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Alcami Corporation

Sample Receipt Processing Technician

Alcami Corporation, Morrisville, North Carolina, United States, 27560

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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?

Location:

US-NC-Morrisville

Job ID:

2025-1898

Category:

Laboratory Support

Position Type:

Full Time

Working Hours:

1st Shift: Monday - Friday, 8:30am - 5:30pm

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 Fresno, conduct inventory ordering, receipt, and management.

On‑Site Expectations

100% on‑site position.

1st Shift: Monday - Friday, 8:30am - 5:30pm.

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 expirationড়িয়ে 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.

Performsisana documentation accurately and completely.

Other duties as assigned.

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Qualifications

High School Diploma or GED required.

2+ years of relevant experience required.

Knowledge, Skills, and Abilities

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.

Travel Expectations

Up to 5% travel may be required.

Physical Demands and Work Environment While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

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