Role - QC Technician
Location - Wrexham, UK
Duration - 6 months
About the Role
To assess all incoming goods requiring Quality inspection as well as perform sampling of raw materials and components. You will also perform, report and review analysis of raw materials and components and work to be performed in accordance with GLP, GMP and Regulatory Requirements.
Responsibilities
* Perform assessment of incoming goods ensuring compliance to site procedures, Industry Standards, Regulatory expectations and GMP requirements.
* Be proficient in reviewing methods against current pharmacopoeial and licence requirements to ensure ongoing compliance.
* Liaise directly with the Supply Chain team to ensure that all incoming goods requiring Quality Assessment are approved within required timeframes and that any issues are escalated appropriately.
* Ensure all raw materials and components requiring analysis are sampled and tested appropriately.
* Entry and review of information in both LIMS and SAP.
* Perform Regular housekeeping and GMP audits of own work areas.
* Participate in internal/external audits/inspections where required.
* Ensure all work is carried out in a safe manner.
* Update and review of departmental documentation.
* Identify out of specification and out of trend results. Actively seek to identifying root cause and corrective actions.
* Highlight non-compliances and communicate as required. Actively engage in providing solutions and identifying appropriate actions.
* Identify and communicate potential or existing problems within the current ways of working. Actively suggest solutions and drive new initiatives.
* Promote accuracy and precision in daily laboratory practices with a ‘right first time’ focus.
* Adhere to relevant SOPs and standards (safety, environmental, GLP and regulatory).
Qualifications
* Relevant experience, preferably in GMP environment
* Worked within a QC incoming pharmaceutical team.
* HND in Scientific discipline or equivalent experience