Sample Receipt Processing Technician

Alcami Corporation•Morrisville, NC

9d•Onsite

About The Position

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are you interested in joining our team? Job Summary As a Materials Control Coordinator, you will facilitate the logging in of laboratory samples and the projects the lab will use for documentation of the analysis. This position provides administrative and organizational support related to materials management activities: receives, processes, and logs in samples and standards, initiates chain of custody tracking and creates projects for laboratory testing, conduct inventory ordering, receipt, and management. On-Site Expectations 100% on-site position. 1st Shift: Monday - Friday, 8:30am - 5:30pm.

Requirements

High School Diploma or GED required.
2+ years of relevant experience required.
Highly organized and detail oriented.
Able to multitask in a fast-paced environment.
Able to work independently, along with ability to work well within a team.
Ability to communicate effectively, both orally and in writing.

Responsibilities

Conducts ordering of required laboratory supplies, obtaining quotes for newly requested materials.
Maintains laboratory consumables storage by organizing, ordering and restocking inventory using FIFO and monitors expiration of consumable goods.
Conducts follow through on outstanding orders.
SAP sample tracking and inventory management
SAP lab tracking
Raw materials release
Components release
In Process Release
Gathers and registers associated documents for received materials.
Stages received materials for laboratory accessibility.
Evaluates and optimizes the quality and efficiency of the processes in the Materials Management area.
Manages laboratory sample storage, chain-of-custody and disposition.
Manages reference standard inventory and storage.
Monitors temperature and humidity of laboratories and chambers, including maintenance and review of chart recorders in labs.
Uses multiple computer software programs to log in, manage, and maintain material status and testing requirements.
Complies with GMP regulations with adherence to SOPS and other regulatory requirements.
Generates and revises SOPs, as needed.
Communicates and collaborates routinely with other departments and clients.
Performs documentation accurately and completely.
Other duties as assigned.