ROLE OVERVIEW Our client is currently looking for a QC Analyst to join a leading pharmaceutical company based in the Essex area. As the QC Analyst, you will be responsible for ensuring the highest standards of quality control in the laboratory, adhering to MHRA and EU GMP Guidelines. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows: 1. Conducting Quality Control testing and documenting laboratory results accurately. 2. Planning and managing testing workloads under the supervision of the Assistant QC Manager. 3. Performing method validations and method transfers as needed. 4. Assisting in Out of Specification (OOS) investigations and maintaining compliance with Standard Operating Procedures (SOPs). ROLE REQUIREMENTS: To be successful in your application to this exciting role as the QC Analyst we are looking to identify the following on your profile and past history: 1. Relevant degree in Chemistry, Biology, or Pharmacy. 2. Proven industry experience in a pharmaceutical Quality Control laboratory. 3. A working knowledge and practical experience with Good Manufacturing Practice (GMP) and laboratory equipment such as titrators and pH meters. Key Words: Quality Control / QC Analyst / Pharmaceutical / Laboratory Testing / GMP / MHRA / EU GMP / SOP / Method Validation / OOS Investigations / Chemistry ...