PAID for Participation Prurigo Nodularis Study (Northridge)

Are you suffering from Psoriasis? Psoriasis is a chronic autoimmune skin condition that leads to the rapid growth of skin cells, resulting in thick, red, scaly patches on the skin's surface. These patches, often referred to as plaques, can be itchy and painful and typically appear on areas such as the elbows, knees, scalp, and lower back, though they can occur anywhere on the body. Northridge Clinical Trials is launching a new research study for individuals with Psoriasis and is in search of qualified participants! We need patient volunteers to help test the effectiveness of a new medication for this condition. The medication will be provided at no cost to you or your insurance. Participants will receive compensation for their time and travel. Additionally, if you refer a friend who qualifies, you can earn a $100 bonus. Call 818-350-7482 Now! Or Apply Here WHY PARTICIPATE? ●Compensation: Get compensated up to $2,100 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 for Psoriasis are given at no cost. TO QUALIFY YOU MUST BE: ●Be at least 18 years of age or older ●Be clinically diagnosed with Psoriasis or have signs of Psoriasis Check out our other studies! ●Moderate to Severe Plaque Psoriasis in Obese Patients ●Prurigo Nodularis ●Hidradenitis Suppurativa ●Acne Vaccine ●Future Studies AND MANY MORE! Northridge Clinical Trials Contact us today at818-350-7482 or visit us at https://northridgetrials.com/ for more details! Advancing Medicine Through Research!

JLA International, Inc., a Leader in Food Safety, is now accepting applications for a Sample Prep Technician position at its facility in Samson, AL. Ideal candidates will possess the following: - A high school diploma or GED (required) - Basic math skills - Good attitude and willingness to work with others - Good communication and organization skills - Strong understanding of aseptic technique in the laboratory - Ability to follow written directions - Ability to regularly lift up to 50lbs above waist level Sample Prep Technician duties include: sample preparation, sample sorting and log-in, performing specific sample testing steps (under supervision), transcribing results, data entry, inventory control, washing glassware, general laboratory cleaning, and other duties as assigned. This is a full-time position and is eligible for standard benefits after a brief waiting period. The laboratory operates weekends, so candidates must be willing to work some weekends. 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#68b8605ca5bd2170ba1f2790 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

PURPOSE OF STUDY: Alastin Skincare is conducting a 14-Week research study to evaluate the effects of an investigational topical body lotion for improving body skin quality. The study Test Product may improve the appearance of your skin but cannot be guaranteed. Study participants will apply the study Test Product twice daily ONLY to the assigned body areas (1 knee & 1 upper inner arm) and use an approved body cleanser and sunscreen for the duration of the study. No products will be used on the untreated side (knee & upper inner arm). To be considered for study participation, you must: • Be a healthy female or male ages 40 to 75 years. • Have Moderate to Severe crepey (crinkly) skin of the upper inner arms & knees. • Have Mild to Severe laxity (loose) skin of the upper inner arms & knees. • Have Mild to Severe skin roughness & dryness of the upper inner arms & knees. • Be willing to use ONLY the study provided Test Product, body cleanser, and sunscreen for the duration of the study (14 weeks). • Be willing to NOT undergo ANY cosmetic procedures on the upper arms & knees for the duration of the study (14 weeks). • Be available to visit the office 5 times during the study period (14 weeks). • Be willing to have photographs taken of your upper arms & knees, and sign a photography release authorizing Alastin Skincare, Inc. to use and/or publish your photographs for promotional purposes. • Be willing to maintain a consistent body weight for the duration of the study. Individuals currently undergoing weight loss treatments can be considered for study participation, provided the dose is stable and a consistent body weight is maintained for the duration of the study (14 weeks). • Meet additional study qualification criteria. Eligible individuals that meet all study qualification criteria and complete ALL study visits will be compensated for their time and travel in the amount of $250 ($50 per study visit) and offered to choose any three (3) Alastin commercially available products, which can be valued at a retail cost up to $700. STUDY LOCATION & CONTACT: Galderma; Alastin Skincare, Inc. 5999 Avenida Encinas, Ste 100, Carlsbad, CA 92008 Lora Colvan, R&D Advisor

