About LTS:

LTS Lohmann Therapy Systems is a premier, global Contract Development and Manufacturing Organization (CDMO) and partner the pharma industry trusts most to deliver innovative oral, transdermal, and intradermal drug delivery systems. From concept to market, launch to lifecycle management, we deliver single source oral and transdermal drug delivery solutions that power partners’ market advantage. Every one of our 1,000 plus members of the LTS family, across three continents, is focused on utilizing our collective strength and innovation to explore new therapeutic opportunities, maximize partner value and improve patient outcomes.

We Care.

We Create.

We Deliver.

Job Summary

As a Product Development (Formulation) Scientist , you will play a key role in the development of innovative oral, transdermal, and intradermal drug delivery systems, with an initial focus on sublingual/buccal films and transdermal patches. You will collaborate closely with senior scientists, project teams, and clients to bring novel therapies to market.

This is a full-time role located in West St. Paul, MN.

***Relocation assistance is not provided for this role.***

What You Will Do:

• Assist senior formulation scientist/R&D manager in development activities from pre-formulation to scale-up, including: Designing and executing experiments, analyzing and interpreting data & writing clear and concise technical reports
• Develop and implement robust analytical methods (HPLC, GC, FTIR, dissolution) to characterize formulations.
• Perform in vitro release testing, including skin permeation studies.
• Collaborate with R&D colleagues across departments (e.g., analytical, process development) to ensure successful project execution.
• Contribute to the development and implementation of new technologies and methodologies.
• Stay abreast of scientific advancements and industry best practices in drug delivery.
• Ensure compliance with all relevant regulations (cGMP, cGLP, USP, FDA).

Your Background:

• Bachelor's degree in a relevant scientific field (e.g., Chemistry, Pharmacy, Pharmaceutical Sciences)
• 1-3 years of experience in a cGMP or cGLP laboratory environment within the pharmaceutical industry (preferred)
• Strong understanding of analytical techniques, particularly HPLC
• Excellent written and verbal communication, presentation, and interpersonal skills
• Proven ability to work independently, prioritize tasks, and meet deadlines
• Strong problem-solving and analytical skills

Preferred Qualifications

• 2-3 years of experience in the development of pharmaceutical dosage forms, with a focus on transdermal and thin oral films
• Experience with polymeric drug delivery systems
• Knowledge of statistical data analysis and QbD principles
• Experience with analytical method development and validation

We Offer

• Competitive compensation and benefits package
• Opportunities for professional growth and development
• A collaborative and supportive work environment
• The chance to contribute to improving patient lives

If this sounds like you, we want to hear from you!

LTS is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.