MAIN DUTIES AND RESPONSIBILITIES
To ensure analysis and recording of QC and stability testing is performed in compliance with the statutory requirements of cGMP.
Responsibility for testing raw materials, in process and finished product samples to ensure that they meet the specifications established in the product licence and internal company specification documents.
Responsible for writing Standard Operating Procedures and their associated risk assessments to ensure that those tasks are performed safely.
Write quality documents e.g. change controls, validation reports, non-conformances and CAPAs where appropriate.
Organise and liaise with external testing laboratories to arrange correct and on time testing to meet production deadlines or suppliers of equipment or chemicals.
Organise and liaise with internal departments such as validation, pharms stores and QA where required.
Maintain an up-to-date awareness of regulatory and scientific developments via courses, meetings and literature.
Undertake work in accordance with company Code of Safety Practice and Quality Systems.
Maintain training records.
Cleaning of laboratories.
Maintenance and calibration of equipment.
- Agency: Cpl Life Sciences
- Contact: Sheldon Grant
- Reference: JO-2109-475716
Website: Cpl Life Sciences
- Posted: 6th September 2021
- Expires: 4th October 2021