We are partnered with aUK-based pharma consultancy who specialise as an advisory firm to life science organisations helping them to achieve and maintain compliance with regulatory and quality standards across the product lifecycle. They predominantly focus on supporting companies in development stage, moving through Phases I-III, and supporting with GMP transition.
They are looking to onboard a Strategic consultant, somebody who can advise and consult a number of Global clients on compliance, and external manufacturing matters. You will act as an external arm of their clients, liaising with and managing CDMO's, and other key Vendors. You will be speaking with key stakeholders including C-suite, and VP level, as well as connecting with entry level and specialists within their clients.
Responsibilities
* CDMO Management and Oversight.
* Vendor Qualification, and Plan of.
* Inspection readiness and Audit management.
* Batch Release and relevant Documentation.
* Work cross-functionally across multiple relevant departments.
* Compile Quality Reports and document findings.
Requirements
* 7+ years' Pharmaceutical QA experience.
* Auditing background/experience.
* Strategic Mindset.
* Clear knowledge of QA Processes.
* Good communicator, confident and self assured.
* Highly organized.
Package
* Remote working model.
* Clear progression Path.
* Friendly and open company culture.
* Competitive salary package.
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