Lab Analyst II - POD (Swing Shift)

Sotera Health•Salt Lake City, UT

2d•Onsite

About The Position

POD Laboratory Analysts are responsible for conducting testing following established procedures using Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) under the supervision of the Study Director. They record data concurrently, maintain the traceability of samples throughout testing, and promptly notify the Study Director of any unforeseen circumstances that arise during testing. This position requires flexibility in schedule and department. You will be trained across many labs and expected to move between them frequently. Hours: M-F Swing Shift Start time between 2/3pm Additional 15% hourly shift differential pay

Requirements

Must have current a role equivalent to a Lab Analyst II; aligned with key duties listed below
A Strong willingness to rotate teams frequently and adapt to consistent change
Repetition of tasks with quality and attention to detail
Ability to follow written procedures
Good documentation practice (GDP)
Critical thinking, problem solving, computer and math skills
Willingness to work in a team environment
High standards of honesty and integrity
Willingness to identify and communicate process improvement ideas
Organized and meets deadlines
Willingness to learn and comprehend difficult tasks
Effective verbal and written communication
Strong work ethic and initiative

Nice To Haves

Demonstrated experience cross training with other sections
Rotational or stretch assignments supporting efforts within the assigned section, or in support of other teams

Responsibilities

Supporting sections requiring additional testing and test support.
Identifying deficits in the necessary employee volume and supplementing the efforts of the section in question.
Rotating consistently among several teams and projects to ensure balanced support across sections. By doing so, POD Laboratory Analysts help maintain high standards of laboratory operations and contribute to the overall efficiency and effectiveness of the testing processes.
Perform testing, both GLP and non GLP; start to finish under supervision of the Study Director
Order supplies and media as needed
Ensure testing is conducted according to approved procedures (SOP, CSS, STP, etc.)
Participate in the collaboration of quality events (unexpected results, deviations, etc.)
Assist with and review controlled documents
Basic computer skills including functional knowledge of Microsoft Office and Outlook
Know and follow applicable regulatory requirements (GMP, GLP, ISO, etc.)
Know and follow company policies and procedures
Complete required training on time
Attend work regularly and reliably
Adhere to all policies and procedures
Perform other duties as assigned