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<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.

Research And Development Manager

<h3>Job Description</h3>
Job Description
Hygiena provides rapid microbiology diagnostic tests and solutions for mission-critical, time-sensitive processes around the world. Hygiena’s proprietary diagnostic technologies enable customers to; prevent illness and save lives, comply with regulations, protect products and brands, run businesses more effectively. Solutions are sold in a wide range of industries globally, but the core focus is food safety. Headquartered in Camarillo, California and with offices around the world, we are actively looking for talented individuals to help grow the business! 
At Hygiena we believe:
<ul>
<li>In providing the highest quality products &amp; service </li>
<li>Being a leader in innovation </li>
<li>Having a compelling desire to improve and win in the marketplace </li>
<li>In contributing positively not only in the workplace, but in our community and environment! </li>
</ul>
With rapid growth comes opportunity. We are looking for a Laboratory Associate I for our Reagent team to join our team in Camarillo!
The Laboratory Associate – Molecular Diagnostics Reagent position is responsible for reagent solution manufacturing, in-process testing, reagent sample collection for in-process testing, product issue investigation, assisting other departments upon request and collaborating with Research and Development (R&amp;D) and Production to ensure all products meet product specifications. This is a full-time, non-exempt/hourly, position.
Responsibilities:
<ul>
<li>Assist Engineering, Quality and Production during filling process as required. Prepare and deliver reagent solutions to filling rooms in the morning and throughout the day as needed.</li>
<li>Prepare and protect reagent Solutions as required to ensure product integrity and quality from start to finish of the manufacturing process including filling process. Continually checks chemical availability ahead of scheduled manufacturing including availability of other supplies and equipment. Prepare and coordinate the preparation and handling of special equipment required for special medias. Maintain all documentation in order, ensures written information is legible and recorded as part of the manufacturing process as required and required forms are completed as part of the SOP.</li>
<li>Maintain an organized and clean work environment in the working Laboratory and other work areas required for product manufacturing, including the sterilization and cleaning of all equipment. Perform pre-inspection of equipment to ensure equipment is properly clean and has been sterilized, correctly by careful review of sterilization print out. Maintain required equipment in good working order and verifies equipment is calibrated.</li>
<li>Ensure compliance with and/or follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seek guidance as necessary.</li>
<li>Actively support and participate in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Safety Manual and Injury Illness Prevention Program (IIPP).</li>
<li>Carry out all responsibilities in an honest, ethical and professional manner.</li>
<li>Must be able to fulfill essential job function in a consistent state of alertness and safe manner.</li>
<li>Handle various other duties as delegated by the Supervisor or Manager</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry or related field, or equivalent education and work experience in a laboratory or manufacturing environment, required.</li>
<li>Recent graduate and/or a minimum of 0-2 years of experience working in a laboratory or manufacturing environment required that includes the following: knowledge of cGMP; aseptic technique</li>
<li>Intermediate knowledge of Microsoft Office (Outlook, Word, Excel, Visio, PowerPoint) and Adobe Acrobat required.</li>
</ul>
Salary Range (applicable to California):
$26.00/ hr. 
Skills/Abilities:
<ul>
<li>Excellent verbal and written communication.</li>
<li>Must be able to use discretion and independent judgement.</li>
<li> Must be able to work in a team environment.</li>
<li>Must be able to pay close attention to details.</li>
<li>Must be able to adapt and adjust to a constant changing environment.</li>
</ul>

Why you’ll want to join our team:
Teamwork as a core value.
At Hygiena, our emphasis on teamwork and cross-functional communication enables us to build stronger bonds within our business.
Be a part of something big.
Hygiena plays a critical role in helping to prevent global health crisis such as foodborne illness, healthcare-associated infections, and other outbreaks.

Giving back to our communities.
Hygiena believes in giving back by supporting local organizations committed to improving the lives of children and youth in our communities.
Benefits and Perks:
<ul>
<li>15 days of PTO &amp; 9 paid company holidays</li>
<li>Medical with HSA employer contribution, Dental, Vision available 1st of the month after start date</li>
<li>Company paid Life Insurance, Short* and Long-Term Disability and an Employee Assistance Program</li>
<li>401(k) with Safe Harbor and Profit-Sharing employer contributions</li>
<li>Tuition Reimbursement program</li>
<li>Charitable Contribution matching</li>
<li>Employee Referral bonus opportunities</li>
</ul>
*State paid short-term disability for California based employees
We are an equal opportunity employer and value diversity. All employment is decided on the basis of qualifications, merit and business need. 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.
Hygiena participates in E-Verify.

