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<h3>Job Description</h3>
Job Description
Job Title:
Science Director – Biophysics
Location: Princeton NJ or Los Angeles CA&nbsp; - must be local to either of these offices or willing to relocate
Vaccination against COVID-19 is a prerequisite for employment at CHDI Management
Salary range: $120,000-220,000.&nbsp; Exact compensation will vary based on experience
Job Description:
CHDI Management seeks an experienced, innovative, and passionate drug discovery scientist to join the preclinical team as Science Director, Biophysics, to support the Foundation’s mission to accelerate meaningful therapies for Huntington’s disease (HD). Partnering with the internal Computational Drug Discovery and Structural Biology Science Director the successful candidate will be a biophysics domain knowledge expert and participate on interdisciplinary teams to advance the understanding of HD biology, to identify and characterize potential HD drug targets and to support the discovery of novel agents for pharmacologic proof-of-concept. The position involves collaborating with internal CHDI scientists, Contract Research Organization (CRO) collaborators, industrial partners and external academic experts.
The position reports to the Vice President, Chemistry
Job Responsibilities:
<ul>
<li>Manage external biophysics resources at CRO partners by providing strategic and technical oversight of biophysical assay deployment across the CHDI project portfolio.</li>
<li>Collaborate with partners including HD biology-focused thematic areas, structural biologists, medicinal chemists and informaticians. Participate as a biophysics domain knowledge expert to interdisciplinary project teams.</li>
<li>Co-develop project workplans as a member of interdisciplinary project teams with strategic line-of-sight to achieve program objectives.</li>
<li>Generate and deliver impactful biophysical data and insight to characterize biomolecular interactions and provide discovery teams with detailed interaction analyses (e.,&nbsp;protein-compound, nucleic acid-compound, protein-protein, and protein-nucleic acid) in cell-free and cellular systems.</li>
<li>Develop and deploy ligand-protein interaction experiments using biophysical methods (e.g. SPR, ITC, NMR, thermal shift, native MS) to measure binding of small molecule hits and leads to potential drug targets.</li>
<li>Design and conduct experiments to deconvolute biophysical mechanisms of active agents to understand residence time, predict efficacy and pharmacology, and select the best molecules for pharmacologic proof-of-concept.</li>
<li>Collaborate with the Research Informatics and Computational Drug Discovery team to prepare, organize, combine and integrate biophysics data and accelerate the development of tool compounds</li>
<li>Identify and partner with external collaborators (CRO, academic) to develop impactful, cutting-edge biophysical methods for their strategic application to projects in support of Foundation objectives.</li>
</ul>
Qualifications:
<ul>
<li>PhD. in Biophysics, Biophysical Chemistry, Chemistry and Chemical Biology or a related discipline.</li>
<li>6 plus years of industry experience in target validation and/or integrated drug discovery projects.</li>
<li>Demonstrated expertise in the use of biophysical methods (SPR, GCII, HTRF, MST, AS-MS, SwitchSense and thermal stability assays such as DSF) for characterization of biomolecular interactions (protein-compound, nucleic acid-compound, protein-protein, and/or protein-nucleic acid).</li>
<li>Experience in designing and building mechanistic assays to support elucidation of novel disease-relevant biology and target validation.</li>
<li>Experience in the application of emerging biophysical methods (e.g., single-molecule fluorescence microscopy, single-molecule force microscopy, magnetic force microscopy to interrogate macromolecular assemblies within their native environment highly preferred.</li>
<li>Experience working in a multidisciplinary team-oriented environment.</li>
<li>Excellent written and oral communication skills.</li>
<li>Experience in oversight of CRO collaborators.</li>
</ul>
About CHDI Foundation, Inc.
CHDI Foundation, Inc. is a privately-funded, not-for-profit, biomedical research organization that is exclusively dedicated to rapidly discovering, accelerating and developing therapies that slow the progression of Huntington’s disease (HD). Our scientists work closely with a network of more than 600 researchers in academic and industrial laboratories around the world in the pursuit of these innovative therapies, providing strategic scientific direction to ensure that our common goals remain in focus. This helps bridge the translational gap that often exists between academic and industrial research pursuits and that adds costly delays to therapy development. In its role as a collaborative enabler, CHDI seeks to bring the right partners together to identify and address critical scientific issues and move drug candidates to clinical evaluation as rapidly as possible. Our activities extend from exploratory biology to the identification and validation of therapeutic targets, and from drug discovery and development to clinical studies and trials. More information about CHDI can be found at&nbsp;<a href="http://www.chdifoundation.org" target="_blank">www.chdifoundation.org</a>
About CHDI Management, Inc.
CHDI Management, Inc. was established in 2002 to provide administrative, management and grant making services to CHDI Foundation, Inc.
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Director, Biophysics (Los Angeles CA or Princeton NJ)

