QC Lab Analyst II - Pharmaceutical Manufacturing

About LTS:

LTS Lohmann Therapy Systems is a global leader in transdermal and oral thin‑film drug delivery technologies. Our teams have pioneered breakthroughs such as the first contraceptive patch, nicotine patch, oral active ingredient film, and Parkinson’s patch. When you join LTS, you become part of a team that continues to shape the future of patient care and bring life‑changing therapies to market.

At LTS, our purpose drives everything we do: We CARE. We CREATE. We DELIVER. We’re committed to fostering an employee experience that reflects our innovation — supportive, collaborative, and empowering. Across our New Jersey and Minnesota locations, you’ll work alongside knowledgeable experts on diverse projects in an environment where every day is different and your contributions truly matter

Quality Control Lab Analyst- Pharmaceutical Manufacturing

Position Overview

Lohman Therapy Systems North America is seeking a highly motivated and detail-oriented Quality Control Lab Analyst to join our growing team. In this role, you will play a critical part in ensuring the quality and safety of our pharmaceutical products by conducting routine analytical testing on in-process and finished goods. You will work independently and as part of a team to maintain high levels of accuracy and efficiency in the laboratory.

• This is a full-time, onsite role located in West St. Paul, MN.
• Working hours are 8:00a – 5:00pm

What You Will Do:

• Conduct routine quality control analysis of in-process and finished goods, including: 
• Bench work such as solution preparation, pH, water content, HPLC, dissolution, and transdermal physical testing.
• Stability testing according to established protocols.
• Environmental monitoring of production clean rooms.
• Equipment cleaning verification.
• Perform QC review of data records. 
• Draft stability program protocols and reports. 
• Maintain a clean and organized laboratory environment. 
• Ensure compliance with all relevant regulations (cGMP, cGLP, USP). 
• Identify and execute continuous improvement opportunities within the laboratory. 
• Troubleshoot analytical instrumentation problems (HPLC).

Your Background:

• Bachelor's degree in Chemistry, Biology, or a related scientific field.
• Minimum 2-4 years of experience in a pharmaceutical manufacturing laboratory environment.
• Strong knowledge of analytical techniques, including pH, water content, and HPLC.
• Experience using chromatographic software (Empower 3 preferred).
• Excellent attention to detail and accuracy.
• Ability to work independently and as part of a team.
• Strong organizational and time-management skills.
• Excellent documentation and record-keeping skills.

Preferred Qualifications

• Experience with aseptic technique and TOC.
• Experience with dissolution and GC.
• Ability to think critically and troubleshoot typical analytical (HPLC) instrumentation problems.

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.