Qualified Person (QP)

SRG's client are looking for an experienced Qualified Person (QP) to join them on a permanent basis at an exciting time for the business as they continue to expand.

You can get further details about the nature of this opening, and what is expected from applicants, by reading the below.

This is a fantastic opportunity for an experienced QP to take on a permanent role with excellent salary and benefits.

Hybrid working options are available.

The role:
Undertake the duties of a Qualified Person as defined in relevant regulatory directives.
Responsibility and performance of Batch Certification and Release of drug product in accordance with requirements of EU Directives and GMP.
Ensure products have been manufactured and tested in accordance with Good Manufacturing Practice (cGMP).
Ensure products manufactured demonstrate compliance with the regulatory requirements.
Working with the Quality Director and site management to ensure that GMP compliance implemented and maintained in accordance with the appropriate legislation, company policies/procedures and in compliance with appropriate manufacturing authorizations.
Review and implement Quality Management Systems in compliance with current GMP and any regulatory updates or observation. Maintain product quality and release by enforcing quality assurance policies and procedures and GMP requirements.
Act as a Subject Matter Expert (SME) to facilitate site compliance with the company’s Quality Management Systems. Support the Quality Assurance department for all compliance inspections of the site e.g. internal audits as well as Regulatory Inspections.
Perform external audits Support the self-inspection schedule for the Company Maintain knowledge of current guidelines and regulatory advancement in line with the role for continued professional development.

The person:
Eligible to undertake the duties of a Qualified Person
A relevant degree qualification (preferably in Chemistry, Pharmacy or Biological Science.)
Experience with FDA, MHRA, EMA and other regulatory agencies.
Prior experience in a pharmaceutical manufacturing environment
Experience in commercial and Investigational medicinal product (IMP).
Experience in steriles, biologics, ideally with advanced therapeutics and experience being on the licences for these products.
Extensive audit experience.
Ability to travel for audits (occasional)