Senior Quality Assurance Leader - GLP/GCP

Evotec WD; Princeton (NJ); Hybrid; USD 76,000 - 127,000; Full time

Benefits offered by this job

Discretionary annual bonus

Medical, Dental & Vision benefits

Short-term & Long-term disability

Company-paid basic life insurance

401k company match

Paid time off & paid holidays

Wellness and transportation benefits

Job summary

Evotec seeks a Senior Quality Management Specialist at the Princeton site to lead quality oversight across discovery activities and ensure GRP, GLP, and GCP compliance. You will drive documentation control, internal audits, and CAPA programs, fostering a culture of quality and continuous improvement within a fast-moving research environment.

You will collaborate with global QA colleagues and site stakeholders to harmonize quality practices, report quality metrics, and support regulatory

Qualifications

• Minimum 3 years of work experience in a Pharmaceutical, Biotechnology or CRO environment.
• Good understanding of GLP and GCP (applied to bioanalytical activities).
• Strong written and verbal communication and teamwork skills.

Responsibilities

• Oversee and maintain GRP across research functions (Protein Sciences, Chemistry, Sample Management, ADME).
• Support GLP and GCP frameworks for bioanalytical activities and provide quality oversight.
• Interpret regulatory requirements and ensure proper implementation across R&D activities.

Skills

Interpersonal skills

Attention to detail

Communication skills

Networking skills

Autonomy

Problem-solving

Education

Master’s degree in Quality Management or Life Sciences

Job description

Evotec seeks a Senior Quality Management Specialist at the Princeton site to lead quality oversight across discovery activities and ensure GRP, GLP, and GCP compliance. You will drive documentation control, internal audits, and CAPA programs, fostering a culture of quality and continuous improvement within a fast-moving research environment.

You will collaborate with global QA colleagues and site stakeholders to harmonize quality practices, report quality metrics, and support regulatory