# Sr. Associate III, Compliance - QRM Lead

Hiring organization: [Biogen](https://career.thegoodapps.co/organizations/biogen)

Canonical page: https://career.thegoodapps.co/jobs/6bc37260-a90f-43f7-bf85-ed71efb18638

Listed on Biogen's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Senior
- Location: Research Triangle Park, NC
- Salary: 111000 – 149000 USD per year

## Summary

This role leads quality risk management and compliance operations at a pharmaceutical manufacturing site, ensuring regulatory readiness and driving continuous improvement across quality systems. It suits experienced quality assurance professionals with pharmaceutical expertise who want to take on operational leadership in a regulated manufacturing environment.

_Our summary, not Biogen's wording._

## Skills named

Change Control, Data Analysis, Quality Management Systems, Risk Management

## Required

- Bachelor's degree in scientific, technical, or relevant discipline
- Minimum 6 years of Quality Assurance experience in pharmaceutical, biotech, or manufacturing
- Strong knowledge of cGMP regulations and global regulatory standards
- Experience with quality systems including risk management, change control, deviation management, and inspection readiness
- Ability to analyze complex data and make decisions under pressure
- Excellent communication, organizational, and stakeholder management skills

## Nice to have

- Master's degree (MBA, MS, or similar) with relevant experience
- Experience leading site-wide or global quality risk management programs
- Strong background supporting regulatory inspections and audit responses
- Demonstrated ability to influence cross-functional teams and drive cultural change
- Advanced knowledge of quality metrics and data-driven decision making

Apply on Biogen's site: https://biibhr.wd3.myworkdayjobs.com/en-US/external/job/Research-Triangle-Park-NC/Sr-Associate-III--Compliance_REQ23507