Sr. Material Coordinator
Juncos, PR, US
Light Industrial
Associate Degree
Full Time, Temporary
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Juncos, PR, US
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Light Industrial
Associate Degree
First Shift (Day)
Job details
Are you ready to take your career to the next level? At Kelly, we have an exciting opportunity for a motivated and detail-oriented individual to join our team in Juncos, PR. As a Sr. Material Coordinator, you will play a crucial role in the coordination and management of materials to support our manufacturing operations.
Responsibilities:
- – Receive, store, dispense, deliver, transfer, reconcile, cycle count, or ship materials in accordance with cGMP procedures and regulations, utilizing multiple systems and/or between multiple sites.
- Proficiently use inventory system(s) to resolve basic system issues within ERP system.
- Utilize various quality, operations, and logistical software applications, including reading, writing access, and verifying cGMP transactions.
- Operate Power Industrial Vehicles (PIV) for the movement of warehouse materials.
- Operate trucks (flat bed or panel) to transport warehouse materials, hazardous materials, or general receiving goods, following Department of Transportation regulations.
- Handle the receipt, delivery, storage, transfer, and shipment of hazardous materials in compliance with Federal guidelines.
- Adhere to OSHA, DOT, and Amgen policies and regulations, as well as any other applicable regulations.
- Identify and report operational issues and opportunities for process improvement to leadership.
- Maintain compliant training records.
- Maintain a clean and safe work environment.
- Prepare for regulatory inspections and audits.
- Serve as a power user of inventory system(s) to effectively troubleshoot and resolve system issues within Amgen’s ERP.
- Serve as a power user of multiple quality, operations, and logistical software applications, with read, write, and owner access.
- Identify and report operational issues and opportunities for process improvement, propose solutions, and assist in addressing them.
- Participate in or lead group or department-specific projects.
- Monitor required training of others and provide training to staff in basic cGMP functions and other areas (such as CFR, DOT, OSHA).
- Monitor work processes to ensure compliance and successful achievement of metric targets.
- Review department’s standard operating procedures, training materials, and validation documents to ensure completeness and accuracy.
- Serve as a point of contact for internal and some external customers regarding daily operational matters.
- Consolidate and report department performance metrics.
- Act as a technical expert in the receipt, storage, dispensing, delivery, transfer, reconciliation, cycle counting, or shipment of materials according to procedures and regulations.
- Demonstrate expertise in the transfer or shipment of hazardous materials in compliance with Federal and approved shipment guidelines.
- Utilize power user skills to effectively troubleshoot and resolve system issues within Amgen’s ERP, suggesting soft and hard code changes for identified efficiencies.
- Identify and report operational issues and opportunities for process improvement to leadership, propose solutions, and lead efforts to address them.
- Participate in or lead group or department-specific or multi-departmental projects.
- Ensure that others receive and maintain required training.
- Train staff in various cGMP and operational functions.
- Regularly review department’s standard operating procedures, training materials, and validation documents to ensure completeness and accuracy, updating as required.
- Act as the primary point of contact for the group to address non-routine operational issues with internal and external customers, including investigation and resolution.
- Consolidate and report department performance metrics.
- Adhere to and enforce cGMP, OSHA, DOT, and Amgen policies and regulations, as well as any other applicable regulations.
- Ensure a clean and safe work environment, which may include serving as a Radiation Safety Officer (RSO) for the functional area.
- Prepare for and participate in regulatory inspections and audits.
- Provide direction to and/or mentor other staff members as needed.
Requirements:
– High school/GED + 2 years of directly related work experience and/or military experience OR?
– Associate’s + 6 months of directly related work experience and/or military experience?
At Kelly, we believe in the power of innovation and teamwork to make a difference in patients’ lives. Join the team as a Sr. Material Coordinator and be part of our mission to deliver life-saving products worldwide. We offer a competitive salary starting at $20.87 per hour and a dynamic work environment where your skills and enthusiasm can thrive.
Take the next step in your career and apply today! We can’t wait to welcome you to the Kelly family and embark on this exciting journey together.
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