Qualified Person (QP) – Sterile Manufacturing

As a Job, the work centres on clinical Trial Authorisation as appropriate. It would suit someone who can bring ownership, clear communication, and practical organisation to the role.

Known job details

• Additional detail: Pension support may be included.

Likely focus of the role

• Clinical Trial Authorisation as appropriate.

Requirements mentioned

• To undertake the duties of Qualified Person.
• To review and evaluate batch records and perform batch certification and release in accordance with Good Manufacturing Practice and the Marketing Authorisation.
• Eligible to be nominated as a Qualified Person EU Directive 2001/83/EC as amended (Medicinal Products for Human Use).