Back to searchSenior QA Officer - Pharmaceutical
Russell Taylor Group Ltd
Posted 16 hours ago, valid for a month
Bolton, Lancashire BL1 1LE, England
£45,000 - £54,000 per annum
Full Time
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Sonic Summary
- The position is for a Senior QA Officer in the pharmaceutical sector, located in the Bolton/North Manchester area.
- This permanent role requires at least 3 years of GMP experience in a similar facility, with a focus on compliance, validation, and quality documentation.
- The salary for this position is competitive and commensurate with experience, although specific figures are not provided in the job listing.
- Key responsibilities include managing quality issues, conducting internal audits, and ensuring adherence to GMP and GDP standards.
- The ideal candidate should possess excellent communication skills and a willingness to work flexible hours while supporting the QA team and other departments.
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 facility
Experience in CAPA, deviation, change controls, OOs, Oot etc
Demonstrated compliance with procedures and policies
The ideal Candidate will have auditing experience (desired)
Excellent team, interpersonal skills, and communication skills (both written and verbal)
Willingness to work flexible hours
Safe adoption of working practises together with an understanding of the needs for precise and accurate documentation
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
