Description
QA Representative sought for 6 month contract in global pharmaceutical company.
Reporting to the QA Group leader your role is to provide assurance that manufacturing is carried out in accordance with cGMO and regulatory commitments. Ensuring that the production records meet the requirements for batch release in accordance with the appropriate SOPs. This will cover the QP release of both veterinary and medicinal products.
In addition you will have QA responsibility for disposition raw materials, evaluation of deviation reports, advising on reprocessing or preventative actions. You will monitor trends and identify issues with purchased materials, review and approve SOPge control documentation, validation protocols and similar.
You will advise on and participate in self-inspections and other manufacturing audits as well as providing training, support and advice and proactive support in the Site Quality systems to product and support teams.
To be successful you will ideally possess a life sciences or related degree and have previous Quality Assurance in a GMP environment within the pharmaceutical industry.