Responsibilities:

• Perform the day-to-day activities in the sample coordination area.
• Maintain and update sample documentation
• Receive and inspect incoming samples
• Independently responsible for pulling samples, actuators, dose indicators, or any other sample configuration or related item and distribute to laboratory staff for testing.
• Independently able to perform stability sets and pulls governing documents
• Independently able to perform and document stability chamber inventory
• Maintains a stability pull calendar for onsite and offsite storage and proactively notifies project staff of upcoming events.
• Independently able to pull and organize samples for shipment to other sites or external groups
• Periodically prepare inventory list and distribute to laboratory management to facilitate disposal of samples that are no longer needed
• May serve as back up to daily chamber monitoring and chart recorder management and documentation

Requirements:

• Two years of GMP pharma experience in a laboratory or sample management role with at least a year of sample management experience.
• Ability to understand and adhere to chemical hygiene and safety requirements while working in a laboratory environment.
• Must possess strong time management and organizational skills and an ability to adapt to a variety of tasks and execute them consistently to a high level of quality.
• Must possess strong communication verbal and written communication skills.