Clinical Laboratory Scientist- Results

Join Us in the Fight Against Alzheimer's Disease Psychosis! Are you or someone you care about dealing with Alzheimer’s Disease? We encourage you to take part in vital clinical trials focused on enhancing research and treatment options for this condition. We are seeking patient volunteers to help evaluate the effectiveness of a new medication for this purpose. The medication will be provided at no cost to you or your insurance. Participants will receive compensation for their time and travel, and if you refer a qualifying friend, you will earn a $100 bonus. Call 480-716-4590 Now! Or Apply Here To qualify, you must: ● Be a male or female, 55 - 95 years of age ● Be diagnosed with Alzheimer's Disease or probable Alzheimer's Disease ● Have a prior history of psychotic symptoms for at least 2 months prior to Screening WHY PARTICIPATE? ●Compensation: Get compensated up to $3,400, with no cost to you or your insurance! ●Comprehensive Support: Regular check-ins and assessments to ensure your health is a priority. Our trial is conducted by experienced healthcare professionals dedicated to your well-being. ●No-cost study medications: Study medications are given at no charge. Check out our other studies! ● Multiple Sclerosis ● Obstructive Sleep Apnea ● Excessive Sleepiness Due to Shift Work ● Narcolepsy and Idiopathic Hypersomnia ● General Anxiety Disorder ● Asthma Treatment ● Cardiovascular Risk Factor Study ● Future Studies AND MANY MORE! Chandler Clinical Trials (CCT) Contact us today at 480-716-4590 or visit us at https://chandlertrials.com/ for more details! Advancing Medicine Through Research!

*$2500 sign on bonus! WORK SCHEDULE 4x10 schedule 3 days between Tuesday and Friday, and each Saturday for a total of 4 days per week, 10 hours per day. Start time: 1:00 pm PST Why Millennium Health? Millennium Health LLC is an accredited specialty laboratory with more than a decade of experience in medication monitoring and drug testing services, helping clinicians monitor the use and misuse of prescription medications and illicit drugs. The testing is used by healthcare professionals to obtain objective information about patients’ recent use of prescription medications and/or illicit drugs and helps monitor the effectiveness of treatment plans. Everyone that joins our team is key to our ability to support the clinicians and patients. GENERAL SUMMARY The Clinical Laboratory Scientist performs a variety of standardized urinalysis tests in a toxicology laboratory for the detection of prescription and illicit drugs using advanced LC-MS-MS technology and approves reports and patient results to ordering physicians. ESSENTIAL FUNCTIONS The following are intended to be examples of the accountabilities for which the person in this position is responsible. This position is not intended to be complete or all-inclusive and does not preclude management from assigning other or related functions for which the individual has demonstrated competency through performance. Responsible for testing and reporting laboratory test results for all test methods approved by CAP, NY and CLIA. Ensures accuracy and quality of test results meeting required turnaround times. Enters testing data and performs a variety of standardized tests on urine samples using advanced LC-MS-MS technology for the detection of prescription and illicit drugs. Evaluate the validity of results obtained, maintain proper records of results, and create a report of results. Maintains quality control and LC-MS-MS chromatographic data before release of results to physicians. Ensures that testing methods follow established quality control procedures; and assists with the preparation of chromatographic data reports prior to release to physicians. Identifies, troubleshoots, documents, and resolves problems with test results. Documents issues using the Laboratory Occurrence Management (LOM) form Acts as a resource and trainer to laboratory technicians and assistants Prepares and maintains reagents and supplies; performs maintenance on laboratory equipment and maintains a laboratory in a clean and orderly condition. Follows safe laboratory practices and participates in operational support activities necessary to maintain and optimize testing capabilities. May oversee the duties of clinical laboratory technicians and assistants who prepare specimens and perform other less complex procedures. The laboratory is actively involved in research and encourages Clinical Laboratory Scientists to participate in research projects. Participates in internal laboratory audits Required to follow all safety procedures, policies, precautions, and Quality Assurance. Other duties as assigned. Ability to ensure HIPAA, Confidentiality and Compliance policies, procedures, and standards