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Formulation Development information

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$13

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$39

How much do formulation development jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for formulation development in Ohio is $21.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.36 and $21.73 per hour, depending on experience, location, and employer.

What is formulation development?

Formulation development is the process of designing and optimizing the composition of a pharmaceutical product, such as a tablet, capsule, or injectable, to ensure its safety, efficacy, and stability. This involves selecting appropriate active ingredients, excipients, and delivery methods to achieve the desired therapeutic effect. Professionals in formulation development work to address challenges like solubility, bioavailability, and manufacturability, while ensuring compliance with regulatory standards. Their work is essential for turning a drug candidate into a viable, market-ready product.

What are the key skills and qualifications needed to thrive in formulation development?

To excel in Formulation Development, a solid background in chemistry, pharmaceutical sciences, or related fields, often with a relevant degree, is essential. Experience with analytical instruments, formulation software, and knowledge of Good Manufacturing Practices (GMP) or regulatory guidelines are typically required. Strong problem-solving abilities, attention to detail, and effective cross-functional communication set top performers apart. These skills ensure the creation of safe, effective, and compliant products that meet both scientific and regulatory standards.

What are some common challenges faced in a formulation development role, and how are they typically addressed?

Professionals in Formulation Development often encounter challenges such as ensuring product stability, achieving desired drug release profiles, and scaling up formulations from the laboratory to manufacturing. These challenges are typically addressed by conducting thorough pre-formulation studies, collaborating closely with analytical and process engineers, and performing iterative testing to optimize formulations. Teamwork and effective communication with quality assurance and regulatory teams are also crucial to ensure products meet both efficacy and compliance standards.

What is the difference between Formulation Development vs Formulation Scientist?

AspectFormulation DevelopmentFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fieldsBachelor's or Master's in Pharmacy, Chemistry, or related fields
Work EnvironmentResearch labs, pharmaceutical companies, R&D departmentsResearch labs, pharmaceutical companies, R&D departments
Industry UsageDesigning and optimizing drug formulations for productionDeveloping and testing drug formulations, conducting experiments

Formulation Development focuses on designing and optimizing drug formulations for manufacturing, while Formulation Scientists conduct experiments and testing to develop these formulations. Both roles require similar educational backgrounds and work environments, but their specific responsibilities differ in scope and focus.

What are popular job titles related to Formulation Development jobs in Ohio?

For Formulation Development jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Formulation Development jobs in Ohio look for?

The top searched job categories for Formulation Development jobs in Ohio are:

Formulation Development jobs near you
Infographic showing various Formulation Development job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $45,147 per year, or $21.7 per hour.

Sr. Scientist, Formulation Development

Hikma Pharmaceuticals PLC

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Hikma Pharmaceuticals rating

8.0

Company rating: 8.0 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical

Job description

Job Title: Sr. Scientist, Formulation Development
Location: Columbus, OH
Job Type: Full time
Req ID: 11881
About Us:
As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our 32 manufacturing plants, three R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.
Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Sr. Scientist, Formulation Development to join our team.
Hikma is expanding its orally inhaled and nasal drug product (OINDP) capability, and we're looking for a formulation scientist who wants to work on technically demanding, high-impact programs from early development through to regulatory submission and launch. This role sits within our growing OINDP formulation team and will be pitched at level depending on your experience. What matters most is depth of knowledge, scientific rigor, and the ability to work at pace across a commercially oriented pipeline.
Key Responsibilities:
  • Design and execute formulation development studies for OINDPs, applying QbD principles throughout
  • Lead or contribute to CMC sections of regulatory dossiers (ANDA, NDA, 505(b)(2) - formulation development reports, excipient justifications, comparability studies. Draft controlled correspondence and responses to project specific deficiency letters as needed.
  • Characterize formulations using methods relevant to OINDP: particle size, aerodynamic performance (NGI/ACI), spray geometry, viscosity, osmolality, and related physical chemistry
  • Support Bioequivalence strategy development, including, IVIVC, biowaiver arguments, and Q1/Q2/Q3 sameness justifications
  • Analyze and interpret experimental data using relevant tools (e.g. JMP, Minitab, Python, or Excel) to draw clear scientific conclusions, identify trends, and define the next cycle of formulation or process development with confidence
  • Collaborate with device/engineering teams on product-device compatibility and human factors considerations
  • Drive tech transfer and scale-up activities, including work with CDMOs
  • Author and review protocols, batch records, and CMC documentation to GMP/GLP standards. Manufacture developmental and clinical (pilot / registration) batches.

Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
  • Bachelor's Degree (Pharmaceutical Sciences, Chemistry, Chemical Engineering) plus a minimum 4 yrs experience with the following:
    • Hands-on OINDP formulation development experience or drug-device formulation is particularly valued. Experience in formulation development of pharmaceutical dosage forms is valued. OR
  • Master's degree (Pharmaceutical Sciences, Chemistry, Chemical Engineering) plus a minimum 2 years of experience with the following:
    • Hands-on OINDP formulation development experience or drug-device formulation is particularly valued. Experience in formulation development of pharmaceutical dosage forms is valued. OR
  • PhD (Pharmaceutical Sciences, Chemistry, Chemical Engineering) plus minimum 1 years of experience with the following:
    • Hands-on OINDP formulation development experience or drug-device formulation is particularly valued. Experience in formulation development of pharmaceutical dosage forms is valued.
  • Working knowledge of ICH guidelines and FDA/EMA expectations for OINDP
  • Experience in working to cGMP and compliance requirements is desirable but not essential.
  • Experience with excipient selection and justification (preservative systems, antioxidants, tonicity agents).
  • Ability to work effectively across formulation, analytical, clinical, QA, operations, IP, and regulatory functions.

Preferred Qualifications:
  • Experience with scale up in GMP environment
  • Experience with regulatory submissions (ANDA / NDA)
  • Knowledge (understanding and interpretation) of analytical characterization techniques
  • Experience with good documentation practices for GMP batches
  • Experience with use of statistical tools in data analysis
  • Knowledge of in-vitro in-vivo correlation

What We Offer*:
  • Annual performance bonus, commission, and share potential
  • Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
  • A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
  • 3 personal days (prorated based on hire date)
  • 11 company paid holidays
  • Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
  • Employee discount program
  • Wellbeing rewards program
  • Safety and Quality is a top organizational priority
  • Career advancement and growth opportunities
  • Tuition reimbursement
  • Paid maternity and parental leave

*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
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