Job Overview:
The Quality Control (QC) Analyst is responsible for ensuring the quality of pharmaceutical substances in a Good Manufacturing Practice (GMP) environment. This role involves performing testing and analysis using various techniques, including Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC). The successful candidate will have excellent analytical skills, attention to detail, and the ability to work independently.
Key Responsibilities:
* Perform testing and analysis of pharmaceutical substances, raw materials, and drug substances in a GMP environment.
* Conduct GC and HPLC analysis, as well as other analytical techniques as required.
* Train on relevant analytical techniques and train other analysts upon qualification.
* Maintain laboratory equipment and calibrate regularly.
* Manage inventory and materials for analysis.
* Verify and review results from other analysts when qualified.
* Ensure accurate data entry into Laboratory Information Management Systems (LIMS).
* Assess testing results and close out batch analyses.
* Meet target dates and update testing status.
* Maintain high standards of laboratory housekeeping.
* Document work accurately.
* Work collaboratively to meet customer expectations and Key Performance Indicators (KPIs).
Requirements:
* High school diploma or equivalent required; bachelor's degree in chemistry, biology, or related field preferred.
* 1+ year experience in QC analysis or related field.
* Excellent analytical skills and attention to detail.
* Ability to work independently and as part of a team.
* Strong communication and documentation skills.