R&D Formulation Associate

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. This is an on-site role in Sugar Land, Texas working Monday - Friday 8:00 AM - 5:00 PM. What the R&D Formulation Associate Does Each Day: Executes compounding activities within the clinical development lab Follows detailed formulations and batch records in processing formulations Sterilize solutions via filtration Assists with sample maintenance and sample collections for development studies Assists in formulation development studies Assists in stability studies Helps testing samples if needed Assists in maintaining lab equipment and keeping lab in good order Ensures all proper policies and procedures/work instructions are followed correctly within new product development Ensures all duties and processes are in adherence with ISO standards, USP, and current good compounding practices Performs change control processes and assist with managing timelines Practices and monitors good documentation practices, including keeping detailed lab notebook Our Most Successful R&D Formulation Associate has: Good coordinating abilities, attention to detail with positive communication skills Excellent organizational skills with ability to manage multiple projects Proficiency in Microsoft Excel and Outlook Minimum Requirements for this Role: Bachelors of Science Degree in Chemistry, Biology, Chemical Engineering or equivalent is required At least 2 years' experience with formulation mixing/processing and aseptic processes in pharmaceutical environment 18+ years of age Able to successfully complete a drug and background check Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Any of the Following Will Give You an Edge: Experience working with controlled substances Experience working with sterile injectable Benefits of Working at Quva: Set, full-time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 17 paid days off plus 8 paid holidays per year Occasional weekend and overtime opportunities with advance notice National, industry-leading high growth company with future career advancement opportunities About Quva: Quva 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. Quva 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.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.