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Manufacturing operations specialist

Cork
beBeeOperations
Operations specialist
Posted: 27 August
Offer description

Job Description

A Manufacturing Operations Specialist with experience in Sterile Manufacturing Operations, Syringe Filling and New Product Introduction is required to join our team. This initial 12 month contract offers a unique opportunity to work on Projects / Programs associated with pre-filled syringe operations.

The ideal candidate will have 3+ years of experience and be responsible for leading problem solving investigations for technical issues as well as owning change controls. They will also be expected to deliver activities on schedule and within budget.

Responsibilities

* Supporting day-to-day operations of the syringe filling area through investigations, identify and deliver corrective actions including continuous improvement projects.
* Communicate and liaise with material/component vendors during project.
* Execute Process Engineering activities to schedule and to the appropriate compliance and safety standards.
* Writing of Process/Operational Control Strategy documents (detailing control over Critical Process Parameters), Failure Mode Effect Analysis (FMEA) and supporting Operator training.
* Coordinating and ownership of deliverables to meet project timelines and cost.
* Generation of hour-by-hour schedules for planning line time and execution of deliverables.
* Provide support where required on the existing Aseptic Syringe Filling Line and supporting processes which includes Debagger / Ebeam / Delid / Deline / Isolator / Syringe filling machine with multi filling technologies.
* Support commercial manufacturing through delivery of key performance metrics (SQDCI).
* Role may require travel to other sites or vendor sites.
* Participate in site GMP regulatory and safety audits.
* Provide technical support to implement process improvements, new product transfers to the site and production.

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.

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