Sr. Associate II, Compliance

Biogen; Milwaukee (WI); On-site; USD 93,000 - 121,000; Full time

Benefits offered by this job

Medical, Dental, Vision, & Life insurances

401(k) with company matched contributions

Tuition reimbursement up to $10,000 per year

Paid Maternity and Parental Leave

Job summary

Biogen is seeking a Sr. Associate II, Compliance in Milwaukee, Wisconsin, to lead compliance and inspection management at the RTP Drug Substance Manufacturing site. The role involves ensuring inspection readiness and driving continuous improvement across quality systems while collaborating with site leadership and global teams.

The ideal candidate will have a Bachelor’s degree in a relevant field and at least 5 years of experience in Quality Assurance, specifically within a highly regulated environment. Benefits include comprehensive health coverage and 401(k) with company contributions.

Qualifications

• Minimum 5 years of Quality Assurance experience in pharmaceutical or biotech.
• Strong knowledge of cGMP regulations and global regulatory standards.
• Ability to manage multiple priorities and make decisions under pressure.

Responsibilities

• Lead site compliance and inspection management activities.
• Ensure the site remains inspection-ready at all times.
• Drive continuous improvement initiatives across quality systems.

Skills

Quality Assurance

Regulatory knowledge (FDA, EMA)

Data analysis

Risk management

Communication

Organizational skills

Problem-solving

Inspection management

Education

Bachelor’s degree in scientific or technical discipline

Tools

Veeva

TrackWise

Power BI

Job description

About This Role

The Sr. Associate II, Compliance plays a critical leadership role in ensuring the RTP Drug Substance Manufacturing site maintains a strong state of compliance and inspection readiness. This position partners closely with Site Leadership and Quality teams to oversee inspection management, data integrity, and quality systems, while driving continuous improvement across local and global processes. This role is instrumental in ensuring adherence to regulatory requirements and strengthening a culture of quality and compliance across the organization.

What You’ll Do

• Lead site compliance and inspection management activities, including planning, execution, and regulatory response coordination


• Ensure the site remains inspection-ready at all times for domestic and international regulatory agencies


• Provide compliance oversight across data integrity, risk management, and quality systems


• Prepare and facilitate site governance meetings and deliver quality metrics using tools such as Veeva, TrackWise, and Power BI


• Drive quality management review processes and lead quality metric governance to support data-driven decision making


• Partner with global quality forums to ensure alignment with the global Quality Management System (QMS)


• Lead and support process and product risk assessments, ensuring timely completion and effectiveness


• Identify and proactively resolve compliance gaps and technical issues


• Champion continuous improvement initiatives across quality systems and processes


• Serve as a key Quality representative on cross-functional teams and site leadership initiatives

Who You Are

You are a proactive and detail-oriented quality professional with a strong foundation in compliance and regulatory expectations. You bring a continuous improvement mindset and thrive in fast-paced, highly regulated environments where collaboration and data-driven decisions are essential.

Required Skills

• Bachelor’s degree in scientific, technical, or relevant discipline


• At minimum 5 years of Quality Assurance experience in pharmaceutical, biotech, or manufacturing environments


• Strong knowledge of cGMP regulations and global regulatory standards (FDA, EMA, etc.)


• Experience with inspection management, compliance oversight, and quality systems


• Demonstrated ability to analyze data, manage risk, and support regulatory interactions


• Excellent communication, organizational, and problem-solving skills


• Ability to manage multiple priorities and make decisions under pressure

Preferred Skills

• Prior experience in Compliance-focused Quality roles


• Experience with quality systems such as Veeva, TrackWise, and Power BI


• Strong knowledge of data integrity principles and regulatory expectations


• Experience supporting global quality initiatives and cross-functional teams


• Proven ability to drive continuous improvement and influence stakeholders

Job Level: Professional

The base compensation range for this role is $93,000.00-$121,000.00.

Benefits

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:

• Medical, Dental, Vision, & Life insurances


• Fitness & Wellness programs including a fitness reimbursement


• Short- and Long-Term Disability insurance


• A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)


• Up to 12 company paid holidays + 3 paid days off for Personal Significance


• 80 hours of sick time per calendar year


• Paid Maternity and Parental Leave benefit


• 401(k) program participation with company matched contributions


• Employee stock purchase plan


• Tuition reimbursement of up to $10,000 per calendar year


• Employee Resource Groups participation

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.