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Logistics Coordinator
2 months ago
BioPhase Solutions is dedicated to connecting skilled professionals with leading organizations in Southern California's scientific sector. We are currently seeking a Supply Chain Associate to support a prominent biotechnology firm in the Orange County region.
Compensation: $24-30/hourPosition Summary:
The Supply Chain Associate will be responsible for executing daily supply chain operations, including the procurement, receipt, storage, and distribution of both GMP and non-GMP materials to facilitate the needs of the office, laboratory, and manufacturing environments.
Key Responsibilities:- Manage the ordering, receiving, storing, and shipping of laboratory, manufacturing, office, and general supplies while ensuring that supply chain areas are organized and compliant with safety and quality standards.
- Collaborate with Project Management, Laboratory, Manufacturing, and Quality Assurance teams to secure necessary documentation for processing orders and managing material transfers.
- Maintain accurate chain of custody and documentation to ensure traceability and adherence to specifications.
- Input purchasing transactions and inventory data into an electronic database while maintaining necessary paper records.
- Monitor lead times and delivery schedules, facilitating communication among all stakeholders.
- Conduct inventory audits to ensure precise counts of all stock items.
- Verify that all received items are accounted for and reject any materials showing signs of damage.
- Work closely with department managers to ensure that ordered materials meet the company's quality and budgetary requirements.
- Uphold workspace organization by implementing the 5S methodology.
- Follow safe work practices and report any unsafe conditions to management.
- This list of responsibilities is not exhaustive and may be expanded as necessary.
- 2-4+ years of relevant industry experience.
- High school diploma or equivalent is required.
- Familiarity with ERP systems, supplier forecasting, supply chain methodologies, and material logistics.
- Understanding of GMP and FDA regulations related to the production of aseptic parenteral products.
- Ability to work independently on routine tasks while requiring guidance on new assignments.