I am working with a global pharmaceutical company with a strong legacy in product innovations and technologies for an experienced Qualified Person (QP) to join their close-knit team and be based at their site just outside of Edinburgh, with a focus on sterile products.
The company is renowned for their staff satisfaction, driving change and wanting the best for both their employees, patients and customers. They are doing very well as a business and growing exponentially at around 10% per year, as a result offering longevity, growth opportunities and job stability. They are also establishing a brand-new state of the art manufacturing site - you will be part of a small team that operate in a transparent, open, supportive and collaborative culture with the goal of ensuring products reach their patients. The company is also keen to continue offering personal development, both personally and professionally.
Qualified Person responsibilities:
Certification and release of medicinal product batches manufactured at the site in accordance with Annex 16 and EU GMP
Managing the UK QMS
Cross-collaboration with other teams e.g. Regulatory Affairs
Representing Quality in projects on both a regional and local scale
Qualified Person Requirements:
Eligibility to act as a QP in the UK (previous experience as QP or trainee QP is preferable)
Life Sciences degree
Strong understanding of UK and EU GMP requirements
Solid foundation in QA and understanding of quality requirements through the whole value chain
Excellent communication skills
If you're interested in this role, click 'apply now' and I will be in touch.
Adecco Lifesciences is acting as an Employment Agency in relation to this vacancy