What are the responsibilities and job description for the Quality Analyst I (Night) position at Astrix?
Our client is a leading manufacturer of encapsulated vitamins and nutritional supplement, seeking two Quality Analyst to join their team!
Title: Quality Analyst I
Location: Portland, OR (Fully Onsite)
Schedule: Night Shift | Sun–Thurs | 10:00 PM–6:30 AM OR Swing 2pm - 1030pm, Mon - Fri
Pay: $22-24/hr
Job Overview
The Quality Analyst I is responsible for reviewing, approving, and releasing incoming raw materials for dietary supplement manufacturing. This role also reviews documentation and analytical data for finished product release while supporting production, purchasing, and customer service teams to resolve material or product discrepancies.
Key Responsibilities
Title: Quality Analyst I
Location: Portland, OR (Fully Onsite)
Schedule: Night Shift | Sun–Thurs | 10:00 PM–6:30 AM OR Swing 2pm - 1030pm, Mon - Fri
Pay: $22-24/hr
Job Overview
The Quality Analyst I is responsible for reviewing, approving, and releasing incoming raw materials for dietary supplement manufacturing. This role also reviews documentation and analytical data for finished product release while supporting production, purchasing, and customer service teams to resolve material or product discrepancies.
Key Responsibilities
- Review and release incoming raw materials and finished products.
- Serve as the Quality Control representative on the production floor.
- Troubleshoot and resolve in-process quality issues and out-of-specifications.
- Perform basic analytical tests and in-process checks per SOPs.
- Review and maintain quality documentation, investigations, and non-conformance reports.
- Communicate quality issues to cross-functional teams promptly.
- Support QC Manager with investigations and corrective actions.
- Train staff on procedures and assist in developing QC/QA methods.
- Prepare raw material and finished product samples for external testing.
- Quality experience in food, manufacturing, production, or health product environments.
- Familiarity with FDA/cGMP standards preferred.
- Experience with non-conformance investigations, documentation review, audits, and raw/finished product checks.
- Prior manufacturing or laboratory environment experience.
Salary : $22 - $24