2 дня назад
Senior Coordinator, Materials Management (Biotech Manufacturing)
21 - 27$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Coordinator, Materials Management (Biotech Manufacturing): Managing GMP and R&D materials, inventory records, warehouse operations, and domestic and international transfers with an accent on hazardous-material handling, cGMP compliance, and import/export documentation. Focus on maintaining accurate inventory, coordinating regulated shipments, monitoring storage conditions, and safely handling chemicals and heavy materials.
Location: San Diego, California, United States; on-site
Salary: $21.17–$27.47 per hour
Company
operates in biotech manufacturing and provides materials management support for GMP and R&D activities.
What you will do
- Receive, identify, quarantine, store, handle, dispense, release, and issue raw materials, APIs, intermediates, reagents, labels, GMP supplies, and packaging materials.
- Maintain paper and electronic inventory records, including expiration and retest dates, cycle counts, batch retesting, and expired-material disposition.
- Monitor refrigerator operation and temperature conditions for stored materials.
- Coordinate domestic and international transfers between STA Pharmaceutical US LLC, clients, and third-party locations.
- Support shipping, receiving, warehouse operations, supply replenishment, and internal GMP inspections.
- Prepare and maintain import/export documentation and operate a forklift when needed.
Requirements
- High school diploma.
- 1–3 years of experience working with chemicals and import/export procedures is preferred.
- Proficiency in DOT and IATA hazardous-material shipping regulations with current certifications.
- Ability to receive training in industrial chemical management and follow established procedures independently.
- Must be medically fit to wear a respirator and lift up to 75 pounds while safely working with hazardous materials.
- Strong verbal and written communication, organization, and reliability.
Nice to have
- Familiarity with dangerous-goods regulations and related cGMP practices.
- cGMP skills.
Culture & Benefits
- On-site work in San Diego.
- Work independently and collaboratively across departments.
- Follow established procedures and maintain up-to-date training and documentation.
- Perform additional job-related responsibilities as assigned.
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