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Quality Engineer I- Chemist
Quality Engineer I- ChemistThatcher • Salt Lake City, UT, US
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Quality Engineer I- Chemist

Quality Engineer I- Chemist

Thatcher • Salt Lake City, UT, US
20 hours ago
Job type
  • Full-time
Job description

Job Details

Job Location

Thatcher Company Inc - Salt Lake City, UT

Position Type

Full Time

Salary Range

$55,000.00 - $65,000.00 Salary / year

Job Shift

Day

Overview

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.

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
  • Qualifications

  • Bachelor's degree in Chemistry, Biology, Engineering, or related scientific field (or equivalent experience).
  • 0–2 years of experience in pharmaceutical, biotechnology, or related regulated industry.
  • Basic understanding of GMP, GDP, and GLP requirements.
  • Strong attention to detail, organizational skills, and ability to follow procedures.
  • Effective written and verbal communication skills.
  • Ability to work collaboratively in a cross-functional team environment.
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    Quality Engineer • Salt Lake City, UT, US