Working for a Pharmaceutical development and manufacturing facility in collaboration with Government, MOD and 3rd party contractors, you will be developing lifesaving pharmaceutical products. This role specialises within the companies downstream processing team as a Unit Manager.
Job Responsibilities:
- Perform a range of routine Production and some non-routine technical procedures and understand the rationale behind the procedures and practices.
- Generate and review documentation with regard to Risk Assessments and cGMP to ensure compliance of the unit with all necessary regulations.
- Ensure the unit is maintained in a compliant state. Work to cGMP following Standard Operating Procedures (SOPs) and Codes of Practice. Keep updated on new rules and regulations.
You:
You’ll have held a similar role within Production within a GMP facility, for this role you will have a proven experience of downstream processing. Experience of continuous improvement, lean and SOPs would be beneficial.
To Apply
Please send your CV to Rebecca