are always adhered to. Ability to ensure administrative, physical, and technical cyber security controls are always adhered to. SECONDARY ACCOUNTABILITIES Remains aware of evolving needs and opportunities, showing flexibility in doing whatever is appropriate to support the Company’s success. Pursues educational opportunities to maintain advanced and up-to-date knowledge in the field. Performs all other related duties as required and assigned and understands that the items in this description are not all-inclusive. Requirements EDUCATION Bachelor’s degree with current California CLS license ASCP license highly preferred EXPERIENCE 1+ years’ experience in high complexity testing; CLIA/CAP environment Must maintain continuing education units required by California Department of Health Services SKILLS/KNOWLEDGE/ABILITIES Knowledgeable in laboratory methods and techniques Knowledgeable of equipment and supplies used in a laboratory Proficient in MS applications (Word/Excel/PowerPoint/Outlook) Strong interpersonal skills and ability to communicate with all levels of employees Effective attention to detail with high degree of accuracy ESSENTIAL PHYSICAL & MENTAL REQUIREMENTS: Sitting (85 %), walking (5 %), standing (10%), and lifting up to 20 lbs. Physical requirements will vary depending on departmental needs. The employee is expected to read and understand standard operating procedures (SOPs) The employee should be able to convert SOP instructions into work-related tasks. The employee must be able to perform simple calculations as required in the SOP The employee must be able to use judgment when there is a deviation in the system and effectively communicate any discrepancy to their supervisor. ADDITIONAL PHYSICAL & MENTAL REQUIREMENTS: The employee is regularly exposed to high pressure/high stress situations, and therefore, must be able to thrive in this type of environment. Must be able to tolerate a moderate noise level. Must be able to work an extended schedule as needed. Benefits Medical, Dental, Vision, Disability Insurance  401k with Company Match   Paid Time off and Holidays  Tuition Assistance  Behavioral and Health Care Resources  POTENTIAL HIRING RANGE: $93,600.00 - $104,000.00 Offers are based on skills, knowledge, and abilities of the selected candidate. Millennium Health is an Equal Opportunity/Affirmative Action Employer and E-verify participant. All qualified applicants will receive consideration for employment without regard to race, color, creed, sex, national origin, disability, gender identity, sexual orientation or protected veteran status. California Employee Privacy Notice - Millennium Health LLC https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm

10x Genomics, Inc. in Pleasanton, CA seeks Document Control Specialist II. Responsibilities: Responsible for managing documentation and records generated during various processes in accordance with the organization’s procedures for commercial and operations functions, including: working closely with Production and R&D to support new production introduction, production batch record change control and BOM setup in electronic document and ERP systems; supporting new and existing documentation, such as SOPs, Work Instruction documents, and training program files; collaborating with subject matter experts to develop new training materials or improve existing documentation, as well as refining standard Quality Management System (QMS) documents; processing document changes, such as Engineering Change Order (ECO), Engineering Change Requests (ECR), and other quality records, adhering to ISO standards; creating and releasing documents, such as batch records, for New Production Introduction (NPI) launches throughout all phases of the release process, including writing Bills of Materials (BOMs) for setup in the electronic documentation and Enterprise Resource Planning (ERP) systems; optimizing all documentation systems, including but not limited to, the Learning Management System (LMS) training system, the PLM platform, and the ERP system; and other duties as assigned. Salary Range $90k - $110k. Education: Bachelor’s degree in Computer Science or related technical field (or foreign equivalent). Requirements: Two (2) years of progressive post-baccalaureate experience in job offered or related positions. Other special requirements: Two (2) years of experience in document control/solutions, electronic storage, and technical writing of content/documentation to meet company standards and target company needs; two (2) years of experience working with document management systems; and two (2) years of experience with PLM system integration. Qualified applicants must send resume to 10x Genomics, Attn: Jana Jensen, 6230 Stoneridge Mall Rd, Pleasanton, CA 94588 quoting job #DCSII.

