Quality Assistant

https://www.teamhorizon.ie/job-search/1407-quality-assistant/quality/dublin/job2024-08-28 10:14:222052-01-12Team Horizon
Job TypeContractor
AreaDublin, IrelandDublinIreland
SectorQuality
Start Date
AdvertiserAshling Guthrie
Job Ref3316
Job Views123
Description

Team Horizon is seeking a Quality Assistant for our client - a Biopharmaceutical manufacturer in Dublin.


 


 


Why you should apply:



  • Work with a company who unleash bold thinking with the power to inspire life-changing medicines. 

  • Become part of a team of professionals working with all aspects of thebusiness from development to commercialization and distribution.

  • You will support the management of the Supplier Quality program and assist in the Supplier approval process and in the management of all Supplier Quality inputs including quality agreements, questionnaires, audits, supplier corrective action reports, supplier notices of change,  change control, etc


 


What you will be doing:



  •  Support the global supplier and material approval processes including migration of site-based processes to the global process.

  • Support the Quality Agreement management process

  • Support Supplier Change Notification process to ensure appropriate change control and regulatory updates have been made prior to making changes.

  • Assist in the preparation of inputs to the Supplier Reviews process, including preparation of data for the review, summarizing the results and status of complaints initiated with suppliers to drive improvement.

  • Assist in the monitoring and reporting of supplier performance indicators and contribute to the quality improvement opportunities within the supply chain.

  • Support Continuous Improvement of the Supplier Quality System

  • Support audits and inspections, as appropriate.

  • Perform all responsibilities in accordance with company policies, procedures, federal regulations and safety requirements.


 


What you need to apply:



  •  Minimum of 1+ years’ experience in Quality with medical device, pharmaceutical, or biologics experience

  • This position requires the individual to understand and follow written SOPs, record all work legibly and in real time; close attention to detail is necessary.

  • The person in this position will receive supervisory direction on all routine and non-routine activities. Routine activities will be unsupervised as training and competency develops. The person in this position must have good organizational skills.

  •  A strong customer focus and ability to prioritize and adapt to business needs

  •  Knowledge of applicable international GXP regulations and standards • Strong business partner with a focus on delivering results.

  • Strong written and verbal communication skills

  • Eagerness to learn and accept challenges


 


 

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