An exciting opportunity for a QA Co-ordinator to join LONZA as Quality Assurance team based in Slough, UK.
The Role
You will co-ordinate site visits by customers and regulatory authorities as well as supporting site compliance by assisting with global, supplier, internal, process and spot audits.
Key Responsibilities
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To maintain the central audit schedule, detailing all global, internal, process, spot, customer audits and regulatory inspections.
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Support and administer all inspection and audit back room activities.
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Provide administrative support to the Quality function.
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Train relevant front and back room personnel in all inspection processes and procedures.
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Develop and maintain role and responsibilities guidance documents for inspection front and back room personnel.
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Support with the co-ordination and tracking of departmental pre‑inspection activities.
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Assist with the creation and administration of QMS inspection and audit records.
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Collate regulatory evidence files.
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Support the set-up and running of all audit types.
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Maintain audit departmental organograms, SOP lists and generic presentations.
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Support and administer preparation and collation of all audit pre-requests.
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Trend and raise CAPAs for internal audits.
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Schedule for supplier and internal audits.
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Support the collation, distribution and tracking of supplier questionnaires and quality agreements
Qualifications
The successful candidate will have –
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Previous work experience in a pharmaceutical manufacturing, GXP or QA environments.
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Previous work experience as an administrator.
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IT literate – MS Office – Word, Explorer, Excel, Access, Outlook.
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Excellent communication skills (verbal and written).
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Accurate data entry skills. Attention to detail.
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Ability to meet deadlines.
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Organisational & planning skills.
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Ability to work in team and solo capacity.
Closing date: 4th April 2016.