We’re Concepta, a fast-growing brand that fuses science-backed cosmetics and supplements with the power of Amazon. Based in Miami, we’re agile, bold, and building something special- products that make a difference and a business model that keeps us sharp. We're expanding, and our next key hire? Someone who knows formulation inside and out, even if they’re not the one mixing the beakers. What You’ll Do: You’ll be the technical lead and liaison between Concepta and our network of contract manufacturers (CMs). You won’t be formulating yourself but you’ll ensure every new skincare, haircare, and supplement product is technically sound, cost-efficient, and aligned with our brand promise. Your responsibilities include: Translating product briefs into technically feasible formulations with our external labs Auditing and evaluating contract manufacturers Advising on ingredient choices, reviewing formulas, and identifying ways to reduce costs Supporting regulatory documentation alongside consultants (you won’t own filings directly) Maintaining clear version histories and formula logic to build a foundation for future IP Helping Concepta prepare for formulation ownership as the brand grows What We’re Looking For: 5+ years in cosmetics or supplements product development Experience working directly with or in contract manufacturing labs Background in formulation development — you understand INCI, specs, and how formulas work Strong communication skills and project ownership Ability to evaluate formulations and spot cost-saving opportunities Based in or willing to relocate to Miami (on-site lab visits required) Nice-to-haves: Experience in startup or indie beauty brands Familiarity with MoCRA and U.S. cosmetic regulatory standards Prior work with celebrity or private label brands Education in Chemistry, Chemical Engineering, or Cosmetic Science What You’ll Get: Strategic ownership of Concepta’s technical development roadmap A seat at the table — work closely with leadership and shape our next bestsellers A fast-paced, high-growth environment that values innovation Opportunity to impact both beauty and nutrition verticals Curious? Apply now or reach out directly to learn more about this role shaping Concepta’s product future.

10x Genomics, Inc. in Pleasanton, CA seeks Sr. Research Associate II. Responsibilities: The Sr. Research Associate II will be a part of the Molecular Biology team working closely colleagues in computational biology, software, chemistry, and microfluidics to optimize and evaluate new assays in spatial multi-omics. More specific duties include: supporting the method development and optimization of novel molecular biology assay schemes for the detection of analytes in situ; collaborating with scientists, engineers, and other researchers in the optimization and troubleshooting of different sample preparation protocols for effectiveness and improved detection of analytes in situ, including in situ assays of tissue section on microscope glass slides; planning, performing, and evaluating data of biological experiments to support, improve, and expand our highly complex and proprietary technologies, products, and solutions; developing procedures, writing technical reports, and maintaining accurate records through diligent experimental observations and data tracking; clearly communicating and presenting results of data and research findings for making critical design decisions; and other duties as assigned. Salary Range $121,264-$130k. Education: Master’s degree in Bioengineering, Biomedical Engineering, or related field (or foreign equivalent). Requirements: Two (2) years of experience in job offered or related positions. Other special requirements: Two (2) years of experience in performing complex multi-step experiments, including NGS library preparation, principle of sequencing technologies, and data analysis; two (2) years of experience in standard molecular biology techniques such as sample preparation, nucleic acid amplification and purification, qPCR, and DNA sequencing; two (2) years of experience in designing novel molecular biology assay schemes and computational analysis of next-generation sequencing data; two (2) years of experience in troubleshooting and optimization of assays; and two (2) years of experience using light and fluorescent microscopy. Qualified applicants must send resume to 10x Genomics, Attn: Jana Jensen, 6230 Stoneridge Mall Rd, Pleasanton, CA 94588 quoting job #SRRAII.

