Site Microbiologist

Who we are

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. 

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 Site Microbiologist at our Waterford site. This is a Permanent Position.

The Site Microbiologist is responsible for the Management of the Microbiology Lab and defines the microbiology strategy for the site in order to meet TEVA Waterford Operational and Quality objectives.

The successful person will be managing the full micro team for the site along with reviewing departmental performance and acting as the site main contact for all micro related queries.

There is no relocation support offered for this role. 

A day in the life of our Site Microbiologist

Responsible for all micro queries and investigations around the site  Liaising with senior management on all queries relating to the micro team Proactively plans for, develops and implement new projects and systems for the micro team on an ongoing basis Being a subject matter expert on all matters relating to micro Supports and drives the Contamination Control Strategy for the site in accordance with Annex 1 requirements Develop and train the micro analysts on the team to the best standards Deliver Customer Service (both internal and external) in accordance with Quality standards, ‘TEVA Best Practices’ and Cost Control. Ensure that operational schedules are met with all batches being ready as needed  Ensure GMP compliant, cost effective systems are developed in place and operational in order to ensure all work carried out by Microbiology personnel is in compliance with required standards conforming to TEVA, cGMP, and Health and Safety, TEVA Best Practice and Environmental requirements. Ensure the team are fully ready for all audits and inspections as required 

Who we are looking for

Are you….

Third Level qualified in Microbiology (essential)

Do you have?

Extensive management experience in a high throughput Laboratory within the Pharma industry? Excellent Knowledge of Regulatory USP/Ph.Eur/JP harmonised microbiological methods, method verification/development ensuring the site is in compliance with all micro regulations Comprehensive Knowledge of Microbiology and Microbiological Techniques in the Pharma Industry Knowledge of Steam Sterilisation and microbiological media. Knowledge of environmental control, routine monitoring and method validation. Understanding of microorganisms and bioburden/contamination control and the risk associated with non-sterile inhalation products. Knowledge of PW systems and microbial control Knowledge of microbial identification methods Good understanding of Contamination Control Strategy and Annex 1 requirements

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