Biobank Technician I

Azenta Life Sciences•Cleveland, OH

21d•$21

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. All we accomplish is grounded in our core values of Customer Focus, Achievement, Accountability, Teamwork, Employee Value and Integrity Job TitleBiobank Technician I Job Description How You’ll Add Value: The regional sites Biobank Technician I is responsible for the whole life cycle from reception, manifesting labeling, retrieving, shipping and discarding of irreplaceable biological and production materials (research samples, products, etc.) as assigned, while maintaining appropriate temperature. 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. The incumbent is also responsible for performing data entry, data analysis, cleaning, maintenance/qualification activities and facilities activities to ensure smooth and continuous functioning of the Biobank operations. What You’ll Do: Perform all functions methodically and in accordance with Policies and Standard Operating Procedures (SOPs). Adhere to FDA Good Practices (GMP, GTP, GLP, GDP), International Organization of Standards (ISO), College of American Pathologists (CAP) standards, International Air Transport Association (IATA) and other regulatory requirements as outlined in SOPs and site location. Handle materials in a manner that maintains required temperatures (+30°C to -196°C) per the project definition and SOPs. Follow all safety requirements for working with infectious and non-infectious 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. Managing the whole life cycle of the samples/materials: Reception Manifesting Registration Retrievals Discard/Shipment Other client specific tasks Investigate and document issues encountered using common and company specific systems. Generate reports and custom reports as assigned/ needed. Work with other team members to help on assigned projects. Proactively manage and drive the resolution of client issues while promoting continuous process improvements. Maintain training file and required documentation. Assist with upkeep of the facility and equipment in a timely manner: Cleaning Keeping track of inventory/consumables Installation Preventive maintenance Calibration Qualification Maintain on-call availability in accordance with schedule set by the employer For sites with a laboratory: Independently operate laboratory equipment Accurately and precisely use of pipettes Proper use of reagent Other duties as assigned What You Will Bring: Bachelor’s Degree (or country specific equivalence) OR Associate Degree + 2 years of relevant experience OR High School Diploma + 4 years of relevant experience (Two years’ experience demonstrating teamwork, self-motivation, detail orientation, and professionalism) Life Sciences degree/experience preferred GMP/GTP/CLIA experience preferred Organized and detail oriented Demonstrate high level of initiative and ability to triage/prioritize and work independently and in teams Ability to maintain confidentiality and make good judgment about what to reveal to customers Strong communication skills, both written and verbal in English and other location’s official languages Ability to read/understand/interpret basic correspondence, instructions, rules, procedures in English and other location’s specific official languages 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. Proficient with Microsoft office suite Microsoft Excel, performing basic and intermediate functions Physical Requirements Reaching, lifting, bending. Ability to lift 50 lbs (~23 kg). 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. Your Working Conditions: The employee will be working in an area with potentially infectious materials The employee will be responsible for maintaining a clean work environment and enforce and follow Universal Precautions for bloodborne pathogens when working in an area considered to be potentially contaminated EOE M/F/Disabled/Vet If any applicant is unable to complete an application or respond to a job opening because of a disability, please email at [email protected] for assistance. Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race, color, age, religion, gender, sexual orientation, gender identity, national origin, disability or veteran status. United States Base Compensation: $21.00 The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience, education (including licensure and certifications), qualifications, performance, and geographic location, among other relevant business or organizational needs. Azenta is a market leader in automated bio sample management solutions and multiomics 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. As a global leader in R&D multiomics services, Azenta Life Sciences, leads the way in providing superior data quality with unparalleled technical support to enable researchers around the world to advance their scientific discoveries faster than ever before. To view more job openings please visit our career site at Careers | Azenta Life Sciences

Requirements

Bachelor’s Degree (or country specific equivalence) OR Associate Degree + 2 years of relevant experience OR High School Diploma + 4 years of relevant experience (Two years’ experience demonstrating teamwork, self-motivation, detail orientation, and professionalism)
Organized and detail oriented
Demonstrate high level of initiative and ability to triage/prioritize and work independently and in teams
Ability to maintain confidentiality and make good judgment about what to reveal to customers
Strong communication skills, both written and verbal in English and other location’s official languages
Ability to read/understand/interpret basic correspondence, instructions, rules, procedures in English and other location’s specific official languages
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.
Proficient with Microsoft office suite Microsoft Excel, performing basic and intermediate functions
Reaching, lifting, bending.
Ability to lift 50 lbs (~23 kg).
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 degree/experience preferred
GMP/GTP/CLIA experience preferred

Responsibilities

Perform all functions methodically and in accordance with Policies and Standard Operating Procedures (SOPs).
Adhere to FDA Good Practices (GMP, GTP, GLP, GDP), International Organization of Standards (ISO), College of American Pathologists (CAP) standards, International Air Transport Association (IATA) and other regulatory requirements as outlined in SOPs and site location.
Handle materials in a manner that maintains required temperatures (+30°C to -196°C) per the project definition and SOPs.
Follow all safety requirements for working with infectious and non-infectious 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.
Managing the whole life cycle of the samples/materials: Reception Manifesting Registration Retrievals Discard/Shipment Other client specific tasks
Investigate and document issues encountered using common and company specific systems.
Generate reports and custom reports as assigned/ needed.
Work with other team members to help on assigned projects.
Proactively manage and drive the resolution of client issues while promoting continuous process improvements.
Maintain training file and required documentation.
Assist with upkeep of the facility and equipment in a timely manner: Cleaning Keeping track of inventory/consumables Installation Preventive maintenance Calibration Qualification
Maintain on-call availability in accordance with schedule set by the employer
For sites with a laboratory: Independently operate laboratory equipment Accurately and precisely use of pipettes Proper use of reagent Other duties as assigned