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Ipsen

QC Technologist

Posted 2 Days Ago
Be an Early Applicant
Dublin
Entry level
Dublin
Entry level
The QC Technologist role involves analyzing API and raw material samples, conducting troubleshooting, maintaining lab standards, updating documents, and ensuring timely delivery of QC data while collaborating with QA personnel. This role requires strong analytical skills and knowledge of GMP regulations.
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Title:

QC Technologist

Company:

Ipsen Manufacturing Ireland Ltd

Job Description:

Ipsen in Ireland is represented by a dynamic state-of-the-art manufacturing facility, creating API for our key products. We currently have an opportunity for a QC Technologist to join our Quality Control team on a 1-year fixed term contract basis. Hours of work:10am-6.30pm Mon-Thurs, 10am-5pm Fri.

The purpose of the QC Technologist role is to perform the analysis of API and raw material samples in a timely manner according to approved analytical procedures. To develop their technical skills through training in diverse techniques. Perform troubleshooting as required.

Essential Duties and Responsibilities

  • Complete the analysis and analytical write up of QC data as required for the testing and release of the following materials: Raw Materials, In-process intermediate samples, API’s, stability samples and environmental samples.

  • Perform analytical troubleshooting as required to ensure all scheduled testing can be completed in line with KPIs.

  • Complete support activities within the lab such as reagent and consumable ordering, stock check and ensuring 5S standards are maintained.

  • Perform all testing activities in line with SOPs and EHS standards.

  • Complete document updates as required through use of Easidoc system.

  • Attend and engage in daily and weekly team meetings to ensure all materials are tested and released on time and to ensure any delays or issues are escalated in a timely manner.

  • Compiling Metrics to display performance for Quality Control Laboratory.

  • Liaise with QA personnel to ensure delivery of QC data in accordance with the production plan.

  • Execution of Quality Connect workflows for Change control, Unplanned event and OOS records. Completing thorough root cause investigations for OOT/OOS results. Determining appropriate Corrective and Preventative actions.

This is a pivotal role for the site, requiring advanced analytical skills ideally at BSc level, and a track record in laboratory testing, ideally in a GMP regulated environment.

#LI-Onsite

IPSEN is committed to equality of opportunity for all staff and applications, individuals are encouraged to apply regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.

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