Senior QC Analyst - Validation

We have a brand new role to join a global quality team where you will be vital in delivering active ingredients that meet the highest pharmaceutical regulatory and compliance standards. The role will initially be for 23 months but may be extended.

* Troubleshoot analytical equipment and technique failures.

* Promote technical skills and quality standards within QC.

* Conduct sample analysis, validation activities, and batch releases.

* Own analytical projects and ensure compliance with GMP and QA standards.

* Collaborate on continuous improvement initiatives and meet corporate quality goals.

You will have a degree in a relevant science field along with proven experience with HPLC, GC FTIR, UV, PXRD, DSC. In addition, you will have a strong understanding of GMP and analytical method validation/transfer principles.

* Competitive hourly rate and retention bonus.

* Professional training and development.

* 36-hour workweek (Monday-Friday).

* Opportunity to contribute to global pharmaceutical innovation.