Senior QC Analyst - NPI

Job Overview

QC Senior Analyst - NPI
Based in Dublin

12- month contract + excellent hourly rate

Excellent opportunity for a Senior QC Analyst with NPI experience to join a leading Biopharmaceutical company in Dublin.

This company has invested millions into their Dublin facility which shows their commitment to employees and the area. This is a superb opportunity to work in a quality control environment supporting new product introductions for a global biopharmaceutical company. Working here will be a fantastic addition to your CV. Working here will give you the opportunity to develop your skills on massive projects with cutting-edge technology and a supportive and friendly team. Your new employer is one of the world's largest biopharmaceutical companies whose products are sold worldwide and make a massive difference to improving patient's quality of life. Working here you will really make a difference.

You will have the opportunity to:

Be responsible for one or more of the following activities in QC including analytical testing, characterisation, sample and data management.
Work across diverse areas within QC with a high degree of technical flexibility.
Plan and perform chemical analytical high volume NPI testing activities within agreed testing time frame.
Perform methods and procedures and a large variety of assays.
Be the QC point of contact for NPI activities and product meetings.
Assist with QC projects and/or QC tasks within projects.
Manage all sample management activities related to NPI activities throughout the site.
Create and approve protocols, sample plans, SOP and documentation related to NPI.
Manage sample shipments and temperature monitoring activities for NPI activities.
Use LIMS data coordination of non-core (NPI) activities.
Contribute to lab investigations as required and approve lab results.
Troubleshoot, solve problems and communicate with stakeholders.
Write protocols and perform assay validation and equipment qualification/ verification.
Introduce new techniques to the lab, including method transfers, reports, validations and protocols.


Relevant experience:

Bachelor's degree in a Science related field is required.
5+ years of bio/pharmaceutical or medical device QC experience within a GMP laboratory.
Experience in both Wet Chemistry and HPLC testing techniques.
Extensive experience in laboratory systems such as sample management LIMS, and Empower software etc.

For more information please don't hesitate to call Aoife on 086 044 3981 to discuss the role in more detail.

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