Verbatim Pharma is working with a global service partner for pharmaceutical and biotech firms, and they help with clinical trial comparators and medicines access programs.
They have a great company culture that is a friendly, energetic and a multi-cultural. The company is home to employees from various backgrounds that speak a range of languages.
If you have a forward-thinking attitude and are ready to go the extra mile then this could be the role for you.
This role will be offered on hybrid basis, working 3 days a week in the office and 2 days at home.
The location will be Reading area and the ideal candidate will need pharmaceutical QA documentation/QMS experience and strong understanding of GMP/GDP.
Main responsibilities:
- Overseeing eQMS and data input
- Helping wider QA team in deviation management and CAPA
- QA Management of documentation, such as SOP’s, Forms, WI’s on electronic system
- Working cross functionally with internal and external stakeholders
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