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QC Manufacturing Support Scientist

QC Manufacturing Support Scientist

  • Location

    London, England

  • Sector:

    Life Sciences

  • Job type:

    Permanent

  • Salary:

    Negotiable

  • Contact:

    Connor Harknett

  • Contact email:

    Connor.Harknett@volt.eu.com

  • Job ref:

    75015-PHARM-CKT_1568020780

  • Published:

    about 1 month ago

  • Expiry date:

    2019-10-09

  • Start date:

    ASAP

  • Consultant:

    #

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 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 compliant QC lab to support the in process testing of AAV products manufactured at the GMP facility. Furthermore, our client will provide a pro-active environment where you will be a part of an effective team working within QC and across company departments where required.

Tasks:

  • Play a vital role in the manufacturing team with environmental monitoring ensuring the clean rooms maintain compliance. Clean room environment is grade D and C.

  • Ensure you are following protocols and SOPs to guarantee effective performance of analytical methods generating valid and reliable data.

  • 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.

  • This role will involve analytical testing programmes according to GXP, with defined schedules and responsibilities.

  • Participate in stability testing and trending of buffers used throughout the production procedure.

  • 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 a Self-motivated individual with the ability to work in a diverse team who are achieving a high standard of work, please do reach out and gain your next career step up!

or 01737 761 697