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Solid Oral Drug Product Formulation Jobs (NOW HIRING)

Servier

Assoc Director, Oral Solid Drug Product

Boston, KY · On-site

$198K - $207K/yr

Role Summary Within MSAT, the Oral Solid Drug Product team is responsible for providing technical ... In-depth knowledge of formulation concepts/techniques across immediate-release and extended-release ...

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How much do solid oral drug product formulation jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for solid oral drug product formulation in the United States is $50.89, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $81.49 per hour, depending on experience, location, and employer.

What is solid oral drug product formulation?

Solid oral drug product formulation involves designing and developing medications in solid forms such as tablets, capsules, or powders that are intended to be taken by mouth. This process includes selecting the appropriate active pharmaceutical ingredients (APIs), excipients, and creating a formulation that ensures stability, efficacy, and patient acceptability. Formulation scientists work to optimize the drug’s bioavailability, manufacturability, and shelf-life while complying with regulatory requirements.

What are some common challenges faced when developing solid oral drug product formulations, and how can they be addressed?

One common challenge in solid oral drug product formulation is ensuring the drug's stability and bioavailability, as active pharmaceutical ingredients (APIs) can sometimes be poorly soluble or degrade during processing. Formulators must carefully select excipients and optimize processing parameters to achieve the desired tablet or capsule characteristics. Collaboration with analytical chemists and process engineers is essential to troubleshoot issues like tablet hardness, dissolution rates, or uniformity. Continuous learning and problem-solving are key, as each formulation may present unique hurdles based on the properties of the API and the intended release profile.

What are the key skills and qualifications needed to thrive as a solid oral drug product formulation scientist, and why are they important?

To thrive as a Solid Oral Drug Product Formulation Scientist, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree. Familiarity with analytical instruments (HPLC, DSC), formulation software, and knowledge of regulatory guidelines (FDA, ICH) are essential, along with experience in Good Manufacturing Practice (GMP) environments. Strong problem-solving, attention to detail, and the ability to work collaboratively with cross-functional teams set outstanding candidates apart. These skills ensure the development of safe, effective, and stable oral drug products that meet regulatory standards and patient needs.

What is the difference between Solid Oral Drug Product Formulation vs Pharmaceutical Scientist?

AspectSolid Oral Drug Product FormulationPharmaceutical Scientist
CredentialsBachelor's or Master's in Pharmacy, Pharmaceutical Sciences, or related fieldsBachelor's, Master's, or PhD in Chemistry, Pharmaceutical Sciences, or related disciplines
Work EnvironmentLaboratories, manufacturing facilities, R&D departmentsResearch labs, development centers, academia, industry
Industry UsageDesigning and developing solid oral dosage forms like tablets and capsulesResearching, developing, and testing new drugs and formulations
Search & Comparison IntentUnderstanding roles in drug formulation and developmentResearching drug development processes and scientific roles

Solid Oral Drug Product Formulation specialists focus on creating and optimizing oral dosage forms, while Pharmaceutical Scientists conduct broader research and development activities across various drug types. Both roles require strong scientific credentials and work in similar environments, but their specific focus areas differ within the pharmaceutical industry.

What other helpful pages are available for Solid Oral Drug Product Formulation?

Other pages related to Solid Oral Drug Product Formulation:

Infographic showing various Solid Oral Drug Product Formulation job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 78% Full Time, 18% Part Time, 2% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $105,849 per year, or $50.9 per hour.

Sr. Principal Scientist, Oral Drug Product Development

Cambridge, MA • On-site

Biogen
Scientific Research and Development Services • 5 - 10K employees
Learn more about Biogenexternal

$188K - $259K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted just now

Biogen rating

9.3

Company rating: 9.3 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

Job description

About This Role
Biogen is seeking a Sr. Principal Scientist, Oral Drug Product Developmentto provide scientific and strategic leadership for the development of small molecule oral drug products. This role leads scientific and engineering efforts supporting formulation and process development across early- and late-stage programs. This technical lead will drive enabling technologies for typically low solubility and low permeability compounds, clinical manufacturing readiness, technology transfer, and commercialization. The Sr. Principal Scientistserves as a senior drug product leader and mentor on cross-functional CMC and asset teams, influencing development strategy, manufacturing readiness, and regulatory submissions. This role will also be responsible for managing external partnerships and advancing new technologies and workflows that strengthen Biogen's oral drug product development capabilities.
What You'll Do
  • Lead formulation design, process development, manufacturability assessment, scale-up, technology transfer, and clinical manufacturing of small molecule oral dosage forms across all stages of development.

  • Develop enabling formulation approaches for challenging compounds, including poorly soluble, poorly permeable, unstable, or complex molecules such as orally delivered peptides.

  • Serve as the senior drug product representative on cross-functional CMC and asset teams, driving alignment across regulatory, quality, manufacturing, analytical, clinical pharmacology, DMPK, and external partner functions.

  • Influence portfolio decisions through assessment of developability, manufacturability, biopharmaceutical performance, technical risk, and investment priorities.

  • Champion technology transfer, clinical manufacturing readiness, and scale-up activities at internal and external manufacturing sites. Provide strategic oversight and establish manufacturing strategies.

  • Mentor and develop scientists and engineers supporting oral drug product development.

  • Oversee completion of drug product sections for regulatory submissions and related technical documentation.

  • Identify and implement new formulation technologies, predictive tools, digital workflows, and best practices that improve development efficiency and portfolio execution.

Who You Are
You are an innovative scientific leader with a passion for advancing drug development processes through rigorous science and data-driven decision-making. You excel at transforming experimental findings into development strategies, using deep technical expertise and sound scientific judgment to solve complex drug product challenges. Your expertise drives you to develop cutting-edge solutions ensuring manufacturability, scalability, and readiness for commercialization. You thrive in collaborative environments, influencing strategic decisions, and fostering alignment across diverse functions. Your mentoring skills inspire teams to achieve excellence, while your forward-thinking approach maximizes Biogen's capabilities in oral drug product development.
Required Skills:
  • PhD in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related scientific discipline with a minimum of 12 years' experience in oral drug product development.

  • Demonstrated track record leading formulation and process development for oral solid dosage forms from early development through clinical manufacturing and/or late-stage development.

  • Experience with scale-up, technology transfer, clinical manufacturing, and external manufacturing organizations.

  • Strong knowledge of CMC development, regulatory expectations, technical documentation, and phase-appropriate development strategies.

  • Proven ability to lead across functions, influence program strategy, manage technical risk, and communicate effectively with diverse stakeholders.

  • Experience mentoring, developing, or leading scientists and engineers.

Preferred Skills:
  • Deep expertise in enabling technologies such as amorphous solid dispersions, spray drying, hot-melt extrusion, lipid-based formulations, modified release, or particle engineering.
  • Experience with late-stage development, commercial readiness, process characterization, or process validation.
  • Experience supporting at least one NDA/MAA or commercial product and regulatory agency interaction experience.
  • Strong understanding and hands on experience with oral solid dose manufacturing unit operations and manufacturability considerations.
  • Experience implementing new technologies, digital tools, knowledge platforms, or best practices across multiple programs.
  • Demonstrated success managing external CDMO/CMO relationships and technology transfer activities.

Job Level: Management
Additional Information
The base compensation range for this role is: $188,000.00-$259,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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About Biogen

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At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.

Industry

Scientific research and development services

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

1978

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