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist – Personal Care &amp; Cosmetics Pay: $100-125k/year DOE + great benefits! Location: Gardena, CA Reports To: R&amp;D Manager -Job Summary: We are seeking a detail-oriented and innovative R&amp;D Chemist to join our R&amp;D team. The ideal candidate will be responsible for formulating and testing personal care and cosmetic products such as skincare, haircare, body care, and color cosmetics. This role plays a key part in developing high-performance, safe, and compliant formulations in line with marketing briefs and regulatory standards. -Qualifications: • Bachelor’s degree in Chemistry, Cosmetic Science, Chemical Engineering, or related field (Master’s preferred). • 5+ years of hands-on lab experience in cosmetic or personal care product formulation. • Strong understanding of regulatory guidelines. • Excellent organizational, documentation, and communication skills. • Ability to work independently and collaboratively in a fast-paced environment. Please send resume to Veronica Vasquez. Thank you! AppleOne Ventura Equal Opportunity Employer / Disabled / Protected Veterans The Know Your Rights poster is available here: <a href="https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf" target="_blank">https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRi…</a> The pay transparency policy is available here: <a href="https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf" target="_blank">https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_…</a> For temporary assignments lasting 13 weeks or longer, the Company is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required. We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team. AppleOne participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program. <a href="https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf" target="_blank">https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Partici…</a> We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications 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. #1111 Company DescriptionThis company offers growth and a great group of people to work with. 
<h3>Company Description</h3>
This company offers growth and a great group of people to work with.

Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Conceive and implement novel experimental approaches to answer scientific questions. Investigate, identify, develop, and optimize new methods and techniques. Contribute to project science in area of expertise. Develop productive collaborations and communications with other groups across science disciplines.
Responsibilities:&nbsp;
<ul>
<li>Design and provide scientific oversight of preclinical PK/TK studies</li>
<li>Conduct data analyses including PK/PKPD analyses, modeling and simulation, literature data analyses</li>
<li>Liaise with research, toxicology, immunology, bioanalytical, clinical development, and regulatory colleagues to generate data and knowledge supporting product development and implementation of translational models</li>
<li>At project level, establish and maintain effective collaborations with key stakeholders to facilitate data integration for biomarker selection, candidate nomination/selection, and human dose prediction</li>
<li>Participate and present at various departmental and cross functional teams</li>
<li>Author regulatory documents including protocols, study reports, exposure-response analyses reports, relevant section of investigator brochures, common technical documents, white papers, and other similar documents</li>
<li>Maintain awareness of emerging literature and science in PK and translational sciences specific to eyecare, aesthetics, and neurotoxin.</li>
<li>Author scientific publications and present at scientific conferences&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree or equivalent education and typically 10+ years of experience, Master’s Degree or equivalent education and typically 8+ years of experience, or PhD (preferably in chemical or biomedical engineering; applied mathematics; quantitative pharmaceutical sciences or a related field or Pharm.D.)&nbsp;with 0-4 years experience.</li>
<li>Possess thorough theoretical and practical understanding of own scientific discipline.</li>
<li>Understanding of small or large molecule drug modalities and relevant analytical methods for measuring drug and biomarker levels in preclinical and clinical study samples</li>
<li>Strong communication skills and the ability to effectively communicate with both internal and external stakeholders, and to audiences of diverse backgrounds</li>
<li>Highly motivated, self-driven and results-oriented person, capable of both leading and being lead</li>
<li>High degree of flexibility in adapting to different projects and personalities as well as excellent networking and relationship-building skills (both internal and external)</li>
<li>Passion for data analysis, solving technical problems and applying new technologies to further scientific goals and answer key scientific questions enabling data informed decision-making</li>
</ul>
Preferred: ​​​​​
<ul>
<li>Hands-on experience with relevant modeling software and programming languages including MATLAB/Simbiology, R, Python, WinNonLin/Phoenix, NONMEM, etc. is desired</li>
<li>Publication record demonstrating PK/PD or systems modeling examples is highly desired</li>
<li>Additional prior experience in an experimental in vitro or in vivo biology field is desired</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, Translational PK

