Laboratory Technician Job Summit area,New Jersey USA,Manufacturing / Production

Position: Laboratory Technician 66361-1

SOKOL GxP Services is seeking a Quality Laboratory Technician to support QC laboratory operations in a GMP/FDA-regulated environment. This role is responsible for managing QC lab material needs, maintaining inventory accuracy, supporting material availability according to the QC schedule, and documenting material handling activities in compliance with GDP requirements.

The ideal candidate will have hands‑on experience with QC inventory management, SAP or LIMS, basic laboratory safety practices, and working knowledge of cGMP expectations. This position works within a team‑based QC shift schedule and supports the timely availability, tracking, stocking, allocation, and condition management of laboratory materials.

Responsibilities

Manage material needs and requirements for QC laboratories.
Maintain and manage QC laboratory inventory.
Perform inventory control activities, including cycle counts, material stocking, scrapping, and related inventory tasks.
Manage material expiry, allocation, and required material storage/condition requirements.
Quantify and maintain materials used in the QC laboratory.
Ensure materials are available on time according to the QC schedule.
Record material handling data clearly, accurately, and in compliance with GDP requirements.
Use ERP or laboratory systems such as SAP or LIMS to support inventory and material management activities.
Work in a team‑based, cross‑functional environment to complete QC tasks according to assigned shift schedules.
Follow basic laboratory safety practices and cGMP requirements.
Work in an environment that may include blood‑derived components.

Requirements

Bachelor's degree with 3+ years of relevant experience, or Associate degree / Medical Technical degree with 4+ years of inventory management experience, or High School diploma / GED with 5+ years of inventory management experience.

Hands‑on experience maintaining and managing QC laboratory inventory is required.

Experience with ERP or laboratory systems is required; SAP or LIMS preferred.

Experience with inventory control activities such as cycle counts, stocking, scrapping, expiry management, material allocation, and material tracking.

Knowledge of cGMP/FDA-regulated industry requirements.

General understanding of cGMPs and GDP documentation expectations.

Basic laboratory safety knowledge.

Technical writing skills and experience.

Proficiency with Microsoft Office applications.

Ability to work within a team‑based QC shift schedule.

Strong attention to detail and ability to maintain accurate documentation.

Background or understanding of biology, chemistry, medical, or clinical practices is a plus.

Benefits

Competitive hourly rate: $28.32 - 35.97/hr (W-2 only, no C2C).

Working hours:

Monday - Friday, regular business hours. 12-month contract with possible extension.

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