Quality Control Chemist - 2nd Shift (Mon-Thu)
Chemistry
Greenville, South Carolina
Professional Direct Hire
Mar 26, 2025
Human Technologies, Inc. has an immediate opening for a Quality Control Chemist (2nd Shift) with a pharmaceutical manufacturer in Greenville, SC. This is a direct-hire, full-time position. The company offers a competitive benefits package and strong opportunities for growth and advancement. The starting salary is approximately $55,000 - $60,000 / year, depending on experience.
2nd shift hours are Monday - Thursday from 4pm - 2:30am
REQUIREMENTS:
Must have Bachelor's degree in Chemistry or a very closely related area of study.
Must have 1+ year of chemistry lab experience. Recent college graduates with a Chemistry major are encouraged to apply.
MUST have HPLC experience (college lab courses are sufficient). Titration and/or wet chemistry experience is a plus.
Strong written and verbal communication skills.
Strong computer skills and laboratory software/systems experience is preferred (Empower, LIMS).
Must be authorized to work in the United States without visa sponsorship.
Local candidates preferred.
JOB SUMMARY:
The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products meet all quality and compliance requirements.
JOB DUTIES:
Shall have an emphasis in HPLC and/or GC methodology and analyses, including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting.
Perform analysis of raw materials, bulk, finished product, and stability samples.
Documentation of all analyses.
Perform routine laboratory functions to support manufacturing/production.
Testing and release of manufactured bulk drug products for packaging.
Maintain a clean and organized workspace within the laboratory; wash labware and pipettes.
Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered.
Assist in documentation review of laboratory notebooks.
Ensure the accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications; following applicable SOP's and safety procedures.
Equal Opportunity Employer
INDPRO
Chemistry
Greenville, South Carolina
Professional Direct Hire
Mar 26, 2025
Human Technologies, Inc. has an immediate opening for a Quality Control Chemist (2nd Shift) with a pharmaceutical manufacturer in Greenville, SC. This is a direct-hire, full-time position. The company offers a competitive benefits package and strong opportunities for growth and advancement. The starting salary is approximately $55,000 - $60,000 / year, depending on experience.
2nd shift hours are Monday - Thursday from 4pm - 2:30am
REQUIREMENTS:
Must have Bachelor's degree in Chemistry or a very closely related area of study.
Must have 1+ year of chemistry lab experience. Recent college graduates with a Chemistry major are encouraged to apply.
MUST have HPLC experience (college lab courses are sufficient). Titration and/or wet chemistry experience is a plus.
Strong written and verbal communication skills.
Strong computer skills and laboratory software/systems experience is preferred (Empower, LIMS).
Must be authorized to work in the United States without visa sponsorship.
Local candidates preferred.
JOB SUMMARY:
The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products meet all quality and compliance requirements.
JOB DUTIES:
Shall have an emphasis in HPLC and/or GC methodology and analyses, including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting.
Perform analysis of raw materials, bulk, finished product, and stability samples.
Documentation of all analyses.
Perform routine laboratory functions to support manufacturing/production.
Testing and release of manufactured bulk drug products for packaging.
Maintain a clean and organized workspace within the laboratory; wash labware and pipettes.
Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered.
Assist in documentation review of laboratory notebooks.
Ensure the accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications; following applicable SOP's and safety procedures.
Equal Opportunity Employer
INDPRO
Job ID: 471042005
Originally Posted on: 3/28/2025