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Senior QA Officer - Pharmaceutical

Russell Taylor
Posted 9 hours ago, valid for 2 days
Location

Bury, Lancashire BL0 0BT, England

Salary

£42,000 - £50,400 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The Senior QA Officer position is located in the Bolton/North Manchester area and is a permanent role with day hours from Monday to Friday.
  • Candidates should have a minimum of 3 years of GMP experience in a pharmaceutical manufacturing setting and a good knowledge of GMP/GDP regulations.
  • The role involves overseeing product quality, managing compliance issues, and supporting the Quality Management System for continuous improvement.
  • The salary for this position is competitive and commensurate with experience, although the exact figure is not specified in the listing.
  • Ideal candidates will possess strong auditing experience, excellent communication skills, and a willingness to adopt safe working practices.
Senior QA Officer, Pharmaceutical Location: Bolton/ North Manchester area Type: PermanentHours: 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 documentationImportant 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.

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.