GMP Biotechnologist

  • Location

    Stevenage, Hertfordshire

  • Sector:

    Life Sciences

  • Job type:

    Blijvend

  • Salary:

    Negotiable

  • Contact:

    Connor Harknett

  • Contact email:

    Connor.Harknett@volt.eu.com

  • Job ref:

    76944-PHARM-CKT_1603871993

  • Published:

    1 maand geleden

  • Expiry date:

    2020-11-27

  • Startdate:

    ASAP

I am actively looking for a GMP Biotechnologist t in Steveange. Please see below.



Looking for the next step up? Looking for a company who can provide an opportunity to play a part in shaping the growth in the Gene therapy market?


I am currently working with one of the top ten global biotechnology companies to watch in 2020, who have real focus on the development and commercialization of unique gene therapies to change lives. They have a strong pipeline with two clinical trials ongoing, where one trial has just moved into phase 3. This allows my client to have a real chance to change the lives of patients by providing directed gene therapy as a life long and potentially curative treatment.

RESPONSIBILITIES:

Be part of the GMP manufacturing operations team responsible for delivering GMP manufacturing batches for clinical studies.

Write SOPs and batch records to support GMP manufacture.

Become fully trained in all areas of the manufacturing process as required and responsible for practical delivery of key process steps.

To be trained in USP/DSP equipment SOPs as required for supporting GMP batch manufacture.

perform the effective transfer of materials/samples/waste into and out of the grade C cleanroom as required by the daily manufacturing plan and daily BOM.

To support GMP Operations in deviations, investigations and change controls as required.




REQUIREMENTS

Must be educated to degree level or equivalent with a pharmaceutical related or biotech related degree.

Prior experience in the pharmaceutical/biotechnology industry, working in a GMP Manufacturing environment at least 1-2 years.

Experience of mammalian cell culture techniques.

Prior experience working with viral vectors ( AAV) and within ATMP's company would be ideal.