Back to searchQA Officer, Pharmaceutical
Russell Taylor Group Ltd
Posted a day ago, valid for a month
Widnes, Cheshire WA8 7ST
£28,000 - £33,600 per annum
Full Time
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Sonic Summary
- The Quality Assurance Officer position is located in Widnes and is a permanent, onsite role with working hours from 9 AM to 5:30 PM, Monday to Friday.
- The role offers a salary that is competitive within the industry, alongside 25 days of holiday plus bank holidays, a company bonus scheme, and a pension plan.
- Candidates must possess a minimum degree in pharmacy, biomedical sciences, or a related scientific field, along with at least 2 years of experience in a GMP/GLP role.
- Key responsibilities include reviewing batch records, archiving GMP documents, assisting in audits, and conducting investigations into deviations and complaints.
- The ideal candidate will have strong administrative skills, attention to detail, and the ability to work effectively both independently and 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 independently
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.
