Alastin Skincare Clinical Research Study (Carlsbad)

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst - 12hr Rotating Shift position at its facility in Buffalo, NY. Ideal candidates will possess the following: - A BS or BA in the biological sciences or related field (required) - Proficiency with data entry and computer applications - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong attention to detail - Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. The pay for this position is $22.25 hourly (plus $2 night shift differential during night time hours) This is a full-time position and is eligible for the following benefits after a brief waiting period: medical, dental, vision, life/AD&D insurance, long- and short-term disability insurance, health and dependent care FSA plans, employee assistance program, 15 days of paid time off per year for sick leave and/or vacation, 6 paid holidays per year, 3 days paid bereavement leave, and 401(k) (with up to 3% employer match after eligibility criteria are met). The schedule for this position is on a rotating shift basis: the first week is Monday-Tuesday and Friday-Sunday, from 2:00pm to 2:00am; the second week is Wednesday-Thursday, from 2:00pm to 2:00am. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from applying. To apply for this position please access the company's job posting at: https://apps.iehlabs.com/applyatieh.html#68e80231cc0681f05966c818 After navigating to the URL listed above, you will be asked to complete optional self-identification surveys and submit your cover letter, resume and references in a combined, single PDF. Equal Opportunity Vets/Disability "Know Your Rights" Poster: https://www.eeoc.gov/sites/default/files/2022-10/EEOC_KnowYourRights_screen_reader_10_20.pdf

Work Location: USA Remote (Prefer PST Time Zone) Work Hours: M - F, 9:00 am - 5:30 pm Pay Rate: $35 - $40 /hr DOE & location This is a non-traditional Human Data Research Analyst role working with an exciting AI start-up based in San Francisco. In this role your responsibilities will involve utilizing your expertise in AI to contribute to the development of optimized AI solutions. Responsibilities: Representing various clients’ software to provide enhanced AI solutions to boost their business productivity. Create Use case scenarios derived from client solutions utilizing tailored AI solutions. Execute delivering your thoughts on the opportunities for improvement. Maintain and improve processes that support the creation of the Use Cases. Attend meetings as appropriate. Independently identify operational inefficiencies and work to mitigate them. Assist with other duties as needed. Keywords provides a competitive compensation package, good benefits and a casual, fun, productive and supportive working environment. We empower people to perform to the best of their ability with our “can do” attitude. We appreciate and embrace flexibility and learn at every opportunity to grow ourselves through experience, training and tackling new challenges. This is what makes us Keywordians. Requirements Cognitive Science, Computer Science or other Masters degree associated with AI Technical aptitude or experience working with AI Experience with Python, SQL, typescript (preferred) Data modeling (preferred) Experience working with and creating Data Visualizations Strong attention to detail Strong Organization skills Critical thinking and problem-solving skills Strong Analytical skills Process Improvement experience Strong aptitude of working with Google sheets, Zoom, and Slack Exemplify the quality of having a "Proactive Approach," attitude which includes a high level of accountability, transparency, and teamwork first & foremost Ability to learn on the job Benefits At KeyWords we provide all our contingent workforce with: Paid Time Off (including sick days and holidays) 401k (3% matching) Medical, Dental and Vision benefits By providing your information in this application, you understand that we will collect and process your information in accordance with our Applicant Privacy Notice. For more information, please see our Applicant Privacy Notice at https://www.keywordsstudios.com/en/applicant-privacy-notice. Role Information: EN Studio: Keywords Studios Location: Americas, United States, San Francisco Area of Work:  Embedded Services Service: Globalize Employment Type: Full Time Working Pattern: Remote

