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<h3>Job Description</h3>
Job Descriptionjob summary: 
This Research Associate contract role offers an exciting opportunity for a scientifically passionate individual to develop critical assays for GMP release, product characterization, and process evaluation of cutting-edge gene therapy products. The ideal candidate will possess a Bachelor of Science degree and at least one year of experience in the pharmaceutical or biotech industry, proficiently performing biologic assays such as PCR, ELISA, and mammalian cell-based assays. You will be instrumental in developing technical documentation, maintaining meticulous records, and collaborating within a dynamic team to advance scientific innovations.
 location: South San Francisco, California job type: Contract salary: $30 - 39 per hour work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Develop assays for GMP release of gene therapy products</li>
<li>Develop assays for product characterization of gene therapy products</li>
<li>Develop assays for AAV/protein/DNA and other materials to assist in evaluation of process change, formulation and stability study</li>
<li>Report project status (development plans, timelines, and results) to supervisor and technical teams.</li>
<li>Write SOP, tech transfer and development reports.</li>
<li>Keep current with all regulatory guidelines, compendia requirements, and technical innovations.</li>
<li>Maintain accurate, error-free records of all analytical development activities timely </li>
</ul>
 qualifications: 
Required
<ul>
<li>Bachelor of Science with 3+ years, or Masters of Science with 1+ years' experience in biopharma industry with proven expertise of a range of physicochemical methodologies for quantifying purity/quality of proteins, viruses, and viral vectors</li>
<li>Extensive experience and knowledge in operating HPLC applied to DNA/RNA, proteins, polymers, detergent and/or viral vectors.</li>
<li>Positive, professional self-starter with a passion for science, innovative technical and analytical skills required to perform at the highest level</li>
<li>Highly motivated and independent yet has successfully worked in a group setting with efficient, flexible and self-motivated work ethic; to be utilized in work planning, executing, and data analyzing.</li>
<li>Excellent clear and concise writing skills for technical reports and documents along with strong verbal communication skills</li>
<li>Proven ability to work in cross-functional teams as a strong team player as well as independently.</li>
<li>Successful history and the ability to handle several fast-paced projects concurrently.</li>
<li>Excellent communication, writing and presentation skills to technical and non-technical audiences.</li>
<li>5+ years of HPLC usage and troubleshooting</li>
</ul>
Preferred
<ul>
<li>Prior experience with AAV or other virus </li>
<li>Experience in analytical method development and separation technologies including multiple modes such as capillary electrophoresis, AUC and mass spectrometric </li>
<li>Proficient working in Microsoft Office Suite </li>
</ul>
#LI-KH1
 skills: MS-EXCEL, Assay Development, Assay Verification, High Pressure Liquid Chromatography (HPLC) 
 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: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Research Associate

<h3>Job Description</h3>
Job Description
Key Responsibilities:
<ul>
<li>Conduct routine and non-routine chemical analysis using HPLC, GC, UV-Vis, FTIR, and other analytical techniques.</li>
<li>Perform method development, validation, and transfer following USP, ICH, and FDA guidelines.</li>
<li>Analyze raw materials, intermediates, and finished products to ensure compliance with specifications.</li>
<li>Prepare and maintain detailed documentation, including test results, validation reports, and lab notebooks, in accordance with cGMP and GLP requirements.</li>
<li>Troubleshoot and maintain analytical instruments, ensuring proper calibration and functionality.</li>
<li>Assist in investigations of out-of-specification (OOS) results, deviations, and corrective actions.</li>
<li>Work collaboratively with Quality Assurance, R&amp;D, and Production teams to support manufacturing and product development.</li>
<li>Stay updated with regulatory changes and industry best practices in pharmaceutical and cosmetic analytical testing.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.</li>
<li>2+ years of experience in a pharmaceutical, nutraceutical, or personal care laboratory performing HPLC and analytical testing.</li>
<li>Strong knowledge of cGMP, USP, ICH, and FDA regulatory requirements.</li>
<li>Experience with analytical instrument troubleshooting and maintenance.</li>
<li>Excellent documentation, data interpretation, and problem-solving skills.</li>
<li>Ability to work independently and in a team-oriented environment.</li>
<li>Strong attention to detail and organizational skills.</li>
</ul>
Company DescriptionOur Professional Division works with clients as a stakeholder in their hiring strategy and process. We facilitate a solid match for our employees and clients, examining the experience and team dynamics required for a great match. Our professional team was handpicked from 25 years of recruiting and staffing experience to build our Professional team to be the best in the industry. We focus on professional placements in your Executive Placement, Accounting &amp; Finance, Human Resources, and Administrative Support areas. We place candidates leveraging direct hire, contract-to-hire, contingent, and “Smart Hire” modalities. 
<h3>Company Description</h3>
Our Professional Division works with clients as a stakeholder in their hiring strategy and process. We facilitate a solid match for our employees and clients, examining the experience and team dynamics required for a great match. Our professional team was handpicked from 25 years of recruiting and staffing experience to build our Professional team to be the best in the industry. We focus on professional placements in your Executive Placement, Accounting &amp; Finance, Human Resources, and Administrative Support areas. We place candidates leveraging direct hire, contract-to-hire, contingent, and “Smart Hire” modalities.

