Lab Analyst - Routine Chemistry (Weekend Shift)

Sotera HealthTaylorsville, UT
9hOnsite

About The Position

Laboratory Analysts conduct testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. Candidates may choose one of the following shift schedules: Friday through Tuesday or Thursday through Monday. These schedules provide consistent weekdays off while supporting weekend coverage needs. A pay differential is included for weekend shifts. All hours worked on Saturday and Sunday are eligible for the additional weekend pay differential. Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry. With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year. Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 8 of the top 10 global pharmaceutical companies.

Requirements

  • Technical
  • 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
  • High school diploma or equivalent required

Nice To Haves

  • Bachelor’s degree in a scientific field preferred

Responsibilities

  • 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
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