QA Associate (Temp) (Stanhope, NJ)

Are you suffering from Plaque Psoriasis and Overweight? Plaque psoriasis is a chronic autoimmune condition that causes raised, red, scaly patches on the skin, often appearing on the elbows, knees, scalp, and lower back. It occurs when the immune system speeds up the skin cell growth cycle, leading to a buildup of skin cells on the surface. This condition can be itchy, painful, and emotionally distressing. Obesity/Overweight is a medical condition characterized by excess body fat that may negatively impact health. It’s been found that people living with obesity are more likely to develop plaque psoriasis, and those with both conditions may experience more severe symptoms. Obesity can also affect how well treatments for psoriasis work. The connection between the two conditions is likely related to inflammation, as both psoriasis and obesity are associated with increased levels of systemic inflammation. Managing weight through healthy lifestyle choices may help improve psoriasis symptoms and overall quality of life. We are seeking volunteers for a clinical study evaluating the safety and effectiveness of a treatment for Plaque Psoriasis and Overweight. If you or someone you know may be interested, please contact us to learn more about eligibility and potential benefits. Call 818-350-7482 Now! Or Apply Here WHY PARTICIPATE? ●Compensation:Get compensated up to $100 per clinic visit 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 Plaque Psoriasis and Overweight are given at no cost. TO QUALIFY YOU MUST BE: ●Be 18 years of age or older. ●Diagnosed with Plaque Psoriasis and Overweight. Check out our other studies! ●Moderate to Severe Chronic Spontaneous Urticaria ●Type 2 Diabetes, Pre-Diabetes, or Metabolic Syndrome ●Moderate to Severe Psoriasis ●Prurigo Nodularis ●Hidradenitis Suppurativa ●Atopic Dermatitis (Eczema) ●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!

Are you suffering from Prurigo Nodularis? Are you or a loved one struggling with the discomfort of Prurigo Nodularis? We invite you to participate in a groundbreaking clinical trial for a new medication designed to alleviate the symptoms of this challenging condition. Medication comes at no cost to you or your insurance. You will be compensated for the time and travel spent on our study. ALSO, if you refer a friend that qualifies, you will earn a BONUS of $100 Call 818-350-7482 Now! Or Apply Here WHY PARTICIPATE? ●Compensation: Get compensated up to $1,300 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 Prurigo Nodularis are given at no cost. TO QUALIFY YOU MUST BE: ●Be 18 years of age or older ●Have been diagnosed with Prurigo Nodularis for at least 3 months. Check out our other studies! ●Moderate to Severe Plaque Psoriasis in Obese Patients ●Hidradenitis Suppurativa ●Acne Vaccine ●Type 2 Diabetes ●Atopic Dermatitis (Eczema) ●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.