Chemist

<h3>Job Description</h3>
RMA Northern California, part of the RMA Network of top fertility practices in the United States, is currently seeking a Senior Embryologist to join our growing San Francisco practice. Hours will be rotating Monday-Wednesday and Saturday - Wednesday 6am-3:30pm.
 
This position will be responsible for executing all laboratory procedures according to established policies as well as adhering to RMA’s quality assurance/control operating procedures. The ideal candidate will hone previous embryology experience and perform all aspects of clinical embryology independently and in accordance with RMA’s Laboratory Philosophy, Mission, and Performance Standards. 
 
Responsibilities:
<ul>
<li>Follow established policies for IVF procedures, specimen handling, and tissue storage</li>
<li>Maintain quality assurance, quality control, and operating guidelines for lab services</li>
<li>Adhere to quality control policies and documentation requirements</li>
<li>Follow OSHA requirements for safe lab operation</li>
<li>Obtain proficiency to perform all lab services efficiently and reliably on an independent basis</li>
<li>Participate in clinical and research lab operations as directed</li>
<li>Identify problems that may adversely affect patients and facilitate a solution</li>
<li>Participate in lab proficiency testing</li>
<li>Assist Laboratory Director in designing and implementing research protocols </li>
<li>Attend laboratory meetings as requested</li>
<li>Attend continuing education programs as requested</li>
</ul>
 
Requirements: 
<ul>
<li>Bachelor's of Science </li>
<li>4+ years embryology experience</li>
<li>Demonstrate an aptitude for performance of laboratory services</li>
<li>Aptitude to make appropriate judgments regarding clinical significance of laboratory data</li>
<li>Excellent work ethic and motivation to learn lab procedures</li>
<li>High level of listening and counseling skills </li>
<li>Aptitude to work independently and demonstrate good judgment</li>
<li>Ability to access, input, and retrieve information from a computer.</li>
<li>Knowledge of office procedure and office machines (i.e., computer, fax, copier, etc.)</li>
<li>Must be able to work weekends and some holidays.</li>
</ul>
 
IVI-RMA offers a comprehensive benefits package to all employees who work a minimum of 30 hours per week.
<ul>
<li>Medical, Dental, Vision Insurance Options</li>
<li>Retirement 401K Plan</li>
<li>Paid Time Off &amp; Paid Holidays</li>
<li>Company Paid: Life Insurance &amp; Long-Term Disability &amp; AD&amp;D</li>
<li>Flexible Spending Accounts</li>
<li>Employee Assistance Program</li>
<li>Tuition Reimbursement</li>
</ul>
 
About IVIRMA Global: 
IVIRMA is the largest group in the world devoted exclusively to human Assisted Reproduction Technology. Along with the great privilege of providing fertility care to our patients, IVIRMA embraces the great responsibility of advancing the field of human reproduction. IVIRMA Innovation, as one of the pillars of IVIRMA Global, is a renowned leader in fertility research and science. Check out our websites at: <a href="https://rmanetwork.com/" target="_blank">https://rmanetwork.com/</a> &amp; <a href="https://www.ivirma.com/" target="_blank">https://www.ivirma.com/</a> 
 
EEO
 “IVIRMA is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: IVIRMA is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at IVIRMA are based on business needs, job requirements and individual qualifications, without regard to race, color, religion and/or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. IVIRMA will not tolerate discrimination or harassment based on any of these characteristics. IVIRMA encourages applicants of all ages.”

