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Teva Quality Control Administrator 
United Kingdom, England 
453558297

11.08.2024

Key Responsibilities:

  • To comply with company policies, procedures and standards, cGMP, cGLP, H&S, Regulatory and Customer requirements.
  • Generate, update & implement documentation including SOP’s, quality reports, monthly measures, etc.
  • Contribute to the review of laboratory processes to support continuous improvement. (LIR, Deviations etc for Annual report)
  • Communicate effectively with-in QC and across other departments to ensure continuity of activities.
  • Use visual management to reflect measures and KPIs. (Track wise, Studium Trend- Training)
  • To support with Document management systems such as Master documents, controlled documents, Archiving and communicating with external vendor.
  • Reconciliation of departmental credit statements.

Do you have?

  • High school level qualifications with a pass mark in English, Science and Maths
  • Experience of working within an administrative role
  • Specialist knowledge in following areas of Computerised systems (Word, Excel, Power point) ideally Track wise or similar tool

Are you?

  • Well-developed communication skills with the ability to persuade and influence all levels of colleagues.
  • Confident in presenting with strong organisation and planning skills
What We Can Offer
  • 25 paid holidays per year with the option to buy and sell up to 5 days annual leave each year
  • Private healthcare scheme through Bupa
  • A formal training and development programme specific to your role and department
  • Company pension – flexible employee and employer contributions
  • Competitive salary
  • Employee assistance programme
  • A number of health benefits including: Life Assurance, Critical Illness Insurance, Income protection
  • Plus many other flexible benefits via salary sacrifice: Cycle to work scheme, online and in store discounts and much more

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