Sr. Director, Quality Compliance & Regulatory Strategy

Kelly Services; Greenville (SC); On-site; USD 180,000 - 220,000; Full time

Benefits offered by this job

Retirement savings plan

Paid holidays

Transit benefit

Medical benefits

Job summary

Kelly Services seeks a Sr. Director of Quality Compliance (DEA) in Greenville, SC to lead enterprise-wide compliance strategy, governance, audit readiness, and quality risk management.

This onsite leadership role oversees QMS, supplier quality, and inspection readiness, partnering with Manufacturing, Regulatory, and Executive teams to sustain cGMP and DEA compliance. Ideal candidates bring 15+ years in pharmaceutical quality with FDA interactions, and a track record of driving CAPAs and

Qualifications

• Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or related science.
• 15+ years of progressive pharmaceutical quality experience in GMP environments.
• Senior leadership in Quality/Regulatory Compliance with FDA interactions.

Responsibilities

• Develop and implement enterprise quality compliance strategies and policies.
• Lead inspection readiness and manage regulatory inspections.
• Oversee QMS processes including change control, deviations, CAPAs, and document management.
• Drive quality metrics, CAPAs, and risk management across functions.
• Lead cross-functional Quality Compliance teams and report to senior leadership.

Skills

Leadership

Regulatory Affairs

Quality Systems

Audit Readiness

Cross-functional Collaboration

Strategic Thinking

Education

Bachelor's degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or related science

Job description

Kelly Services seeks a Sr. Director of Quality Compliance (DEA) in Greenville, SC to lead enterprise-wide compliance strategy, governance, audit readiness, and quality risk management.

This onsite leadership role oversees QMS, supplier quality, and inspection readiness, partnering with Manufacturing, Regulatory, and Executive teams to sustain cGMP and DEA compliance. Ideal candidates bring 15+ years in pharmaceutical quality with FDA interactions, and a track record of driving CAPAs and