Stability Scientist I

Fresenius Medical Care•Ogden, UT

1d•Onsite

About The Position

This role coordinates stability programs and facilities, reviews data for completeness, and enters it into the stability database. It also assists in laboratory quality and validation projects, including special analyses and stability studies. The position involves coordinating drug and device stability studies, managing stability chamber space and environmental conditions, and maintaining databases and spreadsheets. The Stability Scientist I will also assist drug/device laboratories with stability testing, compare input and output data for correctness, and aid in stability study maintenance and laboratory quality improvement projects. Responsibilities include loading and pulling samples from stability chambers, delivering samples to testing labs, gathering and reviewing stability testing data, and entering data into the stability database. The role involves working closely with the Stability Scientist II, maintaining a clean working area, and building stable internal working relationships. The position typically receives specific instructions and may refer to senior staff for assistance, escalating issues as necessary. Additional duties include compiling and submitting Annual Drug Product Review data, monitoring environmental storage conditions, performing chamber reprofiles, and ensuring annual stability lots are placed correctly. It also involves performing reviews of test methods, instrument qualifications, and software validations. For device stability, the role oversees product levels and inventories, provides reports, and monitors storage conditions. Additional responsibilities may focus on specific departments or locations.

Requirements

Bachelor’s degree in chemistry or closely related science field required
Minimum 1 – 2 years’ stability or laboratory related experience.
Ability to read, analyze, and interpret general business periodicals, professional journals, science journals, technical procedures, or governmental regulations.
Strong oral and written communication skills.
Ability to apply advanced mathematical concept
Ability to solve practical problems and deal with a variety of concrete variables in situations where limited standardization exists
Proficient with PC operating systems, windows a plus
Experience in Microsoft Office applications.

Nice To Haves

Knowledge in cGMP, Drug and device processes a plus.

Responsibilities

Reviews notes and test methods and compare information with final reports to detect errors and ensure completeness and conformity to SOPs and regulatory guidance.
Coordinates drug and device stability studies.
Coordinates stability chamber space and environmental conditions, including product levels and mechanical maintenance.
Maintains data base and spreadsheets.
Assists the drug/device laboratories with stability testing using various techniques as required by respective projects based on current training and capabilities.
Compares input and output data and calculations for correctness.
Assists in stability study maintenance projects and laboratory quality improvement projects.
Loads and pulls stability samples into/from the stability chambers as required by stability SOP’s and protocols.
Delivers samples to the respective testing laboratories testing.
Gathers and reviews data related to stability testing and compiles into respective study files.
Enters respective data into the stability database for review and approval.
Works closely with the Stability Scientist II on stability-related issues/projects.
Maintains general housekeeping of working area, environmental chambers and proximal plant areas.
Builds stable working relationships internally.
Assists with various projects as assigned by direct supervisor.
Other duties as assigned.
Coordinates drug stability studies.
Oversees drug product levels and inventories.
Compiles and submits Annual Drug Product Review data to respective ADPR team leaders.
Monitors drug environmental storage conditions.
Assures proper environmental chamber operation and maintains environmental conditions.
Performs chamber reprofiles for drug chambers as required.
Assures annual (ongoing) stability lots are pulled and placed into stability yearly as specified in the applicable SOP.
Performs annual test method, instrument qualification and software validation reviews in accordance with the respective PM requirements.
Coordinates device stability studies.
Oversees device product levels and inventories.
Provides device-related stability reports and data to respective study leaders as required.
Monitors device environmental storage conditions.
Assures proper environmental chamber operation and maintains environmental conditions.
Performs chamber reprofiles for device chambers as required.
Performs annual test method, instrument qualification and software validation reviews in accordance with the respective PM requirements.