<h3>Job Description</h3>
Job Description
We have an immediate opportunity for a Wildlife Biologist in the Southern and Northern California area. The ideal candidate will be responsible for managing individual project tasks and providing direction to the support staff.
Duties and Responsibilities
<ul>
<li>Ability to multitask with strong organization skills supporting the team and project management</li>
<li>Experience preparing and reviewing application and regulatory documents</li>
<li>Ability to prepare project scopes and proposals</li>
<li>Knowledge preparing and managing project schedules</li>
<li>Attend project and agency meetings</li>
<li>Manage field surveys as needed</li>
<li>Mentor entry-level and junior field staff</li>
</ul>
Background and Education
<ul>
<li>Bachelor’s Degree in natural science, field, Master’s or PhD a plus</li>
<li>3 years’ related work experience including project and task management</li>
<li>Previous experience working with regulatory processes. Must understand the federal Clean Water Act Section 404 and 401; Porter Cologne Water Quality Act; CDFW Fish and Game Code 1602; California ESA 2081; and ESA Section 7 and 10 processes.</li>
<li>Experience with wetland delineations and/or other local flora and fauna field surveys</li>
<li>Knowledge of California biological habitats, species and general conservation biology/ecology</li>
<li>USFWS/CDFW permits and Memoranda of Understanding a plus</li>
<li>Excellent communication and writing skills.</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Biologist, Master’s, PhD, CDFW, USFWS, Species, Flora, Fauna, habitat, 404)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Wildlife Biologist

<h3>Job Description</h3>
Job Description
We have several opportunities for on-call Field Archaeologists to monitor for a project located in the Ontario area.
· Willing to work 6:30 am to approximately 3:30 pm (1 to 4 days per week for the next 3 weeks or longer).
· Willing to work on Saturdays if needed.
· Have a BA or higher degree in Archaeology/Anthropology.
· Have around 2 years’ experience in CRM, monitoring experience desired.
(Archaeologist, anthropologist, archaeology, anthropology, CRM, cultural resources management)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

On Call Field Archaeologist

<h3>Job Description</h3>
Job Description
We have an immediate opportunity for a full-time architectural historian in the Northern California area. This position will require fieldwork.
Job Responsibilities
<ul>
<li>Conducting archival research</li>
<li>Prepare historic context, applying National Register criteria.</li>
<li>Prepare architectural history components of NHPA and CEQA technical reports</li>
<li>Document Architectural resources on California DPR 523 records and History American Building Survey (HABS) / Historic American Engineering Record (HAER) / Historic American Landscape Survey (HALS), and other duties as assigned</li>
<li>Excellent written and oral communication</li>
<li>Knowledge of GIS and basic understanding of cultural resources mapping and date collection</li>
<li>Previous field experience</li>
<li>Travel within Northern California as required</li>
</ul>
Education and Experience
<ul>
<li>Master of Arts (evidence of completion or nearly completed) in Historic Preservation, Public History, Architecture, Architectural History or closely related</li>
<li>1-2 years of experience</li>
<li>Proficiency with Microsoft Suite</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Architectural, Historian, GIS, Historic Preservation, Cultural Resources, CEQA, NHPA)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Architectural Historian

