Senior QC Chemistry Associate — Release & Stability Lead

Biogen; Milwaukee (WI); On-site; USD 69,000 - 90,000; Full time

Benefits offered by this job

Medical, Dental, Vision, & Life ins.

Fitness & Wellness programs

Disability insurance

Vacation and holidays

Stock purchase plan

Tuition reimbursement

Job summary

Biogen’s Quality Control team in Milwaukee, WI seeks a qualified Associate III to support QC Chemistry, ensure cGMP compliance, and drive timely release and stability testing. You will collaborate with supervisors, managers and peers to coordinate test results and support global QC initiatives.

The role emphasizes leadership in cross-functional teams, troubleshooting analytical methods, and maintaining data integrity while applying FDA/EMEA guidelines.

Qualifications

• Bachelor's or Associate degree (+2 years lab experience) in biological/chemistry/life sciences.
• HPLC experience.
• Knowledge of FDA/EMEA regulations and compliance.
• Demonstrated instrument/method troubleshooting skills.

Responsibilities

• Performs release and stability testing.
• Authors or reviews investigational protocols and validation documents.
• Supports transfer, method development, and validation projects with Analytical Technology/Development.
• Provides leadership through project management and laboratory investigations.
• Maintains data integrity and supports cross-functional site teams.
• Mentors peers and contributes to development of team members.

Skills

Analytical thinking

Problem solving

Communication

Leadership

Education

Bachelor's or Associate degree in life sciences

Tools

HPLC

LC-MS

Dissolution

Karl Fischer

GC

Job description

Biogen’s Quality Control team in Milwaukee, WI seeks a qualified Associate III to support QC Chemistry, ensure cGMP compliance, and drive timely release and stability testing. You will collaborate with supervisors, managers and peers to coordinate test results and support global QC initiatives.

The role emphasizes leadership in cross-functional teams, troubleshooting analytical methods, and maintaining data integrity while applying FDA/EMEA guidelines.