Entry-Level Associate Scientist - GMP Lab Analytics

Eurofins; Lancaster (Lancaster County); Presencial; USD 45.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical, dental, vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Descripción de la vacante

Eurofins USA BioPharma Services in Lancaster, PA is seeking an entry-level analytical chemist to perform analyses of APIs and finished pharmaceutical products using various instruments. You will set up and validate analytical methods, prepare samples, and document work for GMP compliance.

Position is full-time, Monday–Friday, with overtime as needed. The role emphasizes learning new techniques, working independently as well as in a team, and contributing to a safety-conscious laboratory

Formación

• Bachelor's degree in chemistry or related field, or equivalent directly-related experience.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsabilidades

• Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products.
• Run the instrumentation independently including various chromatographic systems.
• Prepare samples for analysis and run instrumentation with minimum supervision.
• Set up and validate new analytical or related processes used by the department.
• Prepare standards and samples for analysis.
• Execute method transfer protocols.
• Document work as required for GMP compliance.
• Perform monthly maintenance of laboratory equipment.

Conocimientos

Strong computer skills

Excellent communication

Attention to detail

Independent & team player

Learn new techniques

Educación

Bachelor's degree in chemistry

Herramientas

Chromatography instruments

Descripción del empleo

Eurofins USA BioPharma Services in Lancaster, PA is seeking an entry-level analytical chemist to perform analyses of APIs and finished pharmaceutical products using various instruments. You will set up and validate analytical methods, prepare samples, and document work for GMP compliance.

Position is full-time, Monday–Friday, with overtime as needed. The role emphasizes learning new techniques, working independently as well as in a team, and contributing to a safety-conscious laboratory