ON DEMAND PHARMACEUTICALS INC

Open

Sterile Operator / Pharmacy Technician

Location
NMMC Tupelo - Tupelo, MS 38801
Last seen
Aug 7, 2026

About the role

On Demand Pharmaceuticals (ODP) ( www.ondemandpharma.com ) is changing the way we make and distribute medicines—by providing them to anyone, anywhere, anytime. We are creating innovative systems to enable our vision to produce critical medicines at the point of care and to secure the pharmaceutical supply chain. As a young organization, ODP offers an exciting opportunity for passionate professionals to make a difference in the world while developing career paths for advancement. ODP is seeking a GMP Sterile Operator / Pharmacy Technician to support our team. Role Summary: Under the direct supervision of the Licensed Pharmacist and according to law and standard procedures, manufactures and/or compounds finished drug product, including associated tasks such as cleaning, packaging, sterilization, etc. and performs other technical duties as assigned. Demonstrates leadership in the training of new employees through the trainee's thorough and efficient attainment of competencies. Responsibilities: Prepares finished drug products (503a compounding, 503b compounding, and/or cGMP manufacturing) Completes sterilization and release testing of finished compounded products Prepares finished drug products for delivery to hospital partner and/or shipping to other customers Inspects and unpacks deliveries of products and places them into inventory or storage Assists with the development and implementation of state-of-the art processes and workflows Assists with training of new employees Audits and maintains drug/supply inventory Execute R&D, technical transfers and production records/documentation Support production operations, including participation in equipment and facility commissioning/qualification/validation activities Able to author, review and revise Standard Operating Procedures Facilitate deviation investigations, CAPAs, and change controls. Ensures compliance with USP 795/797/800, cGMP, Mississippi Board of Pharmacy, and other appropriate regulatory body rules and regulations Perform other tasks as required to support production and development schedules Adhere to standard operating procedures, company policies and site safety requirements