Job Ref: 213956411

Date: 2021-06-11 12:08:52

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Are you a skilled Administrator with a great attention to detail?

If so you may be interested in this new opportunity for a leading medical company just outside of High Wycombe.

Training can be provided but experience in Audit, Compliance, Quality Assurance etc would be ideal.There is also an opportunity for you to undertake formalised professional development qualifications.

What will I be doing?

Working within the Clinical Governance, Quality Assurance and Regulatory Affairs Team you will be involved in maintaining an effective documentation system supporting quality & regulatory standards within the business. This will involve ensuring the day-to-day management & co-ordination of technical documentation review and retention, collecting required reports at necessary timepoints, supporting technical query requests and the initiation and maintenance of supplier assessment reviews. You will assist, support, and actively participate in the review and issue of Standard Operating Procedures (SOP) and you will develop the skills necessary for investigation and accurate documentation of customer complaints. You will actively contribute to and support the team in taking notes during meetings.

What skills and qualifications do I need?

* Demonstrable accuracy and attention to detail

* Possess good written & oral communication skills

* Proven IT skills including Microsoft platforms e.g., TEAMS, Word, Excel, PowerPoint

* Ability to build and maintain professional relationships with internal and external customers

* Ability to prioritise, plan and organise workload and working to deadlines

* Strong numerical skills

* Maintain legible, accurate and timely records

* Able to deliver independently as well as working within a multi-disciplinary team environment.

* A willingness to develop knowledge & expertise in Clinical Governance, Quality Assurance & Regulatory Affairs

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