R&D Pharmaceutical Formulation Scientist

Meds • Elmhurst, IL

1d • Onsite

About The Position

Meds.com is a rapidly growing consumer technology firm operating a suite of healthcare businesses, including our flagship brand BlueChew. Our mission is to better patients' lives through innovative healthcare solutions. With a team of 300 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. BlueChew is 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. You 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. Join our team in Elmhurst, IL - we're looking for someone who truly values and enjoys working in the lab, not just tolerates it.

Requirements

• Education: BS, MS, or PhD in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field.
• Experience: 3–6 years of experience in pharmaceutical formulation or compounding.
• Technical Knowledge: Deep understanding of excipient functionality, flavor chemistry, and the physical chemistry of solid dosage forms.
• Regulatory Familiarity: Knowledge of FDA regulations and USP compounding standards.
• The Startup Mindset: You are comfortable working in a fast-paced environment where priorities can shift, and you enjoy the "build" phase of a product.

Nice To Haves

• Specific experience with chewable tablets, gummies, or oral disintegrating tablets (ODTs) is a major plus.
• Experience in an R&D setting preferred.

Responsibilities

• Lead the end-to-end development of new products, focusing on active ingredient compatibility, texture, and flavor masking.
• Optimize and scale existing formulations to improve stability and patient experience.
• Develop compounding protocols and manufacturing processes that can transition seamlessly from the R&D lab to large-scale pharmacy production.
• Ensure all formulations meet USP <795> (non-sterile compounding) and USP <797> standards where applicable, maintaining meticulous documentation for quality assurance.
• Conduct and oversee stability testing, dissolution studies, and ingredient assays to ensure product integrity.
• Take ownership of projects from concept through pilot scale, ensuring smooth transfer to production and clear communication with cross-functional teams
• Utilize analytical tools (e.g. HPLC, dissolution testing) to generate meaningful insights that guide formulation decisions and scale-up readiness
• Work across multiple oral dosage forms – including chewables, gummies and ODT’s to improve taste, texture and patient experience
• Apply practical, hands-on problem solving to overcome formulation challenges, using data and experimentation rather than theoretical approaches
• Partner with raw material suppliers to source high-quality APIs and excipients, staying ahead of industry trends in pharmaceutical compounding.
• Ensure all formulations comply with regulatory standards and guidelines.
• Understand 21 CFR FDA drug compliance requirements
• Perform HPLC stability testing, dissolution testing, and other necessary tests to ensure the efficacy and safety of formulations.
• Create prototypes and samples for further testing and evaluation.
• Analyze data and interpret results to guide formulation development.
• Document all experiments and results accurately and comprehensively.
• Ensure all formulations meet internal quality standards.
• Implement and maintain quality control processes throughout the formulation development phase.
• Work collaboratively with cross-functional teams, including quality control, regulatory affairs, and production.
• Communicate project status, challenges, and results to stakeholders effectively.
• Stay updated with the latest advancements in pharmaceutical formulation and regulatory requirements.
• Manage multiple projects simultaneously, ensuring timelines and budgets are met.
• Identify potential risks and develop mitigation strategies.
• Prepare project reports and presentations for internal and external stakeholders.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level