Lead Toxicology Sample Extraction

LabRulez; South Brunswick (NJ); Ibrido; USD 70.000 - 100.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical insurance

Dental coverage

Vision coverage

401(k) with company match

Paid vacation and holidays

Descrizione del lavoro

Eurofins Scientific is seeking a Sample Extraction Manager for Medical Device studies in South Brunswick, NJ. You will oversee extraction activities for toxicology studies, supervise staff, and ensure studies follow GLP, SOPs, and safety guidelines.

The role requires coordinating study workflows, translating client requirements into detailed prep instructions, and maintaining accurate documentation to support regulatory submissions. Excellent leadership and communication are essential.

Competenze

• Bachelor’s degree in toxicology, biology, chemistry, pharmaceutical sciences, or related field preferred.
• Significant supervisory experience in a regulated lab environment.
• Experience overseeing test article extractions and sample prep.
• Strong organizational and documentation skills.

Mansioni

• Supervise Sample Preparation Scientists and other extraction staff.
• Coordinate staffing to meet study schedules and priorities.
• Develop clear extraction instructions and worksheets for each prep.
• Ensure adherence to GLP, SOPs, and safety procedures.
• Review calculations, preparation records, and supporting documentation.
• Assist in deviations investigations and CAPA activities.
• Provide hands-on support for extractions when needed.

Conoscenze

Leadership

Communication

GLP knowledge

Quality control

Formazione

Bachelor's degree in toxicology/biology/pharmaceutical sciences

Descrizione del lavoro

Eurofins Scientific is seeking a Sample Extraction Manager for Medical Device studies in South Brunswick, NJ. You will oversee extraction activities for toxicology studies, supervise staff, and ensure studies follow GLP, SOPs, and safety guidelines.

The role requires coordinating study workflows, translating client requirements into detailed prep instructions, and maintaining accurate documentation to support regulatory submissions. Excellent leadership and communication are essential.