Reference Standard Development Stability Management Inventory Manager

Keywords StudiosIndianapolis, IN
Onsite

About The Position

The Reference Standard Development Stability Management Inventory Manager will manage the inventory of stability samples. In addition, the individual will label, initiate stability studies, pull stability samples according to schedule, deliver or ship the samples to the corresponding receiver and reconcile inventory in the data management system. The individual will also manage the inventory of GMP/clinical trial materials which can include shipping to multiple receivers.

Requirements

  • An Associate degree in chemistry or related field and/or significant pharmaceutical industry experience or equivalent significant applicable experience.
  • Excellent communication (oral and written) and attention to detail
  • Strong computer and organizational skills, and experience with Microsoft Office Suite
  • Ability to work independently and as part of a team, have self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies
  • No applicable drug allergies
  • Must be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements
  • Previous inventory experience is required.

Nice To Haves

  • cGMP Lab or pharmaceutical science experience would be preferred.

Responsibilities

  • Receive, store, label, forecast, submit, and deliver samples
  • Support domestic and international shipping of material
  • Conduct annual inventory of stored material
  • Maintain documentation for stability studies in electronic system or logbook
  • Support the client's work requests as needed

Benefits

  • Medical, dental and vision benefits
  • Paid time off (including sick and select holidays)
  • 401(k) enrollment with 3% employer matching
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