Senior Quality Management Specialist — Growth & Impact

Evotec SE; Princeton (NJ); On-site; USD 94,000 - 127,000; Full time

Benefits offered by this job

Competitive salary

Bonus potential

Comprehensive benefits

Job summary

Evotec seeks a Senior Quality Management Specialist to drive quality systems at a site in Princeton, NJ. You will oversee GRP, GLP, and GCP, maintain documentation, and support audits and regulatory inspections while guiding CAPAs and investigations.

The role emphasizes a strong quality culture, cross-functional collaboration, and training to ensure data integrity and risk-based quality practices across discovery functions.

Qualifications

• Master’s degree in Quality Management or Life Sciences is required.
• At least 3 years’ experience in Pharmaceutical/Biotech/CRO environments.
• Strong knowledge of GLP and GCP in bioanalytical contexts (biomarkers, LC-MS).
• Excellent written and verbal communication; proactive and detail‑oriented.
• Ability to work autonomously in a matrix, fast-moving setting.

Responsibilities

• Oversee and maintain GRP, GLP, GCP frameworks across discovery functions.
• Manage documentation systems, policies, and records per company requirements.
• Plan, coordinate, and perform internal audits and sponsor inspections.
• Lead CAPA tracking, investigations, and root cause analyses.
• Foster quality culture and provide training on data integrity and risk-based quality.

Skills

GLP/GCP knowledge

Quality management

Regulatory compliance

Education

Master's degree in Quality Management or Life Sciences

Job description

Evotec seeks a Senior Quality Management Specialist to drive quality systems at a site in Princeton, NJ. You will oversee GRP, GLP, and GCP, maintain documentation, and support audits and regulatory inspections while guiding CAPAs and investigations.

The role emphasizes a strong quality culture, cross-functional collaboration, and training to ensure data integrity and risk-based quality practices across discovery functions.