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Semi Solid Formulation Scientist Jobs (NOW HIRING)

LGM Pharma, LLC

FORMULATION SCIENTIST

Rosenberg, TX · On-site

$87K - $105K/yr

Lead formulation development, optimization, and scale-up activities for semi-solid and liquid ... Design, execute, analyze, and document formulation and process development studies using scientific ...

TechData Service Company LLC

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Formulation Scientist

Alameda, CA · On-site

$40 - $60/hr

The applicant also must possess a solid track record of working in a high potency lab, deep ... Design formulation development studies including lab scale and scale-up manufacturing processes for ...

Viatris

Lead Formulation Scientist

Morgantown, WV

Demonstrates comprehensive understanding of solid oral dosage form development, process ... Ability to solve problems with a variety of concrete variables through semi-standardized solutions ...

Viatris

Lead Formulation Scientist

Morgantown, WV · On-site

Demonstrates comprehensive understanding of solid oral dosage form development, process ... Ability to solve problems with a variety of concrete variables through semi-standardized solutions ...

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How much do semi solid formulation scientist jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for semi solid formulation scientist in the United States is $37.61, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $43.51 per hour, depending on experience, location, and employer.

What are some common challenges faced by Semi Solid Formulation Scientists when developing new topical products?

Semi Solid Formulation Scientists often encounter challenges related to achieving the desired texture, stability, and efficacy of topical products such as creams, gels, and ointments. Balancing the formulation to ensure proper drug release, patient acceptability, and shelf-life stability can be complex due to interactions among active ingredients and excipients. Additionally, scaling up formulations from laboratory to production scale while maintaining consistency and regulatory compliance requires careful planning and collaboration with manufacturing and quality teams.

What jobs can I do with pharmaceutical science?

A Semi Solid Formulation Scientist can pursue roles such as formulation scientist, research and development scientist, quality control analyst, or manufacturing specialist in the pharmaceutical industry. These positions involve developing, testing, and improving drug formulations, often requiring knowledge of chemistry, stability testing, and regulatory standards. Skills in laboratory techniques and familiarity with Good Manufacturing Practices (GMP) are essential for these roles.

What are the key skills and qualifications needed to thrive as a Semi Solid Formulation Scientist, and why are they important?

To thrive as a Semi Solid Formulation Scientist, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree and experience in formulation development. Familiarity with analytical instruments, formulation software, and Good Manufacturing Practice (GMP) guidelines is crucial. Excellent problem-solving abilities, attention to detail, and effective teamwork and communication skills help distinguish top performers in this role. These competencies ensure the safe, effective, and scalable development of semi-solid pharmaceutical products, meeting regulatory and market demands.

What are Semi Solid Formulation Scientists?

Semi Solid Formulation Scientists are specialized professionals who develop, optimize, and test pharmaceutical products in semi-solid forms, such as creams, ointments, gels, and lotions. They work primarily in the pharmaceutical, cosmetic, or biotechnology industries to ensure these products are safe, effective, and stable. Their role includes researching ingredients, conducting laboratory experiments, and adhering to regulatory guidelines. They also collaborate with other scientists and departments to scale up production and troubleshoot formulation challenges.
FORMULATION SCIENTIST

FORMULATION SCIENTIST

LGM Pharma, LLC

Rosenberg, TX • On-site

$87K - $105K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 25 days ago

Job description

RESPONSIBILITIES:

  • Lead formulation development, optimization, and scale-up activities for semi-solid and liquid pharmaceutical dosage forms, including: (Rectal and vaginal suppositories/pessaries, Creams, gels, ointments, lotions, and topical foams, and Oral and topical liquid formulations)
  • Evaluate and optimize critical process parameters (CPPs) and critical material attributes (CMAs) to ensure robust product performance, manufacturability, scalability, and stability.
  • Design, execute, analyze, and document formulation and process development studies using scientific and risk-based approaches.
  • Apply Quality by Design (QbD) and Design of Experiments (DoE) principles during product and process development activities.
  • Support technology transfer, engineering batches, exhibit/registration batches, pilot-scale activities, and GMP manufacturing operations.
  • Generate and review technical documentation, including: (Experimental protocols, technical reports, Development summaries, Master Batch Records (MBRs), Formula cards, Scale-up and stability documentation)
  • Perform hands-on laboratory and pilot-scale formulation activities (approximately 50–70% bench/lab work depending on project needs).
  • Conduct physical characterization and evaluation of formulations and intermediates, including: (Viscosity/rheology, Appearance and physical stability, Hardness/penetration testing, Melting behavior, Homogeneity and content uniformity, Dispersion/suspension characteristics)
  • Operate and troubleshoot formulation and characterization equipment, including: (Viscometers, Rheometers, Penetrometers, Homogenizers, Suppository testing equipment, and Vertical Franz diffusion cells (IVRT/IVPT))
  • Collaborate cross-functionally with Analytical Sciences, Quality Assurance, Manufacturing, Regulatory Affairs, Purchasing, and Project Management teams to ensure successful project execution.
  • Assist in raw material selection, qualification, and procurement activities.
  • Support evaluation, selection, and implementation of new laboratory and manufacturing equipment.
  • Participate in manufacturing investigations, troubleshooting activities, process improvements, deviations, and CAPA-related support as needed.
  • Ensure all activities are conducted in compliance with: (Current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Data integrity requirements, and Internal quality systems and safety procedures)
  • Effectively manage multiple projects and priorities within aggressive timelines while maintaining high technical quality and attention to detail.
  • Perform other related duties as assigned.

QUALIFICATIONS:

Education & Experience:

    • M.S. in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related scientific discipline required; Ph.D. preferred.
    • Minimum 5 years of pharmaceutical industry experience in formulation development, scale-up, and manufacturing support of drug products; equivalent combination of education and experience may be considered.
    • Strong hands-on experience with semi-solid and liquid dosage forms is required, preferably including suppositories/pessaries and topical dosage forms.
    • Experience supporting process scale-up, technology transfer, engineering batches, and GMP manufacturing activities.
    • Strong understanding of pharmaceutical formulation principles, excipient functionality, and process development.
    • Working knowledge of: (QbD concepts, Design of Experiments (DoE), Pharmaceutical development best practices, and cGMP and GDP requirements)
    • Experience with formulation characterization techniques and laboratory instrumentation commonly used in semi-solid and liquid product development.
    • Ability to independently organize, prioritize, and manage multiple concurrent projects with minimal supervision.
    • Excellent technical writing, verbal communication, and problem-solving skills.
    • Strong attention to detail and commitment to scientific rigor and compliance.
    • Proficiency in Microsoft Office Suite.
    • Flexibility to support evolving project timelines and occasional extended working hours as required.

Physical Requirements:

  • Able to regularly lift up to 25 pounds and navigate active construction or facility expansion sites as needed.


At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.