R&D Chemist I

R D Chemist I LTS Lohmann Therapy - 3.5 West Saint Paul, MN Job Details Full-time $32.00 - $34.50 an hour 1 day ago Qualifications Revenue growth Research design Dissolution testing Stability testing Gas chromatography Empower (software) GLP Technical documentation Pharmaceutical regulatory compliance High-performance liquid chromatographs Laboratory experiments GMP Mid-level Technical report writing Key Performance Indicators Statistical analysis Polymer chemistry Product development projects Bachelor's degree Data management Scientific protocols Pharmaceutical analysis Laboratory compliance management Experimental design 1 year Research & development Communication skills Regulatory compliance management FDA regulations

Full Job Description About LTS:

LTS Lohmann 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 2,000 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 an R D Chemist at LTS Lohmann, you will play a crucial role in supporting product development and ensuring analytical compliance within our cGMP/cGLP laboratory environment. This is a full time, role located in West St. Paul, MN.

What You Will Do:

Conduct analytical testing and analysis to support product development and revenue growth. Ensure adherence to QbD standards and regulatory requirements. Provide analytical support for key performance indicators (KPIs) and scale-up activities. Develop, optimize, and scale up analytical methods for various dosage forms. Create and review technical documentation, including analytical method development reports and standard operating procedures. Perform bench work, such as HPLC, GC, and dissolution.

Your Background:

Bachelor's degree in a relevant science field with 1-3 years of experience. Experience in a cGMP or cGLP laboratory environment. Knowledge of analytical techniques, including HPLC (GC, dissolution & stability testing experience preferred). Proficiency in chromatographic software (Empower 3 strongly preferred). Excellent analytical, technical writing, communication, and data management skills. Ability to design and execute experimental studies, analyze data, and author/review protocols and reports. Strong problem-solving and troubleshooting skills for analytical instrumentation. Understanding of cGMP, cGLP, USP, and regulatory requirements for pharmaceuticals. Highly motivated and self-driven individual with the ability to work independently and multi-task.

Preferred Skills:

2-3 years' experience in the FDA drug/pharmaceutical industry Demonstrated in-depth scientific knowledge & experience in analytical method development, & validation Experience in the development of pharmaceutical dosage forms and polymeric drug delivery systems with emphasis in transdermals. Experience in statistical data analysis and QbD principles An understanding of polymer science, analytical development, drug and formulation characterization, optimization and scale-up 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.