Pharma QC Lab Analyst II — HPLC & Stability

LTS Lohmann Therapie-Systeme AG; West Saint Paul (MN); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive compensation

Professional growth opportunities

Collaborative work environment

Impact on patient lives

Job summary

LTS Lohmann Therapy Systems is seeking a Quality Control Lab Analyst in West St. Paul, MN.

The role focuses on routine QC testing of in-process and finished goods, using pH, water content, HPLC, and dissolution techniques in a fast-paced pharmaceutical manufacturing environment. The successful candidate will perform stability testing, environmental monitoring, data review, and documentation with strict adherence to cGMP, cGLP, and USP standards.

Qualifications

• Bachelor's degree in Chemistry, Biology, or a related field.
• 2–4 years in a pharmaceutical manufacturing lab environment.
• Experience with analytical techniques (pH, water content, HPLC).
• Familiarity with chromatographic software (Empower 3 preferred).
• Strong attention to detail and accuracy.

Responsibilities

• Conduct routine quality control analysis of in-process and finished goods.
• Bench work including solution prep, pH, water content, HPLC, dissolution, and transdermal testing.
• Perform stability testing per established protocols.
• Environmental monitoring of production clean rooms.
• Equipment cleaning verification.
• QC data records review.
• Draft stability program protocols and reports.
• Maintain a clean and organized lab environment.
• Ensure compliance with cGMP, cGLP, and USP.
• Identify and implement continuous improvement opportunities.
• Troubleshoot analytical instrumentation problems (HPLC).

Skills

Analytical techniques

HPLC

pH measurement

Water content analysis

Attention to detail

Independence

Teamwork

Documentation

Time management

Education

Bachelor's degree in Chemistry or Biology

Tools

Empower 3

Job description

LTS Lohmann Therapy Systems is seeking a Quality Control Lab Analyst in West St. Paul, MN.

The role focuses on routine QC testing of in-process and finished goods, using pH, water content, HPLC, and dissolution techniques in a fast-paced pharmaceutical manufacturing environment. The successful candidate will perform stability testing, environmental monitoring, data review, and documentation with strict adherence to cGMP, cGLP, and USP standards.