Teva Quality Control Administrator 

United Kingdom, England 

453558297

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

• 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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