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Laboratory Sample Coordinator

4 months ago

Wilson, United States iConsultera Full time

NOTE:

This is a 100% onsite role. Candidate should be flexible to come in earlier if needed.


• Perform stability sample pulls using GLIMS and delivery to the laboratory, adhering to GMP processes and procedures.

• Perform receipt of stability samples from production units.

• Perform shipment of stability samples to external testing laboratories.

• Perform build and setup of stability studies in GLIMS.

• Able to clearly represent individual status/accomplishments.

• Actively promotes an inclusive culture.

• Properly documents, investigates, and identifies proactive measures to ensure right first-time achievements.

• Understand and apply Data Integrity concepts.

Qualifications

Education Minimum Requirement:

• Bachelor's degree in Science, Chemistry, Biochemistry, Biology, or related science field.

Required Experience and Skills:

• Minimum of one (1) year of experience in Laboratory GMP regulated environment.

• Two (2) plus years in a pharmaceutical manufacturing and cGMP environment

• GLIMS experience

• Technical communication (written & presentation) skills.

A successful candidate will exhibit: -

• Understanding of the fundamental business drivers for the company and apply this knowledge in their own work.

• Ability to interpret Company Quality Policies and Guidelines for daily application.

• Understanding and active application of regulatory/compliance requirements, including GMP and related regulations, and ability to interpret those regulations for implementation in the workplace.

• A knowledge of theories, processes, and procedures in the Quality Laboratory.

• Strong technical writing capabilities.