QA Leader — Regulated Pharma (On-Site Pomona)

Bimeda; Pomona (CA); On-site; USD 120,000 - 150,000; Full time

Benefits offered by this job

Health Insurance (medical, dental, or/

401(k) plan for retirement savings

Paid time off (vacation, sick leave, &

Life insurance

Employee assistance program

Job summary

Bimeda in Pomona, CA is seeking a QA Manager to lead quality systems and ensure regulatory readiness across cGMP, QSR, and GDP. The role supervises QA Associates and works with multiple departments to resolve quality events and drive continuous improvement.

You will manage investigations into non-conformances, coordinate internal and external audits, and prepare for Health Authority inspections while maintaining product delivery timelines and KPIs.

Qualifications

• 5–7 years in a regulated pharmaceutical environment.
• Minimum 2–3 years in a leadership role.
• Bachelor degree in a scientific discipline.
• Strong knowledge of cGMP, QA, regulatory affairs.
• Proven leadership and communication across all levels.
• Ability to manage competing priorities in a fast-paced environment.

Responsibilities

• Lead quality systems and compliance activities for product delivery.
• Oversee investigations, audits, and CAPA programs.
• Ensure product release adheres to regulatory standards.
• Manage QA team and coordinate cross-functional quality initiatives.
• Liaise with Health Authorities and customers on quality matters.
• Monitor KPIs and foster continuous improvement.
• Prepare and respond to inspections and audits.
• Provide direction and development for direct reports.

Skills

Quality leadership

Regulatory compliance

CAPA management

Audits & inspections

Investigations root cause

Education

BSc in life sciences

MS degree preferred

Tools

GxP systems

Documentation control

Job description

Bimeda in Pomona, CA is seeking a QA Manager to lead quality systems and ensure regulatory readiness across cGMP, QSR, and GDP. The role supervises QA Associates and works with multiple departments to resolve quality events and drive continuous improvement.

You will manage investigations into non-conformances, coordinate internal and external audits, and prepare for Health Authority inspections while maintaining product delivery timelines and KPIs.