Senior Validation Specialist
- M4 Corridor
- Permanent
- Commissioning, Qualification and Validation
This vacancy has now expired
Based on the M4 Corridor, they have undergone a massive refurbishment and expansion at their facility here and seem to keep growing.
In this role you will be responsible for the generation and execution of validation strategy, protocols and reports in line with cGMP across facilities/utilities validation. You will be the Subject Matter Expert (SME) for this area, you’ll enjoy working in a very autonomous role where you will set the validation agenda for this area as well as working part of the wider function.
You will have the following experience and qualifications:
- Degree (or equivalent) in a science or related engineering discipline
- Extensive validation experience within the biopharmaceuticals industry
- Demonstrable specific expertise in facilities / utilities validation
- Experience working within a GMP environment including clean rooms and facilities
- Knowledge and understanding of manufacturing operations
- Fermentation
- Purification
- Controlled storage
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We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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Peter
I manage this role.