Senior Embryologist

<h3>Job Description</h3>
Microbiology Section Lab Supervisor Full Time Days Modesto-CA Full-Time (FTE)_Direct Hire
Position: Microbiology Section Lab Supervisor Full Time Days
Job Type: Full-Time (FTE)
Location: Modesto-CA 
Base Salary: $111,758 to $178,700 +Best-in-class benefits
 Job Description:
Position Summary:
 
 *Reporting to the Laboratory Director, the Section Supervisor is a Clinical Laboratory Scientist, (CLS), responsible for supervising one section of the Lab, correctly performing technical procedures and Quality Control, operating and maintaining instrumentation and taking steps necessary to assure quality results and performing other duties as needed. 
 *Every employee of the laboratory at Doctors Medical Center is expected to promote the mission and philosophy of the hospital by acting in a caring, courteous and confidential manner towards patients, visitors, colleagues, and staff by performing their duties and responsibilities according to the expected standards. 
 *Every member of the Laboratory Staff is expected to perform their duties and to accept the responsibility of the accuracy of their work as dictated in their Professional Standards as Clinical Laboratory Scientist or Health Care Workers. 
 *Staff members will maintain confidentiality of all reports, maintain the integrity of identification of patient samples and will perform designated tasks which will enable the laboratory to comply with all regulatory standards of Clinical and Anatomic Laboratories.
Qualifications for Candidates: 
 *Minimum Education: Bachelors Degree - Medical Technology/Biological Science, Medical Technologist Internship
 *Minimum Experience/Skills: One to three years experience preferred.
 *License/Certificates/Credentials: 
 California Clinical Laboratory Scientist license
 ASCP Registry recommended
Physical Demands:
 * Moderate walking, standing.
 * Lift/position up to 30 lbs. 
 * Push/pull up to 50 lbs of force. 
 * Reaching, stooping, bending, kneeling, crouching. 
 * Manual dexterity and mobility. 
 * Touch, auditory and visual perception and acuity. 
 * Adequate vocal pitch and volume.
Skills and Certifications: 
 *California Clinical Laboratory Scientist license
 *ASCP Registry recommended
Candidate Details:
 *2+ to 5 years experience
 *Seniority Level - Mid-Senior
 *Minimum Education - Bachelor's Degree
 *Willingness to Travel - Occasionally

