LivingstonPermanent OpportunityCompetitive SalaryThe CompanyA leading pharmaceuticals company are looking for a QC Coordinator to join their growing team in Livingston. The company are a cGMP facility working on a range of products for the global market.The Role
The successful QC Coordinator will work within the company's QC team on a range of duties in a cGMP environment. Reporting to the Lab Manager you will be responsible for QC sample logistics, including shipments. The role would be suited to someone with previous experience in a QC position who has worked in a GMP/GLP environment. Key responsibilities include; * Shipment of QC samples and materials to approved suppliers * Act as SME for shipments and provide training in process for others* Act as central point of contact for receipt of certificates* Support co-ordination of the storage of QC samples and sample logistics for all testing* Working with Raw Materials Coordinator, maintain raw material specifications to ensure continued compliance, acting as their deputy as required* Immediately escalate and report any deviations to materials, facilities, processes or procedures to line manager and progress QMS in a timely manner* Maintain all QC systems, databases, logs and support the generation of QC trend data* Support QC activities in line with manufacturing schedule, as per rota. This includes provision of overtime cover as required* Shift work and out of hours work as requiredYour ExperienceThe successful applicant will have the following skills/experience;
* A BSc or above in a relevant scientific subject* Experience in raw material testing and sample management and shipping as well as managing external relationships effectively.* Experience working in a GMP environment and working to deadlines, managing conflicting priorities. Next StepsIf you are looking to become a QC Coordinator for a leading pharmaceuticals company in Livingston please apply online.
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