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QP Biologics - Flexible working conditions

Contract Type: Permanent
Location: Dublin
Contact Name: John Reid
Contact Email: johnr@rftgroup.ie

Job Description

QP Biologics – Flexing working conditions

My client a leading Pharmaceutical company now require a QP Biologics to join their expanding team.

The QP is a key member of the Quality Assurance team associated with sterile manufacture of an Advanced Therapeutic Medicinal Product, the Qualified Person (ATMP) is responsible for promoting a culture of Regulatory Compliance and Continuous Improvement within the Quality Department

This is a permanent role based in Dublin and it comes with a good salary with good benefits. There would also be some flexibility regarding working from home.

Responsibilities of QP Biologics
  • Management of batch disposition and material status control activities associated with Advanced Therapeutic Medicinal Product acting as a Qualified Person.
  • Management of review of Batch Manufacturing Records (BMRs).
  • Assisting in, and facilitating, investigations as part of the site Deviation Management System, ensuring effective root cause analysis and assigning of appropriate CAPAs.
  • Management of the Change Control process associated with ATMP manufacture and testing, ensuring controlled implementation of all GMP changes.
  • QA oversight of routine manufacturing, testing and relating activities to ensure on-going cGMP compliance.
  • Ensuring effective participation of the Quality Assurance team in production and other site meetings.
  • Implementation of Key Performance Indicators within the Quality Assurance area to align with company and global quality objectives.
  • Participation in the site Internal Audit programme.
  • Participation in the preparation of, and hosting, external cGMP audits, e.g. from Regulatory Authorities and Global Quality.
  • Participation in the preparation of documentation for regulatory submission and participation in regulatory affairs discussions.
  • Taking a leadership role in promoting a culture of Compliance, Right First Time and Continuous Improvement.
  • Implementing efficiency improvements in Quality Dept on a continuous basis and participating in site projects and initiatives.
  • Communication and liaison with other departments on Quality issues (as required), providing guidance and support to others.
  • Acting as a designee to the QA Manager as required.
  • Supervisory duties for Quality Assurance personnel may be part of the role.

Requirements of QP Biologics:
  • Primary Degree in a scientific discipline
  • Must meet the educational requirements of a Qualified Person as per EU Directive 2001/83/EC.
  • Minimum of 5 years’ experience in the pharmaceutical industry in a Quality role.
  • Experience of sterile manufacture is essential.
  • Experience of biologics manufacture is desirable.


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The RFT Group, BioPharmaceutical Division specialize exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.

For more information please contact John at The RFT Group / www.rftgroup.ie / 01 2302400 or click apply below