QC Coordinator - Raw Materials
iLABS (Innovation Labs) Inc. · Mahwah, NJ · 2 days ago
On-siteQuality Assurance$25/hrFull-time
Responsibilities
- Receive Certificates of Analysis (COAs) from the warehouse and complete all required receiving documentation.
- Remove labels, verify and mark material weights, and assign storage locations when applicable.
- Receive, review, and file microbiological test results with corresponding raw material COAs.
- Review and release raw materials for production use following established quality procedures.
- Review and release extension materials.
- Print, prepare, and complete COAs for extension documentation.
- Request extension forms and supporting documentation from the warehouse as needed.
- Prepare and complete submission forms for in-house laboratory testing.
- Prepare and submit documentation for testing performed by external laboratories.
- Maintain and organize retained samples in both standard and hazardous storage areas.
- Maintain retained sample inventory using Excel, ensuring accurate tracking and inventory control.
- Perform FTIR (Fourier Transform Infrared Spectroscopy) testing on raw materials according to established procedures.
- Organize FTIR test results and attach them to corresponding raw material COAs.
- Cookordiate requests for new raw material standards with the Research & Development department.
- Maintain raw material classification records, labeling systems, and inventory logs using Excel and physical filing systems.
- Manage daily correspondence related to quality activities and distribute emails to the appropriate departments.
- Provide cross-functional support and PTO coverage for various departments as assigned.
- Perform additional duties and special projects as assigned.
Requirements
- Bachelor's degree in Chemistry.
- Experience in quality control, quality assurance, laboratory operations, or a GMP-regulated manufacturing environment preferred.
- Experience in the cosmetics, skincare, pharmaceutical, or personal care manufacturing industry is a plus.
- Working knowledge of Good Manufacturing Practices (GMP) and quality documentation preferred.
- Proficiency in Microsoft Excel, Outlook, and other Microsoft Office applications.
- Experience with laboratory documentation and quality records is preferred.
- Strong organizational skills with exceptional attention to detail.
- Able to manage multiple priorities while maintaining accuracy and meeting deadlines.
- Strong written and verbal communication skills.
- Able to work independently and collaboratively in a fast-paced manufacturing environment.
Benefits
- Comprehensive Health Benefits package (Medical, Dental, Vision, Life, AD&D).
- Competitive 401(k) match.
- Paid time off (Vacation, Sick, Holiday, Summer Fridays).
- Monthly birthday celebrations + other fun activities!
Schedule
Daily subsidized meals iLABS (Innovation Labs) Inc.
Pay
Hourly Rate: $25/hr