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QA Officer, Pharmaceutical

QA Officer, Pharmaceutical

Russell Taylor

Posted a day ago, valid for 19 days

Prescot, Merseyside L35 3XE

Full Time

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Sonic Summary

The position is for a Quality Assurance Officer in the pharmaceutical industry located in Widnes, and it is an onsite role with no remote work options.
This is a permanent position requiring a minimum of 2 years of experience in a GMP/GLP role, along with a degree in pharmacy, biomedical sciences, or a related scientific field.
Key responsibilities include reviewing batch records, archiving GMP documents, assisting in audits, and performing investigations related to deviations and complaints.
The role offers a salary in the range of £30,000 to £40,000, along with benefits such as 25 days of holiday plus bank holidays, a company bonus scheme, and a pension plan.
Candidates should possess strong administrative skills, attention to detail, and the ability to work independently as well as part of a team.

Quality Assurance Officer, Pharmaceutical Location: Widnes, (this is an onsite role and duties cannot be performed from home). Type: Permanent Hours: Working 9-17.30 Monday to Friday Additional: 25 days +BH hols, company bonus scheme (dependant on performance), company pension, onsite parking Major Duties and Responsibilities • Reviewing Batch records and creating the associated checklists to support batch certification• Archiving GMP critical documents in line with company policy• Ensuring current versions of controlled documents are available to site personnel • Assist in Audits • Proactively identifying risks within the QMS and supporting the development of action plans to address and drive continuous improvement • To foster collaborative working with sister departments across the globe • To perform out of specification / out of trend investigations • To perform deviation / complaint investigations • Assisting in the follow up of events and CAPA's • To ensure correct QC samples are taken and sent for UK release testing in a timely manner The Person• Minimum degree in pharmacy, biomedical sciences, or any other scientific degree.• 2 years' experience in a GMP/GLP role.• Experience in CAPA, OOs, OOt, deviations, change controls etc in a GMP setting • Willingness to learn.• Strong administrative skills and the ability to generate clear and concise communication across all departments.• Ability to prioritize work, take initiative when required and to work quickly and accurately.• Attention to detail.• Ability to work in a fast - paced, small company environment.• Great interpersonal skills, a team player but equally comfortable to work independentlyImportant 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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