Quality Assurance Associate - GxP Auditor (Hybrid)

Discovery Life Sciences; Newtown (PA); Hybrid; USD 45,000 - 60,000; Full time

Benefits offered by this job

Dental and Vision package

Life Insurance

Disability Coverage

401(k) Match

Generous Vacation & PTO

Parental Leave

Tuition Reimbursement

Professional Development

Team-Building/Social Events

Employee Referral Program

Colleague Recognition Program

Job summary

Discovery Life Sciences is seeking a Quality Assurance Associate to join the Global Quality & Regulatory team at the Newtown, PA location. This role ensures the integrity, accuracy, and compliance of laboratory and quality system documentation across Specialty Lab Services, applying ALCOA+ data integrity, GDP, and risk-based quality methodologies.

The QA Associate will review globally scientific, technical, and quality records, provide audit support locally and externally, and collaborate with

Qualifications

• Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, Life Sciences, or related scientific discipline.
• 0 to 2 years of experience in Quality Assurance or regulated environments.
• Internship, co-op, undergraduate research, or laboratory experience in a regulated setting.
• Experience supporting audits, document control, or quality systems is a plus.
• Excellent Microsoft Office skills (Word, Excel, PowerPoint, OneNote).
• Basic understanding of GxP, GDP, and ALCOA+ data integrity principles.
• PMP certification or ASQ certifications.
• Strong attention to detail with ability to review technical and scientific documentation.

Responsibilities

• Review GxP-regulated documents for compliance, accuracy, completeness, and quality.
• Support audit readiness and track CAPAs.
• Assist with pre-audit preparation and audit requests.
• Coordinate with global teams to support quality system effectiveness.
• Develop and maintain controlled documents and procedures.

Job description

Discovery Life Sciences is seeking a Quality Assurance Associate to join the Global Quality & Regulatory team at the Newtown, PA location. This role ensures the integrity, accuracy, and compliance of laboratory and quality system documentation across Specialty Lab Services, applying ALCOA+ data integrity, GDP, and risk-based quality methodologies.

The QA Associate will review globally scientific, technical, and quality records, provide audit support locally and externally, and collaborate with