Lead Quality Audits — Pharma Compliance & Supplier Risk

Dr. Reddy's Laboratories; Princeton (NJ); On-site; USD 90,000 - 130,000; Full time

Job summary

A leading pharmaceuticals company is seeking a seasoned Lead Associate for Quality Audits to ensure compliance with regulatory standards in Princeton, New Jersey. The role requires 8+ years of experience in auditing and a strong understanding of pharmaceuticals. You will conduct assessments, drive quality improvement initiatives, and support regulatory compliance oversight. This position demands an M.S. in a relevant field and excellent communication skills.

Qualifications

• 8+ years of progressive experience in auditing pharmaceutical or medical device systems.
• 2 years of internal and external audit management experience.
• Strong writing skills for creating technical documents such as SOPs and audit reports.

Responsibilities

• Conduct assessments on company sites and quality systems for compliance.
• Maintain Supplier management process using quantitative methods.
• Identify areas for process improvement and recommend corrective actions.

Skills

Understanding of pharmaceuticals

Auditing skills

Regulatory compliance knowledge

Excellent communication skills

Strong attention to detail

Education

M.S. in Chemistry, Biology or other life sciences

Auditing Certification

Job description

A leading pharmaceuticals company is seeking a seasoned Lead Associate for Quality Audits to ensure compliance with regulatory standards in Princeton, New Jersey. The role requires 8+ years of experience in auditing and a strong understanding of pharmaceuticals. You will conduct assessments, drive quality improvement initiatives, and support regulatory compliance oversight. This position demands an M.S. in a relevant field and excellent communication skills.