Quality Control Scientist

  • Location

    London, England

  • Sector:

    Life Sciences

  • Job type:

    Blijvend

  • Salary:

    Negotiable

  • Contact:

    Connor Harknett

  • Contact email:

    Connor.Harknett@volt.eu.com

  • Job ref:

    75365-PHARM-CKT_1571642749

  • Published:

    1 jaar geleden

  • Expiry date:

    2019-11-20

  • Startdate:

    ASAP

I'm currently seeking a Quality Control Scientist in London. Please see details below.

Would you like the chance to join an award winning global biotechnology Company who focus on development and commercialisation of innovative gene therapies to change lives? My client has a broad pipeline with one clinical trial ongoing and two more coming in 2019/20 which allows more opportunities to change lives of patients by providing directed gene therapy as a life-long and potentially curative treatment.

This opportunity will allow you to be involved in establishing a GMP/GCLP compliant QC lab to support the in process of bio analytical testing of AAV products manufactured at the GMP facility for pre and post clinical samples. Furthermore, play a vital role in technology transfer and validation of in process and release assays from the development lab and external CROS.

Tasks:

  • You will be tasked on executing a variety of bioanalytical testing methods according to GXP. Your data must be recorded and presented in project team meetings where you innovative ideas/opinions can be expressed.

  • Contributing in analytical and OOS investigations. This will allow a culture of continuous improvement, by you having a keen eye of detail to seek out unusual observations, unexpected findings which will need to be reported to QC manager.

  • Moreover, you will be a part of a QC team in establishing a GMP compliant QC lab to support the in process testing of AAV products.

  • You will need to be able provide guidance to junior members of staff where it is needed to ensure a safe working environment and company processes are followed.

  • Must maintain high level communication with all quality professionals and cross functional departments, while responding to audit findings.

  • Furthermore, this role will provide a flexible working in environment allowing you to set up and deliver on projects successfully.

  • Working within a QMS to include change control systems, deviations and OOS reporting.

  • Furthermore, provide essential input for reporting of data, generation of certificates, protocols, SOPs and internal written reports.


If you are looking for next career step, where you are looking to grow your own career as well as your companies, Please do get in touch!