QA Officer, Pharmaceutical

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

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