
Quality Assurance Specialist I / Analytical Chemist I - Part-Time
14h14 hours agoMedix Biochemica
Maryland Heights, US · Full-time · $40,000 – $55,000
About this role
This dual role combines 20 hours per week in Quality Assurance with 20 hours per week in Analytical Chemistry, supporting Medix Biochemica's quality system and analytical testing operations. The Quality Assurance Specialist I assists in maintaining and continually improving the company's quality system, while the Analytical Chemist Level I generates and interprets routine analytical data for final product release, product stability, and raw materials testing.
Day-to-day responsibilities in QA include documentation review for Good Documentation Practices, receiving and releasing products and materials, reorganizing files and folders, scanning documents, and drafting documents and reports. In the analytical lab, you will perform routine analytical testing and analysis, assist in analytical assay development as needed, and follow all current SOPs while updating and maintaining written protocols for testing procedures.
You will work in a laboratory environment that requires maintaining notebooks, calibrating and maintaining analytical equipment, and managing inventory of supplies and reagents. The role demands a self-motivated, detail-oriented individual with good time-management and organizational skills who is willing to go above and beyond what is asked.
This part-time position offers the opportunity to build experience across both quality assurance and analytical chemistry functions within a chemical sciences company. The role is ideal for someone seeking a split-focus position that provides exposure to both regulatory compliance and hands-on laboratory analysis.
Requirements
- Self-motivated, hard-working individual willing to go above and beyond
- Detail-oriented with good time-management and organizational skills
- Knowledgeable of Microsoft Office package and a fast, efficient general computer user
- Ability to learn additional programs as needed
- Ability to apply common sense understanding to carry out written, oral, or diagram instructions
- Ability to add, subtract, multiply, and divide in all units of measure, including whole numbers, fractions, decimals, percentages, volumes, and conversion factors
- Ability to sit, stand, walk, use back, leg and arm muscles, use hands, reach, talk, hear, and occasionally lift and/or move over 50 pounds
Responsibilities
- Perform documentation review for Good Documentation Practices (GDP)
- Receive and release products and materials
- Reorganize files and folders and scan documents
- Draft documents and reports, and assist in maintaining records and logs
- Perform routine analytical testing and analysis
- Assist in analytical assay development as needed
- Update and maintain written protocols for testing procedures
- Calibrate and maintain analytical equipment and manage inventory of supplies and reagents
Benefits
- Part-time schedule with 20 hours per week in QA and 20 hours per week in Analytical
- Opportunity to work across both quality assurance and analytical chemistry functions
- Exposure to regulatory compliance and hands-on laboratory analysis
- Reasonable accommodations available for individuals with disabilities
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