About the Role:
We're looking for a Qualified Person (QP) to join a leading pharmaceutical company in South Wales. If you have experience of both commercial and IMP, then you could be the Qualified Person that we've been looking for.
What will you be doing?
As the Qualified Person, you'll be responsible for certifying manufacturing processes and activities performed under Pharma services MHRA licenses. You will review batch manufacturing documents, ensuring compliance with EU GMP and the product specification file/marketing authorisation. You will review batch documents for all operations and will certify medicinal products for use in the EU and outside of the EU. Further to this, you will undertake audits in EU and third countries to ensure that sponsor manufacturing sites are operating in general compliance with EU GMP. If you have the ability to assist with regulatory inspections and client audits, then we want to hear from you.
What skills should you have?
- QA experience within the medicinal products/pharmaceutical industry
- Eligible to act as a Qualified Person for the certification of marketed products and investigational medicinal products
- GMP audit experience (preferably qualified as Lead Auditor)
- Experience working as a QP in the certification of sterile medicinal products
Who will you be working for?
As the Qualified Person, you'll be working for a company in South Wales that delivers unparalleled results to the pharmaceutical industry, working at the forefront in your field. You'll be joining an organisation who are passionate about supporting your personal development, supporting you through any training or CPD you may require. Further to this, as the Qualified Person, there would be potential for you to progress to a line management position dealing with direct reports.
If you have strong analytical and problem solving skills and consider yourself to be a conscientious communicator, then you could be the ideal fit for Qualified Person. If you're interested, contact us, today.