Quality Engineer Job description Job Summary: Supports all quality system and functions. Assists in establishing systems to support the facility to drive continuous improvements and minimize the costs of non-conformance. Plans, schedules, executes and communicates all items regarding quality issues, Deviations, OOS, validations and other projects to the QA Manager and/or other interested parties. Performs all duties associated with compliance-related items for ISO standards and cGMPs. Essential Duties and Responsibilities: Analyze data, process capabilities, customer concerns and expectations and any other leading or lagging indicators, which may be used to improve product and process knowledge. Interact with customers in order to understand and integrate those requirements into manufacturing and quality system requirements. Identify manufacturing and development constraints. Work with management and technical staff in performing root cause failure analysis and implementing corrective and preventive actions to preclude recurrence. Assists facility with quality improvement programs by utilizing Six Sigma tools and Lean techniques, including the education of facility personnel on these tools and techniques. Assumes responsibility for various assigned projects designed to improve product quality, reduce costs and/or validate facility products or processes, including development and implementation of any new or required inspection methods. Participates in FDA, CAPH and Customer quality system audits. Manage the CAPA process including the review and approval to open new CAPAs as well as approving CAPA plans, timelines and verification of effectiveness plans to assure timely completion within the established goal, inclusive of Change Control establishment and maintenance. Lead investigation and root cause analysis to internal deviations, non-conformance reports and OOS. Support validation of facilities and equipment and process. Approve engineering studies and other protocols as required. Oversee Calibration and pest control activities. Performs other duties, as assigned based on business needs. Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules. Exhibits regular, reliable, punctual and predictable attendance. Basic Qualifications: Bachelor’s in Science or Engineering or equivalent experience. 5 Years of experience Preferred Knowledge in Pharmaceutical Manufacturing of Aseptic Products. Skills and Abilities: Excellent writing skills pertaining to SOP, and Data report generation. Experience with Project Management Tools, Quality Risk Management, and Six Sigma problem solving tools. Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description. Able to comply with the company’s safety policy at all times. Able to comply with the company’s quality policy at all times. Working Requirements: Good communication and writing skills to interact with others in a positive and technical manner. Must be able to understand direction and adhere to established procedures.

Job Summary: We are seeking a detail-oriented and motivated Lab Technician to join our Research & Development team. Under the supervision of the Lab Manager, the Lab Technician will assist in the formulation, testing, and production of skincare products, ensuring compliance with quality and safety standards. This role offers an opportunity to work in a fast-paced, innovative environment and contribute to the development of cutting-edge skincare solutions. Key Responsibilities: Prepare, mix, and test batches of skincare formulations, including creams, serums, lotions, and other personal care products. Conduct routine and non-routine testing (e.g., pH, viscosity, stability, odor, and appearance) to ensure product quality and compliance with specifications. Maintain accurate records of experiments, test results, and formulations in lab notebooks or Laboratory Information Management Systems (LIMS). Assist in quality control checks to identify and troubleshoot stability or performance issues. Operate and maintain laboratory equipment, ensuring proper calibration and adherence to safety protocols. Collaborate with formulation chemists, regulatory teams, and production staff to support product development and scale-up processes. Follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) to ensure compliance with FDA and other regulatory standards. Order and manage lab supplies, ensuring a clean and organized workspace. Assist in preparing samples for third-party testing or regulatory submissions, as needed. Qualifications: Associate’s or Bachelor’s degree in Chemistry, Biology, Cosmetic Science, or a related field (or equivalent experience). 1-3 years of experience in a laboratory setting, preferably in cosmetics, skincare, or personal care product manufacturing. Familiarity with lab equipment, testing methods (e.g., pH meters, viscometers), and safety protocols. Knowledge of GLP, GMP, and FDA regulations is a plus. Strong attention to detail, organizational skills, and ability to follow standard operating procedures (SOPs). Proficiency in data collection and basic computer skills (e.g., Microsoft Office, LIMS). Ability to work independently and collaboratively in a team environment. Excellent problem-solving skills and a passion for skincare product innovation. Preferred Skills: Experience with emulsions, surfactants, or color cosmetics. Familiarity with raw material sourcing and product stability testing. Basic knowledge of cosmetic regulations (e.g., Cosmetic Product Notification Portal - CPNP). What We Offer: Competitive salary and benefits package, including health, dental, and vision insurance. Opportunities for professional growth and development in the skincare industry. A collaborative and innovative work environment with hands-on training. Employee discounts on skincare products.

Breathe Easier: Join Our Refractory or Unexplained Chronic Cough Clinical Trials! Are you or someone you care about struggling with a persistent cough? You may be eligible to participate in a clinical trial focused on Refractory or Unexplained Chronic Cough. We’re currently seeking volunteers to help evaluate a new investigational treatment designed to reduce chronic cough symptoms and improve quality of life. There is no cost for the study medication, and participants will be compensated for their time and travel. Call 626-822-6554 Now! Or Apply Here Why Participate? ● Compensation: Get compensated for up to $100/Visit! ● 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. ● Study medications: Study-related medication are given at no cost. To qualify: ● Must be 21 years of age or older ● No diagnosis of RCC=(insufficient improvement in cough after treatment for the underlying conditions(s) contributing to their cough)/UCC(=Unexplained cough for which an underlying condition has not been determined despite adequate investigation with diagnostic test and trials of therapy) ● Diagnosis of respiratory conditions other than RCC/UCC, such as Asthma, COPD, Idiopathic Pulmonary Fibrosis or Bronchiectasis ● Non smokers or vapers Check out our other studies! ●Foot Ulcers ●Vitligo ●Plaque Psoriasis ●Future Studies Pasadena Clinical Trials Your participation can help advance research and improve lives. If you're ready to take action, contact us at 626-822-6554 or visit Pasadena Clinical Trials website for more information. Get Involved Today!