Direct message the job poster from Mason Alexander
We are delighted to be representing a well established pharmaceutical consultancy, on a permanent Qualified Person opening.
This is a fantastic role that will see you work across a range of products at different stages of development, and work within a great Quality Division!
As Qualified Person, you will be responsible for:
* Foster a culture of GMP knowledge and compliance throughout the organisation
* Conduct batch release for investigational medicinal products and commercial products
* Support business development activities, with specific focus on clients requiring IMP expertise
* Develop and maintain quality systems that ensure GMP compliance
* Participate in audit preparation and inspection readiness activities
* Collaborate with Quality Managers and the quality team to meet company and client objectives
* Manage assigned client projects effectively
* Support Senior Management in developing and implementing company vision and strategy
Education & Experience required:
* Educated to degree level in a Scientific Discipline
* Eligible to act as Qualified Person
* IMP Release experience is essential
This is a primarily remote role with travel required to the office in the midlands approximately 1-2 days per month
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Quality Assurance, Science, and Manufacturing
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
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