Teva Quality Control Analyst 

Ireland 

46383480

We would like to invite applications for the role ofat our site in Waterford.

Key Responsibilities:

• Test and analyse components/raw materials/finished product using the correct procedures in order to comply with GMP for Labs/GMP/EH&S/SOP’s and regulatory requirements.
• Identify and make recommendations for improvements as part of a team within or outside the department in order to eliminate non value added activities and ensure continuous improvement
• Deliver Customer Service level of >95% by testing components/raw materials/finished product in an efficient and timely manner
• Complete all QC batch documentation right first time (i.e. correct and in full) in order to achieve Customer Service and GMP.
• Quality and cost of product e.g. highlighting issues and awareness of the cost of re-tests and the cost associated with absenteeism and test failures.
• Organising own work and use of instruments to ensure targets are achieved and efficiency of the laboratory is maximised.
• Review work schedule in advance to ensure all relevant components and equipment are available.
• Prioritise daily work schedule to ensure effective analysis of product and schedule adherence.
• Plan, organise and carry out calibration, maintenance and validation of instruments as required.

Are you….

• Educated to Degree Level in a science related discipline.

Do you have….

• Experience within cGMP environment and the GMP requirements within a laboratory setting

• Knowledge of GMP Policies and Procedures

• Broad experience of analytical techniques including HPLC Calibration Systems(Desirable)

• Operating experience across

  • Chemicals and associated dangers

  • Documentation Compliance

  • Hazards in the workplace

  • Lab procedures

  • Products & Test Methods

  • Stability Testing

  • Calibration, maintenance & validation of laboratory instruments

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