Senior Administrator in United Kingdom
United Kingdom |
GBP £12.05 per hour, PAYE |
Contract
Mane are recruiting for a Senior Administrator in Llanberis for a 6 month contract initially which may be extended or an opportunity for temp/perm. Your main focus will be to quality check information that comes back from the lab. We are looking for someone experienced with Excel and someone who has used Pivot tablet and V look up.
The Conformance Data Reviewer will request assays, review and summarise the data from them, support the approval, or otherwise of critical raw materials.
In addition, they will liaise with Production Control, Manufacturing Ops, and RM planning , to achieve the required turnaround times to support the business needs, whilst maintaining the highest Quality.
What are my responsibilities?
*To direct the testing group, via the completion of work instructions, to carry out the testing required to approve critical raw materials.
*To review and summarise the data resulting from the above testing, and disposition it in relation to QC specifications.
*Communicate effectively with RM planning, production control, the laboratory, Tech Ops and QA Release, as appropriate, to fulfil the above tasks in a timely manner and in line with business needs.
*Assist the Supervisor / Manager in updating procedures and paperwork as required.
*To prioritise work in line with business requirements.
*Ensure compliance at all times with the relevant standard operating procedures.
*Ensure compliance at all times with company Health, Safety and Environmental policies and procedures.
*Maintain confidentiality at all times.
What do I need to qualify for the role?
*A science /technical background
*A knowledge and understanding of the Immulite systems
*Basic computer skills such as knowledge of Word, Access and Excel
*Awareness of working in GMP environments
If you have the relevant experience please apply to this advert.
The Conformance Data Reviewer will request assays, review and summarise the data from them, support the approval, or otherwise of critical raw materials.
In addition, they will liaise with Production Control, Manufacturing Ops, and RM planning , to achieve the required turnaround times to support the business needs, whilst maintaining the highest Quality.
What are my responsibilities?
*To direct the testing group, via the completion of work instructions, to carry out the testing required to approve critical raw materials.
*To review and summarise the data resulting from the above testing, and disposition it in relation to QC specifications.
*Communicate effectively with RM planning, production control, the laboratory, Tech Ops and QA Release, as appropriate, to fulfil the above tasks in a timely manner and in line with business needs.
*Assist the Supervisor / Manager in updating procedures and paperwork as required.
*To prioritise work in line with business requirements.
*Ensure compliance at all times with the relevant standard operating procedures.
*Ensure compliance at all times with company Health, Safety and Environmental policies and procedures.
*Maintain confidentiality at all times.
What do I need to qualify for the role?
*A science /technical background
*A knowledge and understanding of the Immulite systems
*Basic computer skills such as knowledge of Word, Access and Excel
*Awareness of working in GMP environments
If you have the relevant experience please apply to this advert.