A Qualified Person (QP) is required by Careerwise Recruitment to work for our Limerick based biotech client.
Role of this position
- Support major investigations, ensuring all product deviations are closed prior to batch release
- Reviews and approves Product Quality Reviews
- Reviews and approves new and revised master manufacturing records.
- Participates in cross functional teams as Quality/Qualified Person representative
- Participate in third party/supplier audits, as required
- Provide additional QP support to quality related issues, as required
- Qualified Person status achieved with min 3 years of relevant work experience acting as Qualified Person, named on a Manufacturing and Importation Authorisation (MIA).
- Biologics manufacturing experience desirable.
- Aseptic / Sterile Drug Product manufacturing experience desirable.
Please call Michael O'Connor today for further information on 091-452410 or email email@example.com
CareerWise Recruitment (In Search of Excellence)