Job Description

Responsibilities

• Taking a lead role in a transition to any new document management systems, including the evaluation of new documentation structures and categorization for BRC Storage & Distribution and all other Management Systems that may be required.
• Ensure current certifications (ISO9001:2015, ISO17025 & GMP) are kept up to date and the requirements for annual re-certifications are met.
• Have an overview and work alongside the Laboratory Team to ensure any internal or external quality complaints are investigated within the required timeframe of 48 hours along with full written explanation to all involved once complete.
• Conduct regular audits to ensure all controlled documents are being completed correctly along physical checks also being actioned
• Completing and filing of any Non conformances
• Tracking of agreed KPIs, preparation of reports on agreed performance criteria for the QC department, along with the preparation of Ad Hoc reports as required to senior management and across site.
• Ensure maximum co-operation and communication between Quality Control and other departments, to ensure optimum performance levels consistent with the achievement of business plans.

Benefits

• 21 Days holiday but 8 bank holidays pro rata
• Felxible Working Employer
• Staff discounts on products and hardware
• Perkbox acceess; a platform designed to enrich our employee's experience both inside and outside of work.
• Employee Assistance Programme
• Cycle to Work scheme
• Life Assurance
• Discounted Gym Membership
• On-Site Mental Health First Aiders
• Free on-site parking

Required Knowledge, Skills, and Abilities

Computer literate. Leadership / management experience. High attention to detail. Able to use own initiative. Good level of written English. Experience in Quality Management Systems. Qualified to Lead Auditor level for ISO9001 (in addition, other accreditations preferable). 2-3 Year’s Experience within Industry Specifically working with Quality Management Systems.