Microbiology Section Lab Supervisor

<h3>Job Description</h3>
We are looking for a meticulous and dedicated scientist with hands-on laboratory experience in assay development who can work effectively in a fast-paced environment to ensure that the highest-quality clinical assays are developed and launched for our patients. The right candidate maintains a broad knowledge of state-of-the-art principles and theories and can work well in an exciting, stimulating, and creative environment. Primary Responsibilities 
<ul>
<li>Design experimental plans and execute complex end-to-end laboratory experiments including nucleic acid extraction from FFPE tissue, NGS library preparation, hybrid capture and sequencing. </li>
<li>Collaborate with assay development team to design, develop, and validate assays for commercial launch. </li>
<li>Communicate and discuss results with a multidisciplinary group of bioinformaticians, statisticians, automation engineers, and reagents/quality control scientists. </li>
<li>Write protocols, document results, make data driven decisions, and present findings at scientific meetings. </li>
<li>Creatively contribute to development activities and advance the assay through design control processes to meet product requirements and project milestones. </li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in molecular biology, biochemistry, or closely related field with 4-6 years experience in assay development for the life science industry </li>
<li>Master’s in molecular biology, biochemistry or closely related field, with 2+ years of industry experience. </li>
</ul>
Knowledge, Skills, And Abilities 
<ul>
<li>Must have hands-on experience with molecular biology techniques, including nucleic acid extraction and quantitation, PCR/qPCR, library fabrication, sample quality control, hybrid capture, and sequencing. </li>
<li>Proficiency working with FFPE tissue and RNA specifically is highly desired. </li>
<li>Must be able to handle manual work/pipetting involving high throughput sample testing. </li>
<li>Experience in optimizing laboratory methodologies and addressing complex problems that are unique when working with FFPE tissue. </li>
<li>Demonstrated success in applying independent scientific judgment in experimental design and analysis. </li>
<li>Experience in writing clear experimental designs, reports, and operating protocols. </li>
<li>Must have excellent communication, organizational, record-keeping, planning, attention to detail, and time management skills. </li>
<li>Experience developing or executing assays using automated liquid handlers is preferred. </li>
<li>Experience in data analysis using Excel and/or other data analysis tools; proficiency in programming languages such as python is a plus. </li>
</ul>
Physical Demands &amp; Work Environment 
<ul>
<li>Duties are typically performed in an office and laboratory setting. </li>
<li>This position requires the ability to perform repetitive motions during pipetting and samples processing. </li>
<li>This position requires the ability to use a computer keyboard, communicate over Zoom/telephone and read printed material. </li>
<li>Laboratory activities require periods of standing while working and occasionally lifting heavy objects. </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 $96,400—$120,500 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 
<ul>
<li> BBB announcement on job scams</li>
<li> FBI Cyber Crime resource page</li>
</ul>

Assoc Scientist R&D, RNA Assay Development

<h3>Job Description</h3>
Job Description
Team 360 Staffing, on behalf of DK Law, is looking for a Senior Settlement Negotiator to join their legal firm.
At DK Law, they don’t just represent their clients. They stand with them-all the way.
They are modern injury and accident attorneys who go all the way for every client, from every background. At the heart of their work is a simple but powerful belief: every client’s experience matters, and they honor it as if it were their own. From the very first call to the final resolution, they approach every case with the mindset that it’s going the distance.
That same mindset fuels their workplace culture. They’re a team of purpose-driven professionals who care deeply, move fast, and never lose sight of the human side of what they do. If you're passionate about making an impact, growing with a team that values excellence and empathy, and being part of something bigger, they’d love to meet you.
 They are searching for a Senior Negotiator &amp; Demand Writer to lead a team and tackle big cases in pre-litigation.
Responsibilities
<ul>
<li>Conduct settlement negotiations with insurance companies and defense firms to resolve personal injury claims, focusing on maximizing recoveries for our clients.</li>
<li>Review and analyze demands to identify key issues, damages, and liability, ensuring a thorough understanding of each case.</li>
<li>Develop negotiation strategies and tactics to achieve optimal settlements, considering factors such as policy limits, coverage issues, and defense firm positions.</li>
<li>Effectively communicate with insurance company adjusters, defense counsel, and other stakeholders to negotiate settlements, resolve issues, and address concerns.</li>
<li>Maintain accurate and detailed records of all negotiations, including correspondence, phone calls, and meetings.</li>
<li>Monitor and update case status, ensuring timely and efficient resolution of claims.</li>
<li>Work closely with attorneys, paralegals, and other support staff to ensure seamless coordination and effective communication throughout the negotiation process.</li>
</ul>
Skills:
<ul>
<li>5+ years of experience in Personal Injury Law, preferably in a demand writing, demand negotiation or case management role</li>
<li>Bilingual (English &amp; Spanish)</li>
<li>Experience negotiating high value cases</li>
<li>Excellent written and verbal communication skills</li>
<li>Proficiency using Microsoft Office</li>
</ul>
Benefits offered by DK Law:
<ul>
<li>Opportunities for growth and advancement</li>
<li>Competitive pay, based on experience</li>
<li>Firm-paid Dental and Vision Insurance</li>
<li>Firm-paid Life Insurance</li>
<li>Medical Insurance</li>
<li>Free Parking</li>
<li>401k</li>
<li>PTO</li>
</ul>
Team 360 Staffing recruits on behalf of DK Law, and they are committed to being an equal employment opportunity provider in accordance with all applicable laws.

