that all costs are considered. Providing routine internal commercial and progress reporting in accordance with management time requirements Maintain systems to see that QualityManagementSystem ISO 9001 and 14001 are implemented. Progress all sales opportunities. Develop and pursue new and existing sales leads Ensure No Claims are made on more »
To conduct the administrative aspect of the Technical Department taking responsibility for the day-to-day management of some or all of the following; QMS, HACCP, Legislation, Customer Specifications, Raw material specification. · Technical kpi generation and interpretation, including, non-conformance, customer complaints, microbiological performance · Helping to develop and maintain change more »
prototype algorithmic functions based on data analysis and experimental findings. Additionally, you'll play a role in maintaining adherence to the ISO 13485 qualitymanagementsystem and collaborate effectively with other engineers to support research and development initiatives and the overall project goal Better patient outcomes! What skills and experience more »
company procedures and policies to ensure smooth delivery of our service Producing reporting on time and to agreed standards Adhering to the companys qualitymanagementsystem and recycle correctly and responsibly Experience & Skills UK Driving Licence (required) Experience in electrical repair, maintenance, servicing & installations, preferably within the public sector A more »
East London, London, United Kingdom Hybrid / WFH Options
SOUTH WEST RECRUITMENT
employment as and when required. You will also receive a full company induction that will include many areas such as GDPR the DBF QualityManagementSystem and all other systems and soft skills training. About the Company Leading the way in Customer Interaction & process management the company are an international more »
be able to hold their own within a QMS. The ideal candidate must have at least two years of experience in a Pharmaceutical QualityManagementSystem and understand and be able to complete QMS activities including: Change control Deviations CAPA QMRs Recalls Returns Training The role involves: Review, update and … bona fide reviews, reviewing Technical Agreements etc. Requirements: Experience/knowledge in the following is useful – Sage, Outlook, Microsoft 365, import of pharmaceuticals, pharmaceutical QMS or PLPI would be useful but not essential. The company has a MIA for PLPI as well as a WDA with a single QMS, so more »