Senior QA Lead, cGMP Compliance & Audits

Siegfried USA, LLC; Pennsville Township (NJ); On-site; USD 82,000 - 110,000; Full time

Job summary

Siegfried USA, LLC is hiring for a Quality Assurance role located in Pennsville Township, New Jersey. This position ensures compliance with regulatory standards and leads internal audits while maintaining quality management systems.

The ideal candidate should have a BA/BS in a relevant field and between 3-5 years of quality assurance experience in pharmaceutical manufacturing. The salary range for this position is between $82,000 and $110,000.

Qualifications

• 3-5 years of experience in QA in a pharmaceutical manufacturing environment required.
• Thorough knowledge of cGMP in active pharmaceutical ingredient (API) manufacturing is preferable.

Responsibilities

• Reviews, approves, and tracks executed production records.
• Reviews and approves production and QC investigations.
• Conducts, writes, and reviews quality related investigations as appropriate.
• Responsible for cGMP compliance of assigned manufacturing operations.
• Hosts customer and internal audits, as needed.
• Participates in inspections by regulatory authorities.

Skills

Excellent communication skills

Conscientious and detail oriented

Excellent computer skills (MS Office 365)

Team player

Self-manage daily work and set priorities

Manage projects and prioritize appropriately

Adhere to deadlines

Education

BA/BS degree in microbiology, biology, chemistry, or engineering

Job description

Siegfried USA, LLC is hiring for a Quality Assurance role located in Pennsville Township, New Jersey. This position ensures compliance with regulatory standards and leads internal audits while maintaining quality management systems.

The ideal candidate should have a BA/BS in a relevant field and between 3-5 years of quality assurance experience in pharmaceutical manufacturing. The salary range for this position is between $82,000 and $110,000.