QC Technician Incoming Materials

4 weeks ago

Oxford, United Kingdom Pharmiweb Full time

Job description:
 

We want you to feel inspired every day. We’re future-focused and our business is growing. We succeed together through passion, commitment and teamwork, and so can you.

 

We are currently recruiting for a QC Technician Incoming Materials to join the Quality Control team.  The purpose of this role is to ensure that incoming raw materials are tested and released in time to meet manufacturing demands and are compliant with regulatory requirements.

 

Quality Control (QC) is made up of the microbiology and raw materials teams. Raw materials make sure incoming materials are of suitable quality. Microbiology test the manufacturing environment and its products to make sure they are free of harmful microorganisms

 

Your responsibilities in this role would be:

 

  • Test and release incoming raw materials ensuring that quality and time targets are met
  • Maintain the QC Chemistry laboratory to GMP standard and keep test equipment calibrated and maintained for optimal use
  • Maintain relevant SOPs, Quality Control PlansGINs and other documentation to ensure compliance with required standards
  • Represent the QC department in communications with manufacturing and supply chain particularly in ensuring uninterrupted raw material flow
  • Represent the company in communications with external testing laboratories and suppliers ensuring test results and quality information is provided
  • Raising and progressing Quality Records (e.g. Deviations, Investigations, Change Controls, CAPAs) within a timely manner

  

We are looking for:

 

  • Knowledge of CMP requirements with specific reference to documentation and laboratory activities in order to ensure compliance is maintained.
  • Knowledge of practical and theoretical chemistry techniques in order to enable effective and accurate material testing
  • Computer literate, especially with MS Office (Excel, Word, etc.)
  • Relevant raw material and chemistry experience
  • Good knowledge of GMP requirements required in a pharmaceutical company 

 

About Us:

 

OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies.

 

OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.

 

What’s in it for you:

 

  • Highly competitive total reward packages
  • Wellbeing programmes
  • Development opportunities
  • Welcoming, friendly, supportive colleagues
  • A diverse and inclusive working environment
  • Our values are: Responsible, Responsive, Resilient, Respect
  • State of the art laboratory and manufacturing facilities

 

Collaborate. Contribute. Change lives

 


We offer:

 

 

 

Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies.  

 

 

 

Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patient’s cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients’ cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy).  

 

Oxford Biomedica collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Oxford Biomedica's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise.

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