Home
Bolton
Lean manager
Senior QA Specialist, Pharmaceutical

Senior QA Specialist, Pharmaceutical

Russell Taylor

Posted a month ago, valid for 6 days

Bolton, Lancashire BL5 3XP, England

£40,000 - £48,000 per annum

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

The Senior QA Specialist position is located in the Bolton/North Manchester area and is a permanent role with daytime hours from Monday to Friday.
The role offers a salary of £40,000 to £50,000, along with an annual performance bonus, health assurance, and company-run incentives.
Candidates must have a minimum of 3 years of GMP experience in a similar pharmaceutical facility and a good knowledge of GMP/GDP related manufacturing.
Responsibilities include managing site quality issues, overseeing product quality, and supporting the Quality Management System for continuous improvement.
The ideal candidate will possess strong auditing experience, excellent interpersonal skills, and a commitment to precise documentation.

Senior QA Specialist, Pharmaceutical Location: Bolton/ North Manchester area Type: PermanentHours: Days (Monday - Friday), parking onsite Additional: Annual performance bonus, health assured and company ran incentives . • 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.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.

Apply now in a few quick clicks

Senior QA Specialist, Pharmaceutical

Continuous Improvement Manager

QESH & Continuous Improvement Manager

QHSE Manager