testing, training and development, promotion, transfer, compensation, benefits, educational assistance, termination, layoffs, social and recreational programs, and retirement. Toeroek is committed to making employment decisions based on valid requirements, without regard to age, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation, or any other applicable status protected by state or local law.
Applicants with disabilities may contact Toeroek Associates, Inc., Human Resources via telephone, fax, e-mail, and other means to request and arrange for accommodations. If you need assistance to accommodate a disability, you may request an accommodation at any time. Please contact Human Resources at <a href="mailto:hr@toeroek.com" target="_blank">hr@toeroek.com</a>.

Chemical Weapons Convention (CWC) National Security Analyst

<h3>Job Description</h3>
Job Description
Job Title: Research Scientist IV
Grade: 27
Salary: $101,809-$121,484
The Research Foundation for Mental Hygiene, Inc. (RFMH) is currently seeking a qualified candidate to serve as a full time Research Scientist IV. The position holder (Whitaker Scholar) will be developing clinical, teaching, and research skills in the Whitaker Scholar Program for Developmental Neuropsychiatry. In this capacity, the Scholar will provide consultation and direct service to improve the care of persons having both developmental disorders and/or emotional/behavioral problems. The Scholar will develop didactic sessions for child psychiatry Fellows. The Scholar will take a role in the development of clinical research studies on autism spectrum disorder and co-morbid psychiatric disorders and in systematic reviews on topics of interest to the Scholar.
Duties and Responsibilities:
<ul>
<li>The Scholar will attend a weekly program meeting, weekly supervision with mentors, and attend Child Psychiatry Research and Division meetings. </li>
<li>The Scholar will attend trainings on autism and other developmental disorders. </li>
<li>The Scholar will provide consultations to clinics/services on complex cases involving developmental disabilities. </li>
<li>The Scholar will develop didactic presentations and conduct systematic reviews on topics of interest to the Scholar.</li>
</ul>
Minimum Qualifications:
<ul>
<li>Bachelor's degree and five years of professional research experience in an appropriate field or master's degree in an appropriate field may substitute for one year of experience, or Ph.D. in an appropriate field may substitute for an additional year of experience.</li>
<li>Applicant must have completed both general and child/adolescent psychiatry residence training. </li>
<li>Applicant must have a minimum of one publication that demonstrates an interest in autism and developmental disorders. </li>
</ul>
 Preferred Qualifications:
<ul>
<li>Applicant must be fluent in at least one language besides English </li>
<li>Applicant must have worked and volunteered with persons with neurodevelopmental disabilities in the past.</li>
</ul>
Work Location: 1051 Riverside Drive, New York, NY 10032
To Apply: Submit an application through our website at <a href="https://nyspi.applicantpro.com/jobs/" target="_blank">https://nyspi.applicantpro.com/jobs/</a>. Please note only applications submitted through our website will be considered.
The Mission of the Research Foundation for Mental Hygiene, Inc. (RFMH) is to promote the mental health of all New Yorkers, with a focus on providing hope and supporting recovery for adults with serious mental illness and children with serious emotional disturbances. Applicants with lived mental health experience are encouraged to apply. RFMH is deeply committed to supporting underserved individuals, organizations, and communities. To this end, RFMH is focused on implementing activities and initiatives to reduce disparities in access, quality, and treatment outcomes for underserved populations. A critical component of these efforts is ensuring that RFMH is a diverse and inclusive workplace where all employees' unique attributes and skills are valued and utilized to support the mission of the Agency. RFMH is an equal opportunity/affirmative action employer.
The Research Foundation is a private not-for-profit corporation and is not an agency or instrumentality of the State of New York. Employees of the Research Foundation are not state employees, do not participate in any state retirement system, and do not receive state fringe benefits. Excellent Benefits Package. Employer/Minority/Women/Disabled/Veteran Employer. VEVRAA 41 CFR 60-300.5(a) compliant.
 Job Posted by ApplicantPro

Research Scientist IV

<h3>Job Description</h3>
Job Description
POSITION SUMMARY: 
Natera is seeking an innovative Staff Scientist, Product Development to join Natera's Oncology Product Development Team. We are looking for a meticulous and dedicated candidate with experience in next generation sequencing (NGS) assay development that can work effectively in a fast-paced environment to ensure that the highest quality clinical assays are developed and launched for our patients.
PRIMARY RESPONSIBILITIES:
<ul>
<li>Lead technical projects and associate timelines and deliverables as a subject matter expert and represent the assay development group in cross-functional project teams</li>
<li>Drive planning, design, execution, and reporting of feasibility, development, verification and validation studies for CLIA assays under the design control quality system</li>
<li>Collaborate closely with Research scientists, Automation engineers, Software engineers, Biostatisticians, Bioinformatics and Data Science team to develop, validate and launch new and innovative molecular assays</li>
<li>Communicate and document experimental data, scientific findings, and recommendations to R&amp;D and other functions including Lab Operations, Scientific Affairs, Product Management, Quality, and Regulatory groups</li>
<li>Provide regular updates at project team and departmental meetings on project progress, outcomes, and next steps to ensure alignment and transparency</li>
<li>Write SOPs, study protocols and reports, manufacturing and QC documents etc</li>
<li>Be flexible to handle multiple tasks and priorities, and perform other duties as assigned</li>
</ul>
QUALIFICATIONS:
<ul>
<li>MS. or PhD in genetics, molecular biology, biochemistry or a closely related field. PhD with a minimum of 8 years relevant experience, OR a MS degree and minimum 10 years of relevant experience</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>Must have hands-on experience with next-generation sequencing (NGS) and DNA/RNA molecular biology - experience with Illumina required, other technologies (e.g. PacBio, Oxford Nanopore, Ultima, Element, etc.) a plus</li>
<li>Must have experience with nucleic acid technologies relating to PCR, multiplex PCR, NGS, epigenetics/methylation analysis, target enrichment. Experience with liquid biopsy is a plus</li>
<li>Hands-on experience with high-throughput sample processing and automated liquid handling systems in a CLIA-regulated lab required</li>
<li>Experience working under Design Control, authoring study plans, protocols and reports is highly desired</li>
<li>Strong interpersonal and communication skills required</li>
<li>Knowledge of statistical methods and techniques to establish acceptance criteria for analytical studies is desired</li>
<li>Proficient in data analysis using tools such as Excel, JMP, R, Python required, combined with a strong drive for analyzing and interpreting data</li>
<li>Ability to manage multiple priorities in a fast-paced, dynamic environment</li>
<li>Exceptional communication and presentation skills with meticulous attention to detail</li>
<li>A proactive, solutions-oriented mindset and demonstrated success in collaborative and individual projects</li>
<li>Demonstrated ability to write clear project plans, study protocols and reports, and SOPs</li>
</ul>
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.San Carlos, CA $148,000—$185,050 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit <a href="http://www.natera.com" target="_blank">www.natera.com</a>.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents. 
Link: <a href="https://www.natera.com/notice-of-data-collection-california-residents/" target="_blank">https://www.natera.com/notice-of-data-collection-california-residents/</a>
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information: - BBB announcement on job scams - FBI Cyber Crime resource page

