Biobank Technician I

Azenta•Indianapolis, IN

11d•$19

About The Position

At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer-focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships. Azenta Life Sciences is a global leader in the life sciences space with headquarters in Burlington, MA, and offices and operations worldwide. We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally. We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the largest installed base managing over 1 billion samples globally. How You’ll Add Value The Biobank Technician I is responsible for registering, labeling, retrieving, and discarding irreplaceable biological and production materials (research samples, products, etc.) as assigned, while maintaining appropriate temperatures. The incumbent is accountable for performing all assigned tasks with full attention and accuracy to maintain the integrity of the material and the storage processes.

Requirements

High School Diploma or equivalent
Two years’ experience demonstrating teamwork, self-motivation, detail orientation, and professionalism
Ability to read/understand/interpret basic correspondence, instructions, rules, procedures in English language
Ability to make decisions and judgements based on reasoning
Ability to perform tasks with care, is thorough and checks work for accuracy and completeness
Strong attention to detail for repetitive tasks
Ability to use Microsoft Excel, performing basic and intermediate functions
Reaching/lifting/bending.
Ability to lift 50 pounds
Extended periods of standing or sitting
Right- and left-hand finger dexterity
Ability to discern colors or use of color correction glasses
Ability to work with refrigerants (e.g., dry ice and LNs) using proper PPE

Nice To Haves

Life Sciences experience preferred
GMP/GTP/CLIA Experience, preferred
Strong communication skills, both written and verbal

Responsibilities

Perform all functions methodically and in accordance with Standard Operating Procedures (SOPs).
Adhere to FDA Good Practices (GMP, GTP, GLP, GDP), International Organization of Standards (ISO), College of American Pathologists (CAP) standards and other regulatory requirements as outlined in SOPs.
Handle materials in a manner that maintains required temperatures (+30oC to -196oC) per the project definition and SOPs.
Follow all safety requirements for working with infectious and noninfectious biological materials, radioactive materials, chemical compounds, and drug products.
Utilize the Company Inventory Management System for all sample handling tasks and ensure chain of custody and audit trails for all activities are proactively maintained.
Register samples into the inventory management system. This includes: Scanning of sample barcodes. Quality checking information on the material being registered against project and shipment manifest specifications. Overlay or place a new label onto materials as required per the project specification.
Store materials at required temperatures in designated storage units for the specified category of the material.
Retrieve and package materials requested for lab services, outbound shipments, and discards.
Perform quality control checks.
Perform discard quality checks
Investigate and document issues encountered in registration or retrieval of materials using common and company specific systems.
Generate location management reports.
Assist with upkeep of the facility.