Senior Settlement Negotiator

<h3>Job Description</h3>
Job Description
About the Role The Assay Scientist plays a key role in advancing research and development initiatives focused on genomic technologies and molecular diagnostics. This position combines hands-on laboratory experimentation with data analysis to support the development of innovative genomics-based assays and products. The ideal candidate will have experience in NGS, bioinformatics, and cancer genomics, with a strong drive to contribute to translational research and product development in clinical and research applications.
Responsibilities
<ul>
<li>
Lead research projects to validate genomic technologies for detecting genomic rearrangements in clinical and translational applications
</li>
<li>
Design and implement development plans for future genomics-based products, services, and applications
</li>
<li>
Perform molecular biology and genomics experiments, including sample preparation, sequencing, and assay optimization
</li>
<li>
Analyze high-throughput genomic data using standard and custom bioinformatics tools
</li>
<li>
Interpret experimental results and propose actionable next steps to cross-functional stakeholders
</li>
<li>
Collaborate with internal teams including R&amp;D, bioinformatics, and product development to support project goals
</li>
<li>
Engage in technical discussions with external collaborators and scientific partners
</li>
<li>
Monitor scientific and technological trends in cancer diagnostics, genomics, and molecular biology
</li>
<li>
Deliver internal technical presentations and contribute to departmental knowledge-sharing sessions
</li>
<li>
Represent the team by presenting research findings at external scientific meetings and conferences
</li>
<li>
Identify potential challenges in research projects early and implement solutions or escalate appropriately
</li>
<li>
Participate in regular lab and R&amp;D team meetings, promoting a collaborative and innovation-driven environment
</li>
<li>
Support additional projects and initiatives as assigned
</li>
</ul>
Qualifications
<ul>
<li>
PhD or MS in Molecular Biology, Genomics, Bioinformatics, Biochemistry, or related field
</li>
<li>
Hands-on experience with next-generation sequencing (NGS) workflows and data analysis
</li>
<li>
Proficiency in using bioinformatics tools and scripting languages (e.g., Python, R, Bash)
</li>
<li>
Strong understanding of genomic rearrangements, chromatin biology, and cancer genomics
</li>
<li>
Proven ability to interpret and present complex genomic data to diverse audiences
</li>
<li>
Experience working in cross-functional research or development teams
</li>
<li>
Excellent written and verbal communication skills
</li>
<li>
Demonstrated ability to manage multiple projects and meet deadlines
</li>
</ul>
Desired Qualifications
<ul>
<li>
Experience with Hi-C or chromosome conformation capture technologies
</li>
<li>
Familiarity with clinical assay development or regulatory standards for molecular diagnostics
</li>
<li>
Background in technology transfer or product commercialization
</li>
<li>
Publication record in peer-reviewed scientific journals
</li>
<li>
Experience presenting at national or international scientific conferences
</li>
<li>
Knowledge of single-cell genomics or spatial transcriptomics
</li>
<li>
Previous involvement in industry academic collaborations
</li>
</ul>

