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As a Quality Lab Technician at Baxter, you will be part of a team ensuring patient safety and compliance by performing microbiological sampling, testing, and audits. The role involves evaluation of products and processes within a dynamic manufacturing environment, contributing directly to saving and sustaining lives. Responsibilities include reporting results, training across multiple areas of the department, and adapting to evolving protocols.
Job Responsibility:
Perform microbiological sampling and analysis and on solutions, sets, devices, controlled environments and plant water
Must perform tests and document results
Must perform product sampling
Must perform functional testing of product
Must be familiar with and follow all specifications, SOPs, and forms that pertain to the above area
Must perform department audits as required
Must assist with the running of protocols
Must perform departmental audits as required
Write protocol and final reports.
Requirements:
Associate’s degree in a related subject area or equivalent work experience plus 1 year related experience
Mathematical proficiency
Knowledge of measurement methods
Ability to perform correct sampling techniques
Ability to pay attention to details
Ability to perform SPC techniques
Effective oral and written communications skills
Ability to communicate with different levels within the organization
Ability to work with computer systems
Must be able to use weight scales
Ability to react quickly and efficiently to non-standard conditions on line
Ability to assist in protocol evaluation performed in particular area or responsibility
Audiometric testing and hearing protection required
Candidates must meet visual acuity requirements
Ability to work in unfavorable conditions
Ability to lift above the shoulder up to 20 pounds
Ability to lift, push, pull up to 25 pounds
Ability to climb on ladders
Ability to reach above shoulder
Ability to bend/stoop
Ability to stand for long periods of time
Low absenteeism
Knowledge of specification system
Work well without close supervision
Ability to review specification and SOP changes
Ability and willingness to cross-train within the area
Ability to write SOPs for area of responsibility
Able to write in-process retentions on defective product
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