We touch the lives of over 200 million patients every day, and billions every year.
After all, everyone needs healthcare or medication at some point.
Yet until today, you may not have heard of us.
We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.
We would like to invite applications for the role of Quality Control Analyst at our site in Waterford.
This will be a fixed term contract position ending 31st December 2025.
This is also a 2 cycle shift position- Monday to Friday 6-2 and 2-10.
A Quality Control Analyst is responsible for carrying out testing duties, to supply quality product to the customer on time and in full in order to meet the objectives of the department.A Day In The Life Of A Quality Control AnalystKey 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.
Who We Are Looking ForAre 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