Associate Scientist

<h3>Job Description</h3>
Job Description
USALCO is a leading provider of aluminum-based component products used in water treatment, pulp and paper manufacturing, the making of catalysts for oil refining, the housing market and other sectors. 
The Chemical Operator reports to the Plant Manager or Production Supervisor, depending on shift allocation. The position requires a detail-oriented, self-starter who: - incorporates safety and quality into every decision while performing day-to-day tasks, - can efficiently operate and maintain chemical processes and equipment to meet manufacturing specifications and achieve maximum productivity without compromising safety or quality, - will actively seek out opportunities for process improvement and take full responsibility for collaborating with management and peers to implement approved changes in a timely manner. 
The holder of this plant position must be a positive-natured, task-oriented individual with chemical manufacturing experience, significant mechanical aptitude, and a high level of computer literacy. This person must be personally and professionally motivated to work constructively with team members at all levels within the company, to execute job responsibilities with a sense of urgency and to support plant and business initiatives, as well as consistently strive to increase the safety, the quality, and the productivity of the site. 
The Chemical Operator will be assigned responsibilities in all areas of plant operations, including product manufacturing, equipment maintenance, analytical testing, bulk loading and unloading, and utilization of the company computer systems.
Essential Functions:
<ul>
<li>Operating chemical processes and equipment to safely manufacture quality products.</li>
<li>Apply all plant safety rules, work guidelines / practices, and procedures.</li>
<li>Recommending and being actively involved in implementing improvements and adjustments to processes, equipment, and procedures.</li>
<li>Updating and maintaining daily QC data and process samples.</li>
<li>Utilizing computers for quality control, inventory control, transportation documents, and other processing purposes.</li>
<li>Providing physical labor where needed.</li>
<li>Working changing shifts as needed.</li>
</ul>
Other Responsibilities:
<ul>
<li>Keeping all process areas, the laboratory and equipment clean and operational.</li>
<li>Loading tanker trucks and preparing them for shipment.</li>
<li>Operating mobile equipment</li>
<li>Maintaining laboratory equipment according to procedure and inventory as required.</li>
<li>Providing production support to all departments as needed.</li>
<li>Developing and applying improvements in processes, equipment and procedures.</li>
<li>Performing additional responsibilities and tasks as directed by management.</li>
</ul>
Requirements:
<ul>
<li>A High School Diploma.</li>
</ul>
<ul>
<li>Significant mechanical and experience and aptitude.</li>
</ul>
<ul>
<li>Preferred 3-5 years Chemical manufacturing experience.</li>
</ul>
<ul>
<li>Basic college coursework in subjects such as math, chemistry, and statistics.</li>
</ul>
<ul>
<li>The right individual has a can-do attitude, the ability to be part of a team while operating independently, and consistently performs to very high standards.</li>
</ul>
USALCO is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. As a general policy, USALCO does not offer employment visa sponsorships upon hire or in the future.

Chemical Operator

<h3>Job Description</h3>
Job Description
Are you ready to be a part of breakthrough research?
Cedars-Sinai offers scientists unparalleled access to ground breaking technologies, facilities, and resources for conducting research related to an impressive range of diseases and disorders, from cancer, cardiology, and digestive diseases, to genetics, genomics, neurosciences, and women's health. You can continue your career journey with us!
The Chute laboratory studies hematopoietic stem cells and the regulation of hematopoietic stem cell fate through the microenvironment, or niche. Our laboratory also studies the mechanisms that govern malignant transformation of hematopoietic stem cells to leukemia stem cells.
The Research Associate I will perform a variety of clinical specimen collecting, handling, transporting, processing, and storing protocols. Incumbent will need to operate crucial laboratory equipment to process specimens and assists, maintains, and organizes patients’ clinical electronic data files. This position is also responsible for keeping accurate and detailed records of clinical samples, data, maintains and supervises storage units, lab equipment, and stock of lab supplies. Incumbent observes laboratory safety standards and procedures. This role will be able to perform routine cellular, micro- and molecular biology procedures including, but not limited to Western, Northern blot, DNA/RNA, PCR, protein extraction, cell culture, Immunohistochemistry, and staining. This position does not have supervisory responsibilities.
Primary Duties and Responsibilities:
<ul>
<li>Performs a variety of routine laboratory tasks and procedures.</li>
<li>May assist with animal husbandry.</li>
<li>Maintains lab equipment and related records.</li>
<li>Transports, processes and logs samples.</li>
<li>Maintains computer database with relevant clinical information.</li>
<li>Performs lab maintenance duties, including glassware cleaning and sterilization.</li>
<li>Maintains stocks of general lab materials, and places orders for lab equipment and supplies.</li>
<li>Assists new students and fellows at the laboratory.</li>
<li>Observes and follows safety standards and procedures.</li>
</ul>
 Qualifications
Education:
<ul>
<li>Bachelor's degree in Biological sciences is required.</li>
</ul>
Experience and Skills:
<ul>
<li>Understanding of general research objectives.</li>
<li>Knowledge of database management, computers, and presentation and imaging software.</li>
<li>Experience with routine laboratory procedures and experimental protocols.</li>
<li>Must possess digital literacy to include, but not limited to, Excel and Word.</li>
</ul>
 About UsCedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents. About the TeamCedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most. Req ID : 11001 Working Title : Research Associate I - Chute Lab - Division of Hematology &amp; Cellular Therapy Department : Research - General Medicine Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $19.50 - $29.87

