{"id":1693572,"url":"https://alion.io/job/meds-rd-pharmaceutical-formulation-scientist","title":"R&D Pharmaceutical Formulation Scientist","company":{"id":678593,"name":"Meds","domain":"meds.com","url":"https://alion.io/company/meds-2","size_band":"201-500","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Lever","truth_index":{"grade":"B","score":79,"open_postings":7,"ghost_share":0,"stale_share":0.857,"repost_share":0,"time_to_fill_p50_days":33,"computed_at":"2026-10-23T05:54:15Z"}},"role":"Biotech","role_family":"Biotech","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Elmhurst, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":69000,"max_usd":142000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":638},"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"HPLC","optional":false}],"status":"live","first_seen_at":"2026-10-01T23:17:33Z","employer_posted_date":"2026-10-01","last_verified_at":"2026-10-23T19:59:12Z","board_verified":true,"closed_at":null,"days_open":21,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":21},"description":"Overview\nMeds.com is a rapidly growing consumer technology firm operating a suite of healthcare businesses, including our flagship brands BlueChew and MOD. Our mission is to better patients' lives through innovative healthcare solutions. With a team of over 500 professionals across various specialties, we've built scalable pharmacy, telemedicine, and e-commerce platforms using cutting-edge technology. As we continue our accelerated growth trajectory, we're launching new products to expand our patient base and accelerate growth. Join us in tackling exciting challenges at the intersection of healthcare and technology.\nWe're looking for a hands-on R&D Formulation Scientist to drive the next generation of products. Based out of our state-of-the-art laboratory located within our company-owned pharmacy in Elmhurst, IL, you will be the bridge between initial concept and commercial scalability.\nYou won't just be tweaking existing formulas; you will be experimenting with novel delivery systems, improving taste profiles, and ensuring the stability and efficacy of medications that reach hundreds of thousands of users.\nJoin our team in Elmhurst, IL - we'relooking for someone who truly values and enjoys working in the lab, not just tolerates it.\nResponsibilities:\nFormulation Development: Lead the end-to-end development of new products, focusing on active ingredient compatibility, texture, and flavor masking.\n\nPortfolio Support: Optimize and scale existing formulations to improve stability and patient experience.\n\nBench-to-Pilot Scaling: Develop compounding protocols and manufacturing processes that can transition seamlessly from the R&D lab to large-scale pharmacy production.\n\nRegulatory Compliance: Ensure all formulations meet USP (non-sterile compounding) and USP standards where applicable, maintaining meticulous documentation for quality assurance.\n\nAnalytical Testing: Conduct and oversee stability testing, dissolution studies, and ingredient assays to ensure product integrity.\n\nTake ownership of projects from concept through pilot scale, ensuring smooth transfer to production and clear communication with cross-functional teams\n\nUtilize analytical tools (e.g. HPLC, dissolution testing) to generate meaningful insights that guide formulation decisions and scale-up readiness\n\nWork across multiple oral dosage forms - including chewables, gummies and ODT’s to improve taste, texture and patient experience\n\nApply practical, hands-on problem solving to overcome formulation challenges, using data and experimentation rather than theoretical approaches\n\nVendor Collaboration: Partner with raw material suppliers to source high-quality APIs and excipients, staying ahead of industry trends in pharmaceutical compounding.\n\nRegulatory Compliance:\nEnsure all formulations comply with regulatory standards and guidelines.\n\nUnderstand 21 CFR FDA drug compliance requirements\n\nTesting and Analysis:\nPerform HPLC stability testing, dissolution testing, and other necessary tests to ensure the efficacy and safety of formulations.\n\nCreate prototypes and samples for further testing and evaluation.\n\nAnalyze data and interpret results to guide formulation development.\n\nDocument all experiments and results accurately and comprehensively.\n\nQuality Control and Assurance:\nEnsure all formulations meet internal quality standards.\n\nImplement and maintain quality control processes throughout the formulation development phase.\n\nCollaboration and Communication:\nWork collaboratively with cross-functional teams, including quality control, regulatory affairs, and production.\n\nCommunicate project status, challenges, and results to stakeholders effectively.\n\nStay updated with the latest advancements in pharmaceutical formulation and regulatory requirements.\n\nProject Management:\nManage multiple projects simultaneously, ensuring timelines and budgets are met.\nIdentify potential risks and develop mitigation strategies.\n\nPrepare project reports and presentations for internal and external stakeholders.\n\nQualifications\nEducation: BS, MS, or PhD in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field.\n\nExperience: 3-6 years of experience in pharmaceutical formulation or compounding (R&D setting preferred).\n\nChewable Expertise: Specific experience with chewable tablets, gummies, or oral disintegrating tablets (ODTs) is a major plus.\n\nTechnical Knowledge: Deep understanding of excipient functionality, flavor chemistry, and the physical chemistry of solid dosage forms.\n\nRegulatory Familiarity: Knowledge of FDA regulations and USP compounding standards.\n\nThe Startup Mindset: You are comfortable working in a fast-paced environment where priorities can shift, and you enjoy the \"build\" phase of a product.\n\nExperience writing scientific protocols, study plans, and technical reports to support research, development, and regulatory activities.\n\nWork Environment\nLaboratory and office settings.\n\nMay require handling of hazardous materials and adherence to safety protocols.\n\nCollaboration with team members and departments to achieve project goals.\n\nPerks\n100% company-paid Medical, Dental, and Vision premium coverage for employees, plus.\n\nShort-Term Disability and Life Insurance\n\n401(k) with company match\n\nComplimentary daily lunch provided on-site","description_format":"text","description_chars":5293,"description_truncated":false,"requirements":{"experience_years_min":3,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":["Life 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