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Position Title: Scientist / Senior Scientist – Vaccine Formulation and Characterization Location: Baird Research Park, 1576 Sweet Home Road, Buffalo, NY 14228 Company Overview: POP Biotechnologies, Inc. (POP BIO) is a biotechnology company developing novel vaccine and drug delivery technologies based on its proprietary cobalt-porphyrin–phospholipid (CoPoP) liposome platform. POP BIO’s technology enables highly immunogenic particulate vaccine formulations and is currently advancing multiple vaccine candidates into clinical development in collaboration with international partners and public health agencies. Position Summary: POP BIO seeks to hire one or more motivated scientists to support the production, characterization, and analytical development of vaccine materials, including recombinant proteins, lipids, and liposomal formulations. The ideal candidate will have experience with one or more of the following: biophysical and biochemical characterization techniques, vaccine immunoassays, and formulation development. This position offers opportunities to contribute to translational research, manufacturing process optimization, grant preparation, and technology commercialization. We are looking for candidates with expertise in one or more of these areas: Protein and Antigen Production Express, purify, and characterize recombinant proteins and peptides Conduct analytical characterization, including SDS-PAGE, Western blot, and chromatography (SEC, HIC, IEX). Perform quantitative and qualitative assays to assess protein purity, yield, and conformation. Analytical Assay Development Develop, optimize, and perform immunoassays, including: ELISA for quantitation of concentrations in vaccine formulations. Slot blot for assessing antigen conformation and epitope integrity. Establish assay validation parameters (specificity, linearity, accuracy, precision, robustness) in accordance with internal standards. Maintain detailed assay SOPs and training materials. Lipid and Liposome Characterization Support the synthesis, purification, and analytical characterization of functionalized lipids, including cobalt-porphyrin–phospholipids (CoPoPs) and related lipid conjugates. Conduct physicochemical analyses of lipids and formulations using UV-Vis spectroscopy, HPLC, LC-MS, and elemental analysis. Manufacture and characterize liposomes, including particle sizing (DLS), zeta potential, encapsulation efficiency, and stability under various storage conditions. Develop and document standardized liposome production procedures for scale-up and reproducibility. Vaccine Formulation Development Prepare and optimize vaccine formulations incorporating HA and NA antigens into CoPoP liposomes or other delivery systems. Evaluate antigen–liposome binding, particle morphology (TEM), and stability. Collaborate with internal and external teams to support process development for GMP-ready formulations. Commercialization and Grant Development Assist in the preparation of grant applications, reports, and technical documents for NIH, CEPI, and other funding agencies. Participate in meetings with collaborators, funding agencies, and potential commercial partners. Contribute to technical writing, data presentation, and preparation of manuscripts, posters, and presentations. Qualifications: M.S. with ≥3 years of relevant experience preferred; at least B.S. for consideration. Ph.D. in Biochemistry, Molecular Biology, Immunology, Pharmaceutical Sciences, or related discipline would be a plus Hands-on experience with protein purification, analytical biochemistry, and vaccine immunoassays. Experience with liposome preparation, nanoparticle characterization, or lipid chemistry preferred. Strong analytical and technical writing skills; ability to draft and edit experimental protocols and grant sections. Excellent organization, attention to detail, and data management skills. Ability to thrive in a collaborative, fast-moving research environment. Preferred Skills: Experience with mammalian or insect expression systems for recombinant protein production. Familiarity with laboratory operations and immunological assay workflows. Prior experience in technology transfer, regulatory documentation, or early-stage biotech development is a plus. Compensation: Commensurate with experience. Includes salary, benefits, and potential for performance-based bonuses. To Apply: Submit a cover letter and CV to jrsmyth@pop.bio with the subject line “Scientist – Vaccine Formulation and Characterization.”

*$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

Join the Fight Against Osteoarthritis of the Knee! Are you experiencing pain, stiffness, or swelling in your knee due to Osteoarthritis? You may be eligible to participate in a clinical trial to help advance new treatments for Knee Osteoarthritis. Call (480) 382-7909 Now! Or Apply Here Why Participate? ● Compensation: Get compensated up to $950 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. ● Free Study Medications: Study medication is provided at no cost. To Qualify: ● 50–80 years old ● Clinical diagnosis of OA (Osteoarthritis) Check Out Our Other Studies! ● Psychosis associated with Alzheimer’s disease ● Active Psoriatic Arthritis ● Cirrhosis ● Diabetic Peripheral Neuropathy Pain ● Plantar Fibromatosis (PFI) - Ledderhose Disease ● Prurigo Nodularis ● Metabolic Associated Steatohepatitis (MASH) ● Future Studies Scottsdale Clinical Trials Interested? Don’t miss the chance to make a difference! For more information about upcoming clinical trials and to see if you qualify, visit Scottsdale Clinical Trials or call us at (480) 382-7909.