Exciting opportunity as a QA Co-ordinator at LONZA

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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
  • 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
Qualifications

 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:  4th April 2016.

 

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