Job Description
Verbatim Pharma is working with a global service partner for pharmaceutical and biotech firms, assisting with clinical trial comparators and medicines access programs.
They have a great company culture that is friendly, energetic, and multicultural. The company is home to employees from various backgrounds who 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 a hybrid basis, working 3 days a week in the office and 2 days at home, located in the Reading area. The ideal candidate will need pharmaceutical QA documentation/QMS experience and a strong understanding of GMP/GDP.
Main responsibilities:
1. Overseeing eQMS and data input
2. Helping the wider QA team in deviation management and CAPA
3. QA Management of documentation, such as SOPs, Forms, and WIs on the electronic system
4. Working cross-functionally with internal and external stakeholders
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