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Quality Systems Supervisor

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

Job Description

Quality Systems Supervisor

My client a leading Pharmaceutical company now require a Quality Systems Supervisor
to join their expanding team.

The Quality Systems Supervisor will provide oversight and management of elements of the Quality Management System (QMS), which includes, but not limited to, change control, deviations, CAPAS, documentation, supplier quality management and GMP training.

This is a permanent position based in Dublin and comes with a strong salary and benefits package.

Quality Systems Supervisor
  • Supervisory duties for Quality Systems personnel within the Quality Systems group.
  • Provide oversight and management of the supplier approval programme and the external audit schedule.
  • Participate in the internal audit schedule.
  • Administration/co-ordination of risk assessments.
  • Develop and write SOP & Controlled Documents.
  • Be a key member of the onsite audit team during external cGMP audits, e.g. from Regulatory Authorities and Global Quality.
  • Assisting in, and facilitating, investigations as part of the site Deviation Management System, ensuring effective root cause analysis and assigning of appropriate CAPAs.
  • Assist and co-ordinate the preparation of reports in relation to Annual Product Reviews for all products manufactured on site.
  • To ensure that the systems with a GMP impact are maintained as per written procedures.
  • Assist and co-ordinate implementation of global standards and procedures into the site Quality Systems.
  • To actively support the development/implementation and continuous improvement of the Quality Management Systems.
  • To be cross-trained in multiple quality systems.
  • Participate in other projects as directed by the Quality Systems & Compliance Manager.

Requirements of Quality Systems Supervisor
  • A minimum of 7 years working within quality in the pharmaceutical industry.
  • A minimum of 5 years' experience in a people management role is desirable.
  • Experience working in finished product pharmaceuticals/biologics, including analytical chemistry, quality assurance, quality control, development, and/or manufacturing areas.
  • Thorough understanding of quality systems and cGMP's.

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