Are you an experienced QA Batch Record Reviewer? Do you have experience working within a GMP-regulated manufacturing environment? If so, this could be the role for you!
We are partnered with a leading manufacturing business in Hampshire who are looking to hire a QA Batch Record Reviewer to support their Quality Assurance team.
This role is essential in ensuring manufacturing documentation is accurate, complete and fully compliant with GMP and regulatory standards, helping to support the timely release of high-quality products.
This role is offered for 6 months initially, with the potential to extend. You will be able to work either 06:00-14:00, or 07:00-15:00 Mon-Fri.
Key Responsibilities
- Review batch records, production documentation, cleaning logs and associated GMP records.
- Ensure documentation is complete and compliant to support product release.
- Work closely with Production, Compounding and Quality teams to resolve documentation queries.
- Investigate batch record discrepancies and elevate observations where appropriate.
- Support the implementation and continuous improvement of batch record review procedures.
- Perform SAP transactions and maintain accurate quality records.
- Assist with deviations, investigations and CAPA activities.
- Collect and analyse quality KPI data to support continuous improvement initiatives.
Qualifications
- Previous experience within Quality Assurance, GMP Compliance or other pharmaceutical or FMCG manufacturing.
- Experience working in a regulated manufacturing environment.
- Strong attention to detail and documentation review skills.
- SAP knowledge is advantageous.
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively across multiple departments.
- Experience in a GMP manufacturing environment; relevant professional certification is beneficial.
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