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 & 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.
#PharmaceuticalChemist #QCLaboratory #AnalyticalChemist #GMPJobs #HPLC #PharmaCareers #ChemistJobs #QualityControl
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 a...
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 & 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.
#PharmaceuticalChemist #QCLaboratory #AnalyticalChemist #GMPJobs #HPLC #PharmaCareers #ChemistJobs #QualityControl
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