Quality Assurance Specialist

2 months ago

Cirencester, Gloucestershire, United Kingdom Corin Full time
Quality Inspector Job Description

Corin is seeking a skilled Quality Inspector to join our team at our manufacturing head office site in Cirencester. As a Quality Inspector, you will play a crucial role in ensuring that our products meet the highest standards of quality and safety.

Key Responsibilities:
  • Inspect raw materials and semi-finished products to ensure they meet the agreed specification.
  • Verify product quality using standard metrology equipment, including Shadowgraphs, Coordinate Measuring Machine (CMM), Callipers, Micrometres, etc.
  • Identify and disposition non-conforming products.
  • Ensure accuracy and compliance with Good Documentation Practice (GDP) for records, including Process Inspection Sheets, Goods Inwards Inspection Sheets, and associated documentation.
  • Record output from inspection activities on the corresponding software, Mestec, Sage.
  • Conduct inspection activities across all areas of the business, including Clean Room, Goods Inwards, Manufacturing Cells, and Final Inspection.
  • Ensure compliance with training activities and support buddy training as required.
  • Ensure that all equipment used is suitable for calibration and is free from damage before use.
  • Retrieve items due for calibration promptly and as per the list supplied.
  • Conduct periodic checks on inspection equipment, including light levels, callipers before use, etc.
  • Undertake other related duties as required, including review of completed batch records (DHR) and release for stock, following documented Work Instructions and Checklists.
  • Liaise with all departments as necessary to resolve and clarify any points of issue resulting from DHR Review and publish regular updates as needed.
  • Perform transactional activities within relevant systems, Sage and QPulse, in support of batch disposition and recording of non-conformance data for trending purposes.
  • Maintain records to ensure safe storage with efficient and effective retrieval, including co-ordination of off-site records.
  • Adhere to Quality Management System (QMS) requirements in line with Corin's ISO13485 QMS & Good Manufacturing Practice (GMP) FDA21 CFR Part 820.
  • Ensure that process and timeline requirements for Corrective & Preventive Actions (CAPA) are met following Corin's Standard Operating Procedures (SOPs) and in support of Corin's Global Objectives for CAPA.

Corin provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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