Thatcher Company
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 - DOE
Great benefits package, including health, dental, life insurance, paid time off, and paid holidays
Significant profit sharing/retirement plan which is 100% employer paid
Excellent career opportunities with a growing company
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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 - DOE
Great benefits package, including health, dental, life insurance, paid time off, and paid holidays
Significant profit sharing/retirement plan which is 100% employer paid
Excellent career opportunities with a growing company
#J-18808-Ljbffr