QC Sample Coordinator (Wednesday-Sunday 2nd Shift)

Eurofins•Sanford, NC

9h•Onsite

About The Position

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services. The QC Sample Coordinator will coordinate and perform workflow for laboratory operations support of multiple cGMP laboratories. This role involves timely and accurate cGMP compliant processing of incoming and outgoing samples and reference materials, accessioning samples into LIMS Sample Management, and initiating sample chain-of-custody. The position requires ensuring the on-time availability of samples and reference standard material in accordance with Sample Management SOPs, assisting with process improvement initiatives, and ensuring data integrity and traceability. The role also involves generating and maintaining records in a regulatory compliant manner, contributing to the oversight of the Sample Management laboratory, and operating effectively in both team and individual settings. Excellent written and oral communication skills, effective day-to-day task management, strong organizational skills, and attention to detail are essential. The role also includes maintaining laboratory 5S organization and performing additional duties as needed. This role is on-site in Sanford, NC.

Requirements

Bachelor’s degree in Scientific discipline or associate’s degree and 0-1 years of industry experience or equivalent.
Ability to utilize email, word processing and spreadsheet software.
Ability to compute basic arithmetic operations: addition, subtraction, multiplication, and division.
Authorization for employment in the United States.

Nice To Haves

Moderate understanding of ICH Guidelines as they pertain to Stability Studies and programs.
Knowledge of GMPs, safety regulations and data integrity preferred.
Proven fundamental use of LIMS systems
Knowledge of material receipt and inventory control.

Responsibilities

Coordinate and perform workflow for laboratory operations support of multiple cGMP laboratories.
Timely and accurate cGMP compliant processing of incoming and outgoing samples and reference materials.
Accession samples into LIMS Sample Management and initiates sample chain-of-custody.
Successfully complete all responsibilities for on-time availability of samples and reference standard material in accordance with Sample Management SOPs and other associated SOPs.
Assist with the implementation of process improvement initiatives.
Ensure data integrity and traceability.
Generate and maintains records in a regulatory compliant manner.
Contribute to oversight of Sample Management laboratory.
Ability to independently follow standard protocols, performs associated tasks without errors per applicable SOPs.
Assist in distribution of all samples destined for various QC laboratories.
Perform sample aliquoting in a Biosafety cabinet using aseptic techniques as needed.
Support inventory control of all retain, reference and reserve samples, including stability samples.
Support for timely and effective investigation of area deviations or corrective actions.
Interact with other functional areas and/or vendors to resolve problems, enhance processes and service delivery.
Work through Protocol questions, issues, escalations and changes with relevant project team members.
Coordinate information and communications for designated projects at the site level, including identification and escalation of discrepancies as needed.
Operate effectively in both a team and individual setting.
Provide excellent written and oral communication skills.
Initiate and manage day-to-day tasks effectively.
Utilize excellent organizational skills and attention to detail.
Maintain laboratory 5S organization, perform additional duties as needed