QC Analytical Scientist

Eurofins•Sanford, NC

21h•Onsite

About The Position

This role performs routine and non-routine analytical testing of pharmaceutical products, raw materials, validation, stability, and process samples within a GMP-regulated laboratory. Independently manage testing priorities, operate and maintain analytical instrumentation, evaluate data for accuracy and compliance, and ensure complete and accurate documentation. Collaborate closely with Quality Operations and may interact with manufacturing, engineering, environmental health and safety, technical services, research teams, and external laboratories as needed. Responsibilities also include supporting investigations, corrective actions, inventory management, material ordering, and maintaining laboratory compliance while delivering reliable, high-quality analytical results that support site operations. Utilize laboratory instruments and equipment in accordance with established procedures to include but not limited to appearance hoods, pH meters, conductivity meters, Solo VPE, Osmometers, UV-VIS, HPLC, UPLC, TOC and conductivity, and various other instruments. Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.).

Requirements

BS in Chemistry or Biochemistry with a minimum of 2 years of experience working in a laboratory environment, QC laboratory preferred.
Experience working with analytical standards, reagents, and laboratory instruments.
Successful hands-on analytical testing experience in a Good Manufacturing Practices also cGMP environment.
Understanding and performing analytical testing and the use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity.
Capability to perform complex mathematical problems and perform complex data analysis.
Accurate pipetting skills.
Strong organizational skills and ability to multi-task across projects and activities.
Must be self-motivated and work with minimal direction.

Nice To Haves

Empower 3, LIMS
Demonstrate proficiency in computerized systems, such as Laboratory Information Management System.

Responsibilities

Perform routine and non-routine analytical testing of pharmaceutical products, raw materials, validation, stability, and process samples within a GMP-regulated laboratory.
Independently manage testing priorities, operate and maintain analytical instrumentation, evaluate data for accuracy and compliance, and ensure complete and accurate documentation.
Collaborate closely with Quality Operations and may interact with manufacturing, engineering, environmental health and safety, technical services, research teams, and external laboratories as needed.
Support investigations, corrective actions, inventory management, material ordering, and maintaining laboratory compliance.
Deliver reliable, high-quality analytical results that support site operations.
Utilize laboratory instruments and equipment in accordance with established procedures to include but not limited to appearance hoods, pH meters, conductivity meters, Solo VPE, Osmometers, UV-VIS, HPLC, UPLC, TOC and conductivity, and various other instruments.
Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.).