Research Associate I - Chute Lab - Division of Hematology & Cellular Therapy

<h3>Job Description</h3>
Job Description
Join Dr. Athanasia Panopoulos and her research group as a Project Scientist in the Cedars-Sinai Regenerative Medicine Institute!
The Cedars-Sinai Board of Governors Regenerative Medicine Institute brings together research faculty and clinicians to provide a true "bench to bedside" organization. Regenerative medicine is a new and developing field that aims to restore function in diseased or aged tissues through either revitalizing existing cells or transplanting new ones. At the Board of Governors Regenerative Medicine Institute, researchers are turning stem cells into therapies for treating a multitude of prevalent diseases and conditions.
The Panopoulos Laboratory at the Cedars-Sinai Regenerative Medicine Institute is a seeking a highly motivated postdoc to join our new, dynamic research group. The laboratory studies fundamental and clinically relevant research questions that are at the intersection of the fields of stem cell biology, blood cell development, and cancer. The long-term research goals of the Panopoulos Laboratory are to harness the power of stem cells to provide innovative and clinically relevant advances in targeted cancer therapeutics and regenerative medicine. Our work focuses on utilizing human somatic cell reprogramming to identify and target novel embryonic mechanisms that are exploited in cancer, and as an avenue to discover fundamental aspects of normal and aberrant hematopoietic development. To learn more, please visit Panopoulos Research Lab | Cedars-Sinai
Are you ready to be a part of breakthrough research?
The Project Scientist will plan and conduct experiments with pluripotent stem cells and cancer cells. The Project Scientist works independently and in cooperation with the Principal Investigator to make significant and creative contributions to a research or creative project in any academic discipline. The Project Scientist may be an ongoing member of a research team or may be employed for a limited period of time to contribute high-level skills to a specific research or creative program. Project Scientists are not required to carry out independent research or to develop an independent research reputation and do not have teaching responsibilities. Ordinarily, the Project Scientist title will carry out research or creative programs as well as administration of day-to-day lab operations with supervision by a member of the Professorial Series.
Primary Job Duties and Responsibilities:
<ul>
<li>May assist in preparation of grant proposals, submissions, publications and presentations but is not responsible for generating grant funds.</li>
<li>May serve as PI for certain grants as approved by supervising member of the Professorial Series.</li>
<li>May participate in publications and presentations as author or co-author.</li>
<li>May develop, adapt and implement new research techniques and protocols.</li>
<li>Assists in lab experiments.</li>
<li>Analyzes, interprets, summarizes and compiles data.</li>
<li>May lead or train Staff Research Associates and Research Fellows.</li>
<li>Will assist in day-to-day laboratory activities.</li>
<li>Appointees on an academic trajectory will be expected to commit a portion of their time to developing an independent range of research.</li>
</ul>
 Qualifications
Education:
<ul>
<li>Doctorate Degree required.</li>
</ul>
Experience and Skills:
<ul>
<li>No experience is required. Completion of postdoctoral appointment in the area of specialization, as applicable.</li>
<li>Demonstrated significant, original, and creative contributions to a research or creative program or project.</li>
<li>Experience in organ-on-chip and/or cell signaling is a plus.</li>
<li>Expertise in one or more of the following areas is required: primary and mammalian cell culture, flow cytometry, animal work/bone marrow transplantation, basic techniques in cell biology, molecular biology, and biochemistry.</li>
<li>Knowledge of PI’s area of research specialization.</li>
<li>Scheduling flexibility, including evening, weekend, and holiday rotation commitment, may be necessary. Travel may be required.</li>
<li>Function efficiently and cooperatively with a team of faculty, research associates, technicians, and students.</li>
<li>Excellent written and oral communication skills are essential.</li>
</ul>
 About UsCedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents. About the TeamCedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most. Req ID : 11092 Working Title : Project Scientist - Panopoulos Lab - Regenerative Medicine Institute Department : Research - RMI Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : EXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $66,560 - $133,120

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