Quality Auditor

PE Global is currently recruiting for a Quality Specialist/Auditor for a leading multi-national Pharma client based in Moorgate, London.
This is an initial 6 months contract position offering hybrid work.
37.5 hours per week.
Pay Rate is from £*****ph up to £*****ph PAYE.
Depending on experience.
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***
Duties of the role/Responsibilities
As a Quality Specialist, you will be responsible for the final review of clinical batch records to ensure compliance with GMP and conformance with regulatory filings.
The compilation and approval of this data pack and presentation to the QP for final release is the core function of the role.
Conducts routine audits of data, information, procedures, equipment and systems (including computer systems), and/or facilities to ensure the compliance with SOPs and GMPs and worldwide regulations.
Review and approve production and analytical documentation accompanying the release of API, Safety Assessment or clinical supply lots (bulk and packaged) to ensure conformance to appropriate regulatory requirements.
Communicates and resolves audit comments with client areas.
Issue reports summarizing deficiencies and work with areas to execute remedial action.
Notify appropriate management of inspection result.
Education/Experience
Experience should be in the pharmaceutical/chemical industry or government drug-regulatory agency with a working knowledge of cGMP regulations.
Existing experience in a QA or similar role in a GMP environment
Effective communications (oral/written) and interpersonal skills are necessary.
Confidence to work with minimal supervision, and a keen eye for detail.
Interested candidates should submit an updated CV.
Please click the link below to apply, alternatively send an up to date CV to
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***