QC Analyst

We are currently looking for a QC Analyst to join a leading company based in the Kent area. As the QC Analyst you will be responsible for the analysis of pharmaceutical raw materials, APIs, and finished products to ensure compliance with internal and regulatory specifications. Daily tasks will involve general chemical analysis including stability testing, various laboratory support activities, documenting analytical data, writing reports and SOPs all in accordance with cGMP.

1. As a QC Analyst you will be involved in Performing analytical testing using GC, HPLC, KF, FTIR and other required techniques in accordance with written procedures.

2. You will be required to record data into appropriate records and notify the line manager of any OOS, OOT, OOE or questionable results

3. You will create and update documents in accordance with cGMP and company procedures

1. Relevant degree in a chemistry or related science discipline.

2. Proven industry experience in Pharmaceutical QC testing and GMP (ideally small molecule) and analytical testing using GC, HPLC, KF, FTIR.

3. Experience in completing OOS investigations, deviations, CAPA, and Change Controls

Key Words: GC / HPLC / TLC / FTIR / QC / Quality Control/ QC Scientist/ GMP / API / Raw materials / Chemistry / analytical /