Pharma QC Analyst: Dissolution & Analytics

Bora Pharmaceuticals; Maple Grove (MN); On-site; USD 52,000 - 65,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Professional development opportunities

Retirement plan

Job summary

Bora Pharmaceuticals in Minnesota is hiring a QC Analyst to provide analytical and technical support for testing raw materials, in-process materials, stability samples, and drug products. You will perform dissolution and related testing with attention to accuracy and compliance with cGMPs.

You'll document results in electronic systems, maintain lab safety, operate HPLC/UV/FTIR instruments, and collaborate with a team to meet testing timelines and quality standards.

Qualifications

• Bachelor's degree in chemistry or related science field or high school diploma with 4 years of laboratory experience in pharma preferred.
• Experience working in a laboratory environment is preferred, preferably in the pharmaceutical industry.

Responsibilities

• Performs testing on raw materials, in-process materials, finished products, and stability samples to support department testing timelines.
• Performs dissolution testing, including system setup, sample introduction, analysis, and cleanup.
• Maintains electronic laboratory notebook documentation and ensures timely corrections.
• Operates and maintains basic lab equipment and instrumentation (e.g., dissolution, UV) with supervision.
• Communicates atypical and out-of-specification results to management.
• Ensures a clean, safe, and compliant laboratory environment.

Skills

Documentation accuracy

Team collaboration

Analytical thinking

Education

Bachelor's degree in chemistry or related science field

High school diploma + 4 years lab experience

Tools

HPLC

UV

FTIR

Microsoft Word

Microsoft Excel

Job description

Bora Pharmaceuticals in Minnesota is hiring a QC Analyst to provide analytical and technical support for testing raw materials, in-process materials, stability samples, and drug products. You will perform dissolution and related testing with attention to accuracy and compliance with cGMPs.

You'll document results in electronic systems, maintain lab safety, operate HPLC/UV/FTIR instruments, and collaborate with a team to meet testing timelines and quality standards.