QA Officer
other jobs SmartSciences Job
Added before 4 Days
- England,East of England,Hertfordshire
- Full Time, Permanent
- Salary negotiable
Job Description:
QA Officer - Pharmaceutical Manufacturing (St Albans)
Are you a quality-focused professional with an eye for detail and a drive for compliance? Smart4 Sciences is partnering with a leading pharmaceutical company in St Albans to recruit a QA Officer who will play a pivotal role in maintaining and strengthening their Quality Management System (QMS).
Working alongside the Quality Systems Manager, you’ll ensure the QMS is inspection-ready, compliant with MHRA, GMP, GDP, and ISO standards, and aligned with regulatory requirements. This is a hands-on role where you’ll oversee documentation, supplier quality, regulatory submissions, and continuous improvement initiatives, while supporting audits and driving operational excellence.
Key Responsibilities*Implement and maintain the QMS to meet MHRA, GMP, GDP, and ISO standards
*Conduct self-inspections, internal audits, and manage CAPAs
*Manage controlled documents including SOPs, batch records, and manufacturing logs
*Review and update specifications, methods, and product artwork
*Support regulatory submissions and assist during MHRA/FDA inspections
*Prepare Product Quality Reviews (PQRs) and risk assessments
*Manage deviations, change controls, and investigation reports
*Oversee supplier quality, vendor agreements, and handle supplier complaints
*Report monthly Quality KPIs and contribute to continuous improvement initiatives
What We’re Looking For*Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or Quality Management
*Strong knowledge of GMP, GDP, ISO standards, and MHRA/FDA requirements
*Experience in pharmaceutical or regulated GMP environments
*Hands-on experience with QMS operations, document management, and audit preparation
*Familiarity with batch documentation (BPR/BAR review) and ERP systems such as SAGE
*Excellent attention to detail, organisation, and problem-solving skills
*Strong communication skills, both written and verbal
Personal Attributes*Accurate, efficient, and adaptable
*Strong team player with a collaborative mindset
*Professional, resilient, and committed to continuous improvement
*High ethical standards and integrity
This is a fantastic opportunity to step into a role where your expertise will directly shape compliance, quality culture, and operational success. If you’re ready to make an impact, apply today or reach out for a confidential chat.
Are you a quality-focused professional with an eye for detail and a drive for compliance? Smart4 Sciences is partnering with a leading pharmaceutical company in St Albans to recruit a QA Officer who will play a pivotal role in maintaining and strengthening their Quality Management System (QMS).
Working alongside the Quality Systems Manager, you’ll ensure the QMS is inspection-ready, compliant with MHRA, GMP, GDP, and ISO standards, and aligned with regulatory requirements. This is a hands-on role where you’ll oversee documentation, supplier quality, regulatory submissions, and continuous improvement initiatives, while supporting audits and driving operational excellence.
Key Responsibilities*Implement and maintain the QMS to meet MHRA, GMP, GDP, and ISO standards
*Conduct self-inspections, internal audits, and manage CAPAs
*Manage controlled documents including SOPs, batch records, and manufacturing logs
*Review and update specifications, methods, and product artwork
*Support regulatory submissions and assist during MHRA/FDA inspections
*Prepare Product Quality Reviews (PQRs) and risk assessments
*Manage deviations, change controls, and investigation reports
*Oversee supplier quality, vendor agreements, and handle supplier complaints
*Report monthly Quality KPIs and contribute to continuous improvement initiatives
What We’re Looking For*Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or Quality Management
*Strong knowledge of GMP, GDP, ISO standards, and MHRA/FDA requirements
*Experience in pharmaceutical or regulated GMP environments
*Hands-on experience with QMS operations, document management, and audit preparation
*Familiarity with batch documentation (BPR/BAR review) and ERP systems such as SAGE
*Excellent attention to detail, organisation, and problem-solving skills
*Strong communication skills, both written and verbal
Personal Attributes*Accurate, efficient, and adaptable
*Strong team player with a collaborative mindset
*Professional, resilient, and committed to continuous improvement
*High ethical standards and integrity
This is a fantastic opportunity to step into a role where your expertise will directly shape compliance, quality culture, and operational success. If you’re ready to make an impact, apply today or reach out for a confidential chat.
Job number 3656524
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