Role Overview
We are currently looking for a QC Analytical Scientist to join a leading Biopharmaceutical Manufacturing company based in the South of the UK. As the QC Analytical Scientist you will be responsible for undertaking chemical and biochemical analyses to support the manufacture of pharmaceutical products in compliance to GMP regulations.
Key Duties and Responsibilities
1. You will be responsible for the testing of raw materials, finished products, in-process and stability samples.
2. You will apply various chemical and biochemical techniques for enzyme analysis including HPLC and UPLC, Gel electrophoresis, and Western blotting
3. You will write quality records, devise CAPAs and execute protocols and investigations (OOS procedures) to troubleshoot QC issues.
4. You will take an active role in the training of junior staff work collaboratively with wider teams to ensure the smooth running of the Analytical QC department.
Role Requirements
1. Relevant degree in a life sciences discipline relating to Chemistry, Biochemistry, Analytical Chemistry, etc.
2. Proven industry experience working in an analytical pharmaceutical GMP environment.
3. A working knowledge and practical experience testing raw materials and finished products using HPLC.
Key Words: Analytical | HPLC | Chemistry | Pharmaceutical | FTIR | QC | Quality Control | GMP | CAPA | OOS | OOT | Change Control | SOP | Biopharmaceutical | UPLC | Gel Electrophoresis | Graduate | BSc | MSc | CDMO | Analytical Scientist