Job Summary
This is a challenging and rewarding role that requires a high level of expertise in pharmaceutical quality assurance. As a Process Quality Excellence Specialist, you will play a critical role in ensuring compliance with regulatory requirements and improving quality processes.
The successful candidate will have experience working in a global pharmaceutical environment and be familiar with international regulations, including ICH GCP, GLP, and PV. They will be responsible for supporting the development of quality and compliance infrastructure, collaborating with stakeholders to ensure compliance, and participating in audit and inspection planning.
Salary Details
The hourly rate for this role is £20.03 (PAYE) or £27.27 per hour (Umbrella). This is a competitive salary that reflects the importance of this role in ensuring compliance and improving quality processes.
Responsibilities
This role includes:
* Developing and implementing quality and compliance procedures.
* Collaborating with stakeholders to ensure compliance with regulatory requirements.
* Participating in audit and inspection planning.
* Managing Study Specific Training activities within the Learning Management System (LMS).
About Our Client
Our client is a global biopharmaceutical company dedicated to creating value for people living with severe diseases in immunology and neurology. This role offers an opportunity to contribute to the company's mission and make a meaningful impact in the industry.
Essential Qualifications
The ideal candidate will have strong pharmaceutical experience, preferably in a global quality assurance or clinical development setting. In-depth experience of GCP, including hands-on experience in global GCP audits and/or inspections, is essential. FDA/EMA inspection readiness experience is also required.