Laboratory Associate I

<h3>Job Description</h3>
Job DescriptionSalary: $110,000 - $120,000/year 
Job Overview
BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, and recombinant cell lines for drug discovery. We are seeking an exceptional scientist, with a strong background in enzymology, enzyme kinetics, protein/protein interactions, and fluorescence and luminescence-based assays.
 
We are seeking a highly skilled Senior Scientist I with deep expertise in antibody generation to join our Molecular and Cellular Biology team. This position plays a critical role in driving research and development efforts, with a primary focus on the design, expression, engineering for multiple targets, purification, and optimization of antibodies, including phage display, single B cell isolation, humanization, and stable cell line generation. The ideal candidate will have strong industry experience and be adept at independently designing and executing experiments at a high standard.
 
Responsibilities:
<ul>
<li>Lead and execute projects related to antibody generation, including: 
<ul>
<li>Antibody design and engineering (e.g., humanization, affinity maturation, bispecific antibody)</li>
<li>Molecular cloning and vector design</li>
<li>Transient and stable expression in mammalian system</li>
<li>Antibody purification using affinity chromatography and other techniques</li>
</ul>
</li>
<li>Develop and optimize stable cell lines for antibody production</li>
<li>Utilize fermentation systems for antibody expression (small- to mid-scale)</li>
<li>Evaluate and integrate new technologies to enhance R&amp;D capabilities</li>
<li>Participate in team meetings, project planning, and cross-functional collaborations</li>
</ul>
<ul>
<li>Design and perform cell-based functional assays to characterize antibody activity</li>
<li>Present research findings internally and externally, including at scientific conferences</li>
<li>Maintain rigorous documentation and ensure high standards of data integrity</li>
<li>Maintaining excellent working relationships with partners throughout the company.</li>
<li>Maintaining updated and well-organized lab notebooks.</li>
<li>Other tasks and duties as assigned.</li>
</ul>
Requirements: 
<ul>
<li>A Ph.D. degree in Molecular Biology, Cell Biology required.</li>
<li>Minimum 3 - 5 years industry experience focused on antibody generation required</li>
<li>The candidate must have proven experience performing enzyme kinetics and assay optimization.</li>
<li>Proven track record in antibody discovery and development, including engineering and functional validation</li>
<li>Extensive experience with phage display, mammalian cell culture, sterile technique, and molecular biology methods</li>
<li>Proficiency in downstream processing including protein purification and analytical characterization</li>
<li>Strong problem-solving skills and ability to manage multiple projects in parallel</li>
<li>Excellent written and verbal communication skills</li>
<li>Team-oriented with a collaborative mindset and attention to detail</li>
</ul>
Benefits!
<ul>
<li>401k with 4% company match</li>
<li>Medical/Dental/Vision health insurance plans</li>
<li>Vacation and paid holidays</li>
<li>Companywide lunches provided quarterly</li>
</ul>
 
BPS Bioscience is an equal opportunity employer, without regard to race, color, religion, age, gender, sexual orientation, disability, or any other characteristic protected by applicable law.

Sr. Scientist I, Molecular and Cellular Biology

<h3>Job Description</h3>
Job Description
We are currently seeking a Research Associate III, Cell Line Development for a prominent Pharmaceutical client of ours. This position is in Oceanside, CA. Details for the position are as follows:
Job Description:
<ul>
<li>Pay: 53.00-56.00/hr.</li>
<li>Length of Assignment: 1 year to start with potential for extension.</li>
<li>Working hours: Mon-Fri, 8:30am-5pm or 8:00am-5pm type of business hours; occasional weekend hours (will have notice).</li>
<li>Seeking a highly motivated, team-oriented individual to design and execute experiments to support cell culture and clone development for our rapidly growing biologics pipeline.</li>
<li>Must have cell line development experience.</li>
<li>Participate in end-to-end Cell Line Development pipeline projects, including activities from vector design and construction to clonal cell lines ready for Master Cell Bank generation.</li>
<li>Support CLD activities including clone selection, technology development, media development, process optimization, and process characterization studies.</li>
<li>Support process improvements for increased speed and efficiency to generate highly productive, high quality, robust cell lines that meet all regulatory requirements with high quality documentation.</li>
<li>Hands-on laboratory operations such as molecular biology, shake flask, bench scale bioreactor and Client culture platforms.</li>
<li>Experience with mammalian cell culture (CHO) and automation/high-throughput technologies for mammalian cell line generation and process optimization preferred.</li>
</ul>
Company DescriptionThe Fountain Group is a nationwide staffing firm with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort. Browse our website below for additional information on our company. The Fountain Group “We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people.” 
<h3>Company Description</h3>
The Fountain Group is a nationwide staffing firm with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort.\r\n\r\nBrowse our website below for additional information on our company.\r\n\r\nThe Fountain Group\r\n\r\n“We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people.”

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