Senior Formulation Scientist (Oral Solids)

EPM Scientific; Houston (TX); On-site; USD 100,000 - 135,000; Full time

Benefits offered by this job

Medical coverage

Dental and vision coverage

Paid time off

401(k) matching

Wellness programs

Job summary

A leading pharmaceutical company in Houston is seeking a Senior Scientist in Formulation Development to advance solid oral drug products. The role involves designing formulations, conducting experiments, and collaborating cross-functionally to enhance product quality. A Ph.D. or Master's degree and 5-7 years of relevant experience are required, along with strong communication skills. This position offers a comprehensive benefits package.

Qualifications

• 5-7 years of experience in pharmaceutical formulation development with a focus on solid oral dosage forms.
• Experience in product development and scale-up, including regulatory filings.
• Strong communication and documentation skills.

Responsibilities

• Design and develop robust non-sterile formulations for small molecule drug products.
• Execute formulation experiments and analyze data.
• Collaborate with cross-functional teams and support technology transfer activities.

Skills

Pharmaceutical formulation development

Cross-functional collaboration

Data analysis

Experiment design

Regulatory compliance

Education

Ph.D. or Master's degree in Pharmaceutical Sciences, Chemistry, or related field

Job description

Overview

This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$100,000.00/yr - $135,000.00/yr

Join a mission-driven, people-first pharmaceutical company as a Senior Scientist in Formulation Development, where you'll play a pivotal role in advancing solid oral drug products from concept to commercialization. This position offers the opportunity to lead technical efforts in formulation design, collaborate cross-functionally, and contribute to the development of high-quality, affordable medications that improve patient lives.

Key Responsibilities

• Design and develop robust non-sterile formulations (e.g., tablets, capsules) for small molecule drug products, ensuring scalability and regulatory compliance.
• Execute formulation experiments, analyze data, and optimize processes to support preclinical through commercial development stages.
• Collaborate with cross-functional teams including Analytical, Regulatory, Quality, and Manufacturing to ensure seamless project execution.
• Support technology transfer activities to internal and external manufacturing sites, including drafting protocols and overseeing scale-up batches.
• Contribute to regulatory submissions (e.g., ANDA, NDA, 505(b)(2)) by preparing technical documentation and responding to agency queries.
• Apply advanced formulation techniques and scientific principles to solve complex development challenges.
• Stay current with industry trends and emerging technologies to enhance formulation strategies and product performance.

Qualifications

• Ph.D. or Master\'s degree in Pharmaceutical Sciences, Chemistry, or related field.
• Minimum of 5-7 years of experience in pharmaceutical formulation development, with a strong focus on solid oral dosage forms.
• Demonstrated experience in product development and scale-up, including support for regulatory filings and product launches.
• Proficiency in experimental design, data analysis, and process optimization.
• Familiarity with cGMP, ICH guidelines, and FDA regulatory expectations.
• Strong communication and documentation skills; ability to work independently and collaboratively in a fast-paced environment.

Benefits

Enjoy a comprehensive benefits package that supports your health and well-being, including medical, dental, and vision coverage, paid time off, 401(k) matching, wellness programs, and more.