<h3>Job Description</h3>
Job Description
At Areté, we are on the forefront of developing innovative solutions, with great minds from all backgrounds, to help solve the nation’s most complex security challenges. We strive for an inclusive, collaborative team environment that approaches differences as opportunities for innovation and excellence. As an employee-owned company, we foster an atmosphere that propels diverse career opportunities and professional growth. 
Discover your future with us. 
We are seeking junior-, mid-, and senior-level Scientist with a strong background in Signal and Image Processing, Physical Science, Applied Math, and/or Scientific Computing. The successful candidate will join a staff of signal/image processing scientists and software engineers that support the development of signal and image processing algorithms and software. In this position you will develop and prototype new algorithms or enhancements to existing algorithms and work with software engineers to implement the algorithms into robust and highly performant software. The position requires knowledge of classical signal processing techniques. 
The successful candidate may ultimately be utilized in one or more of the following areas: ocean remote sensing, signal/image processing, state estimation, detection and tracking, computer vision, machine learning, physics-based modeling, data analysis, and sensor characterization. This role requires a passion for solving challenging technical problems in a collaborative environment. This is a full-time, exempt, non-supervisory position is based in our Northridge, CA office.
We have an impressive range of benefits, programs, and perks that we offer:
Health &amp; Wellness:
<ul>
<li>Medical, Dental &amp; Vision Insurance</li>
<li>Life and Long-Term Disability (LTD)</li>
<li>Vision Reimbursement</li>
<li>Fitness Reimbursement</li>
</ul>
Financial:
<ul>
<li>401(k) Retirement Plan Contributions</li>
<li>Employee Stock Ownership Plan (ESOP)</li>
<li>Continuing Education Assistance</li>
</ul>
Work-Life Balance:
<ul>
<li>Flexible Scheduling</li>
<li>Paid Time Off (PTO)</li>
<li>Paid Parental and Bereavement Leave</li>
</ul>
What We Value:
<ul>
<li>Creativity and innovation in solving challenges</li>
<li>Integrity and responsibility in all actions</li>
<li>Collaboration across teams and specialties</li>
<li>Responsiveness in fast-paced environments</li>
<li>Passion for national security and excellence</li>
</ul>
Experiences and Background We Look For (required skills)
<ul>
<li>Qualified candidates will have a BS, MS, or PhD in a STEM discipline</li>
<li>Demonstrated classical signal/image processing experience </li>
<li>Experience programming in Python, C, C++, MATLAB or similar languages</li>
<li>Intellectual curiosity and a desire for continuous learning</li>
<li>Ability to work with minimal supervision and collaborate with small teams</li>
<li>Excellent written and verbal communication skills</li>
<li>Willingness to work onsite in the office 100%</li>
<li>Must be able to obtain and maintain a TS/SCI security clearance and meet customer-specific security screening requirements </li>
</ul>
Nice to Have (preferred skills)
<ul>
<li>Experience working in a Linux environment</li>
<li>Physics-based modeling and simulation experience</li>
<li>Remote sensing experience utilizing Electro-Optics or Synthetic Aperture RADAR </li>
<li>Computer vision, image and data fusion, image classification or automated target recognition</li>
<li>Parallel programming experience (threads, MPI, CUDA, etc.) </li>
<li>Active Top Secret Clearance</li>
</ul>
The salary range for this role depends on the candidate’s level of experience:
<ul>
<li>Scientist 1: $90,000 - $120,000 [required BS degree or higher]</li>
<li>Scientist 2: $105,000 - $135,000 [minimum experience of BS+2 years, OR MS+0 years]</li>
<li>Staff Scientist: $120,000 - $150,000 [minimum experience of BS+5 years, MS+3 years, or PhD+0 years]</li>
</ul>
However, Arete considers several factors when extending an offer of employment, including but not limited to the position and associated responsibilities, a candidate’s work experience, education/training, and key skills.
Other Considerations
Areté is committed to the principles of equal employment opportunity and nondiscrimination, and we believe every person has the right to be treated with fairness, dignity, and equal consideration. 
Areté is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, marital status, national origin, age, veteran status, disability, or any other characteristic protected by applicable federal, state, or local law.
U.S. citizenship is required to meet position eligibility. Successful passage of a criminal background screen is required to meet position eligibility. 
Selected applicants will be subject to a government security investigation and must meet eligibility requirements for access to classified information.
Areté will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the Los Angeles Fair Chance Initiative for Hiring.
Successful passage of a Department of Transportation (DOT) drug test is required to meet position eligibility.
If you are a qualified individual with a disability or a disabled veteran, you have the right to request an accommodation if you are unable or limited in your ability to use or access our website because of your disability. To request an accommodation, please contact Areté Human Resources at 818-885-2200 for assistance.

