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Quality and Validation Engineer-Cleanroom Manufacturing

Job description

Quality and Validation Engineer-Cleanroom Manufacturing


Excellent salary plus benefits

37.5 Hours week with early finish on Friday

Are you an experienced Quality Engineer looking for an exciting opportunity with a fast growing pharmaceutical manufacturer. This is a superb opportunity to join a growing company at exactly the right time

The position offers excellent working conditions, job security and really superb job satisfaction.

Part of the goal of the position will be the moving the cleanroom operations over to a new purpose built facility (very local to current site) so there is something really worthwhile and exciting to work towards.

The role

  1. Full time permanent position working Mon-Fri working in the pharmaceutical/cleanroom manufacturing sector
  2. Focusing on the quality system for a range of products and focusing on the cleanroom operation
  3. Internal and external audits of Quality System.
  4. Assist in moving the cleanroom to a new purpose built facility

The person

  • Working experience to include practical application of ISO 13485, ISO 14971, ISO 14644 and FDA Quality System Regulation CFR 21 Part 820.
  • GMP experience mandatory. .
  • Applied technical knowledge of Qualitative and Quantitative data analysis, and statistical tools.
  • Project Management experience/qualifications

Reference Number: BBBH182081

To apply for this role or to be considered for further roles, please click "Apply Now" or contact Nick Smith at Rise Technical Recruitment.

Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles.

The salary advertised is the bracket available for this position. The actual salary paid will be dependent on your level of experience, qualifications and skill set. We are an equal opportunities employer and welcome applications from all suitable candidates.