Quality Officer

You have the chance to join a market leading organisation in a business critical, interactive role. As the Quality Officer you will be supporting the adherence to the Quality Management System throughout the engineering & manufacturing process by effectively managing documentation & updating SOPs.

Client Details

This market leading company manufacture an array of specialist products including pharmaceuticals & as the Quality Officer you will be instrumental in ensuring their process consistency. You will be working to ensure GMP/EHS regulatory compliance is met across the site & championing best practice processes. This role is initially on a 12 month interim basis & will be based in the Leicestershire area.

Description

You will be working as part of a Quality team focused on quality assurance, change management & process improvement. The role will involve interaction with different internal functions; using data compiled from audits & internal reporting to put corrective measures in place.

Key Responsibilities:

• Creation and Maintenance of regulatory documents and the control of associated processes and procedures.
• Compliance with Change control (CMR and ECC) and the creation, update, submission and Maintenance of related documents.
• Coordination and supervision of GMP service providing contractors, including the collation, checking and filing of all of the GMP data that they produce.
• Verification of data and ensuring it is correctly entered on the systems.
• Ensuring Quality Improvement Reports are raised if necessary.
• Ensuring documented compliance control of associated Contractor GMP processes.
• Regulatory, customer and internal audit support, including collating and presenting drawings, documents and data.
• Raise and complete QIRs, CAPAs and all associated documents on behalf of the Department
• Collating and reporting Plant Engineering Compliance Data to daily meetings and Monthly QA Review.

Profile

A Quality Officer/Professional who is available to start at short notice for a 12 month assignment & who has the following:

• Ideally a recognised Engineering/Technical Qualification
• Experience working in a GMP regulated/FMCG industry
• An understanding of GMP related regulations & EHS standards
• The ability to develop documentation or recording systems
• Excellent collation and interpretation of detailed data skills
• PC literate (MS Office, Enovia and SAP experience would be advantageous)
• Strong interpersonal & team working skills

Job Offer

Circa £16 - £19 per hour