Chemist

Trioptus

Wilson, NC

JOB DETAILS
SALARY
$18–$22 Per Hour
SKILLS
Analysis Skills, Assays, Assembly Equipment, Biotech and Pharmaceutical, Chemistry, Cleaning Equipment, Communication Skills, Current Good Manufacturing Practice (cGMP), Data Quality, Detail Oriented, Disassemblers, Documentation, Documentation Standards, Drug Products, Equipment Maintenance/Repair, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), Hand Tools, High Performance Liquid Chromatography (HPLC), Housekeeping/Cleaning, IR (Infrared), Identify Issues, Instrumentation, Laboratory Analysis, Laboratory Information Management System (LIMS), Laboratory Management, Laboratory Systems, Lift/Move 20 Pounds, Maintain Compliance, Manufacturing, Operational Support, Operations, Problem Solving Skills, Procedure Development, Quality Control, Quality Metrics, Regulatory Compliance, Resource Utilization, Safety Compliance, Safety Process, Supply Chain, Test Equipment, Testing, UV/VIS (Ultraviolet-Visible Spectroscopy), United States Drug Enforcement Agency (DEA)
LOCATION
Wilson, NC
POSTED
4 days ago

Job Title: Chemist Level 1

Category: Manufacturing / Supply Chain

Location: Wilson, NC 27893

Schedule: Monday Thursday, 7:00 AM 6:00 PM (10-hour shifts)

Hours: 40 hours/week

Start Date: March 30, 2026 - End Date: September 30, 2026

Position Summary

The Chemist Level 1 performs routine analytical testing and GMP documentation in a cGMP-regulated laboratory environment. This position supports quality control activities by executing laboratory analyses, maintaining analytical instrumentation, and ensuring compliance with cGMP, GLP, DEA, and internal quality standards. The role requires strong attention to detail, adherence to documentation standards, and the ability to work effectively within a team to support daily QC operations.

Key Responsibilities

  • Perform routine analytical testing of drug products, including dissolution, assay/degradant, content uniformity, and identification (ID) evaluations in a cGMP laboratory.
  • Ensure all assigned testing is completed accurately, efficiently, and in alignment with cGMP, GLP, DEA, and company procedures.
  • Enter and review laboratory data in the Laboratory Information System (LIMS) while maintaining complete and accurate documentation consistent with cGMP and data integrity requirements.
  • Operate and maintain analytical equipment such as HPLC, GC, dissolution apparatus, spectrometers, and other lab instrumentation according to established procedures.
  • Perform basic instrument troubleshooting and escalate issues when necessary.
  • Maintain open communication with team members to ensure optimal resource utilization, workflow efficiency, and issue resolution.
  • Assist other laboratory personnel as needed and support team-based workload distribution.
  • Follow established safety procedures and uphold strong housekeeping practices throughout the lab environment.
  • Monitor and replenish laboratory chemicals, reagents, and consumables to support continuous operations.
  • Perform equipment cleaning, assembly/disassembly, and incidental maintenance using small hand tools.
  • Complete additional duties and assignments as required.

Required Skills and Experience

  • Foundational understanding of analytical technologies such as:
    • HPLC, GC, Dissolution, UV/Vis, NIR, IR, AA/AE, or other pharmaceutical testing equipment.
  • Ability to perform precise, accurate testing with strong documentation discipline.
  • Relevant laboratory experience (academic or industry) preferred; minimum 1 year of applicable experience is ideal.
  • Ability to work a 10-hour/day, 4 day workweek (Mon Thurs) with overtime as required.
  • Physical capability to:
    • Lift and maneuver up to 20 lbs
    • Bend, stoop, kneel, twist, or reach as needed for sampling and equipment access
    • Operate industrial hoses, perform manual cleaning (scrubbing/wiping), and assemble/disassemble lab components

Education Requirements

  • BA or BS in Chemistry or a closely related scientific discipline required.

Work Environment

  • Onsite role located at Wilson, NC (QC Lab).
  • Work is performed in a controlled laboratory setting, requiring PPE, safety awareness, and compliance with all regulatory expectations.

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About the Company

T

Trioptus