Exciting opportunity as a QA Co-ordinator at LONZA

• To maintain the central audit schedule, detailing all global, internal, process, spot, customer audits and regulatory inspections.
• Support and administer all inspection and audit back room activities.
• Provide administrative support to the Quality function.
• Train relevant front and back room personnel in all inspection processes and procedures.
• Develop and maintain role and responsibilities guidance documents for inspection front and back room personnel.
• Support with the co-ordination and tracking of departmental pre‑inspection activities.
• Assist with the creation and administration of QMS inspection and audit records.
• Collate regulatory evidence files.
• Support the set-up and running of all audit types.
• Maintain audit departmental organograms, SOP lists and generic presentations.
• Support and administer preparation and collation of all audit pre-requests.
• Trend and raise CAPAs for internal audits.
• Schedule for supplier and internal audits.
• Support the collation, distribution and tracking of supplier questionnaires and quality agreements

 The successful candidate will have –

• Previous work experience in a pharmaceutical manufacturing, GXP or QA environments.
• Previous work experience as an administrator.
• IT literate – MS Office – Word, Explorer, Excel, Access, Outlook.
• Excellent communication skills (verbal and written).
• Accurate data entry skills.  Attention to detail.
• Ability to meet deadlines.
• Organisational & planning skills.
• Ability to work in team and solo capacity.

Closing date:  4^th April 2016.