{"schemaVersion":"jobsearcher.job.v1","id":"4a9658097119c8c1f2af0b3f","url":"https://jobsearcher.com/jobs/4a9658097119c8c1f2af0b3f","canonicalUrl":"https://jobsearcher.com/jobs/4a9658097119c8c1f2af0b3f","title":"R&D Formulation Associate","description":"The R&D Formulation Associate is responsible for supporting the formulation of new products and any new formulations for existing products because of continuous process improvement. The associate will assist in compounding, calibration, lab maintenance, drug filtration, labeling, monitoring/organizing samples for testing, The Formulation Associate will report to the Senior Formulation Scientist. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement.\n\nThis is an on-site role in Sugar Land, Texas working Monday - Friday 8:00 AM - 5:00 PM.\n\nWhat the R&D Formulation Associate Does Each Day:\n\nExecutes compounding activities within the clinical development lab\nFollows detailed formulations and batch records in processing formulations\nSterilize solutions via filtration\nAssists with sample maintenance and sample collections for development studies\nAssists in formulation development studies\nAssists in stability studies\nHelps testing samples if needed\nAssists in maintaining lab equipment and keeping lab in good order\nEnsures all proper policies and procedures/work instructions are followed correctly within new product development\nEnsures all duties and processes are in adherence with ISO standards, USP, and current good compounding practices\nPerforms change control processes and assist with managing timelines\nPractices and monitors good documentation practices, including keeping detailed lab notebook\nOur Most Successful R&D Formulation Associate has: Good coordinating abilities, attention to detail with positive communication skills\nExcellent organizational skills with ability to manage multiple projects\nProficiency in Microsoft Excel and Outlook\nMinimum Requirements for this Role: Bachelors of Science Degree in Chemistry, Biology, Chemical Engineering or equivalent is required\nAt least 2 years' experience with formulation mixing/processing and aseptic processes in pharmaceutical environment\n18+ years of age\nAble to successfully complete a drug and background check\nMust be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas\nAny of the Following Will Give You an Edge: Experience working with controlled substances\nExperience working with sterile injectable\nBenefits of Working at Quva: Set, full-time, consistent work schedule\nComprehensive health and wellness benefits including medical, dental and vision\n401k retirement program with company match\n17 paid days off plus 8 paid holidays per year\nOccasional weekend and overtime opportunities with advance notice\nNational, industry-leading high growth company with future career advancement opportunities\n\nAbout Quva:\n\nQuva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.\n\nQuva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”\n\nCalifornia Consumer Privacy Act (CCPA) Notice for Applicants and Employees\n\nEqual Opportunity Employer\n\nThis employer is required to notify all applicants of their rights pursuant to federal employment laws.\nFor further information, please review the Know Your Rights notice from the Department of Labor.","company":"Quva Pharma","rawCompany":"quva pharma","city":"Houston","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-06-28T03:29:35.555Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"29-2052.00","title":"Pharmacy Technicians","slug":"pharmacy-technicians"},{"code":"29-1051.00","title":"Pharmacists","slug":"pharmacists"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"456110","title":"Pharmacies and Drug Retailers","slug":"pharmacies-and-drug-retailers"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"R&D Formulation Associate","description":"The R&D Formulation Associate is responsible for supporting the formulation of new products and any new formulations for existing products because of continuous process improvement. The associate will assist in compounding, calibration, lab maintenance, drug filtration, labeling, monitoring/organizing samples for testing, The Formulation Associate will report to the Senior Formulation Scientist. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement.\n\nThis is an on-site role in Sugar Land, Texas working Monday - Friday 8:00 AM - 5:00 PM.\n\nWhat the R&D Formulation Associate Does Each Day:\n\nExecutes compounding activities within the clinical development lab\nFollows detailed formulations and batch records in processing formulations\nSterilize solutions via filtration\nAssists with sample maintenance and sample collections for development studies\nAssists in formulation development studies\nAssists in stability studies\nHelps testing samples if needed\nAssists in maintaining lab equipment and keeping lab in good order\nEnsures all proper policies and procedures/work instructions are followed correctly within new product development\nEnsures all duties and processes are in adherence with ISO standards, USP, and current good compounding practices\nPerforms change control processes and assist with managing timelines\nPractices and monitors good documentation practices, including keeping detailed lab notebook\nOur Most Successful R&D Formulation Associate has: Good coordinating abilities, attention to detail with positive communication skills\nExcellent organizational skills with ability to manage multiple projects\nProficiency in Microsoft Excel and Outlook\nMinimum Requirements for this Role: Bachelors of Science Degree in Chemistry, Biology, Chemical Engineering or equivalent is required\nAt least 2 years' experience with formulation mixing/processing and aseptic processes in pharmaceutical environment\n18+ years of age\nAble to successfully complete a drug and background check\nMust be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas\nAny of the Following Will Give You an Edge: Experience working with controlled substances\nExperience working with sterile injectable\nBenefits of Working at Quva: Set, full-time, consistent work schedule\nComprehensive health and wellness benefits including medical, dental and vision\n401k retirement program with company match\n17 paid days off plus 8 paid holidays per year\nOccasional weekend and overtime opportunities with advance notice\nNational, industry-leading high growth company with future career advancement opportunities\n\nAbout Quva:\n\nQuva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.\n\nQuva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”\n\nCalifornia Consumer Privacy Act (CCPA) Notice for Applicants and Employees\n\nEqual Opportunity Employer\n\nThis employer is required to notify all applicants of their rights pursuant to federal employment laws.\nFor further information, please review the Know Your Rights notice from the Department of Labor.","datePosted":"2026-06-28T03:29:35.555Z","dateModified":"2026-06-28T03:29:35.555Z","hiringOrganization":{"@type":"Organization","name":"Quva Pharma","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Houston","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"4a9658097119c8c1f2af0b3f"},"url":"https://jobsearcher.com/jobs/4a9658097119c8c1f2af0b3f"}}