Senior QA Officer, Pharmaceutical
Location: Bolton/ North Manchester area
Type: Permanent
Hours: Days (Monday - Friday), parking onsite
Responsibilities:
Duties will include handling site quality issues including compliance, validation, internal audits, project management & execution, and quality documentation, under the leadership of the Quality Assurance Manager.
This role involves overseeing the quality of all products manufactured or sourced by the company to ensure adherence to GMP, GDP, and documented procedures.
Additionally, the role supports Quality Management in implementing GMP/GDP documentation and in enhancing the Quality Management System (QMS) for continuous improvement.
CAPAs, Deviations, audits, risk assessments, customer complaints & root cause analysis.
Generate SOPS and other quality documentation.
Ensure that the QMS is already in a condition ready to inspect.
Ensure that the internal audit schedule is followed as per procedure.
Manage and maintain the supplier approval process
Create supplier audit documentation
Liase with MHRA relating to quality and compliance matters.
Assist in training of QA team members aswell as potentially helping to support other teams.
Undertake and develop risk assessments.
The Person:
Good knowledge of GMP/GDP related pharmaceutical manufacturing
3 years+ GMP experience in a similar f...