Seattle, WA  USA | Full-time | Permanent   Salary: $135,000 - $158,000 DOE + bonus + equity  Location note: Please note that while Seattle, WA is the preferred location for this position, we can also consider the role to be based in the states of Massachusetts or New York – please state your preferred working location in your cover letter.  We also have a very similar UK-based opening for this position in our Cambridge, UK office. Please see our separate, Cambridge, UK job posting for more details.  Compensation note: The salary range for this role is broad as we are able to consider varying levels of experience.  Any offer made will carefully take into account level of experience (including relevant industry experience), transferable relevant skills and previous relevant achievements.  About us   Riverlane’s mission is to make quantum computing useful, sooner. From advances in material science to complex chemistry simulation for drug design and discovery, quantum computers will help solve some of the world’s most important challenges. Riverlane is building the quantum error correction stack, Deltaflow, to make this happen. It’s a complex problem that requires a range of skills, talent and passion.   We recently raised $75M in Series C funding to accelerate our cutting-edge R&D in quantum error correction (QEC), and are partnering with many of the world’s leading quantum hardware providers and government agencies to make fault-tolerant quantum computing a reality. We’re making remarkable progress and growing fast.     About the role  As quantum computing enters a new phase—the ‘QEC era’— marked by significant advancements in quantum error correction, Riverlane’s customers are integrating Deltaflow with their existing quantum computing control systems, and demonstrating the first steps toward error-correcting capability.  We’re excited to launch this fantastic QEC Applications Scientist opportunity, which will play a critical role in the QEC journey for our customers and partners.  Working closely with Riverlane’s customers and leveraging the learnings from our work with varied quantum computing systems, you will be instrumental in supporting each customer to achieve their first QEC results.    What you will do  As QEC Applications Scientist, you will be responsible for supporting Riverlane’s customers and partners on their QEC experimental journey, starting from their first QEC results. As Riverlane works with many different partners, across all qubit types, you will gain exposure to different qubit architectures, and their respective QEC considerations.   Using these insights, along with your background in quantum computing and quantum error correction, and your proven track record of publications in quantum computing, you will accelerate the progress of Riverlane’s customers and partners toward fault-tolerance.     In this role, you will:   Enable our North America-based customers (predominantly US) with varied qubit architectures to achieve successful QEC demonstrations using Riverlane’s quantum error correction system (Deltaflow)  Use Deltaflow and Riverlane’s software tools for rapid QEC experiment prototyping in collaboration with our customers   Present QEC integration and experimentation results externally, including at conferences and through publications (and other relevant avenues)  Influence Deltaflow’s product development by advocating for the needs of our customers  Work with stakeholders across Riverlane to influence the creation of educational content that can accelerate a new QEC customer’s journey  Champion a culture where Riverlane shares the QEC success stories of customers to benefit the wider QEC community  Requirements What we need   Master’s or PhD in Electrical Engineering, Computer Science, experimental physics (or related field)  Proven experience with quantum error correction or related research and experimentation experience (in industry or academia)   Proven experience with computational tools for scientific research in quantum computing (or related field)  Familiarity with qubit architectures and considerations for NISQ and QEC experiments  Ability and willingness to travel within North America (mainly the US) to customer and partner sites  Strong written and oral communication skills, with the ability to discuss complex ideas with a variety of audiences, in a clear and simple way  Ability to work effectively in a collaborative team environment  A passion for learning and a curious, solution-oriented mindset  Even better if you have   Strong track record of working collaboratively with research and product development teams to enable customers and partners   Experience in stim (strongly preferred) and/or other QEC tools, especially in a quantum computing experimental setting    Familiarity with quantum error correction concepts and protocols  Benefits What can you expect from us   A comprehensive benefits package that includes an annual bonus scheme, private health insurance, life insurance and a contributory retirement fund.   Equity, so that our team can share in the long-term success of Riverlane   Generous annual leave and enhanced family leave   A diverse work environment that brings together experts in many fields (including software and hardware development, quantum information theory, physics and maths) and over 20 different nationalities    A learning environment that encourages individual, team and company growth and learning, including an annual training and conference budget.    How to apply   Please upload a CV and covering letter by clicking 'Apply Now'. Your covering letter should explain why you are applying for the job and what skills and experience you can bring to the role.   We review CVs as we receive them and interview as soon as we have applications that look like a good match (usually within one week). We do not use closing dates. So, please apply as soon as possible to avoid missing out on this role.      If you have any queries, please contact jobs@riverlane.com.      Everyone is welcome at Riverlane. We are an equal opportunities employer and encourage applications from eligible and suitably qualified candidates regardless of age, disability, ethnicity, gender, gender reassignment, religion or belief, sexual orientation, marital or civil partnership status, or pregnancy and maternity/paternity.   Studies have shown that women tend to apply to jobs if they meet all or almost all of the requirements whereas men apply even if they meet only some of the requirements. If that sounds like you then please apply – we are happy to review your application and let you know if we think you might be a good fit.   If you need any adjustments made to the application or selection process so you can do your best, please let us know. We will be happy to help.