QC Analytical Scientist (Sun-Wed)

Eurofins•Sanford, NC

20h•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. The position involves independently managing testing priorities, operating and maintaining analytical instrumentation, evaluating data for accuracy and compliance, and ensuring complete and accurate documentation. Collaboration with Quality Operations and potential interaction with manufacturing, engineering, environmental health and safety, technical services, research teams, and external laboratories is expected. 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. The role requires utilizing laboratory instruments and equipment in accordance with established procedures, including but not limited to appearance hoods, pH meters, conductivity meters, Solo VPE, Osmometers, UV-VIS, HPLC, UPLC, TOC, and conductivity meters, among others. The role is also responsible for the appropriate creation, review, and approval of GMP documentation such as test records, validation protocols/reports, test methods, and equipment records.

Requirements

BS in Chemistry or Biochemistry.
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 (GMP) or 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.
Must be authorized to work in the United States indefinitely without restrictions or sponsorship.

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.
Ensure complete and accurate documentation.
Collaborate closely with Quality Operations.
Interact with manufacturing, engineering, environmental health and safety, technical services, research teams, and external laboratories as needed.
Support investigations and corrective actions.
Manage inventory and material ordering.
Maintain laboratory compliance.
Deliver reliable, high-quality analytical results.
Utilize laboratory instruments and equipment in accordance with established procedures (e.g., appearance hoods, pH meters, conductivity meters, Solo VPE, Osmometers, UV-VIS, HPLC, UPLC, TOC, conductivity meters).
Create, review, and approve GMP documentation (test records, validation protocols/reports, test methods, equipment records).