The Quality Engineer I is an entry-level position that supports quality assurance and quality control functions within a GMP-regulated pharmaceutical environment. This role performs laboratory testing, documentation review, and compliance activities under supervision, ensuring adherence to regulatory requirements and company quality standards.
Base pay range
$55,000.00 / yr - $65,000.00 / yr
Key Responsibilities
- Perform laboratory testing under supervision, including instrumental analyses (GC, HPLC, FTIR), bench-scale chemical analysis, and basic microbiological testing.
- Collect raw materials, finished product, microbiology, and environmental samples.
- Execute validation protocols (IQ / OQ / PQ) and collect data as directed.
- Perform basic Laboratory investigation.
- Oversee batch record review, component disposition, and documentation practices to ensure cGDP standards.
- Manufacturing inspections, equipment setup, and cleanliness verification.
- Collect and trend basic quality and testing data.
- Provide basic support during internal audits and inspection readiness.
- Assist with compiling batch and testing data for PQR / APR reports.
- Follow cGMP, cGDP, cGLP, and chemical safety protocols in daily work.
What's In It For You
Competitive Salary - DOEGreat benefits package, including health, dental, life insurance, paid time off, and paid holidaysSignificant profit sharing / retirement plan which is 100% employer paidExcellent career opportunities with a growing companyJ-18808-Ljbffr