Experienced Underground Utility Locator (Fairview)

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!

SCHEDULE: Night Shift This position offers four 10 hour shifts with an 8pm PT start time. The 4 days will be between Tuesday and Sunday. Hours worked between 9pm and 4am will receive a 10% night shift differential. Additionally, if scheduled to work hours on both Saturday and Sunday, a $200 weekend differential will be provided. LOCATION: San Diego, CA While the work schedule will be mostly remote, employee needs to live within the San Diego area to come onsite for occasional training. 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, Data Review will review chromatographic data and calculated results obtained from 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 EIA; applies toxicological and chromatographic rule sets to determine acceptability of results; requests additional testing as necessary; 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 is not intended to be complete or all-inclusive and does not preclude management from assigning related functions for which the individual has demonstrated competency through performance. Responsible for testing to troubleshoot result issues. Reports 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 reviews chromatography and calculated results from a variety of standardized tests on urine samples using advanced LC-MS-MS technology and EIA for the detection of prescription and illicit drugs. Evaluates the validity of results obtained, maintains proper records of results and creates a report of results. Maintains quality control and LC-MS-MS chromatographic data prior to release or results to physicians. Ensures that testing methods follow established quality control procedures. Identifies, troubleshoots, documents and resolves test result issues. Documents issues using the Laboratory Occurrence Management (LOM) form. Acts as a resource to laboratory technicians, laboratory assistants and associate scientists. 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, clinical laboratory assistants and associate scientists who prepare specimens or perform other less complex procedures. Participates in internal laboratory audits. 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 SKILLS/KNOWLEDGE/ABILITIES 2+ years’ experience in high complexity testing; CLIA/CAP environment Must maintain continuing education units required by California Department of Health Services 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 Bachelor’s degree with current California CLS license ASCP license highly preferred ESSENTIAL PHYSICAL & MENTAL REQUIREMENTS: Physical: Primary functions require sufficient physical ability to work in an office setting and operate office equipment. Continuous sitting and upward and downward flexion of neck; fine finger dexterity; fast paced data entry with finger pressure to manipulate keyboard. Have the ability to speak and listen to customers on fast-paced phone calls. Mental: The employee is expected to read, understand, and retain SOPs. Be able to convert SOP instructions into work-related tasks. Use judgment when there is a deviation and effectively communicate any discrepancy to their Manager. 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: Hourly Position: $45-$50 10% Night Shift Differential applied to hours worked between 9pm and 4am $200 Weekend differential is added per weekend worked 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, religion, 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.

*$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 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.

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.