Inventory Specialist — GMP & Radioactive Materials

OpenKrill; United States; À distance; USD 50 000 - 75 000; Plein temps

Avantages offerts par ce poste

Hybrid work options

Performance bonus

Equity incentives

Generous vacation

Résumé du poste

Telix Pharmaceuticals is seeking an Inventory & Receiving Specialist to support GMP-compliant receipt, inspection, and inventory processes. You will handle radioactive isotopes and customer samples, log inventory in systems, and ensure items are staged for production.

Strong Excel/Outlook skills, safety awareness, and precise organization are required. Role involves collaboration with QA and production teams, adherence to safety procedures, and participation in supplier audits.

Qualifications

• High school diploma required; advanced degree preferred in business or supply management.
• Proficiency with Excel and Outlook; strong organizational skills and attention to detail.
• Comfort working around radioactive isotopes with safety precautions.

Responsabilités

• Receive and log goods per GMP SOP.
• Inspect items and resolve discrepancies, notify owners.
• Check in radioactive isotopes after training and maintain inventory records.
• Log inventory in control systems and stage goods for production.
• Maintain vendors list and ensure minimum quantities are met.
• Support supplier audits and retrieval of samples.

Connaissances

Excellent interpersonal skills

Excellent organizational skills

Detail-oriented

Safety awareness around radioactive材料

Team collaboration

Formation

High school diploma

Associate's or Bachelor's Degree in Business or Supply Management

Outils

Excel

Outlook

Description du poste

Telix Pharmaceuticals is seeking an Inventory & Receiving Specialist to support GMP-compliant receipt, inspection, and inventory processes. You will handle radioactive isotopes and customer samples, log inventory in systems, and ensure items are staged for production.

Strong Excel/Outlook skills, safety awareness, and precise organization are required. Role involves collaboration with QA and production teams, adherence to safety procedures, and participation in supplier audits.