QC Lab Analyst I - Raw Materials

LTS Lohmann Therapy • West Saint Paul, MN

3d • Onsite

About The Position

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. LTS is hiring a Quality Control (QC) Analyst -I to support routine testing of raw materials and in-process goods in a cGMP pharmaceutical manufacturing environment. In this role, you will perform analytical bench testing, document and review results against specifications, and help ensure production areas and equipment meet cleanliness and environmental monitoring requirements.

Requirements

• Bachelor’s degree in a relevant science field.
• At least 1–2 years of experience in a pharmaceutical manufacturing laboratory environment (or similar regulated lab environment).
• Ability to work independently, multi-task, and meet aggressive timelines.
• Knowledge of analytical techniques including HPLC/GC and FTIR.

Nice To Haves

• Experience using chromatographic software (Empower 3 strongly preferred).
• Working knowledge of cGMP, cGLP, USP, and pharmaceutical regulatory requirements.
• Experience with aseptic technique and TOC.
• Ability to think critically and troubleshoot typical analytical (HPLC) instrumentation issues.

Responsibilities

• Conduct routine quality control testing of in-process goods and raw materials in accordance with SOPs, master specifications, and cGMP regulations.
• Perform bench testing such as solution preparation, pH, FTIR, HPLC, and viscosity testing.
• Test excipients and production materials according to USP/Ph Eur/FCC monographs and in-house methods.
• Document and assess data against established specifications following cGMP and GDP expectations.
• Perform QC review of data records.
• Support production by performing routine environmental monitoring of cleanrooms and verifying equipment cleaning procedures.
• Maintain a high level of productivity, accuracy, and attention to detail; adjust priorities as needed.
• Support inventory and cleaning activities for the QC laboratory.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level