Material Handler - Full Time

Base pay $30.00/hr - $32.00/hr
Material Handler — Rahway, NJ Material Handler
Overview
Individual will be responsible for sub-division and preparation of shipment of GMP materials in the GMP Sample Repository. Workflows will be executed in accordance with relevant standard operating procedures and conform to current Good Manufacturing Practices (cGMPs). The employee will ensure all required documentation associated with material receipt, order processing and shipping is accurately prepared and maintained. Additionally, all relevant databases will be updated accordingly.
Responsibilities Provide functional support for all GMP Sample Repository activities such as receiving and processing (label, store subdivide, and ship) all GMP material for distribution to preclinical or clinical studies and commercial reference standards in accordance with SOPs, cGMPs, and federal and regulatory guidelines.
Order chemicals and supplies, execute receipt, subdivision and shipment of GMP materials, and perform documentation management for Distribution & Logistics records.
Interact with RY site shipping, transportation companies, brokers, etc. to facilitate and ensure shipments.
Generate shipping documentation and hazardous goods packages according to DOT/IATA guidelines.
Compile transportation details of shipments for confirmation and distribution and maintain open communication with recipients to convey shipment details, ensuring smooth deliveries.
Demonstrate high levels of customer support with Sample Repository and Reference Standard staff and in conducting all business activities with other sites and external parties.
Role is based in Rahway, NJ; onsite 5 days per week.
Qualifications Experience operating in a GMP environment, with material handling, documentation, data generation and data reporting.
Good computer skills, able to quickly learn and implement area-specific software/database systems.
Effective interpersonal, organizational, and communication skills (written and oral); high attention to detail. Able to work independently and in team or group settings.
Aptitude to manage time, priorities, and personal effort to achieve productivity.
Desirable working knowledge of country-specific shipping regulations.
Education requirements BA/BS in a science-related field is preferred but not required.
Experience Operating in a GMP environment with material handling, documentation, data generation and data reporting.
Job details Seniority level: Associate
Employment type: Full-time
Job function: Manufacturing, Distribution, and Quality Assurance
Industries: Staffing and Recruiting and Pharmaceutical Manufacturing

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