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Pfizer Bioprocessing Technician in Grange Castle, Ireland

Applications will close 08 April 2020.

One Site, Multiple Opportunities!

The Bioprocessing Operations Unit is a manufacturing area at Pfizer Grange Castle that is currently delivering multiple New Product Introduction projects. Your role will be in the Bioprocessing Manufacturing Suites where you will be directly involved in the manufacture of Vaccines and Biotherapeutics as part of a diverse team of welcoming and supportive colleagues.

We work with downstream manufacturing processes including Chromatography, Ultrafiltration/Diafiltration, Conjugation, Viral Filtration and Sterile Filling.

This is an exciting permanent opportunity to join a world class facility which is dedicated to bringing therapies to the market that will significantly improve patients' lives.

About the Role

  • Responsible for execution of all tasks associated with the preparation for and production of Pfizer products in cGMP environment ensuring full attention to detail and excellent documentation skills.

  • Assist in maintaining a safe, cGMP compliant work environment at all times

  • Responsible for completion of tasks according to Standard Operating Procedures and batch records (paper and electronic).

  • Perform initial troubleshooting of issues identified during routine operations.

  • Assist with the investigation of and operations deviations through QTS system, engaging with all relevant personnel and functions as appropriate.

  • Assist where necessary with the training of colleagues in SOPs, process execution and equipment operation.

  • Provide input into the creation and maintenance of area SOPs and batch records.

  • Seek opportunities for Continuous Improvement and embrace Pfizer's 'Own It' culture to own and drive any activities associated with delivering these improvements.

  • Use Lean Tools as part of daily operations (Standard Work, 5S, Method 1, 2 etc.) to optimize efficiency and drive the culture of Continuous Improvement and Zero Defects.

  • Assist in Facility and Equipment start up and Validation activities. Provide input on equipment installation, start-up, operation and troubleshooting to support introduction of new products into sustaining operations.

About You

To be successful in this role you will require:

  • Prior experience working in a regulated environment

  • Working knowledge of production operations with a strong focus on attention to detail and compliance to all regulatory standards

  • An ability to work independently, and as a member of a team in a dynamic, fast-paced environment that requires flexibility and initiative.

  • Flexibility to work 24/5 and 24/7 shift patterns as required.

In order to be considered for this position you need to be legally eligible to work in Ireland.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Due to high volume of applications we will be contacting successful candidates only.

#LI-PFE

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Manufacturing

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