Staff Scientist, Product Development

<h3>Job Description</h3>
Job Description
Under general supervision, the Chemical Process Engineer provides characterization of process optimization strategies and/or troubleshooting of operational issues in operations, manufacturing, pilot plant, or capital projects environments. The engineer applies basic engineering principles to the design and implementation of system modifications, experiments, and capital projects. This role involves organizing, analyzing, and presenting interpretations of results for operational issues or engineering projects of minor scope and complexity.
FUNCTIONS:
<ul>
<li> Provide solutions to a variety of technical problems of moderate scope and complexity. </li>
<li> Under general supervision, evaluate, select, and apply standard engineering techniques and procedures. Assistance will be provided for unusual problems. </li>
<li> Perform assignments with clear and specific objectives, requiring investigation of a limited number of variables. </li>
<li> Initiate and complete routine technical tasks. </li>
<li> Serve as a technical expert for equipment or systems, focusing on troubleshooting operations. Actively engage in daily operations when required to meet schedules or resolve complex problems. </li>
<li> Routinely audit the operational performance and regulatory compliance of equipment or systems of significant complexity. </li>
<li> Collaborate with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance, and/or validation departments to develop system modification requirements and recommendations. </li>
<li> Work under the direct supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints. </li>
<li> Collaborate with consultants, architects, and engineering firms to develop standard design documents. </li>
<li> Obtain and evaluate quotes for equipment modifications or installations. </li>
<li> Generate project cost estimates and schedules. </li>
</ul>
Requirements
EDUCATION:
<ul>
<li> Master’s degree OR Bachelor’s degree in Engineering with at least 2 years of Engineering experience. </li>
<li> Chemical Engineering, Mechanical Engineering, or Electrical Engineering preferred. </li>
</ul>
PREFERRED QUALIFICATIONS:
<ul>
<li> Working knowledge of pharmaceutical/biotech processes. </li>
<li> Familiarity with validation processes and documentation in a highly regulated environment. </li>
<li> Ability to operate specialized laboratory equipment and computers. </li>
<li> Ability to interpret and apply GLPs and GMPs. </li>
<li> Ability to apply engineering science to production processes. </li>
<li> Strong problem-solving and applied engineering skills. </li>
<li> Basic technical report writing, verbal communication, and technical presentations. </li>
<li> Knowledge of validation protocol execution requirements. </li>
<li> Demonstrated skills in analytical problem solving, technical (equipment-specific) skills, and computer literacy.</li>
</ul>
Benefits
<ul>
<li>1st Shift</li>
<li>1 year contract with possible extension </li>
</ul>

Chemical Process Engineer

<h3>Job Description</h3>
Job Description
Only open to candidates with U.S. work authorization
We are on the hunt for a passionate and precise Embryologist to join a dynamic team in San Francisco! If you thrive in a fast-paced, high-tech lab environment and are excited to play a key role in helping individuals and families grow, this is your moment.
What Youll Do:
 Perform all aspects of IVF lab work: ICSI, embryo culture, cryopreservation, biopsies, assisted hatching, and more
 Collaborate with physicians and clinical staff to ensure outstanding patient care
 Maintain lab records, equipment, and QA processes with meticulous attention to detail
 Participate in research, meetings, and training initiatives
What Youll Bring:
 Bachelors in Biological Sciences (Masters preferred)
 2 - 3+ years of clinical embryology experience
 Expertise in ICSI, embryo culture, and cryo techniques
 Team player with excellent communication and problem-solving skills
 Willingness to work occasional weekends/holidays
Perks &amp; Benefits:
 Competitive salary + sign-on + relocation
 Medical, dental, vision, 401(k) match
 Generous PTO and holidays
 Tuition assistance &amp; professional development
 The opportunity to help build families every single day
Compensation:
$150,000 - $200,000 DOE + Sign-on Bonus + Relocation Assistance
To express interest or request more information, please submit your resume or CV to <a href="mailto:hr@ivfnomads.com" target="_blank">hr@ivfnomads.com</a>. Kindly include your availability for a brief introductory call.

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