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Senior bioprocess engineer - contract position

Cork
beBeeProcessEngineer
Engineer
Posted: 5 July
Offer description

Job Opportunity: Process Engineer

We are seeking an experienced PROCESS ENGINEER to join our team in Waterford. This is a 12-month contract position, offering the opportunity to work on pre-filled syringe operations and contribute to the growth of our biopharmaceutical and medical device client.

The ideal candidate will have at least 3 years of experience in Sterile Manufacturing Operations, Syringe Filling, and New Product Introduction. They will be responsible for leading projects and programs associated with pre-filled syringe operations, including filter test development, fill weight cycle development, cleaning verification, and documentation generation.

The successful candidate will also be responsible for supporting day-to-day operations of the syringe filling area, investigating issues, and delivering corrective actions. They will communicate and liaise with vendors during project execution and execute process engineering activities to schedule and compliance standards.

Requirements:

* Honours degree in an Engineering discipline
* Strong problem-solving skills
* 3 or more years' relevant experience in a highly regulated GMP environment
* Experience of Sterile Manufacturing Operations would be an advantage
* Experience in syringe filling would be a distinct advantage
* Experience in new product introduction would be a distinct advantage

Key Responsibilities:

* Supporting day-to-day operations of the syringe filling area
* Leading problem-solving investigations for technical issues
* Liaising with vendors during project execution
* Executing process engineering activities to schedule and compliance standards

Benefits:

* Opportunity to work on pre-filled syringe operations
* Contribution to the growth of our biopharmaceutical and medical device client
* Chance to develop skills in Sterile Manufacturing Operations and New Product Introduction

Others:

* Must hold a valid working visa for Ireland
* Role may require travel to other sites or vendor sites
* Participation in site GMP regulatory and safety audits

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