Chemist C
Job in
Durham, Durham County, North Carolina, 27701, USA
Listed on 2026-08-05
Listing for:
Careers Integrated Resources Inc
Full Time
position Listed on 2026-08-05
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
QC Chemist C
QC Chemist C will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. Will work as a member of the stability team to effectively execute QC analytical testing using established (official and/or in-house) test procedures. This role will entail 80% - 100% of their work being performed at the bench level. The Chemist C will be responsible for review of analytical documents, investigations, maintain the GLP status in lab.
Responsibilities include:
- Perform assigned in-process, finished product and stability product testing, using various wet chemicals, physical and instrumental techniques (HPLC, UPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per Finished Product methods.
- Independently plan and execute testing to meet established time-lines. Perform complicated testing with little supervisory direction.
- Assist with the preparation or review of Test Procedures, SOPs, Protocols, and CoAs as assigned.
- Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately.
- Perform maintenance and calibrations of laboratory instruments/equipment with little supervisory direction/training.
- Perform troubleshooting and investigations under the direction of a supervisor.
- Assist in drafting deviation reports as assigned.
- Comply with all regulatory/in-house requirements (may include but not limited to safety, house keeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
- Review of analytical documents
- Investigation for OOS/OOT/Deviation and other lab related events
Preferred qualifications:
- Knowledge of EMPOWER Chromatography Data System and LIMS
- QC experience in Generic Pharmaceutical industries would be preferable
- Experience in a cGMP environment is required
- Knowledge and use of Good Documentation practices
- Knowledge of USP/ICH/FDA guidelines
- Team player who will assist junior colleagues
- Willing to work flexible hours to meet product deliverables
- Ability to learn quickly and have decision making skills that adhere to regulatory practices is required
Education and experience:
- BS or MS in Chemistry or Pharmaceutical Sciences, or related field
- Minimum 5+ years of experience in Pharmaceuticals and Analytical testing is desirable
- Preference shall be given for experience in Inhalation testing on a variety of Inhalation products
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