Overview
Are you an experienced QC professional who has worked within a cGMP environment?
SRG have a fantastic opportunity to join a successful and expanding organisation in the Central Belt of Scotland.
Responsibilities
* Development of quality systems, in particular those relating to QC activities of the Quality Department
* Review and approve data such as Environmental Monitoring and QC testing
* Assist with stability study management
* Approve and release incoming Raw Materials
* Management of QMS for QC investigations
* Support analytical method technical transfer and validation
* Carry out a range of analysis such as Environmental Monitoring, endotoxin, bioburden, pH and analytical chemistry based methods
* Support the ongoing maintenance and management of subcontract facilities
* Trending QC data
* Ensure all QC processes are compliant with cGMP guidance
Skills
* Able to work well as part of a team
* Time management and planning
Requirements
* Experience in QC release and/or stability testing would be beneficial or experience of similar techniques and lab work
* Experience of working in a GMP regulated environment would be beneficial
* Experience of helping manage a QMS and assist with investigations
Please apply online or contact Emma for more information if you feel you have the relevant skill and experience to be considered for this role.
Seniority level
* Associate
Employment type
* Full-time
Job function
* Science
Industries
* Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr