Bio-Technician II

General Atomics•Poway, CA

22h•Onsite

About The Position

Under general supervision, this position is responsible for the operations necessary to support development activities for clinical diagnostic products. The individual works with an interdisciplinary team, maintains project notes and Design History Files, and presents updates to the Research and Development team and management. Additionally, the role involves participating in the development of standard operating procedures for the project and conducting laboratory experiments in a safe and regulated manner.

Requirements

Associate's degree in related discipline and one or more years of related experience working in an academic or industrial biology or microbiology laboratory.
General understanding of biological/microbiological theories and principles.
Working knowledge of laboratory protocols, and regulatory and safety requirements.
Ability to interpret data and identify and analyze issues, contributing solutions to moderately complex problems.
Good interpersonal, verbal and written communication skills to explain general to mid-level information and effectively communicate with all levels of employees.
Ability to maintain the confidentiality of sensitive information.
Ability to use basic office/scientific software and knowledge of basic computer operations and applications.
Ability to work both independently and in a team environment is essential.
Ability to work extended hours as required.

Nice To Haves

Bachelor’s degree in a related discipline is preferred.

Responsibilities

Participates in an interdisciplinary team performing life sciences research and development experiments in the laboratory.
Prepares buffers, stock solutions and operates laboratory equipment needed for research and development.
Analyzes experimental data and participates in design of experiments to be performed in the laboratory
Maintains and updates a variety of confidential and sensitive electronic and/or hard copy project records and/or files.
Presents findings during research and development meetings.
Completes and submits various good manufacturing practices (GMP), safety, and regulatory related documents as required.
Assists with scale manufacturing of developed products with testing to assure that product specifications are met.
Maintains strict confidentiality of sensitive information.
Other duties as assigned or required.
Responsible for observing all laws, regulations, and other applicable obligations wherever and whenever business is conducted on behalf of the Company.
Expected to work in a safe manner in accordance with established operating procedures and practices.