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Senior Director, Quality
Atlanta, GA, US
Scientific
Bachelors Degree
Full Time, Direct Hire
Manager (Manager/Supervisor)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Atlanta, GA, US
Manager (Manager/Supervisor)
Full Time, Direct Hire
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Senior Director, Quality
Metro Atlanta, GA, Fully onsite, Monday-Friday 8am-5pm
Salary Range: $180,000-$245,000/year
Relocation Assistance provided and bonus potential
About the Role
A leading biopharmaceutical organization is seeking a proven Senior Director of Quality to lead and evolve a high-performing, multi-site Quality function. With an FDA-approved commercial product and a growing clinical pipeline, this company is at the forefront of personalized medicine. This role offers the opportunity to drive strategic initiatives, shape enterprise-wide quality systems, and directly impact the delivery of life-changing therapies to patients.
What You’ll Do
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Lead and align Quality operations across manufacturing and R&D sites, ensuring compliance with cGMP and global regulatory standards
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Develop and execute corporate quality strategy in close collaboration with cross-functional leaders across Manufacturing, Regulatory, Clinical, and Commercial teams
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Oversee Quality Assurance, Quality Control, Quality Systems, Validation, Compliance, and Training functions
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Serve as the primary Quality lead during regulatory inspections and third-party audits
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Manage CMO relationships to ensure alignment with internal quality standards
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Drive continuous improvement, quality risk management, and inspection readiness initiatives
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Lead Quality Management Reviews, track quality KPIs, and support organizational growth through proactive quality leadership
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Develop, mentor, and inspire a team of 100+ professionals to foster a culture of accountability and operational excellence
What You Bring
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Bachelor’s degree in a scientific or technical discipline required; advanced degree (MS, PhD, or MBA) preferred
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15+ years of QA/QC experience in the biopharma or biologics industry
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10+ years in leadership roles within regulated cGMP environments, ideally overseeing multiple locations
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Deep understanding of FDA, EMA, and ICH regulatory expectations
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Demonstrated success navigating audits and building robust enterprise-level quality systems
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Strong communication, leadership, and strategic thinking skills
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Experience with cell therapy, personalized medicine, or immunotherapies is a strong plus
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Willingness to travel up to 40% as needed
Work Environment
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Combination of office, cleanroom, and lab settings
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Must be able to occasionally gown for cleanroom entry and lift up to 25 lbs
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May involve handling of biologics with appropriate PPE provided
This is a high-impact leadership opportunity for a quality-focused professional looking to contribute to a rapidly growing organization committed to patient-centered innovation. If you are passionate about elevating standards and driving meaningful outcomes in the biopharmaceutical space, we encourage you to apply.
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