QC Chemist

Location: Olmsted County, MN

We are proud to partner with a leading CDMO specializing in pharmaceutical development and manufacturing to hire a QC Chemist. In this important role, you will join a skilled team dedicated to supporting drug development from early research through commercial production—helping to accelerate the path to market with accuracy and compliance.

Key Responsibilities

• Design and refine small-scale synthetic processes, methodologies, and formulations for labeled products, including small molecules, peptides, and antibodies.
• Conduct regular analytical testing of labeled products utilizing techniques like TLC, HPLC, and spectroscopy.
• Collaborate with development teams to generate and maintain Chemistry, Manufacturing, and Controls documentation for client projects.
• Provide subject matter expertise to production teams regarding synthetic processes and troubleshooting.
• Accurately document laboratory experiments, author standard operating procedures, and prepare technical reports.
• Support investigations into deviations occurring during product development or manufacturing activities.
  
  

Qualifications & Experience

• Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline.
• At least 3 years of hands-on experience in analytical testing, method development, or product labeling within pharmaceutical or biotech environments.
• Familiarity with analytical techniques including TLC, HPLC, and spectroscopy; experience with complex labeling or conjugation is advantageous.
• Strong organizational and analytical skills, with the ability to interpret and present data effectively.
• Ability to prioritize tasks, manage multiple assignments, and anticipate potential issues.
• Excellent communication and teamwork skills, with the capacity to collaborate across departments.
• Self-motivated with the ability to work independently and meet project deadlines.
• Flexibility to work extended hours or occasional weekends as needed.
• #INDBH