SRG are working with a pharmaceuticals company who develop & manufacture novel medicines to improve the outcomes & wellbeing of patients, unable to take traditional dose forms. Based in West Yorkshire, we are looking to recruit a QC Validation Analyst on a 12-month initial contract to aid the team during a key period of growth.
This would be a great opportunity to join a highly experienced team, in a cGMP environment that can also offer flexible working hours.
The Role:
As the QC Validation Analyst, you will be responsible for ensuring the quality & compliance of raw materials & finished products by performing analysis on samples relevant to the release of products.
Key responsibilities will include:
1. Conducting validation activities in accordance with cGMP regulations.
2. Performing QC analysis of raw materials, in-process & finished products.
3. Participating in out-of-specification / failure investigations and corrective actions.
4. Reviewing external testing data to ensure accuracy & regulatory compliance.
The Person:
1. A degree or similar qualification in Chemistry or a relevant field.
2. Previous method or cleaning validation experience within a GMP environment.
3. Prior experience of HPLC would be advantageous, but not essential.
4. Keen eye for detail and accuracy – with the ability to understand, review and write documents & procedures.
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