Signal and Image Processing Scientist

<h3>Job Description</h3>
Job DescriptionSalary: $138,000.00 - $148,000.00 
Summary We are seeking a highly motivated and experienced scientist to join our Bioanalytical team in Pre-clinical Department. This Senior Scientist II position will play a role in the bioanalytical LC-MS/MS method development, validation and sample analysis for the quantification or qualification drugs and metabolites in biological matrices under GLP and non-GLP guidelines to support nonclinical and clinical studies. This position is also responsible for communication/presentation of bioanalytical results with relevant team members. 
 
Responsibilities
<ul>
<li>Develop and validate LC-MS/MS methods for the quantitation of drugs/metabolites in biological matrices under GLP and non-GLP guidelines to support nonclinical and clinical studies at different developmental stages.</li>
<li>Serve as study director/principal investigator with responsibility for study binder review.</li>
<li>Lead and/or supervise bioanalytical activities.</li>
<li>Maintain, operate, and troubleshoot API5500 LC-MS/MS instruments and other analytical equipment.</li>
<li>Study and recommend new techniques in sample purification, analysis, and automation.</li>
<li>Write and revise departmental SOPs, validation and analytical protocols and reports.</li>
<li>Ensure adherence to protocols, SOPs and GLP guidelines.</li>
<li>Ensure data integrity and compliance with applicable regulatory guidelines.</li>
<li>Analyze technical data to draw conclusions.</li>
<li>Assist in the preparation of any regulatory submissions.</li>
<li>May provide training to new and less experienced departmental staff.</li>
<li>Maintain research records and lab notebooks in a concise, legible and complete manner.</li>
</ul>
 
Preferred Requirements
<ul>
<li>B.S. or M.S. in Analytical Chemistry or other related disciplines.</li>
<li>At least 10 years of CRO or relevant industrial hands-on experience in bioanalytical method development/validation and sample analysis using LC-MS/MS techniques in a regulated bioanalytical environment.</li>
<li>In-depth knowledge of LC-MS/MS techniques and sample preparation are a must.</li>
<li>Prior experience serving as a study director/principal investigator. This experience includes development of study protocols, SOPs, validation and analytical reports; preparation and/or review of study binders ensuring compliance.</li>
<li>Proficiency with software such as Sciex Analyst, Microsoft Word, Excel, and PowerPoint as well as online quality management and document handling systems.</li>
<li>Experience with liquid handling programming.</li>
<li>Strong communication skills, as well as the ability to be a team player. </li>
</ul>
 
Arthrosi Therapeutics is an equal opportunity employer. All applicants will be considered foremployment without attention to the following: race, color, sex, sexual orientation, gender,gender identity, religion, national origin, citizenship and/or immigration status, pregnancy,genetic information including family medical history, physical or mental disability, child orspousal support withholding, military or veteran status, medical condition, marital status, AIDS/HIV, natural hair styles, political activities or affiliations, domestic violence, assault, orstalking victim status, application for or enrollment in Medi-Cal, lawful conduct occurringduring nonworking hours away from the employers premises, credit report or creditinformation, prior non-conviction arrest record, and any other protected class, in accordancewith applicable federal, state, and local laws.

Senior Scientist II, Bioanalytical

<h3>Job Description</h3>
Dynamic start-up medical device firm seeks individual to join its r&amp;d organization. Responsibilities will be broad based, sharing responsibilities with the VP of R&amp;D. This may include overseeing early feasibility study submission and submissions for the European Union. 
This is a hands-on technical management role. The technology consists of implants and catheter delivery systems to treat mitral valve regurgitation. This firm has about 20 employees and is currently conducting clinical trials OUS.

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