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Executive Pharmaceutical Formulation Development Jobs

FORMULATION SCIENTIST

Rosenberg, TX · On-site

$87.50K - $105K/yr

Lead formulation development, optimization, and scale-up activities for semi-solid and liquid pharmaceutical dosage forms, including: (Rectal and vaginal suppositories/pessaries, Creams, gels ...

Collaborate effectively within Pharmaceutical Development and cross-functional project teams ... formulation development. * Experience or exposure to Process Analytical Technology (PAT), and/or ...

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Executive Pharmaceutical Formulation Development information

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$35K

$93.2K

$197.5K

How much do executive pharmaceutical formulation development jobs pay per year?

As of May 31, 2026, the average yearly pay for executive pharmaceutical formulation development in the United States is $93,160.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,000.00 and $100,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Executive in Pharmaceutical Formulation Development, and why are they important?

To thrive as an Executive in Pharmaceutical Formulation Development, you need a strong background in pharmaceutical sciences, drug development processes, and regulatory guidelines, usually supported by an advanced degree in pharmacy, chemistry, or a related field. Familiarity with laboratory instrumentation, formulation technologies, quality management systems, and cGMP compliance is essential, along with certifications such as Six Sigma or Lean Manufacturing being advantageous. Leadership, problem-solving, and effective communication are critical soft skills for driving innovation, managing cross-functional teams, and ensuring project success. These skills and qualifications ensure that new pharmaceutical products are developed efficiently, meet regulatory standards, and address market needs.

What are some common challenges faced in Executive Pharmaceutical Formulation Development roles, and how are they typically addressed?

Professionals in Executive Pharmaceutical Formulation Development often encounter challenges such as ensuring batch-to-batch consistency, addressing stability issues, and meeting stringent regulatory requirements. These challenges are typically managed through robust analytical testing, cross-functional collaboration with quality assurance, and continuous process optimization. The role also demands staying updated with the latest regulatory guidelines and leveraging teamwork to troubleshoot and resolve formulation setbacks efficiently. Regular communication with R&D, manufacturing, and regulatory teams is essential for timely project delivery and compliance.

What are Executive Pharmaceutical Formulation Development professionals?

Executive Pharmaceutical Formulation Development professionals are responsible for overseeing and coordinating the design, development, and optimization of pharmaceutical formulations. They lead teams in creating safe and effective dosage forms, such as tablets, capsules, or injectables, ensuring compliance with regulatory standards. Their work involves collaborating with research, analytical, and manufacturing teams to bring new drug products from concept to market. Additionally, they troubleshoot formulation issues, manage timelines, and contribute to documentation required for regulatory submissions.

What is the difference between Executive Pharmaceutical Formulation Development vs Pharmaceutical Formulation Scientist?

AspectExecutive Pharmaceutical Formulation DevelopmentPharmaceutical Formulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related field; experience in formulation developmentBachelor's or Master's in Pharmacy, Chemistry, or related field; entry to mid-level experience
Work EnvironmentSenior role in R&D departments, overseeing projects, strategic planningHands-on laboratory work, experimental formulation testing
Employer & Industry UsagePharmaceutical companies, biotech firms, contract research organizationsResearch labs, pharmaceutical companies, academia

In summary, Executive Pharmaceutical Formulation Development roles focus on strategic oversight and project management in formulation development, often requiring leadership experience. In contrast, Pharmaceutical Formulation Scientists are primarily involved in experimental work and formulation testing. Both roles are essential in drug development but differ in responsibilities and seniority.

More about Executive Pharmaceutical Formulation Development jobs
What cities are hiring for Executive Pharmaceutical Formulation Development jobs? Cities with the most Executive Pharmaceutical Formulation Development job openings:
What are the most commonly searched types of Pharmaceutical Formulation Development jobs? The most popular types of Pharmaceutical Formulation Development jobs are:
What states have the most Executive Pharmaceutical Formulation Development jobs? States with the most job openings for Executive Pharmaceutical Formulation Development jobs include:
Infographic showing various Executive Pharmaceutical Formulation Development job openings in the United States as of May 2026, with employment types broken down into 91% Full Time, 2% Part Time, 4% Temporary, 1% Contract, and 2% Nights. Highlights an 66% Physical, 7% Hybrid, and 27% Remote job distribution, with an average salary of $93,160 per year, or $44.8 per hour.

R&D Pharmaceutical Formulation Scientist

Meds

Elmhurst, IL

Full-time

Posted 8 days ago


Job description

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. 

What You'll Do
  • Formulation Development: Lead the end-to-end development of new products, focusing on active ingredient compatibility, texture, and flavor masking. 

  • Portfolio Support: Optimize and scale existing formulations to improve stability and patient experience. 

  • Bench-to-Pilot Scaling: Develop compounding protocols and manufacturing processes that can transition seamlessly from the R&D lab to large-scale pharmacy production. 

  • Regulatory Compliance: Ensure all formulations meet USP <795> (non-sterile compounding) and USP <797> standards where applicable, maintaining meticulous documentation for quality assurance. 

  • Analytical Testing: 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 

  • Vendor Collaboration: Partner with raw material suppliers to source high-quality APIs and excipients, staying ahead of industry trends in pharmaceutical compounding. 

Regulatory Compliance:  

  • Ensure all formulations comply with regulatory standards and guidelines.  

  • Understand 21 CFR FDA drug compliance requirements  

Testing and Analysis:  

  • 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.  

Quality Control and Assurance:  

  • Ensure all formulations meet internal quality standards.  

  • Implement and maintain quality control processes throughout the formulation development phase.   

Collaboration and Communication:  

  • 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.  

Project Management:  

  • 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.  

Qualifications 

  • 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 (R&D setting preferred). 

  • Chewable Expertise: Specific experience with chewable tablets, gummies, or oral disintegrating tablets (ODTs) is a major plus. 

  • 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. 

Work Environment 

  • Laboratory and office settings.  

  • May require handling of hazardous materials and adherence to safety protocols.  

  • Collaboration with team members and departments to achieve project goals. 

We are looking for top talent that wants to make a measurable impact in an exciting, fast-paced environment in our Elmhurst, IL Lab (fully onsite). 
 
 
 
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